Device and method for slowing or stopping myopia progression

Abstract

A device and method for providing ocular photo-bio-stimulation to an eye of a user and protecting a macula of an eye of a user.

Description

DEVICE AND METHOD FOR SLOWING OR STOPPING MYOPIA PROGRESSION BACKGROUND OF THE INVENTION

[0001] Guide:

[0002] For the purpose of assisting in navigating this comprehensive patent application, thefollowing main sections with page numbers are provided. It is important to note that due to common, supportive, and overlapping teachings, while the patent application is divided into sections, certain teachings are taught in multiple sections.

[0003] Page 1: Background of the Invention

[0004] Page 13: Summary of Invention

[0005] Page 29: Brief Description of the Drawings

[0006] Page 38: Definitions

[0007] Page 55: Ocular Photo-Bio-Stimulation with Inventive Embodiments

[0008] Page 62: Ocular Photo-Bio-Stimulation Cell Phone Case

[0009] Page 70: Ocular Photo-Bio-Stimulation Electronic Display Screen with ControllableLighted Border

[0010] Page 75: Ocular Photo-Bio-Stimulation Electronic Display Screen with FixedLighted Border Edge

[0011] Page 80: Ocular Photo-Bio-Stimulation Steering Wheel, dashboard, or instrumentpanel of a Vehicle

[0012] Page 88: Ocular Photo-Bio-Stimulation Light, Lamp or Light Box

[0013] Page 91: Eyewear and Optics for Providing Ocular Photo-Bio-Stimulation

[0014] Page 135: Lenses or Optics Comprising a Defocus Zone for Ocular Photo-Bio-Stimulation Therapy

[0015] Page 146: Chromatic Aberration Focused Lens for Ocular Photo-Bio-Stimulation

[0016] Page 172: Sunglass Lens or Sunglass Optic or Filtered lens or Filtered optic thatProvides Ocular Photo-Bio-Stimulation

[0017] Page 208: XR Devices for Ocular Photo-Bio-Stimulation

[0018] Page 258: A System and App for a Computerized Device Comprising an OcularPhoto-Bio-Stimulation Light Source

[0019] Page 268: Fixation Target Macula Protection

[0020] Page 302: ClaimsField of the Invention

[0021] The current invention relates, in part, to ocular photo-bio-stimulation therapy, abiological technique to control or influence the activity of neurons or other cell types in, on or about the eye with light. As used herein ocular photo-bio-stimulation is an umbrella category of which photobiomodulation, optogenetics and phototherapy are forms thereof. The current invention relates, in part, to photobiomodulation therapy, which includes the utilization of non- ionizing electromagnetic energy to trigger photochemical changes within cellular structures. The current invention relates, in part, to optogenetics. Optogenetics is a biological technique to control the activity of neurons or other cell types with light. The current invention relates, in part, to phototherapy, also known as light therapy or bright light therapy, which is a treatment that uses controlled exposure to artificial or natural light to treat medical conditions.

[0022] A description of the anatomy of the eye will help understand the inventiondescribed herein.

[0023] The Eye’s Retinal Layer

[0024] In reference to FIG. 1, retinal cones are photoreceptor cells in the retina that givehumans color vision and help them see fine details. They are cone-shaped, with a pointed tip at the top and a circular bottom, and are concentrated in the center of the retina, in an area called the macula, the center of which is called the fovea. There are ~6M cones.

[0025] In further reference to FIG. 1, retinal Rods make up more than 95% ofthe photoreceptors. There are ~125M rods, and they pool signals to provide high sensitivity for dark-adapted vision, say starlight, which appears monochromatic. A lack of color vision is the hallmark of rod-mediated vision. Rods are absent within 350 μm of the fovea but reach a peak density in an annular region at about 20 degrees eccentricity.

[0026] In further reference to FIG. 7, rhodopsin is the opsin of the rod cells inthe retina and a light-sensitive receptor protein that triggers visual phototransduction in rods.

[0027] In further reference to FIG. 1, intrinsically photosensitive retinal ganglioncells (ipRGCs), also called photosensitive retinal ganglion cells that contain melanopsin (ipRGC) or called (mRGcs), are retinal ganglion cells (RGCs), which are neurons in the retina that transmit visual information from the eye to the brain. They are located near the inner surface (the ganglion cell layer) of the retina of the eye. It receives visual information from photoreceptors via twointermediate neuron types: bipolar cells and amacrine cells. Retinal ganglion cells collectively transmit image-forming and non-image forming visual information from the retina to several regions in the thalamus, hypothalamus, and mesencephalon, or midbrain. There are about 1.2 to 1.5 million retinal ganglion cells in the human retina. The melanopsin-containing retinal ganglion cells (mRGCs) represent only between 0.3% and 0.8% of the total ganglion cells of the retina.

[0028] In further reference to FIG. 7, melanopsin, a G family coupled receptor, is foundwithin the ganglion cell layer in the retina and plays an important role in non-image-forming visual functions, including hormone secretion, entrainment of circadian rhythms, cognitive and affective processes.

[0029] In further reference to FIG. 9, melatonin is a natural hormone that is mainlyproduced by your pineal gland in your brain. It plays a role in managing your sleep wake cycle and circadian rhythm.

[0030] In further reference to FIG. 1, Amacrine cells are nerve cells in the vertebrateretina that act as interneurons, or local circuit neurons, to connect two projection neurons. They are located in the inner nuclear layer of the retina and are the first neurons in the visual system to fire action potentials. Amacrine cells are named for their presumed lack of an axon. They come in many shapes and sizes and are synaptically active in the inner plexiform layer (IPL).

[0031] In further reference to FIG. 1, dopaminergic amacrine cells (DACs) serve as thesole source of retinal dopamine, and dopamine release in the retina follows a circadian rhythm and is modulated by light exposure. Dopaminergic amacrine cells (DACs) make up less than 1% of all amacrine cells in the retina. DACs are the main source of dopamine in the retina and are one of the rarest cell types in the retina, with a density of about 10–100 per mm. DACs are the first retinal neurons to be identified neurochemically. They have long primary dendrites, a sparse dendritic arbor, and an axon that usually emerges from the soma or primary dendrite. Their dendritic fields are irregular, often elongated or asymmetric.

[0032] In further reference to FIG. 1, the optic nerve head (optic disk) is composed ofneural, vascular, and connective tissues. The convergence of axons of retinal ganglion cells (RG) at the optic disc creates the neuroretinal rim that surrounds the cup, a central shallow depression in the optic disc.

[0033] In further reference to FIG. 2, the macula is a small, round area in the center of theretina, the light-sensitive layer of tissue at the back of the eye. It is about 5 millimeters across and aquarter of a millimeter thick, and is responsible for central vision, color vision, and fine detail. The macula is the part of the retina used when looking directly at objects, such as when reading or recognizing faces at a distance.

[0034] In further reference to FIG. 2, the fovea centralis, or fovea, is a small depressionwithin the neurosensory retina where visual acuity is the highest. The fovea itself is the central portion of the macula, which is responsible for central vision.

[0035] In reference to FIG. 1, retinal rods & cones are photoreceptors in the retina thatdetect light and convert it into signals that the brain can use for vision.

[0036] In reference to FIG. 4, it shows the eyes retina diameter and retinal zones of theretina relative to the center of the fovea: posterior zone (or central zone) (radius<10 mm), midperiphery zone (radius=10−15 mm), and far-periphery zone (radius>15 mm.

[0037] In reference to FIG. 5, it shows pupil size relative to ambient light, by way ofexample only, a pupil size can be 3.5 mm at 550 lux, 4.2 mm at 350 lux, 5.2 mm at 150 lux, 5.03 mm at 40 lux, and 5.4 mm at 2 lux.

[0038] In reference to FIG. 11, myopia (nearsightedness or shortsightedness), is a commoneye disease that causes light rays to bend and focus in front of the retina instead of on it. This makes distant objects appear blurry, while nearby objects appear normal. There is a silent epidemic of myopia in the world. It is forecasted that by 2050 approximately 50% of the world’s population will be myopic. The number of myopes forecasted is approximately 5 billion. Hyperopia (farsightedness) is a common vision condition in which you can see distant objects clearly, but objects nearby may be blurry. With hyperopia the eye focus of the light rays is behind the retina. Astigmatism is a common eye problem that occurs when the cornea or lens of the eye is an abnormal shape, causing light to bend differently as it enters the eye. This refractive error results in distorted or blurred vision at any distance and can make it difficult to see fine details. Presbyopia is a refractive error that causes the eye to lose its ability to focus on close objects as it ages. It is also known as age-related farsightedness. Presbyopia occurs when the eye’s lens loses its elasticity and can no longer focus light correctly on the retina. This makes it harder to read, thread a needle, or do other close-up tasks. Symptoms include blurry close-up vision, eyestrain, headaches, difficulty focusing on crafts and hobbies, and needing brighter lighting for clearer near vision. Dry macular degeneration (AMD) is a common eye disorder that affects the macula, the part of the retina that gives the eye clear vision. It is a chronic condition that usually develops in both eyesand is caused by a metabolic disorder, genetics, and environmental factors. As people age, the macula thins and the light-sensitive cells in it slowly break down, causing blurred or reduced central vision. AMD is referred to as age related macular degeneration and as such begins centrally within the macular area of the retina. Diabetic retinopathy (DR) is a chronic eye condition that occurs when high blood sugar from diabetes damages the retina’s blood vessels. The damaged blood vessels can swell, leak, or bleed, which can lead to blurry vision, dark areas, and difficulty seeing colors. This usually begins peripheral to the macular area of the retina. Retinitis pigmentosa (RP) is a rare genetic disorder that affects the retina, the light-sensitive part of the eye at the back. RP causes the retina’s photoreceptor cells to gradually break down over time, leading to vision loss. Symptoms often start in childhood or adolescence and include night blindness and peripheral vision loss. This may begin in the far and mid-periphery of the retina and progresses centrally from the peripheral retina.

[0039] In reference to FIG. 6, the visible light wavelength spectrum is the segment of theelectromagnetic spectrum that the human eye can view. More simply, this range of wavelengths is called visible light. Typically, the human eye can detect wavelengths from 380 to 700 nanometers.

[0040] In reference to FIG. 7, light sensitivity spectrum for melanopsin, rhodopsin isshown. Regarding the spectral sensitivity of human vision, the maximum spectral sensitivity ofthe human eye under daylight conditions is ~555 nm (yellow / green arrowhead), while at night the peak shifts to ~507 nm (green arrowhead), near the peak of rhodopsin (dashed blue-green line with a peak at 505 nm). Circadian photoreception mediated by melanopsin-expressing, intrinsically photosensitive ganglion cells integrate light information, but is most sensitive to a distinct blue portion of the spectrum (dashed blue line). The human retina also contains macular xanthophylls (X), yellow pigments found to be composed of two chromatographically separable components (i) lutein and (ii) zeaxanthin, whose absorption spectrum is a broad band (~100 nm width) with a spectral center between the short and medium-long wavelength photoreceptor pigments of the retina (peak ~460 nm). Rhodopsin, a visual pigment found in photoreceptor rods, has a peak sensitivity to blue-green light at around 500 nanometers (nm). This means that rhodopsin absorbs green-blue light most strongly, which gives it a reddish-purple appearance. The peak for melanopsin is ~ 480nm. In addition, between 25 and 33 % of all light entering the eye is absorbed by pigment granules in the RPE and the choroid. The naturally occurring pigment melanin, contained within pigment granules in the RPE and the choroid, and to a lesser extent hemoglobinin red blood cells, absorbs excess and scattered light to improve visual acuity. This serves to protect photoreceptors from photic injury and is thought to function as a quencher of free radicals and suppressor of photosensitized molecules.

[0041] In reference to FIG. 8, longitudinal chromatic aberration (LCA) is a lens’sinability to focus on different color wavelengths in the same focal plane. It occurs when different wavelengths of light disperse from a lens at different points along the optical axis, creating a circle of confusion. This results in unintentional color fringes, even in the center of an image, and colored areas where not all three colors are in focus. The eye’s natural longitudinal chromatic aberration (LCA) is an optical imperfection in the human eye that causes images projected onto the retina to blur. It occurs because the eye’s refractive index varies with wavelength, causing the eye’s focal power to change by almost 2 diopters (D) across the visible spectrum. This chromatic difference of focus causes short wavelengths to focus in front of long wavelengths, which is known as LCA. Optical lens material’s longitudinal chromatic aberration (LCA) decreases as Abbe number increases. Abbe number is a measure of how much light a lens disperses, and lenses with higher Abbe numbers disperse less light and produce less chromatic aberration. Chromatic aberration is inversely proportional to the Abbe number, meaning that as Abbe number decreases, chromatic aberration increases.

[0042] In reference to FIG. 9, Brain – melatonin, serotonin, dopamine, studies show thatdopamine production and release increases with light and decreases with darkness, while melatonin does the opposite. Seasonal Affective Disorder (SAD) is a type of depression that occurs in a seasonal pattern, often during the fall and winter months when there is less sunlight.

[0043] In reference to FIG. 10, serotonin and dopamine are neurotransmitters that act aschemical messengers between nerve cells in the brain and other parts of the body. They are often called “happy hormones” because they both play a role in positive mood and emotion. Brain Serotonin (5-HT) is a chemical messenger that the body produces naturally and acts as a neurotransmitter and hormone. It is involved in many physiological functions, including the central nervous system: mood, memory, anger, fear, appetite, stress, addiction, sexual pleasure, sleep, pain perception, and central respiratory drive and pupil dilation. Serotonin is a chemical messenger that affects wellbeing and happiness. Many antidepressants increase serotonin levels in the brain. Serotonin is found in the eye, where it acts as a neuromodulator in the retina and is present in human tears. Eye serotonin is found in the A17 cell, where it co-exists withGABA. Serotonin receptor signaling pathways are specific to the retina, and activating these receptors can help prevent photoreceptor degeneration. Serotonin is also involved in retinal physiology, physiopathology, and photoreceptor survival. Sunlight entering the eyes can stimulate the retina, which then signals the brain to produce serotonin. Brain dopamine is a chemical messenger in the brain that helps nerve cells communicate with each other. It is produced in the brain and acts on cells in other parts of the brain. Dopamine plays a role in many body functions, including motivation, pleasure, movement, memory, and mood. Dopamine is known as the feel-good hormone. Dopamine levels that are too high or too low can be associated with diseases like Parkinson’s disease, restless legs syndrome, and attention deficit hyperactivity disorder (ADHD). Low dopamine levels can also lead to symptoms like anxiety, sadness, difficulty sleeping, and low sex drive. Eye dopamine (DA) is a neurotransmitter in the retina that plays a role in visual signaling, development, and refractive development. It is found in the retinas of all vertebrates, including humans, and is released from dopaminergic amacrine cells in the retina’s inner plexiform layer. DA levels are dependent on light and retinal image contrast. Attention- deficit / hyperactivity disorder (ADHD) is one of the most common and most studied neurodevelopmental disorders in children. “Neuro” means nerves in cases. Scientists have discovered there are differences in the brain, nerve networks and neurotransmitters of people with ADHD. ADHD is a long-term (chronic) brain condition that causes executive dysfunction, which means it disrupts a person’s ability to manage their own emotions, thoughts and actions. ADHD makes it difficult for people to: manage their behavior, pay attention, control overactivity, regulate their mood, stay organized, concentrate, and / or follow directions and sit still. Kids usually receive a diagnosis during childhood and the condition often lasts into adulthood. However, effective treatment is available. Left untreated, ADHD can cause serious, lifelong complications. According to the Centers for Disease Control and Prevention, almost 11% of U.S. children between the ages of 2 and 17 have received an ADHD diagnosis representing an estimated 6 million children ages 3 to 17 years. Worldwide, 7.2% of children have received an ADHD diagnosis. It is estimated that adult ADHD affects more than 8 million adults (or up to 5% of Americans). Many medical conditions are linked to low levels of dopamine including attention deficit hyperactivity disorder (ADHD), Parkinson’s disease, Alzheimer’s, restless legs syndrome,depression, schizophrenia, brain fog, mood swings, chronic fatigue and muscle spasms. Low levelsof serotonin may be associated with many health conditions including depression and other moodproblems such as anxiety, sleep problems, digestive problems, suicidal behavior, obsessive- compulsive disorder, post-traumatic stress disorder and panic disorders.

[0044] Exposure to blue light wavelengths stimulates the body's production ofserotonin and dopamine, both in the eye and possibly the brain. Also, very bright intense red light has been found to stimulate serotonin and dopamine. Serotonin is an inhibitory neurotransmitter that affects mood, appetite, sleep, temperature regulation, and some social behavior. 95% of the body’s serotonin is generated in the intestine. Dopamine is an excitatory neurotransmitter that regulates motivation. A low dopamine level can contribute to ADHD, as well as memory loss, low sex drive, poor digestion, muscle spasms, restless legs syndrome, Parkinson’s Disease, poor cognition, as well as an increase in myopia. Dopamine is produced in serval areas of the brain. Some dopamine is generated in the retina of the eye by the rods and / or ganglion cells more so than the cones.

[0045] Norepinephrine, also called noradrenaline, is both a neurotransmitter and ahormone. As a neurotransmitter, it's a chemical messenger that helps transmit nerve signals across nerve endings to another nerve cell, muscle cell or gland cell. It regulates arousal and attention. Norepinephrine helps regulate arousal, attention, cognitive function, and stress reaction. Dopamine is converted into norepinephrine in the body.

[0046] Research findings suggest that green light wavelengths can alleviate or reduce painby stimulating cone cells, which then initiate a signaling pathway that results in the activation of opioid receptors in the DRN. It is believed that green lighting can stimulate the release of endogenous endorphins and stimulate the cannabinoid system which results in improved moods and higher pain tolerance. By way of example, it is thought that green light can reduce the pain associated with migraines and other types of pain.

[0047] The “ISO sunglass traffic light test” refers to a standardized procedure outlined inthe ISO 12312-1, which measures how well a pair of sunglasses allows a wearer to distinguish between traffic light colors, ensuring they meet safety requirements for driving by not significantly altering the visibility of red, yellow, and green lights: essentially testing the sunglasses’ ability to accurately transmit the necessary wavelengths of light for traffic signal perception. Key points about the ISO sunglass traffic light test include: The test is based on the ISO 12312-1 standard, which covers requirements for general use sunglasses, including those worn while driving. The test assesses the “luminous transmittance” of the sunglasses at specific wavelengthscorresponding to red, yellow, and green light, ensuring a sufficient level of light passes through the lenses to accurately perceive traffic signals. The ANSI sunglass traffic light test is of a similar type test. It is critical for a sunglass lens / optic / eyewear to pass such testing to show that, when worn by a wearer / user, they are safe to drive when wearing and driving. Thus, the appropriate color balance of light being transmitted to the eye through the sunglass lens is critical for safe driving. Description of Related Art

[0048] While ocular photo-bio-stimulations have been tested before, a need forimprovement exists within the art. For example, U.S. Patent No.10,444,505 B2 teaches a head mounted display comprising a light emitting source and an optical waveguide adapted to collect light emitting from the light emitting source and to guide the collected light to the eye. U.S. Patent No.10,444,505 B2 further teaches the use of blue green wavelengths of light within the range of 460nm and 520nm directly targeting intrinsically photosensitive retinal ganglion cells (ipRGC), more specifically the melanopsin ganglion cells, and indirectly targeting rods. However, U.S. Patent No.10,444,505 B2 does not teach a means for maximizing the number or ganglion cells and rods stimulated. The larger number of melanopsin ganglion cells and rods that are stimulated the greater the physiological response. This prior art is silent as to how to stimulate certain areas of the mid peripheral and far peripheral retina that are not normally stimulated when light is shined into an eye. The teachings included herein will show that an estimated 20% - 30% of each eye’s retina is not normally stimulated when looking straight ahead. U.S. Patent No.5,923,398 teaches off axis photon stimulation of a person’s eye, provided by a light field which provides biological or psychological benefits. This art teaches embedded or fixed light delivery elements such as fiber optic members that deliver off axis stimulation to peripheral areas of the retina. The cosmetics of the device leave much to be desired. Furthermore, anyone looking at an individual wearing such a device would look bizarre as the wearer’s eye lids, and eyes, would appear lighted. Both U.S. Patents 10, 444,505 B2 and 5,923,398 teach the use of eye tracking for the purpose of identifying the location of the pupil of the eye. Thus, there is a need for a simplified and more cosmetically desirable way to provide photo-bio-stimulation to the eye or eyes of a user. The inventive embodiments taught herein solve that need. The invention disclosed herein teaches various embodiments of electronic displays, optics, lenses, extended reality and modified extended reality that are not taught by any known art.

[0049] U.S. Patent No. 3,826,751 teaches a selective optical filter having a transmittance ofwavelengths in the wavelength range between 625nm and 875nm, which is manageable from zero up to any desired value, while reducing the near infrared transmittance. Materials are shown that can be used for sunglasses. Subsequent, external dying (with methods known in the art) can be used to lower the transmission of the shorter wavelength portion of the visible spectrum. Various light curves showing different light wavelength spectrums are shown. U.S. Patent No.3,826,751 is silent regarding amount of light intensity (lux) (or lumens) being transmitted from the sunglass lens to stimulate dopamine in the eye of the wearer, and silent as to the light intensity (lux) that strikes the retina of the eye of the wearer. The patent is silent as to time of day when worn, silent regarding color balance transmission, and silent regarding the proper color balance of light wavelengths transmitted to the eye needed to pass the ANSI or ISO traffic light / signal test. The current invention is an improvement over that technology.

[0050] U.S. patent no. 5,083,858 teaches the design of a tinted lens that filters andtransmits light that approximates the absorption curve for rhodopsin. However, 5,083,858 does not teach a tinted lens that transmits filtered light that approximates the absorption curve for melanopsin. Further, US 5,083,858 does not teach a filtered lens capable of reducing the overall visible light transmission below 40% or 30% while approximating the absorption curve of rhodopsin, among other differences. U.S. patent No.5,083,858 is silent regarding amount of light intensity (lux) (or lumens) being transmitted from the sunglass lens to stimulate dopamine in the eye of the wearer, and silent as to the light intensity (lux) that strikes the retina of the eye of the wearer. The patent is silent as to time of day when worn, silent regarding color balance transmission, and silent regarding the proper color balance of light wavelengths transmitted to the eye needed to pass the ANSI or ISO traffic light / signal test. The current invention is an improvement over that technology.

[0051] U.S. patent no. 11,086,145 B2 teaches additional examples of tinted filtered lensesthat have a light transmission peak of 465nm or 495nn and also have a light transmission range within the wavelength range of 400nm – 490nm of 70% and outside of 400nm – 490nm being less than 70%. Once again, U.S. patent no.11,086,145 B2 does not teach filtered tinted lenses having the overall visible light transmission being less than 40% or 30%, among other differences. The current invention is an improvement over that technology. U.S. patent No.11,086,145 B2 teaches light intensity (lux) leaving the sunglass lens of at least 200 lux (but not the lumens) and limits thelight intensity lux to no more than 300 lux. It is also silent as to the light intensity (lux) that strikes the retina of the eye of the wearer. The patent is silent as to time of day when worn, silent regarding color balance transmission, and silent regarding the proper color balance of light wavelengths transmitted to the eye needed to pass the ANSI or ISO traffic light / signal test. The current invention is an improvement over that technology.

[0052] EP 3,528,036 A1 teaches tinted filtered lenses that have an absorption spectrum thatapproximates the absorption curve of melanopsin, while also showing other tinted lenses that predate EP 3,528,036. However, the overall visible light transmission is not less 40% or less, or 30% or less, among other differences with the current invention. EP 3,528,036 is silent regarding amount of light intensity (lux) (or lumens) transmitted from the sunglass lens to stimulate dopamine in the eye of the wearer, and silent as to the light intensity (lux) that strikes the retina of the eye of the wearer. The patent is silent as to time of day when worn, silent regarding color balance transmission, and silent regarding the proper color balance of light wavelengths transmitted to the eye needed to pass the ANSI or ISO traffic light / signal test. The current invention is an improvement over that technology. The current invention is an improvement over that technology.

[0053] U.S. Publication No. 2024 / 0036357 A1 teaches a photochromatic lens that in anactivated state is that of a photochromic sunglass having overall visible light transmission between 40% and 55%, with the light transmission within the range of 450nm and 510nm being less than 50%. Figure 3 of U.S.2024 / 0036357 lays out the light transmission by nanometer and when calculated teaches an overall visible transmission of 42.13%. Figures 3 and 4 show that the overall visible light transmission would be greater and not less than 42.13%. Figures 1, 2 and 3 of 2024 / 0036357 A1 show that the light transmission within the range of 450nm and 510nm is always less than 50%. U.S. Publication No.2024 / 0036357 is silent regarding amount of light intensity (lux) (or lumens) being transmitted from the sunglass lens so to stimulate dopamine in the eye of the wearer, and silent as to the light intensity (lux) that strikes the retina of the eye of the wearer. The patent application is silent as to time of day when worn, silent regarding color balance transmission, and silent regarding the proper color balance of light wavelengths transmitted to the eye needed to pass the ANSI or ISO traffic light / signal test. The current invention is an improvement over that technology.

[0054] U.S. Patent No. 11,065,468 teaches a wide range of wavelengths falling within therange of 450nm- 530nm, 460nm – 560nm, and preferably 480nm – 520nm. U.S. Patent No. 11,065,468 teaches a light transmission within the range of 480nm – 510nm of 50% or more. Further, this art teaches overall visual transmission of 18% - 43%, 8% - 17%, and 3% - 8%. U.S. Patent No.11,065,468 is silent regarding amount of light intensity (lux) (or lumens) being transmitted from the sunglass lens, and silent as to the light intensity (lux) that strikes the retina of the eye of the wearer. The patent is silent as to time of day when worn, silent regarding color balance transmission, and silent regarding the proper color balance of light wavelengths transmitted to the eye needed to pass the ANSI or ISO traffic light / signal test. The current invention is an improvement over that technology.

[0055] U.S. Publication No. 2022 / 0397774 A1 teaches a transmitted 30 nanometer, limited,light wavelength range of 465nm – 495nm, which is less than 50% of the absorption curve of melanopsins or rhodopsin. U.S. Publication No.2022 / 0397774 A1 does, within the limited / narrow 30 nanometer light wavelength range, show the ability for the tinted filtered lens to transmit over 32% of light within 465nm and 495nm, and also for the tinted filtered lens to have an overall visible transmission of 18% or less. However, the light transmission performance of the tinted lens of U.S. Publication No.2022 / 0397774 A1, within the wavelength range of 465nm and 495nm and the overall visible transmission percentage of the tinted lens, is due to utilizing such a narrow 30 nanometer wavelength range within 465nm and 495nm. The limited 30 nanometer wavelength range, while advantageous for achieving less than an 18% overall visible light transmission of the tinted lens, significantly limits the ability of the tinted lens to transmit sunlight blue light intensity (lux) from sunrise to sunset, as well as the amount of blue light intensity (lux) that is transmitted through the tinted lens. This is due to the fact that as the sun moves in the sky throughout the day, the percentage of blue light wavelengths in sunlight reduces from morning until night. Thus, if the lens only transmits blue light within a limited wavelength range of 465nm – 495nm, as opposed to a broader wavelength range of 450nm to 510nm, the amount of blue light intensity (lux) will be significantly reduced as sunlight moves from sunrise, to morning, to midday, to afternoon, to sunset (see Figures 70 - 73). U.S. Publication No.2022 / 0397774 A1 is silent regarding amount of light intensity (lux) (or lumens) being transmitted from the sunglass lens to stimulate dopamine in the eye of the wearer, and silent as to the light intensity (lux) that strikes the retina of the eye of the wearer. The patent application is silent as to time of day when worn, silentregarding color balance transmission, and silent regarding the proper color balance of light wavelengths transmitted to the eye needed to pass the ANSI or ISO traffic light / signal test. The current invention is an improvement over that technology. SUMMARY OF THE INVENTION

[0056] Embodiments disclosed herein can provide ocular photo-bio-stimulation throughlight stimulation of specific wavelengths to the eye’s retina, and, in some embodiments, to the entire eye’s retina, the retina peripheral to the fovea, and / or the retina peripheral to the macula. In certain embodiments, the light stimulation is targeted at or to the rods. In other embodiments, the light stimulation is targeted at or to the ganglion cells. In still other embodiments, it is targeted at or to the rods and the ganglion cells. When ganglion cells are mentioned herein, the ganglion cells targeted or stimulated are the melanopsin containing ganglion cells (ipRGCs) or can also be called mRGCs.

[0057] According to embodiments of the current invention described herein, for thepurpose of stimulating dopamine production in the eye and / or brain of the user / wearer, and for the amount of dopamine produced and for longevity of dopamine to remain active, the brighter the light intensity (lux) delivered to the eye’s retina through a tinted filtered lens throughout the day, the better the dopamine outcome for the user / wearer. Various embodiments of a sunglass lens taught herein take in to account: time of day, the amount of sunlight lux striking the sunglass lens, the amount of light intensity (lux) leaving the sunglass lens transmitted within a specified range of light wavelengths needed to stimulate dopamine in an eye of the user / wearer, the overall visible light transmission of the sunglass lens, the percentage of light transmission within a defined range of light wavelengths that cover the majority of the absorption curves of melanopsin and rhodopsin as well as certain of the cone opsins, the width of a range of wavelengths of light within the range of 450nm – 520nm, the color balance of light wavelengths needed to be transferred from the sunglass lens to the eye of the wearer, and the ability of the sunglass lens to pass the ISO and / or ANSI traffic light test. As can be understood, embodiments taught herein must balance numerous components that contribute to the ability of the sunglass lens to cause the production of dopamine or increase the production of dopamine in the eye’s retina of the wearer of the sunglass lens, while also providing the appropriate level of clear distance and / or (near) vision clarity for the wearer of the sunglass lens, and further provides the appropriate color balance of light wavelengths transmitted from the sunglass lens to the eye of the wearer of the sunglass lens, so that either thewearer of the sunglass lens subjective measurements or the sunglass lens by way of objective measurements can pass the ISO and / or ANSI traffic light test.

[0058] Embodiments herein teach the stimulation of the rods and / or ipRGCs with specificlight wavelengths. The retina of the human eye contains 100+M rods, 1M ganglion cells but fewer than 7,000 ipRGCs which are the ganglion cells that contain melanopsin. ipRGCs are less sensitive to photic stimulation and their response kinetics are slow compared to that of rods and cones. Response latency is inversely related to stimulus intensity and under dim light conditions ipRGCs can take many seconds to reach a peak response; the response may also persist for minutes after stimulus termination. However, ipRGCs are similar to rods and cones in that they show adaptation by adjusting their sensitivity according to lighting conditions. While slow to respond to dim light conditions, ipRGCs appear capable of responding to the capture of a single photon of light. It has been estimated that the membrane density of melanopsin is about a thousand times lower than that of photopigments in the outer segments of rod and cone photoreceptors; this relatively low density may account for the poor absorption rate of ipRGCs. The capture of a single photon in an ipRGC generates a large and prolonged membrane current, greater than that recorded in rod photoreceptors but also 20-fold slower.

[0059] In aspects, embodiments disclosed herein teach stimulating both the rods andipRGC. Several embodiments teach exciting both rods and ipRGC with ocular photo-bio- stimulation light. The rods become excited first and then the ipRGC, in cases. The rods outnumber the ipRGC and thus provide a significant amount of initial stimulation and response, however the stimulation effect of the ipRGC outlives that of the rods and thus the long term stimulation effect can be due to that of the ipRGC being stimulated.

[0060] Melanopsin photopigment expressed in intrinsically photosensitive retinal ganglioncells (ipRGCs) plays a crucial role in the adaptation of mammals to their ambient light environment through non-image-forming (NIF) visual responses. ipRGCs are structurally and functionally distinct from classical rod / cone photoreceptors and have unique properties including single-photon response, long response latency, photon integration over time, and slow deactivation.

[0061] The efficiency of melanopsin is comparable to that of rod and cone. ipRGCs,however, lack specialized photopigment-concentrating organelles (such a rod / cone outer segments) to maximize the probability of photon capture. As a result, the probability of absorbing a photo by ipRGCs is greater than 1 million times lower than in rods or cones for a given area of photostimulation. Consequently, even though the ipRGC phototransduction cascade has high amplification, melanopsin photoreception is much less sensitive than that of rods and cones. Once the threshold for melanopsin activation has been reached, however, the intrinsic light response scales with stimulus intensity over several decimal orders and is remarkably persistent, being sustained over long durations of constant illumination.

[0062] Many of the embodiments herein teach a wide wavelength range within that of450nm – 520nm for ocular photo-bio-stimulation. The wider range can provide light wavelengths needed to activate different photoreceptors in the retina, e.g., most of the ipRGCs and rods, in addition to partially excite the S- and M- cones, all implicated to have different and important functions due to the visual and non-visual effects of the light striking them.

[0063] As the time of the ocular photo-bio-stimulation lasts, the retina becomes lesssensitive and the excitation of the retina moves from a first highest sensitivity at 510nm to a lower sensitivity at 480nm, in aspects. By way of example only; 1 second of exposure at 510, then 10 seconds of exposure at 500nm and then 100 seconds of exposure at 460nm. Thus, the longer the exposure from the ocular photo-bio-stimulation light source, the light wavelengths that provide maximum stimulation of the retina change over time.

[0064] The wide range of light wavelengths that overlap melanopsin and rhodopsinabsorption curves allow for more light of different spectral quality to the eye and these different (more) wavelengths cause the eye to enable different physiological functions, all contributing towards better eye health, brain / cognitive health, or overall health, by way of example.

[0065] Cyan light (blue green) wavelengths (~495nm – 520nm) have been found tocontribute more towards increasing choroidal thickness which is an important parameter in treating / stopping myopia.

[0066] Blue light wavelengths (~450nm - 495 nm or ~450nm- 500nm) are helpful for theeye, by way of reducing the eye’s axial length, another important factor when treating myopia and stopping its progression. Also, blue light increases one’s alertness, improves cognitive function and other beneficial neurological functions. This occurs due to the stimulation of or one or more of dopamine, serotonin or norepinephrine in the brain.

[0067] Blue light (~465nm-495 nm) has been found to be good for non-visual pupillaryreflex, i.e., keeping the pupil constricted or small, thus, to maximize clear vision, while looking through a tinted sunglass lens.

[0068] Moreover, more blue light is needed to maintain a healthy circadian rhythm in thelens’ wearer.

[0069] Embodiments disclosed herein that are directed to increasing dopamine in anindividual’s eye’s retina or one or more of dopamine, serotonin or norepinephrine in the brain of the individual whose eye was stimulated attempt to use wavelength ranges that cover the peak sensitivities for melanopsin (480nm) and also for rhodopsin (500nm). Given that rhodopsin of Rods is 20 times faster to react than melanopsin of ipRGCs, but that melanopsin has much longer reactive staying power than the reaction of rhodopsin, combined with the fact that rods are 10+ times the number of ipRGCs, is the reason various embodiments disclosed herein use light wavelengths within the light wavelength ranges of at least one of 480nm + / - 30nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, 500nm + / - 30nm, or 650nm + / - 30nm or 700nm + / - 30nm. The lower level of 480nm + / - 30nm is to capture direct stimulation of melanopsin by ipRGCs and indirect stimulation of melanopsin by rods.

[0070] In certain embodiments when generating dopamine in the eye (or one or more ofdopamine, serotonin or norepinephrine in the brain) via the eye light, the invention utilizes light wavelengths that strike the eye’s retina which fall within the wavelength range of the following at least one of: 480nm + / - 30nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, 500nm + / - 30nm, 650nm + / - 30nm, or 700nm + / - 30nm, which would include blue, bluish green and green wavelengths. These light wavelength ranges can be generated by light emitters, filtered optics or filtered lenses.

[0071] FIG. 77 presents the light transmission spectrum of the inventive embodimentfiltered lens or filtered optic, or sunglass lens or sunglass optic, overlapped with the light absorption spectra of two photoreceptors: ipRGCs (containing melanopsin) and rods (containing rhodopsin) photoreceptors. The light passing through the inventive embodiment lens, in particular, the light between the light wavelength range of 450nm and 510nm, transmitted towards the eye of the wearer will stimulate / activate the melanopsin and / or the rhodopsin in the ipRGC and rods photoreceptors, respectively.

[0072] The brighter the ocular photo-bio-stimulation light, the higher intensity this light is,and, in aspects, the best case for generating dopamine. It has been found that a minimum light intensity of 400 lux striking eye’s retina, within the wavelength range of 450nm – 520nm, is required to effectively generate dopamine in the eye’s retina and / or one or more of dopamine, serotonin or norepinephrine in the brain. When taking into consideration that the eye’s tissues (depending upon age) absorb or attenuate up to 60% of blue light (e.g., 25% for a 9 year old, 50% for a 25 year old, 60% for a 60 year old), and further that eyewear and sunglasses sit approximately 13mm from the cornea of the eye, in many, but not all, embodiments taught herein, it is believed the various inventive embodiments disclosed herein will allow one or more of 400 lux or more, 450 lux or more, or 500 lux or more, light to be transmitted from the lens or eyewear (within the wavelength range of 450nm to 510nm) for what is needed to stimulate dopamine production in the eye of the wearer / user of lens / eyewear designed to stimulate dopamine production in the eye and / or the brain. The amount of the ocular photo-bio-stimulation light intensity of lux required at the ocular photo-bio-stimulation light source needed to achieve the desired physiological response of the patient or subject can be one or more of: 250 lux or more, 500 lux or more, 1,000 lux or more, 2,000 lux or more, and so on. The ocular photo-bio- stimulation light intensity can be expressed in lumens given off by the ocular photo-bio- stimulation light source. When considering the light radiating in a cone light manner from the ocular photo-bio-stimulation light source to strike the eye and face of the user or subject, the number of lumens given off from the ocular photo-bio-stimulation light source can be one of 10 lumens or more, 25 lumens or more, 50 lumens or more, 100 lumens or more, 200 lumens or more, and so on. The exact amount of lux or lumens needed to be radiated from the ocular photo-bio- stimulation light source can depend upon various attenuation factors, each causing attenuation of the light intensity as it travels from the ocular photo-bio-stimulation light source to strike the retina of the eye of the patient or subject. In embodiments disclosed herein the desired physiological response of the patient or subject is the increased production or the production of dopamine in the patient or subject’s eye’s retina. To achieve the production of dopamine in most, but not all, embodiments, the desire is to have enough light intensity given off from the ocular photo-bio- stimulation light source so that when taking all attenuation into account a minimum of 350 lux or more, or 400 lux or more, by way of example, strikes the retina of the patient or subject’s eye. In certain other embodiments the desired physiological response of the patient or subject is one ormore of, the production of either dopamine, serotonin or another hormone in the brain that acts like dopamine or serotonin. To achieve the production of or one or more of dopamine, serotonin or norepinephrine in the brain that acts in a similar way, in most, but not all, embodiments, the desire is to have enough light intensity given off from the ocular photo-bio-stimulation light source so that when taking all attenuation into account a minimum of one or more of: 350 lux or more, or 400 lux or more, or 500 lux or more, strikes the retina of the patient or subject’s eye.

[0073] It has been reported that higher intensity of light (brighter light) is needed to affectthe generation of retinal dopamine and improve the brain function with regards to cognitive functions, alertness, mood, and reduce sleepiness. It has been reported that under photopic conditions more retinal dopamine is generated. ipRGCs and rods have been implicated as being responsible for the retinal dopamine generation. It is noteworthy that rod photoreceptors have recently been found to be active under sustained bright light conditions, which is contrary to the conventional thinking that rods respond only under scotopic conditions.

[0074] Inventive embodiments taught herein teach a filtered lens or filter optic, or sunglasslens or sunglass optic, comprising a light transmission curve that approximates (by way of coverage) most of, or a vast majority of, or all of, the light absorption curve of melanopsin and also, in aspects, approximating over 75% or more of the light absorption curve of rhodopsin. In certain embodiments the light transmission curve of the filtered lens or filtered optic, or the sunglass lens or sunglass optic, can approximate (by way of covering) all of the light absorption curves of melanopsin and rhodopsin. As used herein the word coverage means having one light transmission curve overlayed over a light absorption curve and seeing or measuring the extent of how the light transmission curve covers the light absorption curve, or that of the absorption spectra within the absorption curve spectra. And in certain cases, it can also be the reverse of having the light absorption curve overlayed over that of the light transmission curve.

[0075] In embodiments of the filtered lens or filtered optic, or sunglass lens or sunglassoptic, they can comprise light transmission within the wavelength range of 450nm – 510nm of 50% or greater, while maintaining an overall visible light transmission through the filtered lens or filtered optic, or sunglass lens or sunglass optic, of 40% or less or 30% or less. This balance of having a high transmission within the wide wavelength range of 450nm – 510nm or even 450nm – 520nm, while providing overall visible light transmission so to qualify as a class 2 or class 3 sunglass lens or sunglass optic, and at the same time providing UV and HEV protection, is one ofthe strong inventive attributes of the embodiments described herein. This is needed in order to provide light intensity of 400 lux or greater of the blue light wavelengths to stimulate the production of dopamine in the eye and / or brain of the wearer while wearing category 2 and category 3 sunglasses throughout most, if not all, daylight hours in the sun.

[0076] The narrow wavelength range of only 30 nanometers, as seen in some existingsunglass eyewear, significantly reduces the amount of blue light that is transmitted to the eye of the wearer for producing dopamine, as the sunlight color changes from majority blue in the morning to majority red in the late afternoon. The inventive embodiments described herein can have greater than 30 nanometers of wavelength range within the wavelength range of 450nm – 510nm or 450nm – 520nm (thus up to 60 nanometers to 70 nanometers), which can provide far more blue light lux throughout the day in sunlight for the production of dopamine while at the same time allowing for a darkened sunglass having an overall visible light transmission of 30% or less. Thus, in embodiments, the current invention can qualify as either a category 2, or category 3, sunglass lens.

[0077] As the day proceeds from dawn to noon to dusk, the predominant sunlight colorsmove from the majority of blue in the morning to the majority of red in the afternoon. (See, FIGs. 70-73.) In the morning, blue light represents approximately 30% or more of the visible spectrum. In midday, blue light represents approximately 20% of the visible spectrum. In the afternoon, blue light represents approximately 10% of the visible spectrum, and at sunset blue light represents approximately 5% or less. Thus, as the day proceeds from morning to noon to afternoon to sunset, it becomes more difficult for a filtered lens or filtered optic or a sunglass lens or sunglass optic to transmit blue light within the wavelength range of 450nm – 510nm to stimulate dopamine in the eye and / or one or more of dopamine, serotonin or norepinephrine in the brain (see FIG.74). This occurs because as the day progresses the blue component of sunlight decreases. The narrower the wavelength range of the tinted lens or optic that transmits the blue light, such as that of 30 nanometers within 465nm – 495nm (see, e.g., U.S. US2022 / 0397774 A1), the less light intensity (lux) of the required blue light wavelengths is transmitted and available to stimulate dopamine throughout the day, compared to anything greater than 30nm, such as 60 or 70 nanometers taught with the inventive embodiments described herein. As discussed, this is due to the level of blue light in sunlight that changes from a high in the morning to a low at sunset.

[0078] Conventional sunglasses transmit low amounts of blue light and thus as the dayprogresses most conventional sunglasses actually in the afternoon inhibit the production of dopamine in the eye and / or one or more of dopamine, serotonin or norepinephrine in the brain, while in all cases all known conventional sunglasses dramatically reduce the light intensity lux needed for the production of dopamine in the eye and / or one or more of dopamine, serotonin or norepinephrine in the brain of the user / wearer as the day proceeds from morning to sunset, with afternoon and sunset being the worst. Certain conventional sunglasses actually inhibit the production of dopamine in the eye and / or one or more of dopamine, serotonin or norepinephrine in the brain from the time they are worn by a wearer. In most cases, the vast majority of the time conventional sunglasses are worn, they reduce the amount or production of dopamine in the eye and / or the brain.

[0079] The most popular sunglass categories are those of class 2 and class 3. Certain of theembodiments disclosed herein qualify as being class 2 or class 3 sunglasses (see, FIG.76). However, unlike conventional sunglasses (which cannot perform in the manner according to the current invention), certain of the inventive filtered lens or filtered optic embodiments, or sunglass lens or sunglass optic embodiments, taught herein can transmit 400 lux or more within the wavelength range of 450nm – 510nm from morning until midafternoon, or even in certain embodiments taught herein, from sunrise to sunset (see, e.g., FIG.74).

[0080] Thus, there is a pressing need for a filtered lens or filtered optic or sunglass lens orsunglass optic that transmits a meaningful / safe / effective amount of blue light within a range that stimulates and / or excites melanopsin and / or rhodopsin, while at the same time protecting the eye from sunlight. This will allow the eye to produce dopamine and possibly cause the production of dopamine and serotonin in the brain throughout the day, while at the same time protecting the eye from the sun.

[0081] A filtered lens or filtered optic, or sunglass lens or sunglass embodiment, taughtherein, can transmit light within the wavelength range of 450nm to 510nm, thus stimulating melanopsin and / or rhodopsin the eye’s retina. In embodiments, the lens or optic transmits blue light such that it covers the full light absorption curve of melanopsin, or the vast majority of the light absorption curve of melanopsins, and 75% or more of the light absorption curve for rhodopsin. These embodiments have benefits in stimulating the production of dopamine in the eye and / or the brain of the user / wearer over conventional sunglasses.

[0082] By way of example only, if the sunlight intensity is, by way of example only,20,000 lux during midday, the embodiment of a filtered lens or filtered optic, or sunglass lens or sunglass optic, taught herein can, by way of example only, have a light transmission of 50.5% within the range of 450nm – 510nm and would transmit 20% of the visible spectrum due to midday sunlight. Therefore, if the filtered lens or filtered optic embodiment has an overall visible transmission of 50.5% and transmits 20% of the light intensity from the sun due to it being midday, the transmitted light intensity would be 20,000 lux X 50.5% X 20% for a total of 2,020 Lux. In certain other embodiments of the invention, a light transmission range can be within 450nm – 520nm, and in still other embodiments of the invention the light transmission range can be within 440nm – 510nm, or 440nm – 520nm. By increasing the wavelength range it is possible to cover the changing color of sunlight as the day progresses from sunrise to sunset, thus optimizing the transmission of blue wavelengths of light that can stimulate / excite melanopsin and rhodopsin.

[0083] Embodiments allowing filtered transmitted blue light wavelength ranges beingeither between 450nm - 510nm or 440nm - 510nm or 440nm - 520nm, have to do with limiting the amount of HEV (High Energy Violet) light on one end of the range and the level of green light wavelengths on the other end of the wavelength range. In still another embodiment, the filtered lens or filtered optic, or sunglass lens or sunglass optic, comprises a transmission curve or spectra that includes the absorption peaks of melanopsin of approximately at around 480nm and rhodopsin at approximately around 500nm, while also protecting the eye of the wearer from UV wavelengths at 400nm or below and reducing HEV light wavelengths from 400nm to 440nm to being at a transmission peak height of 40% or less or 30% or less.

[0084] In another embodiment, the sun light intensity, by way of example only, is 20,000lux during midday (blue light being 20% of sunlight during midday) and the filtered lens or filtered optic or sunglass lens or sunglass embodiment, by way of example only, has a light transmission of 50.5% but within a much more limited wavelength range of 465nm to 495nm (which does not cover the full absorption spectrum of melanopsin and rhodopsin), but rather half (or less than half) of the absorption spectrum, wherein the transmitted light intensity would be 20,000 lux X 50.5% X 20% still obtaining a total of 2,020 lux “midday.” However, as the day proceeds to “midafternoon,” and the blue color of the sunlight reduces and becomes more red, embodiments having the limited light transmission spectrum from 465nm to 495 nm will provide less blue light intensity needed to produce or stimulate dopamine in the eye and / or the brain of the user / wearerwhen compared to embodiments having a light transmission wavelength range from 450nm – 510nm, that cover the vast majority of the absorption spectrum of melanopsin and 75% or more of rhodopsin. To further emphasize this point, later in the “late afternoon” as the blue light of sunlight decreases even further, this difference in the amount of light intensity lux providing dopamine production or stimulation between an embodiment having light transmission within the range of 465nm to 495nm compared to an embodiment having light transmission within the rage of 450nm – 510nm, will become even more pronounced in favor of the embodiment having light transmission within the range of 450nm – 510nm, in aspects. By way of example, it is estimated that in the morning approximately 30% of blue light from the sun is located within 450nm – 510nm, by noon approximately 20% of blue light from the sun is within 450nm – 510nm, by midafternoon approximately 10% is within 450nm -510nm, and by sunset less than approximately 5% within 450nm – 510nm.

[0085] As used herein, in embodiments when light wavelengths are generated by way offiltered optics or filtered lenses, the peak spectral curve of the wavelength range that strike the eye’s retina fall within the wavelength range of at least one of: 480nm + / - 30nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, 500nm + / - 30nm, 650nm + / - 30nm, or 700nm + / - 30nm.

[0086] In certain embodiments disclosed herein, when a filtered optic or filtered lens isused, the overall light transmission through the filtered optic or filtered lens can be 50% or less, while the light transmission within the predominant transmitted filtered wavelength range being transmitted to the eye can be 50% or more. In certain cases, the pupil of the eye enlarges when looking through the filtered optic or filtered lens and constricts when looking absent of the filtered optic or filtered lens.

[0087] In certain embodiments disclosed herein, when a filtered optic or filtered lens isused, the overall light transmission through the filtered optic or filtered lens can be 40% or less, while the light transmission within the predominant transmitted filtered wavelength range being transmitted to the eye can be 40% or more. In certain cases, the pupil of the eye enlarges when looking through the filtered optic or filtered lens and constricts when looking absent of the filtered optic or filtered lens.

[0088] In certain embodiments disclosed herein, when a filtered optic or filtered lens isused, the overall light transmission through the filtered optic or filtered lens can be 30% or less, while the light transmission within the predominant transmitted wavelength range being transmitted to the eye can be 40% or more. In certain cases, the pupil of the eye enlarges when looking through the filtered optic or filtered lens and constricts when looking absent of the filtered optic or filtered lens. In other embodiments the pupil of the eye remains constricted due to a higher percentage of blue light wavelengths being transmitted. Still in other embodiments taught herein the pupil is tricked by way of a modulation of the light source thus permitting blue light wavelengths to strike the retina before the pupil constricts. This then can be repeated over and over again.

[0089] As used herein, in embodiments when light wavelengths are generated by way of alight emitter(s) if in a dark room with no ambient lighting the wavelength range that strikes the eye’s retina fall within the wavelength range of at least one of: 480nm + / - 30nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, 500nm + / - 30nm, 650nm + / - 30nm, or 700nm + / - 30nm.

[0090] As used herein, in embodiments when light wavelengths are generated by a lightemitter(s) if ambient lighting is present (including that of artificial light or sun light) the blended light wavelengths of the light emitter(s) and also the ambient light comprises wavelengths of light that strike the eye’s retina falling within the wavelength range of at least one of: 480nm + / - 30nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, 500nm + / - 30nm, or 650nm + / - 30nm, or 700nm + / - 30nm.

[0091] It should be understood that when interpreting embodiments utilized herein unlesstotal darkness is specified, it should be assumed that there is ambient light and thus the light wavelengths striking the retina are blended by the light from the light emitter and the ambient light. The same is true with a filtered optic or filtered lens. In most but not all cases the filtered optic or filtered lens is located 12+mm from the eye of the wearer unless the filtered optic or filtered lens is that of a contact lens or intraocular lens. An exception to this interpretation would be that of the use of a virtual reality device or a modified reality device whereby the device is sealed from ambient light.

[0092] In still other embodiments, a light wavelength(s) from either a filtered optic, filteredlens, light emitter(s), and / or light emitter(s), combined with ambient light that strikes the retina of the eye, are selected so that the radiation peak of these wavelengths falls between the peak melanopsin sensitivity (480nm, and rhodopsin sensitivity (500nm)). Thus, the spectral curve peak of these wavelengths falls within the range of 480nm and 500nn. In these embodiments this occurs whether the wavelengths were generated by a filtered optic, filtered lens, light emitter, and / or light emitter, combined with ambient light.

[0093] In still other embodiments, the light stimulation is targeted at or to the cones, rodsand ganglion cells. In certain embodiments the objective of ocular photo-bio-stimulation is to increase dopamine within the eye. In certain embodiments the objective of ocular photo-bio- stimulation is to increase dopamine within the eye’s retina. When increasing dopamine in the eye and / or retina, ocular photo-bio-stimulation blue light or blue green light having wavelengths within the range of 450nm to 510nm can be used, or, for increasing dopamine in the eye and / or retina, ocular photo-bio-stimulation red light wavelengths of 650nm + / - 30nm or 700nm + / - 30nm can be utilized. In certain embodiments the objective of ocular photo-bio-stimulation is to increase dopamine within the eye’s retina and the brain. In still other embodiments the objective of ocular photo-bio-stimulation is to reduce pain. In still other embodiments the objective of ocular photo- bio-stimulation is to reduce the severity of a headache. When reducing pain by ocular photo-bio- stimulation, green light having wavelengths within the range of 530nm + / - 20nm can be utilized. In still other embodiments the use of light wavelengths in the range of 650nm + / - 30nm or 700nm + / - 30nm can improve mitochondria function and / or reduce age related inflammation in the eye of the user. In other embodiments the objective is to improve mitochondria function and / or reduce age related inflammation in the eye’s retina of the user.

[0094] In still other embodiments, the objective of ocular photo-bio-stimulation is toincrease the number or healthy mitochondria present within the ocular photo-bio-stimulation, the area of the retina in which the ocular photo-bio-stimulation has targeted. When increasing healthy mitochondria by way of ocular photo-bio-stimulation, red light having wavelengths within the range of one of 650m to 700nm, 650nm + / - 30nm, 700nm + / - 30nm, or 830nm + / - 30nm, can be utilized. Such ocular photo-bio-stimulation, according to the present invention, increases retinal mitochondrial function and attenuates oxidative stress thus increasing the number of healthymitochondria within the area of the retina being treated. This can be important for treating, by way of example only, diabetic retinopathy, macular degeneration, and / or retinitis pigmentosa.

[0095] In still other embodiments, the objective of ocular photo-bio-stimulation is toincrease the alertness of the individual being treated with ocular photo-bio-stimulation. When increasing alertness by way of ocular photo-bio-stimulation, blue light having wavelengths within the range of 450nm to 510nm can be utilized. In still other embodiments the objective of ocular photo-bio-stimulation is to increase the slowing down, to slow the progressing of, or to stop myopia of the individual being treated with ocular photo-bio-stimulation. When slowing down or stopping myopia by way of ocular photo-bio-stimulation, blue light having wavelengths within the range of 450nm to 510nm, or red light within the wavelength range of 650nm + / - 30nm or 700nm + / - 30nm can be utilized. Such ocular photo-bio-stimulation wavelengths can be applied to a large portion of the eye’s retina to stimulate the ipRGC ganglion cells and / or rods, or to the ganglion axons of the optic nerve head for the purposes of generating increased retinal dopamine.

[0096] In still other embodiments, the objective of ocular photo-bio-stimulation is to treator correct a neurological abnormality of the individual being treated with the ocular photo-bio- stimulation. When correcting a neurological abnormality by way of ocular photo-bio-stimulation, blue light having wavelengths within the range of 450nm to 510nm can be utilized. Neurological abnormalities that may be treatable by ocular photo-bio-stimulation are by way of example only: Alzheimer’s, cognitive disorders, ADD, ADHD, depression, anxiety, and / or Parkinson’s disorder.

[0097] In still other embodiments the objective of ocular photo-bio-stimulation is toprevent myopia from occurring with the individual being treated with the ocular photo-bio- stimulation. In still other embodiments the objective of ocular photo-bio-stimulation is to treat or correct an ocular abnormality of the individual being treated with ocular photo-bio-stimulation. When correcting an ocular abnormality, the use of the appropriate light wavelengths must be employed when treating with ocular photo-bio-stimulation. Ocular abnormalities that may be treatable by ocular photo-bio-stimulation are by way of example only: myopia, AMD, dry AMD, diabetic retinopathy, retinal degenerative disease, glaucoma, optic neuropathy, cataract, and / or meibomian gland disfunction leading to dry eye.

[0098] For all embodiments provided herein for providing ocular photo-bio-stimulation,light wavelengths predominantly fall within the wavelength range of at least one of 480nm + / - 30nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm,495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, 500nm + / - 30nm, 650nm + / - 30nm, or 700nm + / - 30nm, which can be utilized inthe above will depend upon the type of ocular photo-bio-stimulation that is desired to produce the desired physiological response. Thus, for any embodiment disclosed within this invention disclosure, any of the above ranges of wavelengths can be applied over and beyond what may be stated.

[0099] In certain other embodiments which reduce any visual unpleasantness from flickerfor the driver or user, the ocular photo-bio-modulation light source can be modulated light wavelength ranges between blue (450nm – 495nm) and bluish green / cyan (495nm – 520nm).[000100] In still other embodiments which reduce any visual unpleasantness from flicker, theocular photo-bio-modulation light source can be modulated within light wavelength ranges between blue (450nm – 495nm) and green (495nm- 570nm).[000101] In certain embodiments the light can be flickered or modulated when providingocular photo-bio-stimulation therapy to the eye’s retina. In other embodiments the light is devoid of a flicker. For embodiments that stimulate the production of dopamine in the eye’s retina or an increase in the production of dopamine, the ocular photo-bio-light source can flicker or be modulated at a rate of 1Hz – 15Hz. In certain embodiments the range is between 10Hz to 12Hz.[000102] In certain embodiments the light can be flickered or modulated when providingocular photo-bio-stimulation therapy to the brain. In other embodiments the light is devoid of a flicker.[000103] For embodiments that stimulate the production of dopamine in the brain or anincrease in the production of dopamine in the brain, the ocular photo-bio-light source can flicker or be modulated at a rate of 40Hz + / - 20Hz. In certain embodiments the range is between 40Hz – 65Hz.[000104] In certain embodiments that cause the brain to increase alertness, the ocular photo-bio-light source can be flickered or modulated at a rate of 40Hz + / - 10Hz.[000105] In certain embodiments that cause the brain to increase cognitive ability, the ocularphoto-bio-light source can be flickered or modulated at a rate of 40Hz + / - 10Hz.[000106] For embodiments that stimulate the production of serotonin in the brain or anincrease in the production of serotonin in the brain, the ocular photo-bio-light source can flicker or be modulated at a rate of 3Hz – 20Hz. In certain embodiments the range is between 5Hz + / - 10Hz.[000107] For embodiments that stimulate the production of norepinephrine in the brain or anincrease in the production of norepinephrine in the brain, the ocular photo-bio-light source can flicker or be modulated at a rate of 3Hz – 10 Hz.[000108] In embodiments, a second eyewear to be worn by a wearer, wherein the secondeyewear when worn is in optical communication with a first eyewear worn by a wearer, wherein the second eyewear comprises a filtered lens or filtered optic, wherein the filtered lens or filtered optic of the second eyewear predominantly transmits light wavelengths within the range of at least one of: 480nm + / - 30nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, 500nm + / - 30nm, or 650nm + / - 30nm, to an eye of the wearer, wherein the first eyewear comprises a first eyewear lens for optically correcting the distance vision of the wearer, and wherein the filtered lens or filtered optic of the second eyewear is distinct from first eyewear lens.[000109] Embodiments include the overall transmission of the first and second eyewearfiltered lens or filtered optic that cause the pupil of the eye of the wearer to constrict or remain smaller in size compared to when wearing conventional sunglasses where the pupil of the eye will enlarge in size. However, in certain embodiments, it is more important to provide more ocular photo-bio-stimulation as opposed to maximum vision clarity. In these embodiments, it is necessary to trick the wearer’s retinal neurological feedback that causes the pupil to constrict while still providing blue light within the range of 450nm – 530nm, preferably 480nm + / - 20nm to strike the wearer’s / user’s retina. This can occur when, for example, utilizing an XR eyewear approach that comprises modulating the image being seen by the wearer of the XR eyewear; the image modulating between, by way of example only, black and blue, thus causing the pupil of the eye to enlarge and then constrict and enlarge and then constrict. By example only, as soon as the pupil enlarges exposing the retina to blue light thus causing the pupil to constrict, then as soon as the pupil constricts exposing the retina to black light (or a black image) causing the pupil to enlarge and so on. The transmission of light wavelengths is within the range of at least one of: 480nm + / - 30nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm,495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, 500nm + / - 30nm, 650nm + / - 30nm, or 700nm + / - 30nm, providing ocular photo-bio-[000110] However, in most cases when the eye’s retina is exposed to blue light within therange of 450nm to 530nm, preferably 480 nm + / - 20 nm, the pupil of the eye constricts or remains constricted. The constriction of the pupil when viewing through a filtered optic or filtered lens allows for the user / wearer of the filtered lens / optic to have improved or maximum vison clarity. However, in certain embodiments it is more important to provide ocular photo-bio-stimulation as opposed to maximum vision clarity. In these embodiments it is necessary to trick the wearer’s retinal neurological feedback that causes the pupil to constrict while still providing blue light within the range of 450nm – 530nm, preferably 480nm + / - 20nm to strike the wearer’s / user’s retina.[000111] Various embodiments taught herein take in to account: time of day, the amount ofsunlight lux striking the sunglass lens, the amount of light intensity (lux) leaving the sunglass lens transmitted within a specified range of light wavelengths needed to stimulate dopamine in an eye of the user / wearer, the overall visible light transmission of the sunglass lens, the percentage of light transmission within a defined range of light wavelengths that cover the majority of the absorption curves of melanopsin and rhodopsin as well as certain of the cone opsins, the width of a range of wavelengths of light within the range of 450nm – 520nm, the color balance of light wavelengths needed to be transferred from the sunglass lens to the eye of the wearer, and the ability of the sunglass lens to pass the ISO and / or ANSI traffic light or signal test. Embodiments taught herein must balance numerous components that contribute to the ability of the sunglass lens to cause the production of dopamine or increase the production of dopamine in the eye’s retina of the wearer of the sunglass lens, or cause the production or increase the production of one or more of dopamine, serotonin, norepinephrine in the brain, while also providing the appropriate level of clear distance and / or near vision clarity for the wearer of the sunglass lens. And the invention can further provide the appropriate color balance of light wavelengths transmitted from the sunglass lens to the eye of the wearer of the sunglass lens, so that either the wearer of the sunglass lens by way of subjective measurements or the sunglass lens by way of objective measurements can pass the ISO and / or ANSI traffic light test.[000112] An embodiment can be that of a filtered lens or filtered optic or sunglass lens orsunglass optic that transmits a higher percentage of blue light and bluish green light wavelengths within the wavelength range of one or more of 480nm + / - 30nm or 530nm + / - 20nm, than a lens or optic comprises an average visible light transmission percentage within the range of 380nm – 780nm and passes the ISO 12312-1 sunglass traffic light / signal test.[000113] In embodiments, biofeedback can be utilized to confirm that one or more of,increased dopamine, serotonin, or norepinephrine, is being produced within the brain of a patient having ocular photo-bio-stimulation therapy. Such biofeedback can be comparing one or more of: increased blink rate of the eye(s) of the patient being treated, increased diameter of pupil(s) of the patient being treated, and / or increased heart rate of the patient being treated to that of a base line for the same activity prior to the ocular photo-bio-stimulation therapy.[000114] In embodiments, one or more of a timer, geolocation, an alarm (such as by way ofexample only, sound, vibration, light, or image), and / or wireless or wired communication to notify a remote third party, can be incorporated or associated with eyewear providing ocular photo-bio- stimulation therapy. BRIEF DESCRIPTION OF THE DRAWINGS[000115] The accompanying drawings illustrate certain aspects of some of the embodimentsof the present invention and should not be used to limit or define the invention. Together with the written description the drawings serve to explain certain principles of the invention.[000116] FIG. 1 shows background information for purposes of explaining the inventionherein.[000117] FIG. 2 shows background information for purposes of explaining the inventionherein.[000118] FIG. 3 shows background information for purposes of explaining the inventionherein.[000119] FIG. 4 shows background information for purposes of explaining the inventionherein.[000120] FIG. 5 shows background information for purposes of explaining the inventionherein.[000121] FIG. 6 shows background information for purposes of explaining the inventionherein.[000122] FIG. 7 shows background information for purposes of explaining the inventionherein.[000123] FIG. 8 shows background information for purposes of explaining the inventionherein.[000124] FIG. 9 shows background information for purposes of explaining the inventionherein.[000125] FIG. 10 shows background information for purposes of explaining the inventionherein.[000126] FIG. 11 shows background information for purposes of explaining the inventionherein.[000127] FIG. 12 shows an embodiment of the current invention as described herein.[000128] FIG. 13 shows an embodiment of the current invention as described herein.[000129] FIG. 14 shows an embodiment of the current invention as described herein.[000130] FIG. 15 shows an embodiment of the current invention as described herein.[000131] FIG. 16 shows an embodiment of the current invention as described herein, with theinvention shown at the top of the steering wheel.[000132] FIG. 17 shows an embodiment of the current invention as described herein.[000133] FIG. 18 shows an embodiment of the current invention as described herein.[000134] FIG. 19A-F shows an embodiment of the current invention as described herein.[000135] FIG. 20A-C shows an embodiment of the current invention as described herein.[000136] FIG. 21A-D shows an embodiment of the current invention as described herein.[000137] FIG. 22 shows an embodiment of the current invention as described herein.[000138] FIG. 23A-B shows an embodiment of the current invention as described herein.[000139] FIG. 24 shows an embodiment of the current invention as described herein.[000140] FIG. 25A-C shows an embodiment of the current invention as described herein.[000141] FIG. 26 shows an embodiment of the current invention as described herein.[000142] FIG. 27 shows an embodiment of the current invention as described herein.[000143] FIG. 28 shows an embodiment of the current invention as described herein.[000144] FIG. 29 shows an embodiment of the current invention as described herein.[000145] FIG. 30 shows an embodiment of the current invention as described herein.[000146] FIG. 31 shows an embodiment of the current invention as described herein.[000147] FIG. 32 shows an embodiment of the current invention as described herein.[000148] FIG. 33 shows an embodiment of the current invention as described herein.[000149] FIG. 34 shows an embodiment of the current invention as described herein.[000150] FIG. 35 shows an embodiment of the current invention as described herein.[000151] FIG. 36 shows an embodiment of the current invention as described herein.[000152] FIG. 37 shows an embodiment of the current invention as described herein.[000153] FIG. 38 shows an embodiment of the current invention as described herein.[000154] FIG. 39 shows an embodiment of the current invention as described herein.[000155] FIG. 40 shows an embodiment of the current invention as described herein.[000156] FIG. 41 shows an embodiment of the current invention as described herein.[000157] FIG. 42 shows an embodiment of the current invention as described herein.[000158] FIG. 43 shows an embodiment of the current invention as described herein.[000159] FIG. 44 shows categories of sunglasses.[000160] FIG. 45 shows information related to the invention described herein.[000161] FIG. 46 shows information related to the invention described herein.[000162] FIG. 47 shows information related to the invention described herein.[000163] FIG. 48 shows information related to the invention described herein.[000164] FIG. 49 shows information related to the invention described herein.[000165] FIG. 50 shows information related to the invention described herein.[000166] FIG. 51 shows information related to the invention described herein.[000167] FIG. 52 shows information related to the invention described herein.[000168] FIG. 53A-D shows an embodiment of the current invention as described herein.[000169] FIG. 54A-B shows an embodiment of the current invention as described herein.[000170] FIG. 55A-I shows an embodiment of the current invention as described herein.[000171] FIG. 56 shows an embodiment of the current invention as described herein.[000172] FIG. 57 shows an embodiment of the current invention as described herein.[000173] FIG. 58 shows an embodiment of the current invention as described herein.[000174] FIG. 59A-B shows an embodiment of the current invention as described herein.[000175] FIG. 60A-B shows an embodiment of the current invention as described herein.[000176] FIG. 61 shows an embodiment of the current invention as described herein.[000177] FIG. 62A-C shows an embodiment of the current invention as described herein.[000178] FIG. 63 is a graph showing functionality of the current invention as describedherein.[000179] FIG. 64 is a graph showing functionality of the current invention as describedherein.[000180] FIG. 65 is a graph showing functionality of the current invention as describedherein.[000181] FIG. 66 is a graph showing functionality of the current invention as describedherein.[000182] FIG. 67 is a chart showing improvements provided by the current invention overconventional eyewear.[000183] FIG. 68 is a chart showing improvements provided by the current invention overconventional eyewear.[000184] FIG. 69 shows sunlight spectrum at a point of time during the day.[000185] FIG. 70 shows sunlight spectrum at a point of time during the day.[000186] FIG. 71 shows sunlight spectrum at a point of time during the day.[000187] FIG. 72 shows sunlight spectrum at a point of time during the day.[000188] FIG. 73 shows sunlight spectrum at a point of time during the day.[000189] FIG. 74 is a chart showing improvements provided by the current invention overconventional eyewear.[000190] FIG. 75 is a chart showing improvements provided by the current invention overconventional eyewear.[000191] FIG. 76 shows sunglass categories.[000192] FIG. 77 is a graph showing improvements provided by the current invention overconventional eyewear.[000193] FIG. 78 is a graph showing improvements provided by the current invention overconventional eyewear, including an embodiment of the invention as described herein.[000194] FIG. 79 shows how blue light transmission through the eye changes as a personages.[000195] FIG. 80 shows how the power of the source light and / or distance of the light fromthe eye can affect the lux at the cornea and the retina.[000196] FIG. 81 shows how the power of the source light and / or distance of the light fromthe eye can affect the lux at the cornea and the retina.[000197] FIG. 82 shows how the power of the source light and / or distance of the light fromthe eye can affect the lux at the cornea and the retina.[000198] FIG. 83 shows how different light wavelengths can differently affect S Cones,Melanopsin, Rhodopsin, M Cones, and L Cones.[000199] FIG. 84 shows how different light wavelengths can differently affect S Cones,Melanopsin, Rhodopsin, M Cones, and L Cones.[000200] FIG. 85 shows how different light wavelengths can differently affect S Cones,Melanopsin, Rhodopsin, M Cones, and L Cones.[000201] FIG. 86 shows ocular photo-bio-stimulation, wherein by way of example, any typeof electronic display can provide light within the wavelength range of 450 nm – 510 nm, having a light intensity of 400 lux or greater when striking the retina of the human eye. The time of treatment can be, by way of example only, 10 minutes or less, twice per day. The patient can play games (including with distance removed other people receiving treatment), use e-mail, or perform e-communication, while receiving ocular photo-bio-stimulation therapy. A computer application can be used to manage such light therapy. In aspects, the lenses being worn can be any type of myopia control lenses (e.g., Essilor Stellest Lens (H.A.L.T.), Zeiss Myocare, HoyaDims Miyosmart, Sightglass Vision (contrast reduction / diffusion), or chromatic aberration focused lenses or chromatic aberration refocused lenses. The lenses can be cleared or filtered.[000202] FIG. 87 shows that a combination can be used to stimulation the production ofdopamine in the eye and / or brain of the user, the brightness level in lux is preferably turned up to display up 1,000 lux (or more ore less) or greater brightness intensity, such as up to 2,000 lux.[000203] FIG. 88 shows an example of an embodiment described herein, such as a cellphone, tablet computer, laptop computer, desktop computer, electronic display, which can be used along with a computer application embodiment. It can be used for ocular photo-bio-stimulation for myopia control or prevention. It can also be used for treating neurological neurotransmitter deficiency disorder, such as deficiencies of one or more of: dopamine, serotonin, or norepinephrine in the brain. The device can include optional sensors that sense a distance from the screen compared to the user’s face or eyes and can adjust the brightness of the screen up or down to maintain a preferred level of lux display light. It can be used with or without a lens or optic wornby the user receiving ocular photo-bio-stimulation light. The display can show blue, green, and red wavelength bands (or white light) providing ocular photo-bio-stimulation to the user.[000204] FIG. 89 shows an example of an embodiment described herein, such as a cellphone, tablet computer, laptop computer, desktop computer, electronic display, which can be used along with a computer application embodiment. It can be used for ocular photo-bio-stimulation for myopia control or prevention. It can also be used for treating neurological neurotransmitter deficiency disorder, such as deficiencies of one or more of: dopamine, serotonin, or norepinephrine in the brain. The device can include optional sensors that sense a distance from the screen compared to the user’s face or eyes and can adjust the brightness of the screen up or down to maintain a preferred level of lux display light. It can be used with or without a lens or optic worn by the user receiving ocular photo-bio-stimulation light. In aspects, the computer application system generated display can provide a programmable border, color wavelengths, and programmable intensity. The border can be of any shape or size, and can all or partly be programmable. The display screen can have content that shrinks and a blue or blue green border within the wavelength range of 450 nm – 510 nm provides ocular photo-bio-stimulation to the user.[000205] FIG. 90 shows an example of an embodiment described herein, such as a cellphone, tablet computer, laptop computer, desktop computer, electronic display, which can be used along with a computer application embodiment. It can be used for ocular photo-bio-stimulation for myopia control or prevention. It can also be used for treating neurological neurotransmitter deficiency disorder, such as deficiencies of one or more of: dopamine, serotonin, or norepinephrine in the brain. The device can include optional sensors that sense a distance from the screen compared to the user’s face or eyes and can adjust the brightness of the screen up or down to maintain a preferred level of lux display light. It can be used with or without a lens or optic worn by the user receiving ocular photo-bio-stimulation light. In aspects, the computer application system generated display can provide a programmable border, color wavelengths, and programmable intensity. The border can be of any shape or size, and can all or partly be programmable. The display screen can have content that shrinks and a blue or blue green border within the wavelength range of 450 nm – 510 nm provides ocular photo-bio-stimulation to the user.[000206] FIG. 91 shows an example of an embodiment described herein, such as a cellphone, tablet computer, laptop computer, desktop computer, electronic display, which can be used along with a computer application embodiment. It can be used for ocular photo-bio-stimulation for myopia control or prevention. It can also be used for treating neurological neurotransmitter deficiency disorder, such as deficiencies of one or more of: dopamine, serotonin, or norepinephrine in the brain. The device can include optional sensors that sense a distance from the screen compared to the user’s face or eyes and can adjust the brightness of the screen up or down to maintain a preferred level of lux display light. It can be used with or without a lens or optic worn by the user receiving ocular photo-bio-stimulation light. In aspects, the computer application system generated display can provide a programmable border, color wavelengths, and programmable intensity. The border can be of any shape or size, and can all or partly be programmable. The display screen can have content that shrinks and a blue or blue green border within the wavelength range of 450 nm – 510 nm provides ocular photo-bio-stimulation to the user. The light can be amplified by additional emitters. Thus, the light wavelengths striking the eye of the user of the electronic display can be blended to include light wavelengths given off by the added light emitters shown on the bottom of the phone pictured. This can affect the response as shown in the inset graph. Thus, in embodiments, blue and / or blue green light emitters (e.g., with the range of 450 nm – 510 nm) can be attached to the display and controlled, for example, by a computer application. This can allow for adding additional light transmission within the range of 450 nm – 510 nm to the light being transmitted by they display to the user, thus blending additional blue and / or blue green (cyan) light to the wavelengths of light being display on the display.[000207] FIG. 92 shows that a computer application can be used to manage the device. Inaspects, children (or people of any age) in different locations can compete with one another with games while receiving ocular photo-bio-stimulation light therapy.[000208] FIG. 93 shows that a computer application can be used to manage the device. Inaspects, children (or people of any age) in different locations can compete with one another with games while receiving ocular photo-bio-stimulation light therapy. In aspects, as the eye follows the animated image around the display, blue light within the range of 450 nm to 520 nm strike different regions of the eye’s retina. This photo-therapy can be performed monocularly or binocularly. The affect can be seen, by way of example, in the inset graph.[000209] FIG. 94 shows that a computer application can be used to manage the device. Inaspects, children (or people of any age) in different locations can compete with one another with games while receiving ocular photo-bio-stimulation light therapy. In aspects, as the eye follows the animated image around the display, blue light within the range of 450 nm to 520 nm strike different regions of the eye’s retina. This photo-therapy can be performed monocularly or binocularly. The light can be mostly blue light, in examples.[000210] FIG. 95 shows an example of a cell phone display providing ocular photo-bio-stimulation light through a lens or optic to a user. The lens or optic can be any one of: Sightglass Vision (diffusion / contrast reduction) myopia control lens; Hoya Miyosmart (D.I.M.S. technology) myopia control lens; Essilor Stellest (H.A.L.T. technology) myopia control lens; Zeiss Myocare (alternating focus and defocus) myopia control lens; a chromatic aberration focus lens.[000211] FIG. 96 shows an example of a cell phone display providing ocular photo-bio-stimulation light through a lens or optic to a user. In this embodiment, as shown, a Fresnel lens or optical having optical power (or plano power) is in a central zone for correcting the wearer’s BVA centrally, with a peripheral zone outside of the central zone comprising increased plus optical power (or reduced minus optical power) compared to the central optical power of, for example, 0.50D to 5.00D. This optic can be housed or supported with fit-over eyewear, disposable eyewear, static cling that attached to the subject’s lenses or held on its own, or supported by an eyeglass frame or other lens.[000212] FIG. 97 shows an example of a cell phone display providing ocular photo-bio-stimulation light through a lens or optic to a user. The lens or optic can be the patient’s conventional lens to correct his or her myopia to 20 / 20 vision or their best visual acuity.[000213] FIG. 98 shows “Rod Distribution Relative to Macula and Fovea,” as backgroundinformation for the invention disclosed herein.[000214] FIG. 99 depicts an ocular photo-bio-stimulation light source and fixation targetaspect, according to embodiments of the current invention as described herein.[000215] FIG. 100 depicts an ocular photo-bio-stimulation light source and fixation targetaspect, according to embodiments of the current invention as described herein.[000216] FIG. 101 shows a chart regarding aspects of a full protective image and a blendedprotective image, according to embodiments of the current invention as described herein.[000217] FIG. 102 depicts aspects of a full protective image and a blended protective image,according to embodiments of the current invention as described herein.[000218] FIG. 103 depicts an example of an eye and eye anatomy for backgroundinformation purposes.[000219] FIG. 104 depicts aspects of a full protective image and a blended protective image,according to embodiments of the current invention as described herein.[000220] FIG. 105 depicts aspects of a full protective image and a blended protective image,according to embodiments of the current invention as described herein.[000221] FIG. 106 depicts aspects of aligning a fixation target, according to embodiments ofthe current invention as described herein.[000222] FIG. 107 depicts aspects of aligning a fixation target, according to embodiments ofthe current invention as described herein.[000223] FIG. 108 depicts aspects of aligning a fixation target, according to embodiments ofthe current invention as described herein.[000224] FIG. 109 depicts examples of ocular photo-bio-stimulation light therapy and relatedequipment.[000225] FIG. 110 depicts examples of ocular photo-bio-stimulation light therapy butprotecting the fovea and at least a portion of the macula, according to embodiments of the current invention as described herein.[000226] FIG. 111 depicts examples of ocular photo-bio-stimulation light therapy butprotecting the fovea and at least a portion of the macula (and at least a portion of the surrounding retina), according to embodiments of the current invention as described herein.[000227] FIG. 112 depicts aspects wherein the light source can modulate, according toembodiments of the current invention as described herein.[000228] FIG. 113 depicts aspects wherein the light source can provide blended light,according to embodiments of the current invention as described herein.[000229] FIG. 114 depicts aspects wherein the fixation target size can be adjusted, accordingto embodiments of the current invention as described herein.[000230] FIG. 115 depicts aspects of ocular bio-photo-stimulation light emitters, usedaccording to embodiments of the current invention as described herein.[000231] FIG. 116 depicts aspects of ocular bio-photo-stimulation light emitters, usedaccording to embodiments of the current invention as described herein.[000232] FIG. 117 depicts aspects of ocular bio-photo-stimulation light source(s), usedaccording to embodiments of the current invention as described herein.[000233] FIG. 118 depicts aspects of an ocular bio-photo-stimulation light box, usedaccording to embodiments of the current invention as described herein.[000234] FIG. 119 depicts aspects of an ocular bio-photo-stimulation light emitting electronicdisplay, used according to embodiments of the current invention as described herein.[000235] FIG. 120 depicts aspects of an ocular bio-photo-stimulation light emitting electronicdisplay, including additional information regarding a fixation target, according to embodiments of the current invention as described herein.[000236] FIG. 121 depicts aspects of an ocular bio-photo-stimulation light emitting electronicdisplay, used according to embodiments of the current invention as described herein.[000237] FIG. 122 depicts aspects of an ocular bio-photo-stimulation light emitting electronicdisplay, including additional information regarding a fine-tuned fixation point, according to embodiments of the current invention as described herein.[000238] FIG. 123 depicts aspects of eyewear providing eye protection, such as a fixationtarget, according to embodiments of the current invention as described herein.[000239] FIG. 124 depicts aspects of eyewear providing eye protection, such as a fixationtarget, according to embodiments of the current invention as described herein. DETAILED DESCRIPTION OF THE INVENTION[000240] Definitions:[000241] As used herein, ambient light can be that of indoor artificial light or sunlight.Ambient light as used herein can be that which would be in addition to that of a light emitter.[000242] As used herein, ECP stands for Eye Care Professional.[000243] As used herein, ocular photo-bio-stimulation is an umbrella term. Ocular photo-bio-stimulation is a biological non-invasive technique of using light to stimulate a neuron(s) or other cells within, on, or about the eye for the purpose of generating a physiological response within the human body. Such stimulation can directly or indirectly amount to stimulation or inhibition of a biological, neurological or chemical process within the human body.[000244] As used herein optogenetic therapy is broadly defined as a form of photo-bio-stimulation.[000245] As used herein, photo-bio-modulation is broadly defined as a form of photo-bio-stimulation.[000246] As used herein, painting the retina, is defined as causing a light that is providingocular photo-bio-stimulation of the retina to project its wavelengths of light onto the retina of an eye in such a manner that the light paints, covers, or affects, different portions or different neurons of the retina with light wavelengths as the light moves relative to the retina or the retina moves relative to the light.[000247] As used herein, an image is that of a focused or defocused light patTern (or lack ofa light patTern when surrounded with light) that falls on or strikes the retina of an eye of a subject. The eye can see or receive multiple images (or image patterns). It is the brain which consolidates the multiple images into one visual image. Thus as used herein it is possible for an eye to see or receive multiple images while the brain causes the multiple images to appear as one image scene. In certain cases the brain will not cause all multiple images to appear as one image or image scene.As used herein an image can be generated by light or by the absence of light when surrounded bya lighted image (e.g., in the case of a black image by way of example only). A black image can also be generated by the colors of: blue, magenta, and yellow, by way of example.[000248] As used herein, the visible light spectrum is as follows: Visible Light Spectrum(electromagnetic radiation spectrum) can be divided by color: blue / violet (400nm – 450nm), blue (450nm – 495), bluish green (495-520nm), green (521nm - 556nm), yellow (556nm – 590nm), orange (590nm – 625nm), and / or red (625nm – 700nm). However, in a general sense as used herein blue can be from 400nm – 520nm.[000249] As used herein, Blue light wavelengths are considered from 400nm – 500nm, withbluish green being between, 490nm and 520nm, with 450nm to 495nm being bright blue.[000250] As used herein, Cyan light wavelengths are considered to be bluish green andbetween 495 nm and 520 nm.[000251] As used herein HEV stands for high energy violet light. The HEV light within therange of 400nm – 440nm can be harmful to the retina of the eye, and more specifically 410nm – 430nm appears to be the most harmful.[000252] As used herein, UV light, which stands for ultraviolet light has wavelengths whichare less than 400nm in wavelength or said another way 399nm or less.[000253] As used herein, BVA stands for the level of vision when considering the best visualcorrection of a patient’s distance vision needs. For example, that of 20 / 25, 20 / 20, or 20 / 15.[000254] As used herein, a wavelength within the range of, by way of example only, 480nm+ / - 30nm means any single wavelength or wavelengths found within the range of 480nm + / - 30nm.[000255] As used herein, a wavelength within the range of, by way of example only, 530nm+ / - 20nm means any single wavelength or wavelengths found within the range of 530nm + / - 30nm.[000256] As used herein, a wavelength within the range of, by way of example only, 650nm+ / - 30nm means any single wavelength or wavelengths found within the range of 650nm + / - 30nm.[000257] As used herein, a wavelength band or wavelengths band, means one or morewavelengths of light within a certain range.[000258] As used herein, predominantly transmits one or more light wavelengths within therange of at least one of: 480nm + / - 30nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, 500nm + / - 30nm, 650nm + / - 30nm, or 700nm + / - 30nm, to the eye(s) of the wearer, means at least one of the preceding ranges of wavelengths includes the predominant (or most) light wavelengths within that wavelength range transmitted to the eye(s) of the wearer.[000259] As used herein, when referring to wavelengths within the range of X, this is meantto convey that any two or more wavelengths that are within the given range of wavelengths are predominantly or solely emitted or transmitted wavelengths (within the light wavelength range given) for the optic, filter, lens, and / or system, when discussing lighting or transmission. In certain cases, the word predominantly may be omitted, however in all cases the word predominantly should be read in to express the meaning.[000260] As used herein a wavelength band is a band of light wavelengths that runconcurrent with a beginning wavelength and ending wavelength.[000261] As used herein, a transmission peak is the peak light wavelength or wavelengthshaving the highest light transmission that fall within a band of light wavelengths. A transmission peak can be that of a curve or a plateau.[000262] As used herein, a light emitter can be any a component that converts an electricalsignal into a light signal. Light emitters can be, for example only, LEDs, OLEDs, TOLEDs. micro-OLEDs, micro-LEDs, micro-ileds, iLEDs, quantum dots, florescent lights, incandescent lights, and / or the sun.[000263] As used herein, a light source can be any artificial light source that comprises alight emitter or light emitters or a light source can be that of the sun.[000264] As used herein, an electronic display screen can be that of any electronic displayscreen. By way of example only, cell phone display screen, tablet display screen, laptop computer display screen, desktop computer display screen, or television display screen.[000265] As used herein, an optical filter is any device or material that changes the spectraldistribution of a light beam spectrally selectively or non-selectively.[000266] As used herein, an optic is a material that transmits light. An optic can be part of anoptical system. However, a lens can also be an optic. As used herein, an optic can be any kind of optic. Furthermore, a lens can be an optic, or an optic can be a lens.[000267] As used herein, a lens is an optic that focuses or defocuses light. A lens isa transmissive optical device that focuses or disperses a light beam by means of refraction. As used herein, a lens can be any kind of lens. Furthermore, a lens can be of any optical power including plano, unless that an optical power is specified in the disclosure.[000268] As used herein, optical power can be any optical power of a lens or optic includingplano optical power. It is common in the optical industry to refer to lens having no optical power as plano optical power. A lens with optical power (other than that of plano optical power) can refract and focus light to that of a focal point.[000269] As used herein, plano optical power means the lens or optic comprises no opticalpower. When an eye doctor prescribes for a patient a lens comprising no optical power the eye doctor prescribes plano. While the lens may be of a plano optical power (meaning no optical power) the lens in most cases (by way of example only) can comprise a lens structure, diameter, curvature, thickness and ultraviolet protection for the wearer eyes.[000270] As used herein, more minus or less plus optical power can be expressed whencomparing the sphere and cylinder optical power of two different lens zones’ optical powers, or by way of comparing the spherical equivalent of the two different lens zones’ optical powers. The same can be true when comparing two different lenses’ or optics’ optical powers.[000271] As used herein, an eyeglass lens can include or be a transparent optical componentdesigned to enhance visual clarity and provide corrective vision for individuals with refractive errors, such as myopia, hyperopia, astigmatism, or presbyopia. It can be made from various materials, including glass and plastic, and may incorporate special features such as coatings for anti-reflective properties, ultraviolet (“UV”) protection, or light filtration. Eyeglass lenses can be customized to fit a wide range of frame styles and can also include specialized lenses for conditions like photophobia or low vision, catering to diverse visual needs and preferences.[000272] As used herein, the Abbe value, also known as the V-number or constringence, is anumerical value that measures how much light disperses into individual wavelengths as it passes through a transparent material.[000273] As used herein, eyewear means any device used on, in, or about the eye thattransmits or directs light into the eye of the wearer of such eyewear. By way of example only, one of: spectacles, sunglasses, disposable eyewear, goggles, dress eyewear, safety eyewear, sports eyewear, clip on eyewear, fit over eyewear, magnetic attachable eyewear, military eyewear, smart eyewear, XR eyewear, AR eyewear, VR eyewear, MR eyewear, modified reality eyewear, contact lens, intra-ocular lenses, corneal implant, lens or lenses that are housed, supported, attached to eyewear or a frame worn around the eye or eyes of the wearer.[000274] As used herein, optical finishing can be the application of any finish, coating,tinting, to a lens. Such a coating can be by way of example only, hard scratch resistant coat, antireflection coat, spin coat, dip coat, vacuum deposition coat, surface cast.[000275] As used herein a semi-finished lens blank is a lens blank that has one of its surfacespolished.[000276] As used herein a finished lens blank is a lens blank that has both of its surfacespolished and further that optical power can be measured.[000277] As used herein, a filtered optic, is an optic or lens that comprises one or more filtersor is in optical alignment with one or more filters. Such filters can be by way of example only one or more of, interference filter, bandpass filter, absorption filter, notch filter, selective wavelength(s) filter, and / or neutral density filter.[000278] As used herein, a filtered lens is a lens or optic that comprises one or more filters oris in optical alignment with one or more filters. Such filters can be by way of example only one ormore of, interference filter, bandpass filter, absorption filter, notch filter, selective wavelength(s) filter, and / or neutral density filter.[000279] As used herein, optical alignment means that two optics (such as, two optics, twolenses, and / or one optic and one lens) are aligned so that a light ray can pass through each of the two optics.[000280] As used herein, chromatic aberration is aberration caused by the differences inrefraction of the colored rays of the spectrum.[000281] As used herein, longitudinal chromatic aberration (LCA) is a lens’s inability toproperly focus different color wavelengths in the same focal plane.[000282] As used herein, the central retina (macula) is a circular area of the retina that isabout 5mm - 6 millimeters in diameter with the fovea in the center, which is a small area in the center of the retina. The retina is between 30mm to 40mm in diameter.[000283] As used herein, the peripheral retina is any area of the retina that is outside of thecentral retina.[000284] As used herein, the mid peripheral retina is located between the far peripheralretina and the central retina.[000285] As used herein the far peripheral retina is located between the ora serrata and themid periphery of the retina.[000286] As used herein, a biomarker (short for biological marker) is an objective measurethat captures what is happening in a cell or an organism at a given moment[000287] As used herein, a physiological response is a bodily response that can be the resultof direct or indirect neural simulation. The physiological response can be immediate or delayed. By way of example only, slowing myopia may result from stimulating retinal rods and / or ganglion cells with an ocular photo-bio-stimulation light comprising blue light wavelengths within the range of 480nm + / - 30nm. The immediate response, in aspects, can be the increase of dopamine in the eye produced by the amacrine cells, while the delayed response could, for example, be that of slowing myopia. For the purposes of this invention disclosure, both the increasing dopamine and slowing of myopia would be considered physiological responses. Another example would be stimulating dopamine and / or serotonin in the brain.[000288] As used herein, intrinsically photosensitive retinal ganglion cells (ipRGCs), alsocalled photosensitive retinal ganglion cells (pRGC) are ganglion cells containing melanopsin and are a type of neuron in the retina of the human eye.[000289] As used herein, melanopsin-containing retinal ganglion cells (mRGCs) arespecialized ganglion cells that contain melanopsin and are a type of neuron in the retina of the human eye.[000290] As used herein, scotopic light is a type of light that is used to describe vision in dimor dark conditions, also known as scotopic vision or night vision. Scotopic light can be below 0.4 lux.[000291] As used herein, mesopic light or mesopic vision, sometimes also called twilightvision, is a combination of photopic and scotopic vision under low-light (but not necessarily dark) conditions. An example of mesopic light is low light level light provided by public lighting of 0.4 lux up to 10 lux (about 0.6 cd / m2).[000292] As used herein, photopic light, also known as daytime vision, is the visualperception that occurs when the eyes are light-adapted and there is enough brightness. A candle at 1 meter distance gives 1 photopic lux of light. Typical room illumination is in the order of 300-500 lux, whereas outdoor light varies from 1,500 lux on a cloudy day to 100,000 lux on a sunny day.[000293] As used herein, light intensity or luminous intensity is measured in lumens persquare foot (footcandles) or lumens per square meter (lux). Lumens measure the intensity of light emitted by a luminaire, while lux is a measurement of the light that is achieved and perceived. Lux, in some cases, is a more important measurement because it relates brightness to distance from the light source.[000294] As used herein, light transmission is the percentage of all visible light transmissionthrough a lens or optic within a range of wavelengths less than that of the visible spectrum.[000295] As used herein, overall visible light transmission means the same as visible lighttransmission or VLT and is expressed as a percentage. Further, it includes all visible light wavelengths transmitted through a lens or optic, by way of example.[000296] As used herein, the transmission of light wavelengths (within a range of givenwavelengths) is the transmission percentage measured within a given range of light wavelengths through a lens or optic of the overall visible light that is transmitted through the lens or optic. By way of example only, if the overall transmission of visible light through the lens or optic was 2,000lux and only 1,000 lux of light was transmitted through and measured within 480nm + / - 30nm, then the transmission percentage through the wavelength range of 480nm + / - 30nm would be 50%.[000297] As used here in light transmission curve spectra, light transmission curvespectrum, is a light curve that is charted / plotted by light transmission percentages for various wavelengths of light.[000298] As used here in light absorption curve spectra, light absorption curve spectrum, isa light curve that is charted / plotted by light absorption percentages for various wavelengths of light.[000299] As used herein within a range of wavelengths or within a wavelength range meansone or more wavelengths within the given range.[000300] As used herein, dopamine deficiency disorders are any disorder caused by a lack ofthe appropriate amount of dopamine. Low levels of dopamine can affect both physical and mental health.[000301] As used herein, serotonin deficiency disorders are any disorder caused by a lack ofthe appropriate amount of serotonin. Low levels of serotonin can affect one’s mental, behavioral, and emotional health.[000302] As used herein, a fixation target, is a target for the eye to fixate on. In most cases,but not all, the fixation target can be used to align the eye for diagnostic or therapeutic purposes. The fixation target can be aligned with the subject’s eye’s fovea and / or macula. When an eye looks at a fixation target the fixation target imparts an image of the fixation target over part or all of the macula (and / or fovea) of the subject’s eye. As used herein,, a fixation target is the target to which the eye’s macula or fovea of a subject is fixated upon.[000303] As used herein, Extended Reality (XR) is an umbrella term to refer to augmentedreality (AR), virtual reality (VR), mixed reality (MR), modified reality (MoR), and combinations thereof. The technology is intended to combine or mirror the physical world with a “digital world” able to interact with it, giving users an immersive experience by being in a virtual or augmented environment.[000304] Virtual Reality (VR) is a computer-generated environment with scenes and objectsthat appear to be real, making the user feel they are immersed in their surroundings. This environment is perceived through a device known as a Virtual Reality headset or helmet.[000305] Mixed Reality (MR) combines Augmented Reality (AR) and Virtual Reality (VR).While AR overlays digital content onto the real world, and VR immerses the user in a completely virtual environment, MR blends these two, creating interactive environments where physical and digital objects coexist and interact.[000306] Augmented reality (AR) is an interactive experience that visually combines the realworld and computer-generated 3D content.[000307] The distinctions between VR and AR come down to the devices they require andthe experience itself: AR uses a real-world setting while VR is completely virtual.[000308] As used herein, Modified Reality is a modified version of extended reality whichresults in any deviation from Augmented Reality, Mixed Reality, or Virtual Reality, where a portion of one, two or more lighted images are seen with an eye or eyes of a user merged or intertwined or overlapped. Such modified reality can be a modified form of augmented reality, virtual reality or mixed reality.[000309] As used herein, a near eye display is an electronic display that is within 30mm orless (in most cases 20mm or less) of the cornea of the eye of the user. A near eye display can comprise or be aligned and in optical communication with a micro-lens array. The use of a micro- lens array allows for the user to see a clear virtual image from said near eye display. However, in certain cases the near eye display is used to provide defocused light and in these cases a micro-lens array is not utilized.[000310] As used herein, a see-through near eye display is an electronic near eye display thatthe eye of the user can see a real image by looking through. In most cases, the use of a micro-lens array allows for the user to see a clear virtual image from said near eye display. However, a micro- lens array can be fabricated to defocus light or diffuse light.[000311] As used herein, a non-see-though near eye display is an electronic near eye displaythat the eye of the user cannot see a real image through. In most cases the use of a micro-lens array allows for the user to see a clear virtual image from said near eye display. However, a micro-lens array can be fabricated to defocus light or diffuse light.[000312] As used herein, an eyewear apparatus includes any device or apparatus describedherein that filters, treats, changes, enhances, diffuses, focuses, defocuses, transmits, generates, or otherwise is capable of producing or affecting light in such a way that the light can be used for ocular photo-bio-stimulation purposes.[000313] As used herein, a micro-lens array is a structure made up of many small lenses, ormicrolenses, that are arranged in a patterned manner. A micro-lens array can comprise hundreds, thousands or millions of micro-lenses. A micro-lens array as used herein can be for one or more of, providing focused light, defocused light, diffused light, and / or filtered light.[000314] As used herein, a myopia control lens is a specially designed ophthalmic lensintended to slow the progression of myopia (nearsightedness). Unlike standard lenses that only correct vision, myopia control lenses actively influence how light focuses on the retina to reduce the eye’s stimulus to grow longer in axial length.[000315] As used herein, a chromatic aberration focused lens or optic can be that of aperipheral refocused chromatic aberration lens or optic. A chromatic aberration focused lens is a lens or optic where a portion or all of the lens peripheral to the central zone of the lens, focuses one or more of the chromatic aberration wavelength bands (blue, green, red) farther away from the lens or optic. Said another way, while the central zone maintains its normal focus of chromatic aberration wavelength bands, the chromatic aberration wavelength bands peripheral to the central zone focuses farther from the lens or optic than those of the central zone.[000316] As used herein defocused light can be that of one or more of: light that focuses infront of the retinal, behind the retina, is scattered light, and / or dispersed or diffused light.[000317] As used herein when discussing enlarging the pupil diameter it is meant to enlargethe pupil diameter relative to what the pupil diameter would have been if all light (without being filtered or blocked) was permitted to strike the retina of the wearer / user's eye(s).[000318] As used herein, a vehicle can be that of any vehicle. By way of example only, avehicle can be an airplane, car, truck, bus, trolley, ship, train, subway, or tram.[000319] As used herein, the frame of an electronic display can be the other edge or a framethat goes around the outer edge of the display.[000320] As used herein, programable means software, memory, or an electrical componentthat was one or more of, programed during the fabrication of the device, can be programmed after fabrication, can be programed after fabrication remotely, and / or can be programed by the consumer after purchase.[000321] As used herein, a vehicle means any type of vehicle. By way of example only, anautomobile, a car, a truck, a bus, a ship, a boat, an airplane, a trolley, a train, a tram, a spaceship, a motorcycle, etc.[000322] As used herein, a fine-tuned fixation target is a more refined target located withinthe fixation target.[000323] As used herein, a full protective image is the main protective image that coverspart or all of the macula of the eye of the subject. This fully protective image can fall or be provided within a blended protective image (zone) which can circumvent the fully protective image.[000324] As used herein, a blended protective image is a secondary protective image that isa blend of the full protective image and that of the ocular photo-bio-stimulation light or light image.[000325] As used herein, a blended protective image zone is the zone around the zone orarea of the full protective image and between the full protective image and the area or zone of where the ocular photo-bio-stimulation light is applied.[000326] As used herein, being in optical communication means whereby radiated light,reflected light, and / or transmitted light, can travel from one object / lens or optic and through another lens or optic such that they are in optical alignment.[000327] The "ISO 12312-1 sunglass traffic signal test also referred to here within as theISO 12312-1 sunglass traffic light / signal test" refers to a standardized test procedure within the ISO 12312-1 standard, which evaluates the ability of sunglasses to transmit light from traffic signals adequately, ensuring drivers can clearly distinguish between red, yellow, and green lights while wearing them; this test primarily measures the “relative visual attenuation quotient (Q factor)” of the sunglasses across different light wavelengths corresponding to traffic signal colors.[000328] All embodiments disclosed herein, when appropriate, can utilize one or more of thefollowing: bandpass filter, notch filter, selective filter, absorption filter, interference filter, neutral density filter, coating, and / or dye, to achieve the desired wavelength transmission results. When more than one filter is used, it can be referred to herein as a hybrid filter. In certain embodiments a film or optic comprising the appropriate filter can be applied over or in front of an electronic display or optic to allow for the desired wavelengths of light to be transmitted. The film or optic comprising the filter can be attachable and removable from the display screen or built into the screen (or optic).[000329] Myopia, Prevention and Control:[000330] According to the current invention, it is believed that juvenile-onset myopia(nearsightedness) occurs due to accommodative near point stress that generates a force causing an increase in the axial length of the eye. The resulting axial elongation occurs when the eye’s ocular structure is unable to provide an offsetting force equal to or larger than that of the force causing axial elongation. The weakness of the opposing ocular structural is due to a deficiency of dopamine present in the retina.[000331] In reference to FIG. 12, ample retinal dopamine is required to increase choroidthickness and maintain a healthy sclera, both of which generate an offsetting force of resistance to axial elongation of the eye. Thus, the following embodiment provides for the prevention of myopia or slowing or stopping myopia progression.[000332] An embodiment of the invention is that of identifying children susceptible tomyopia and treating them before their myopia develops. A diagnostic test can be performed to determine the level of dopamine in the eye or eyes of a child. By way of example only an ERG (electroretinogram) test can be performed at an early age, (for example) 6 years and older. When such a test is performed one can identify if a child has a dopamine deficiency disorder. Following this, a refractive examination can be performed, whether subjective or objective, using a retinoscope, automatic refractor, or phoropter. Accordingly, the results can be used to identify those children who have 0.75D of hyperopia or less of hyperopia. Such children would include emmetropes. The result of these two tests (electroretinogram and refraction) can then identify which children are susceptible to becoming myopic. In certain cases an additional test for contrast sensitivity can be performed. Low contrast sensitivity can be an indication of a dopamine deficiency. Upon identifying a child that is susceptible of becoming myopic, one can begin treatment for ocular dopamine generation. Such means of treatment are identified in this invention disclosure. By improving the level of dopamine in the retina of the child’s eye, one can offset the development of ocular axial elongation (or myopia).[000333] Said another way, an embodiment for the prevention of myopia is:1) Identify those children 6 years old or older (or even younger) who have low levels ofdopamine in their retina;2) Test those children to identify their BVA (best distance visual acuity) refractive status; and3) If the refractive status of the child is +0.75D or less hyperopia and their ocular dopaminetest indicates low dopamine, begin therapy to increase retinal dopamine.[000334] For those children who already have myopia it is important to stop or slow theprogression of myopia as the child ages. Thus, it is important to increase the level of retinal dopamine in those children. Embodiments for increasing dopamine in the eye’s retina are disclosed herein.[000335] An embodiment of the current invention can be that of a device that is capable ofdetermining a level of dopamine in the eye’s retina of a patient, while also determining a refractive status of the eye. By way of example only, such a device can measure if the patient’s eye comprises dopamine at a level that meets or exceeds “X”, wherein X represents the level of dopamine deficiency, and also measure if the same eye comprises a refractive status that is less than “Y” diopters of hyperopia or is emmetropia or myopic. Another example would be that such a device can measure if the patient’s eye comprises dopamine at a level that meets or exceeds “X”, wherein X represents the level of dopamine deficiency, and also measure if the same eye comprises a best distance refractive correction that measures +0.75D or less of hyperopia.[000336] An embodiment can be an instrument for identifying a child or young adult that issusceptible to developing myopia, wherein the child or young adult is 25 years or younger, wherein the instrument determines if the child or young adult’s eye comprises dopamine at a level that meets or exceeds “X”, wherein X represents the level of dopamine deficiency, and wherein the instrument can also determine if the same eye’s distance refractive correction (being that of the best distance correction optical power) is that of +0.75D or less.[000337] An embodiment can be an instrument for identifying a child or young adult that issusceptible for developing myopia, wherein the child or young adult is 25 years or younger, wherein the instrument determines if the child or young adult’s eye comprises dopamine at a level that meets or exceeds “X”, wherein X represents the level of dopamine deficiency, and wherein the instrument can also measure if the same eye’s refractive correction, being that of the best distance correction optical power, is that of a spherical equivalent that is +0.75D or less hyperopic.[000338] Such a device could determine both the level of dopamine in the retina or eye andthe refractive status simultaneously or in succession. Such a device could be one of, handheld, a tabletop instrument, attachable to a slit lamp bio microscope, or attachable to a phoropter stand. By way of example only, such a device could be a combination ERG instrument and an autorefractor.[000339] An embodiment can be that of an instrument for identifying a child or young adultthat is susceptible for developing myopia, wherein the child or young adult is 25 years or younger,wherein the instrument determines if the child or young adult’s eye comprises dopamine at a level that exceeds “X”, wherein X represents the level of dopamine deficiency, and wherein the instrument can also determine if the same eye’s distance refractive correction (being that of the best distance correction optical power) is that of +0.75D or less.[000340] In determining if the child or an adult’s eye has a dopamine deficiency, thefollowing tests can be performed by:A. ERG (more specifically measuring the B Wave Amplitude of an ERG)B. Measuring contrast sensitivity[000341] An embodiment can be that of an instrument for treating myopia progression,wherein the instrument can determine a level of dopamine in the eye, wherein the instrument can also determine if the eye’s refraction requires an increase in minus optical power. Such an instrument can be that of an electroretinogram (ERG). Such an instrument can be handheld, or table mounted. For testing children, the use of a handheld ERG instrument that uses electrodes connected to the skin of the patient is recommended as opposed to corneal electrodes. By measuring the B wave amplitude, it is possible to determine a level of dopamine in the retina of the eye. A reduction in the B wave amplitude can indicate a dopamine deficiency. In certain cases, the testing of the child’s contrast sensitivity can also give an indication of a dopamine deficiency. Poor contrast sensitivity can be such an indication. The instrument further comprises the ability to provide ocular photo-bio-stimulation. Artificial intelligence (AI) can be incorporated into such an instrument to further help with optimizing such a diagnosis and treatment.[000342] The following is a listing of diagnostic testing and providing myopia control lighttherapy, and such an instrument embodiment could comprise:a. ERG (more specifically measuring the B Wave Amplitude of an ERG)b. Measuring contrast sensitivityc. Measuring Refractive Errord. Measuring or checking the scleral thicknesse. Measuring or documenting the eye’s axial length or elongation, and / orf. Treating with providing ocular photo-bio-stimulation[000343] In certain embodiments the diagnostic and myopia control therapy instrument cancomprise a combination handheld or table mounted instrument that comprises three or more of the following:a. ERG testing (for measuring the B wave amplitude)b. Optical biometer (for measuring the axial length of the eye)c. Auto-refractor (for measuring the refractive error of the eye)d. Contrast sensitivity tester (for measuring the contrast sensitivity of the eye)e. Measurement of scleral thickness of the eyef. Ocular photo-bio-stimulation (for providing light therapy to increase dopamine productionin the retina)g. AI (Artificial Intelligence)h. ML (Machine Learning)[000344] In certain embodiments the diagnostic and myopia control therapy instrument cancomprise a combination handheld or table mounted instrument that comprises four or more of the following:a. ERG testing (for measuring the B wave amplitude)b. Optical biometer (for measuring the axial length of the eye)c. Auto-refractor (for measuring the refractive error of the eye)d. Contrast sensitivity tester (for measuring the contrast sensitivity of the eye)e. Measurement of scleral thickness of the eyef. Ocular photo-bio-stimulation (for providing light therapy to increase dopamine productionin the retina)g. AI (Artificial Intelligence)h. ML (Machine Learning)[000345] In certain embodiments the diagnostic and myopia control therapy instrument cancomprise a combination handheld or table mounted instrument that comprises five or more, six or more, seven or more, or eight or more of the following:a. ERG testing (for measuring the B wave amplitude)b. Optical biometer (for measuring the axial length of the eye)c. Auto-refractor (for measuring the refractive error of the eye)d. Contrast sensitivity tester (for measuring the contrast sensitivity of the eye)e. Measurement of scleral thickness of the eyef. Ocular photo-bio-stimulation (for providing light therapy to increase dopamine productionin the retina)g. AI (Artificial Intelligence)h. ML (Machine Learning)[000346] An embodiment can be that of an instrument for treating myopia progression,wherein the instrument can determine a level of dopamine in the eye, wherein the instrument can also determine if the eye’s refraction requires an increase in minus optical power. Such an instrument can be that of an electroretinogram (ERG). Such an instrument can be handheld, or table mounted. For testing children, the use of a handheld ERG instrument that uses electrodes connected to the skin of the patient is recommended as opposed to corneal electrodes. By measuring the B wave amplitude, it is possible to determine a level of dopamine in the retina of the eye. A reduction in the B wave amplitude can indicate a dopamine deficiency. In certain cases the testing of the child’s contrast sensitivity can also give an indication of a dopamine deficiency. Poor contrast sensitivity can be such an indication. Artificial intelligence (AI) can be incorporated into such an instrument to further help with optimizing such a diagnosis and treatment.[000347] An embodiment can be that of an instrument for preventing or treating myopia,wherein the instrument can determine a level of dopamine in the eye’s retina, wherein the instrument can also determine if the eye’s best distance refraction is +0.75D or less of plus optical power or if the eye requires an increase in minus optical power to maintain its best corrected distance vision. Artificial intelligence (AI) can be incorporated into such an instrument to further help with optimizing such diagnosis and treatment.[000348] An embodiment can be that of an instrument for preventing or treating myopia,wherein the instrument can determine a level of dopamine in a patient’s eye’s retina, wherein the instrument can also determine the optical power required to achieve for the same eye of the patient its best distance vision correction or best distance visual acuity. Artificial intelligence (AI) can be incorporated into such an instrument to further help with optimizing such a diagnosis and treatment.[000349] An embodiment can be that of an instrument for preventing and / or treatingmyopia, wherein the instrument can determine a level of dopamine in a patient’s eye’s retina, wherein the instrument can also determine the optical power required to achieve for the same eye of the patient its best distance vision correction or best distance visual acuity, and wherein the instrument can apply photo-bio-stimulation. Artificial intelligence (AI) can be incorporated into such an instrument to further help with optimizing such diagnosis and treatment.[000350] As disclosed herein, a means for determining an indication of the level of dopaminein the retina of the eye of a patient one or more of the following can be measured; the B wave amplitude of an electroretinogram, the thickness of the choroid and / or sclera. Such thickness can be measured (by way of example only) by a Cirrus HD-OCT 5000. A contrast sensitivity test that indicates low contrast sensitivity can also indicate a dopamine deficiency. Artificial intelligence (AI) can be incorporated into such an instrument to further help with optimizing such diagnosis and treatment.[000351] An embodiment for slowing or preventing myopia can comprise modulation of theimage or light source. Such modulation can be within the range of 5Hz – 15Hz, 10Hz to 20Hz, or 40Hz + / - 20Hz.[000352] An embodiment can comprise a light source or light emitter having a light intensityof at least one of: 300 lux or greater, 500 lux or greater, 1,000 lux or greater, or 5,000 lux or greater. An embodiment can comprise light that strikes the eye of the user or wearer of at least one of: 300 Lux or greater, 500 lux or greater, 1,000 lux or greater, or 5,000 lux or greater.[000353] An embodiment can comprise an ocular-photo-bio-stimulation time of 1 minute to 5minutes, 5 minutes to 30 minutes, or one hour or less. With certain embodiments of eyewear disclosed herein such an ocular-photo-bio-stimulation time can be that of normal daily wear of the eyewear.[000354] Another embodiment of the invention can be a diagnostic test to determine thethickness of the choroid and / or scleral thickness of the eye or eyes of a child. By way of example only an OCT test can be performed at an early age, (for example) 6 years and older. When such a test is performed one can identify if a child has a dopamine deficiency disorder by way of measuring the choroidal and / or scleral thickness and / or testing the child’s contrast sensitivity. Following this, a refractive examination can be performed, whether subjective or objective, using a retinoscope, automatic refractor, or phoropter. Accordingly, the results can be used to identify those children who have 0.75D of hyperopia or less hyperopia. Such children would include emmetropes. The result of these two tests (electroretinogram and refraction) can then identify which children are susceptible to becoming myopic. Upon identifying a child that is susceptible to becoming myopic, one can begin treatment for ocular dopamine generation. Such means of treatment are identified in this invention disclosure. By utilizing ocular photo-bio-stimulation therapy one can stimulate dopamine production in the retina of the eye or eyes, also increase thethickness of the choroid and or sclera of the child’s eye(s), thus offsetting the development of ocular axial elongation (or myopia). A further indication of increased dopamine production can be by way of measuring an increase in the child’s contrast sensitivity. And an additional indication of increased dopamine production can be by way of performing and ERG test whereby the ERG test indicates an increase in the B wave amplitude. Artificial intelligence (AI) can be incorporated into such a diagnostic test to further help with optimizing such diagnosis and treatment.[000355] Said another way, an embodiment for the prevention of myopia is:4) Identify those children 6 years old or older (or even younger) who have low levels ofdopamine in their retina.5) Test those children to identify their BVA (best distance visual acuity) refractive status; and6) If the refractive status of the child is +0.75D or less hyperopia and their choroidal and / orscleral thickness indicates a low dopamine level, begin therapy to increase retinal dopamine and choroidal and / or scleral thickness.[000356] For those children who already have myopia it is important to stop or slow theprogression of myopia as the child ages. Thus, it is important to increase the level of retinal dopamine in those children. Embodiments for increasing dopamine in the eye’s retina are disclosed[000357] Ocular Photo-Bio-Stimulation with Inventive Embodiments[000358] Embodiments disclosed herein can provide ocular photo-bio-stimulation throughlight stimulation of specific wavelengths to the eye’s retina, and, in some embodiments, to the entire eye’s retina, the retina peripheral to the fovea, and / or the retina peripheral to the macula. In certain embodiments, the light stimulation is targeted at or to the rods. In other embodiments, the light stimulation is targeted at or to the ganglion cells. In still other embodiments, it is targeted at or to the rods and the ganglion cells. When ganglion cells are mentioned herein, the ganglion cells targeted or stimulated are the melanopsin containing ganglion cells (ipRGCs) or can also be called mRGCs.[000359] Embodiments herein teach the stimulation of the rods and / or ipRGCs with specificlight wavelengths. The retina of the human eye contains 100+M rods, 1M ganglion cells but fewer than 7,000 ipRGCs which are the ganglion cells that contain melanopsin. ipRGCs are less sensitive to photic stimulation and their response kinetics are slow compared to that of rods and cones. Response latency is inversely related to stimulus intensity and under dim light conditions ipRGCs can take many seconds to reach a peak response; the response may also persist for minutes afterstimulus termination. However, ipRGCs are similar to rods and cones in that they show adaptation by adjusting their sensitivity according to lighting conditions. While slow to respond to dim light conditions, ipRGCs appear capable of responding to the capture of a single photon of light. It has been estimated that the membrane density of melanopsin is about a thousand times lower than that of photopigments in the outer segments of rod and cone photoreceptors; this relatively low density may account for the poor absorption rate of ipRGCs. The capture of a single photon in an ipRGC generates a large and prolonged membrane current, greater than that recorded in rod photoreceptors but also 20-fold slower.[000360] In still other embodiments, the light stimulation is targeted at or to the cones, rodsand ganglion cells. In certain embodiments the objective of ocular photo-bio-stimulation is to increase dopamine within the eye. In certain embodiments the objective of ocular photo-bio- stimulation is to increase dopamine within the eye’s retina. When increasing dopamine in the eye and / or retina, ocular photo-bio-stimulation blue light having wavelengths within the range of 450nm to 510nm can be used, or, for increasing dopamine in the eye and / or retina, ocular photo- bio-stimulation red light wavelengths of 650nm + / - 30nm can be utilized. In certain embodiments the objective of ocular photo-bio-stimulation is to increase dopamine within the eye’s retina and the brain. In still other embodiments the objective of ocular photo-bio-stimulation is to reduce pain. In still other embodiments the objective of ocular photo-bio-stimulation is to reduce the severity of a headache. When reducing pain by ocular photo-bio-stimulation, green light having wavelengths within the range of 530nm + / - 20nm can be utilized. In still other embodiments the use of light wavelengths in the range of 650nm + / - 30nm can improve mitochondria function and / or reduce age related inflammation in the eye of the user. In other embodiments the objective is to improve mitochondria function and / or reduce age related inflammation in the eye’s retina of the user.[000361] In still other embodiments, the objective of ocular photo-bio-stimulation is toincrease the number or healthy mitochondria present within the ocular photo-bio-stimulation, the area of the retina in which the ocular photo-bio-stimulation has targeted. When increasing healthy mitochondria by way of ocular photo-bio-stimulation, red light having wavelengths within the range of one of 650m to 700nm, 650nm + / - 30nm, 700nm + / - 30nm or 830nm + / - 30nm, can be utilized. Such ocular photo-bio-stimulation, according to the present invention, increases retinal mitochondrial function and attenuates oxidative stress thus increasing the number of healthymitochondria within the area of the retina being treated. This can be important for treating, by way of example only, diabetic retinopathy, macular degeneration, and / or retinitis pigmentosa.[000362] For most if not all embodiments provided herein for providing ocular photo-bio-stimulation, light wavelengths predominantly fall within one of the wavelength ranges of 480nm + / - 30nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, 500nm + / - 30nm, 650nm + / - 30nm, or 700nm + / - 30nm, and can be utilized in addition to what is stated within the embodiments. The exact wavelength band of the above will depend upon the type of ocular photo-bio-stimulation that is desired to produce the desired physiological response. Biofeedback or diagnostics involving one or more of, pupil size increase, lid blink rate increase, heart rate increase, or blood oxygen level increase, can be an indication of increased production or stimulation of dopamine or norepinephrine in the brain and in some cases serotonin. An increase in contrast sensitivity, B wave amplitude of an ERG, scleral thickening, and / or slowing of axial length eye growth, can indicate an increase in the production of dopamine in the retina.[000363] Embodiments when light wavelengths are generated by way of filtered optics orfiltered lenses, the peak spectral curve of the wavelength range that strike the eye’s retina falls within the wavelength range of one: 480nm + / - 30nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, 500nm + / - 30nm, 650nm + / - 30nm, or 700nm + / - 30nm.[000364] Embodiments providing ocular photo-bio-stimulation can filter or block damaginghigh energy blue light, UV, and reduce bright light visual discomfort.[000365] Melanopsin photopigment expressed in intrinsically photosensitive retinal ganglioncells (ipRGCs) plays a crucial role in the adaptation of mammals to their ambient light environment through non-image-forming (NIF) visual responses. ipRGCs are structurally and functionally distinct from classical rod / cone photoreceptors and have unique properties including single-photon response, long response latency, photon integration over time, and slow deactivation.[000366] Embodiments disclosed herein that are directed to increasing dopamine in anindividual’s eye’s retina or dopamine in the brain of the individual whose eye was stimulated, attempt to use wavelength ranges that cover the peak sensitivities for melanopsin (480nm) and alsofor rhodopsin (500nm). Given that rhodopsin of Rods is 20 times faster to react than melanopsin of ipRGCs, but that melanopsin has much longer reactive staying power than the reaction of rhodopsin, combined with the fact that rods are 10+ times the number of ipRGCs, is the reason various embodiments disclosed herein use light wavelengths within the light wavelength ranges of 480nm + / - 30nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, 500nm + / - 30nm, 650nm + / - 30nm, and / or 700nm + / - 30nm. The lower level of 480nm + / - 30nm is to capture direct stimulation of melanopsin by ipRGCs and indirect stimulation of melanopsin by Rods.[000367] In certain embodiments, when generating dopamine in the eye or the brain via theeye light, the invention utilizes light wavelengths that strike the eye’s retina, which fall within at least one of the wavelength ranges of: 480nm + / - 30nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / -495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, 500nm + / - 30nm, 650nm + / - 30nm, or 700nm + / - 30nm which would include blue, bluish green and green wavelengths. These light wavelength ranges can be generated by light emitters, filtered optics or filtered lenses.[000368] In embodiments when light wavelengths are generated by way of filtered optics orfiltered lenses, the transmission peak of the wavelength range that strike the eye’s retina fall within one of the wavelength ranges of: 480nm + / - 30nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, 500nm + / - 30nm, 650nm + / - 30nm, or 700nm + / - 30nm.[000369] In embodiments when light wavelengths are generated by way of a light emitter(s)if in a dark room with no ambient lighting, the wavelength range that strike the eye’s retina fall within at least one of: 480nm + / - 30nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm,+ / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, 500nm + / - 30nm, 650nm + / - 30nm, or 700nm + / - 30nm.[000370] In embodiments when light wavelengths are generated by a light emitter(s) ifambient lighting is present (including that of artificial light or sun light) the blended light wavelengths of the light emitter(s) and also the ambient light comprises wavelengths of light thatstrike the eye’s retina fall within one of the wavelength ranges of at least one of: 480nm + / - 30nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, 500nm + / - 30nm, 650nm + / - 30nm, or 700nm + / - 30nm.[000371] It should be understood that when interpreting the embodiments utilized hereinunless total darkness is specified, it should be assumed that there is ambient light and thus the light wavelengths striking the retina are blended by the light from the light emitter and the ambient light. The same is true with a filtered optic or filtered lens. In most but not all cases the filtered optic or filtered lens is located 12+mm from the eye of the wearer unless the filtered optic or filtered lens is that of a contact lens or intraocular lens. An exception to this interpretation would be that of the use of a virtual reality device or a modified reality device whereby the device is sealed or mostly sealed from ambient light.[000372] Examples only of light emitters that emit light wavelengths which significantlyexcite melanopsin and rhodopsin in the retina of the human eye can be, by way of example only, Green LED light, Blue LED light, Cold White LED light, and / or Sunlight.[000373] In still other embodiments, light wavelength from either a filtered optic, filteredlens, and / or light emitter(s), that strikes the retina of the eye are selected so that the radiation peak of these wavelengths falls between the peak melanopsin sensitivity (480nm, and rhodopsin sensitivity (500nm)). Thus, the transmission peak of these wavelengths falls within the range of 480nm and 500nm.[000374] In certain embodiments when a filtered optic or filtered lens is used, the overalllight transmission through the filtered optic or filtered lens can be 50% or less, 40% or less, or 30% or less, while the light transmission within the predominant transmitted filtered wavelength range being transmitted to the eye can be 50% or more. In certain cases, the pupil of the eye enlarges when looking through the filtered optic or filtered lens and constricts when not looking through the filtered optic or filtered lens.[000375] In still other embodiments, the objective of ocular photo-bio-stimulation is toincrease the alertness of the individual being treated with ocular photo-bio-stimulation. When increasing alertness by way of ocular photo-bio-stimulation, blue light having wavelengths within the range of 450nm to 510nm can be utilized. In still other embodiments the objective of ocular photo-bio-stimulation is to increase the slowing down, to slow the progressing of, or to stopmyopia of the individual being treated with ocular photo-bio-stimulation. When slowing down or stopping myopia by way of ocular photo-bio-stimulation, blue light having wavelengths within the range of 450nm to 510nm, or red light within the wavelength range of 650nm + / - 30nm or 700nm + / - 30nm, can be utilized. Such ocular photo-bio-stimulation wavelengths can be applied to a large portion of the eye’s retina to stimulate the ipRGC ganglion cells and / or rods, or to the ganglion axons of the optic nerve head for the purposes of generating increased retinal dopamine.[000376] In still other embodiments, the objective of ocular photo-bio-stimulation is to treator correct a neurological abnormality of the individual being treated with the ocular photo-bio- stimulation. When correcting a neurological abnormality by way of ocular photo-bio-stimulation, blue light having wavelengths within the range of 450nm to 510nm can be utilized. Neurological abnormalities that may be treatable by ocular photo-bio-stimulation are by way of example only: Alzheimer’s, cognitive disorders, ADD, ADHD, depression, anxiety, and / or Parkinson’s disorder.[000377] In still other embodiments the objective of ocular photo-bio-stimulation is toprevent myopia from occurring with the individual being treated with the ocular photo-bio- stimulation. In still other embodiments the objective of ocular photo-bio-stimulation is to treat or correct an ocular abnormality of the individual being treated with ocular photo-bio-stimulation. When correcting an ocular abnormality, the use of the appropriate light wavelengths must be employed when treating with ocular photo-bio-stimulation. Ocular abnormalities that may be treatable by ocular photo-bio-stimulation are by way of example only: myopia, AMD, dry AMD, diabetic retinopathy, retinal degenerative disease, glaucoma, optic neuropathy, cataract, and / or meibomian gland disfunction leading to dry eye.[000378] In embodiments, biofeedback can be utilized to confirm that increased dopamineand / or serotonin is being produced within the brain of a patient having ocular photo-bio- stimulation therapy. Such biofeedback can be comparing one or more of: increased blink rate of the eye(s) of the patient being treated, increased diameter of pupil(s) of the patient being treated, increased heart rate, and / or increased body temperature of the wearer of the patient being treated comparted to that of a base line for the same activity prior to the ocular photo-bio-stimulation therapy.[000379] An embodiment for ocular photo-bio-stimulation can comprise modulation of theimage or light source. Such modulation can be within the range of 5Hz – 15Hz, 10Hz to 20Hz, or 40Hz + / - 20Hz.[000380] An embodiment can comprise a light source or light emitter having a light intensityof at least one of: 300 lux or greater, 400 lux or greater, 500 lux or greater, 1,000 lux or greater, or 5,000 lux or greater, or 10,000 lux or greater. As used herein, the sun is considered to be a light emitter. As used herein, various electronic devices or components, chemical-based devices or components, or electro-chemical devices or components that emit light are considered light emitters. As used herein, sunlight and artificial light each qualify as ambient light.[000381] An embodiment can comprise an ocular-photo-bio-stimulation time of 1 minute to 5minutes, 5 minutes to 30 minutes, or one hour or less. With certain embodiments of eyewear disclosed herein such an ocular-photo-bio-stimulation time can be that of normal daily wear of the eyewear. It has been found that the longer the ocular photo-bio-stimulation the eye becomes more sensitive to lower wavelengths of light, thus there is a shift in retinal sensitivity. It appears the retina becomes less sensitive and thus there is a shift in the direction towards melanopsin absorption curves from that of rhodopsin absorption curves. By way of example only, with one second of light stimulation the retina (which includes melanopsin, rhodopsin, and the cones opsins) is most sensitive at 510nm, for 10 seconds of continuous light stimulation the retina becomes most sensitive at 500nm, and for 100 seconds of continuous light stimulation the retina becomes most sensitive at 480nm. Age also affects the melanopsin absorption curves; at age 20 the peak sensitivity of melanopsin is 488nm and by age 80 the peak sensitivity if 503nm. So, while time of stimulation shifts the retinal sensitivity to the left and lower wavelengths, age shifts the sensitivity of melanopsin to the right.[000382] Biofeedback or diagnostics involving one or more of, pupil size increase, lid blinkrate increase, heart rate increase, and / or blood oxygen level increase, can be an indication of increased production or stimulation of dopamine or norepinephrine in the brain and in some cases serotonin. An increase in contrast sensitivity, B wave amplitude of an ERG, scleral thickening, and / or slowing of axial length eye growth, can indicate an increase in the production of dopamine in the retina.[000383] An embodiment can be that of a filtered lens or filtered optic or sunglass lens orsunglass optic that transmits a higher percentage of blue light and bluish green light wavelengths within the wavelength range of one or more of 480nm + / - 30nm or 530nm + / - 20nm than the lens or optic comprises an average visible light transmission percentage within the range of 380nm – 780nm and passes the ISO 12312-1 sunglass traffic light / signal test.[000384] An embodiment can be that of a filtered lens or filtered optic or sunglass lens orsunglass optic that transmits a higher percentage of blue light and bluish green light wavelengths within the wavelength range of one or more of 480nm + / - 30nm or 530nm + / - 20nm than the lens or optic comprises an average visible light transmission percentage within the range of 380nm – 780nm to qualify for category 2 or category 3 sunglasses and further passes the ISO 12312-1sunglass traffic light / signal test.[000385] An embodiment can be a filtered lens or filtered optic or sunglass lens or sunglassoptic that transmits 40% or greater percentage of blue light and bluish green light wavelengths within the wavelength range of one or more of 480nm + / - 30nm or 530nm + / - 20nm than the lens or optic comprises an average visible light transmission percentage within the range of 380nm – 780nm to qualify for category 2 or category 3 sunglasses and further passes the ISO 12312-1 sunglass traffic light / signal test.[000386] An embodiment can be a filtered lens or filtered optic or sunglass lens or sunglassoptic that transmits 40% or greater percentage of blue light and bluish green light wavelengths within the wavelength range of one or more of 480nm + / - 30nm or 530nm + / - 20nm than the lens or optic comprises an average visible light transmission percentage within the range of 380nm – 780nm to qualify for category 3 sunglasses and further passes the ISO 12312-1 sunglass traffic light / signal test.[000387] Electronic Devices for Ocular Photo-Bio-Modulation or Ocular Photo-Bio-Stimulation[000388] Ocular Photo-Bio-Stimulation Cell Phone Case[000389] FIG. 13 shows an embodiment of the current invention. It shows a cell phone case,which can comprise, among other things, enabling electronics and a blue lighted border that circumvents all or part of the cell phone. The lighted border of the cell phone case can be programmed for one or more light intensity, wavelength, modulation or flicker, start time, and / or end time. The cell phone case can comprise a sensor to measure the distance from a user to the case and the light intensity can be automatically or manually adjusted to provide that appropriate level of light intensity required for the ocular photo-bio-stimulation therapy.[000390] In certain embodiments the cell phone case comprises its own ocular photo-bio-stimulation light source. In other embodiments the cell phone or cell phone case can utilize the light given off by the flashlight of the cell phone. When the cell phone case utilizes the flashlightof the cell phone, the cell phone can comprise light pipes or waveguides. In certain embodiments the inside of the cell phone case is comprised of highly reflective material. The cell phone case can fit around part or all of the cell phone in such a manner whereby there is a space formed between the wall of the cell phone case and the side or sides of the cell phone that extends partially around or fully around the cell phone. Ocular photo-bio-stimulation light can be radiated from the light emitter or emitters through this space.[000391] In certain other embodiments the ocular photo-bio-stimulation light is emittedforward through the front thickness of one or more walls of the cell phone case. In still other embodiments the ocular photo-bio-stimulation light is emitted through the back of the cell phone case. In these embodiments the subject or patient must turn the cell phone case around when receiving ocular photo-bio-stimulation therapy.[000392] In embodiments, the electronic display screen or the housing device which housesthe electronic display screen can identify the distance from the eye of the user and can automatically adjust the intensity of the blue, green, or red-light border to be appropriate for such a distance. In a certain embodiment the electronic display screen or the housing of the electronic display screen can comprise a distance sensor and optionally facial recognition. In addition, the border light intensity can be adjusted automatically or manually depending upon the ambient lighting available in the room or space.[000393] The lighted border can comprise wavelengths within the range of one or more of:441nm or greater, 460nm + / - 20nm, 470nm + / - 20nm, 460nm – 520nm, or 480nm + / - 30nm. The ocular photo-bio-stimulation effect targeted can be one or more of (by way of example only), increased dopamine in the eye; the prevention of, slowing down of, or stopping of myopia; increasing dopamine in the brain; increasing alertness; and / or reducing depression severity.[000394] In certain embodiments a lighted border can comprise wavelengths of light withinthe range of 440nm to 700nm. The lighted border can be a white lighted border. The white light can comprise peaks of light wavelengths of: 460nm + / - 10nm, 525nm + / - 10nm, and / or 620nm + / - 10nm. The transmission peak of 460nm + / - 10nm can be greater than 80%. The transmission peak of 525nm + / - 10nm can be greater than 70%. The transmission peak of 620nm + / - 10nm can be greater than 60%. Such a white lighted border can provide ocular photo-bio-stimulation. The light intensity of lux given off from the lighted border can be 500 lux or more, 1,000 lux or more, 2,000 lux or more, and so on. When considering the light radiating in a cone light manner from thelighted border to strike the eye and face of the user or subject, the number of lumens given off from the lighted border can be 25 lumens or more, 50 lumens or more, 100 lumens or more, 200 lumens or more, and so on.[000395] In certain embodiments an electronic display can comprise wavelengths of lightwithin the range of 440nm to 700nm. The lighted border can be a white lighted border. The white light can comprise peaks of light wavelengths of 460nm + / - 10nm, 525nm + / - 10nm, and / or 620nm + / - 10nm. The transmission peak of 460nm + / - 10nm can be greater than 80%. The transmission peak of 525nm + / - 10nm can be greater than 70%. The transmission peak of 620nm + / - 10nm can be greater than 60%. Such a white lighted electronic display can provide ocular photo-bio- stimulation. The lighted border can comprise wavelengths of light within the range of 440nm to 700nm. The lighted border can be a white lighted border. The white light can comprise peaks of light wavelengths of 460nm + / - 10nm, 525nm + / - 10nm, and / or 620nm + / - 10nm. The transmission peak of 460nm + / - 10nm can be greater than 80%. The transmission peak of 525nm + / - 10nm can be greater than 70%. The transmission peak of 620nm + / - 10nm can be greater than 60%. Such a white lighted border can provide ocular photo-bio-stimulation. The light intensity of lux given off from the lighted border can be 500 lux or more, 1,000 lux or more, 2,000 lux or more, and so on. When considering the light radiating in a cone light manner from the lighted border to strike the eye and face of the user or subject, the number of lumens given off from the lighted border can be 25 lumens or more, 50 lumens or more, 100 lumens or more, 200 lumens or more, and so on.[000396] In certain embodiments an ocular photo-bio-stimulation light source can comprisewavelengths of light within the range of 440nm to 700nm. The lighted border can be a white lighted border. The white light can comprise peaks of light wavelengths of; 460nm + / - 10nm, 525nm + / - 10nm, and / or 620nm + / - 10nm. The transmission peak of 460nm + / - 10nm can be greater than 80%. The transmission peak of 525nm + / - 10nm can be greater than 70%. The transmission peak of 620nm + / - 10nm can be greater than 60%. Such a white lighted ocular photo- bio-stimulation light source can provide ocular photo-bio-stimulation. The light intensity of lux given off from the ocular photo-bio-stimulation light source can be 500 lux or more, 1,000 lux or more, 2,000 lux or more, and so on. When considering the light radiating in a cone light manner from the ocular photo-bio-stimulation light source to strike the eye and face of the user or subject,the number of lumens given off from the ocular photo-bio-stimulation light source can be 25 lumens or more, 50 lumens or more, 100 lumens or more, 200 lumens or more, and so on.[000397] Biofeedback or diagnostics involving one or more of, pupil size increase, lid blinkrate increase, heart rate increase, and / or blood oxygen level increase, can be an indication of increase production or stimulation of dopamine or norepinephrine in the brain and in some cases serotonin. An increase in contrast sensitivity, an increase in the B wave amplitude of an ERG, scleral thickening, and / or slowing of axial length eye growth, can indicate an increase in the production of dopamine in the retina.[000398] Embodiments when light wavelengths are generated by way of filtered optics orfiltered lenses, the transmission peak of the wavelength range that strike the eye’s retina falls within the wavelength range of at least one of: 480nm + / - 30nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, 500nm + / - 30nm, 650nm + / - 30nm, or 700nm + / - 30nm.[000399] In certain embodiments when the intensity of light wavelengths is adjusted by wayof filtered optics or filtered lenses, the transmission peak of the wavelength range that strikes the eye’s retina falls within the wavelength range of 450nm – 520nm.[000400] Embodiments when light wavelengths are generated by a light emitter(s) if ambientlighting is present (including that of artificial light or sun light) the blended light wavelengths of the light emitter(s) and also the ambient light comprises wavelengths of light that strike the eye’s retina falling within one of the wavelength ranges of at least one of: 480nm + / - 30nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, 500nm + / - 30nm, 650nm + / - 30nm, or 700nm + / - 30nm.[000401] In certain embodiments, when light wavelengths are generated by a light emitter(s),and if ambient lighting is present (including that of artificial light or sun light), the blended light wavelengths of the light emitter(s) and also the ambient light comprises wavelengths of light that strike the eye’s retina falling within one of the wavelength ranges of certain embodiments and / or the range of 450nm – 520nm.[000402] In certain embodiments, the range of wavelength band includes the peaks of themost sensitive spectral points of rhodopsin (500nm) and melanopsin (480nm). This way bothrhodopsin and melanopsin can be stimulated or excited. By way of example, by utilizing a filtered optic or lens, that predominantly transmits within the wavelength range of at least one of 460nm – 520nm or 470nm to 520nm, or by utilizing a light source or light emitter that predominately transmits within the wavelength range of at least one of 460nm- 520nm, 470nm to 520nm, or 480nm – 520nm. This would include blue, bluish green and green wavelengths. This can be most beneficial when stimulating the production of increased dopamine in the retina of an eye. This can be most beneficial when stimulating the production of increased dopamine in a brain by way of stimulating the retina of an eye.[000403] The light border can have an intensity of 300 lux or greater. The light border canhave an intensity of 400 lux or greater. The light border can have an intensity of 1,000 lux or greater. The light border can have an intensity of 5,000 lux or greater. The time of ocular photo- bio-stimulation treatment can be 5 minutes to 10 minutes. The time of ocular photo-bio- stimulation treatment can be 10 minutes to 30 minutes. The time of ocular photo-bio-stimulation treatment can be 30 minutes to 1 hour. The time of ocular photo-bio-stimulation treatment can be 30 minutes or more.[000404] The amount of required light intensity given off by an ocular photo-bio-stimulationartificial light source (not the sun) is dependent upon the distance of the light source from the eye of the subject receiving ocular photo-bio-stimulation treatment, the age of the subject, and whether or not the subject is wearing a eyeglass that either filters and / or refracts light. In most, but not all cases, for most handheld devices that give off ocular photo-bio-stimulation, the light intensity needs to be 60 lumens of more leaving the ocular photo-bio-stimulation light source. The preference is for 400 lux of ocular photo-bio-stimulation light or more to strike the retina of the eye of the subject for a period of time in order for the subject to have the desired physiological response.[000405] The lighted border can comprise wavelengths within the range of one of:wavelengths of 530nm + / - 10nm, 530nm + / - 15nm, 530nm + / - 20nm, or 500nm to 550nm. The ocular photo-bio-stimulation effect targeted can be one or more of (by way of example only), reduced pain severity, reduced frequency of headaches, and / or reduced frequency of migraines.[000406] The same embodiment can be provided for a red-light border within thewavelengths of 630nm + / - 20nm, 650nm + / - 30nm, or 650nm – 700nm or 700nm + / - 30nm. The ocular photo-bio-stimulation effect targeted can be that of one or more of (by way of exampleonly), increased mitochondrial health or mitochondrial numbers within the retina of the eye for the purposes of reducing the severity or improving a retinal disease / disorder, such as one or more (by way of example only), dry AMD, retinitis pigmentosa, and / or diabetic retinopathy. In certain cases, the red wavelength border light can also treat or help treat dry eye conditions whereby the tear layer evaporates too quickly.[000407] The border of treatment (e.g., blue light treatment) can appear for a certain timeinterval that can be programed or preset. The intensity of this blue light border can be adjustable or programed to a setting. The intensity can modulate. The intensity can be adjustable or fixed. The light wavelength can be adjusted or fixed. By way of example only, such a border can appear on one’s electronic display screen at 7:00am and remain there until 8:00am when it will disappear / stop. The blue light can cause the user of the electronic display to become more alert. The cell phone case border can act as a design feature allowing for different colored lights that can be programable during the day or at night. In most, but not all, cases, the lighted border is in the front periphery (that faces the user) of the cell phone case that surrounds the cell phone. The light can modulate or flicker. The light can be programable with regards to one or more of: light intensity, wavelength, modulation or flicker, start time, and / or end time. The light can modulate by way of example only, within the range of 5Hz to 15 Hz, 10Hz to 20Hz, or 40Hz + / - 20Hz.[000408] In another embodiment a cell phone case comprises the appropriate enablingelectronics and comprises a green light border. The green light can be comprised of wavelengths of green light, for example within the range of 480nm + / - 30nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm,500nm + / - 10nm, 500nm + / - 20nm, or 500nm + / - 30nm, 650nm + / -30nm, or 700nm + / - 30nm. The border of green light can appear for a certain time interval that can be programed or preset. The intensity of this green light border can be adjustable or programed to a setting. The intensity can modulate. The intensity can be adjustable or fixed. The light wavelength can be adjusted or fixed. By way of example only, such a border can appear on one’s electronic display screen at 7:00am and remain there until 8:00am when it will disappear. The green light can cause the user of the electronic display to have, by way of example only, reduced pain. The cell phone case border can act as a design feature allowing for different colored lights that can be programable during the day or at night. In most, but not all cases the lighted board is in the front periphery (that faces the user) of the cell phone case that surrounds the cell phone. The light can modulate or flicker. The light canbe programable with regards to one or more of: light intensity, wavelength, modulation or flicker, start time, and / or end time. In certain embodiments a diffuser can be placed over the light emitters. In certain embodiments a filter or filters are used so as to permit a higher concentration of wavelengths within the range of at least one of: 480nm + / - 30nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, 500nm + / - 30nm, 650nm + / - 30nm, or 700nm + / - 30nm, to be transmitted from the light source.[000409] In another embodiment a cell phone case comprises the appropriate enablingelectronics and comprises a red-light border. The red light can be comprised of wavelengths of red light, for example only, 660nm + / - 10nm or 650nm + / - 30nm. The border of red-light can appear for a certain time interval that can be programed or preset. The intensity of this red-light border can be adjustable or programed to a setting. The intensity can modulate. The light can modulate or flicker. The intensity can be adjustable or fixed. The light wavelength can be adjusted or fixed. By way of example only, such a border can appear at 10:00 pm and be turned off prior to the user when going to sleep. The red light can cause the user of the electronic display to become more relaxed before going to sleep. The cell phone case border can act as a design feature allowing for different colored lights that can be programable during the day or at night. In most, but not all cases the lighted board is in the front periphery (that faces the user) of the cell phone case that surrounds the cell phone. The light can be programable with regards to one or more of: light intensity, wavelength, modulation or flicker, start time, and / or end time.[000410] An embodiment can be that of a phone case that can provide ocular photo-bio-stimulation therapy, wherein a plurality of light emitters encircle part or all of the cell phone screen, wherein the ocular photo-bio-stimulation light emitters provide one or more light wavelengths within the range of at least one of: 480nm + / - 30nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / -495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, 500nm + / - 30nm, 650nm + / - 30nm, or 700nm + / - 30nm, wherein the plurality of light emitters are controllable, manually or automatically, with regards to one or more of: intensity, on and / or off time, and / or wavelengths band(s), and wherein the intensity of the ocular photo-bio-stimulation light can be automatically adjusted depending upon one or more of: distance from the face of the user or ambient light of theroom or space. The ocular photo-bio-stimulation light can comprise a timer to provide the appropriate level of ocular photo-bio-stimulation therapy.[000411] In certain embodiments the color of the ocular photo-bio-stimulation light can bealternated in a sequence. By way of example only green wavelengths, then blue green wavelengths, then blue wavelengths. In other embodiments, green wavelengths, then blue green wavelengths, then blue wavelengths, then white light. This can be done to maximize the stimulation effect of light wavelength versus time on retinal excitation. Said another way, first (for, in aspects, a short period of time) have the green light wavelengths excite the retina, then the bluish green wavelengths, and the longer the time period have the blue light wavelengths excite the retina. Thus, sequencing strong light intensity of green light wavelengths, then bluish green light wavelengths, and then blue light wavelengths, can provide for the maximum retinal stimulation. By way of example only, emit green for 1 – 5 seconds, emit bluish green for 10 – 60 seconds, then emit blue for 60 seconds, and so on… until the ocular photo-bio-stimulation is ceased.[000412] In certain embodiments the ocular photo-bio-stimulation light can modulate withinthe range of, one of: 5 Hz to 15 Hz, 10Hz to 20Hz, or 40Hz + / - 20Hz. In other embodiments the ocular photo-bio-stimulation light source cannot modulate and thus has zero Hz. In certain embodiments an invisible white light spectral flickering can occur. In certain embodiments by using blue light within the wavelength range of 480nm + / - 30nm and modulating at 40Hz + / - 10 Hz, it can result in a significant improvement of one or more of: depression, cognitive ability, alertness, and decision making of the user. However, visually 40Hz + / - 10Hz can be annoying and distracting for a user. In certain embodiments an invisible spectral flickering can occur. In certain other embodiments which reduces visual unpleasantness for the user, the ocular photo-bio- modulation light source can be modulated within the ranges between blue (450nm – 495nm) and bluish green / cyan (495nm – 520nm). In still other embodiments which reduce any visual unpleasantness, the ocular photo-bio-modulation light source can be modulated within the ranges between blue (450nm – 495nm) and green (495nm- 570nm). The ocular photo-bio-stimulation light can then stimulate, one or more of dopamine, serotonin, and / or norepinephrine in the brain. In certain embodiments by using blue light within the wavelength range of 480nm + / - 30nm and modulation or flickering between 5Hz and 15Hz, or between 10Hz and 12Hz, the invention can be used to stimulate production or increase the production of dopamine in the eye’s retina of the user.[000413] Ocular Photo-Bio-Stimulation Electronic Display Screen with ControllableLighted Border[000414] In certain embodiments a lighted border can comprise wavelengths of light withinthe range of 440nm to 700nm. The lighted border can be a white lighted border. The white light can comprise peaks of light wavelengths of; 460nm + / - 10nm, 525nm + / - 10nm, and / or 620nm + / - 10nm. The transmission peak of 460nm + / - 10nm can be greater than 80%. The transmission peak of 525nm + / - 10nm can be greater than 70%. The transmission peak of 620nm + / - 10nm can be greater than 60%. Such a white lighted border can provide ocular photo-bio-stimulation. The light intensity of lux given off from the lighted border can be one of, 500 lux or more, 1,000 lux or more, or 2,000 lux or more. When considering the light radiating in a cone light manner from the lighted border to strike the eye and face of the user or subject, the number of lumens given off from the lighted border can be one of, 25 lumens or more, 50 lumens or more, 100 lumens or more, or 200 lumens or more.[000415] In certain embodiments an electronic display can comprise wavelengths of lightwithin the range of 440nm to 700nm. The lighted border can be a white lighted border. The white light can comprise peaks of light wavelengths of; 460nm + / - 10nm, 525nm + / - 10nm, and / or 620nm + / - 10nm. The transmission peak of 460nm + / - 10nm can be greater than 80%. The transmission peak of 525nm + / - 10nm can be greater than 70%. The transmission peak of 620nm + / - 10nm can be greater than 60%. Such a white lighted electronic display can provide ocular photo-bio-stimulation. The lighted border can comprise wavelengths of light within the range of 440nm to 700nm. The lighted border can be a white lighted border. The white light can comprise peaks of light wavelengths of: 460nm + / - 10nm, 525nm + / - 10nm, and / or 620nm + / - 10nm. The transmission peak of 460nm + / - 10nm can be greater than 80%. The transmission peak of 525nm + / - 10nm can be greater than 70%. The transmission peak of 620nm + / - 10nm can be greater than 60%. Such a white lighted border can provide ocular photo-bio-stimulation. The light intensity of lux given off from the lighted border can be one of, 500 lux or more, 1,000 lux or more, or 2,000 lux or more. When considering the light radiating in a cone light manner from the lighted border to strike the eye and face of the user or subject, the number of lumens given off from the lighted border can be one of, 25 lumens or more, 50 lumens or more, 100 lumens or more, or 200 lumens or more.[000416] In certain embodiments an ocular photo-bio-stimulation light source can comprisewavelengths of light within the range of 440nm to 700nm. The lighted border can be a white lighted border. The white light can comprise peaks of light wavelengths of 460nm + / - 10nm, 525nm + / - 10nm, and / or 620nm + / - 10nm. The transmission peak of 460nm + / - 10nm can be greater than 80%. The transmission peak of 525nm + / - 10nm can be greater than 70%. The transmission peak of 620nm + / - 10nm can be greater than 60%. Such a white lighted ocular photo- bio-stimulation light source can provide ocular photo-bio-stimulation. The light intensity of lux given off from the ocular photo-bio-stimulation light source can be one of, 500 lux or more, 1,000 lux or more, or 2,000 lux or more. When considering the light radiating in a cone light manner from the ocular photo-bio-stimulation light source to strike the eye and face of the user or subject, the number of lumens given off from the ocular photo-bio-stimulation light source can be one of, 25 lumens or more, 50 lumens or more, 100 lumens or more, or 200 lumens or more.[000417] Biofeedback or diagnostics involving one or more of, pupil size increase, lid blinkrate increase, heart rate increase, and / or blood oxygen level increase, can be an indication of increase production or stimulation of dopamine or norepinephrine in the brain and in some cases serotonin. An increase in contrast sensitivity, B wave amplitude of an ERG, scleral thickening, and / or slowing of axial length eye growth, can indicate an increase in the production of dopamine in the retina.[000418] In reference to FIG. 14, in embodiments, the border of any electronic displayprovides a lighted ocular photo-bio-stimulation therapy border. Such an electronic display can be, by way of example only, one of cell phone display screen, tablet display screen, laptop computer display screen, desktop computer display screen, or television display screen. By way of example only, in certain embodiments the display can be programed to provide for an outer peripheral zone (the lighted border) that provides ocular photo-bio-stimulation wavelengths of light while the central zone provides visual content, which can be in form or illustrations, letters, numbers or visual images (motion or still). The ocular photo-bio-stimulation border light can be programable with regards to one or more of: light intensity, wavelength, modulation or flicker, start time, and / or end time. The light can modulate by way of example only, within the range of one of 5Hz to 15 Hz, 10Hz to 20Hz, or 40Hz + / - 20Hz. The display can comprise a sensor to measure the distance from a user to the display and the light intensity can be automatically or manually adjusted toprovide that appropriate level of light intensity required for the ocular photo-bio-stimulation therapy.[000419] The light border can have an intensity of 400 lux or greater. The light border canhave an intensity of 1,000 lux or greater. The light border can have an intensity of 5,000 lux or greater. The time of ocular photo-bio-stimulation treatment can be 5 minutes – 10 minutes. The time of ocular photo-bio-stimulation treatment can be 10 minutes to 30 minutes. The time of ocular photo-bio-stimulation treatment can be 30 minutes to 1 hour. The time of ocular photo-bio- stimulation treatment can be 30 minutes or more.[000420] In embodiments when light wavelengths are generated by way of filtered optics orfiltered lenses, the transmission peak of the wavelength range that strike the eye’s retina falls within the wavelength range of at least one of: 480nm + / - 30nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, 500nm + / - 30nm, or 650nm + / - 30nm or 700nm + / - 30nm.[000421] In embodiments when light wavelengths are generated by a light emitter(s) ifambient lighting is present (including that of artificial light or sun light), the blended light wavelengths of the light emitter(s) and also the ambient light comprise wavelengths of light that strike the eye’s retina, which fall within one of the wavelength ranges of at least one of: 480nm + / - 30nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, 500nm + / - 30nm, or 650nm + / - 30nm or 700nm + / - 30nm.[000422] By way of example only, when the border light is part of the lighted electronicdisplay, the electronic display can be programed for (by way of example only) 8:00am so that a peripheral lighted border, having a light intensity and light wavelength band, within the electronic display area shows up while the central (non-peripheral border) becomes smaller in overall size. And this lighted border can be programed to turn off at (for example only) 11:00 am so that the central zone which is displaying the content and image(s) for the electronic display increases back to its original size. In this embodiment the electronic display screen or the housing device which houses the electronic display screen can identify the distance from the eye of the user and can automatically adjust the intensity and size and shape of the blue, green, or red-light border to be appropriate for such a distance. In a certain embodiment the electronic display screen or thehousing of the electronic display screen comprises a distance sensor and optionally facial recognition. In addition, the border light intensity can be adjusted automatically or manually depending upon the ambient lighting available in the room or space. In certain embodiments a diffuser can be placed over the light emitters. In certain embodiments a filter or filters are used so to permit a higher concentration of wavelengths within the range of one of 480nm + / - 30nm, 530nm + / - 20nm, or 650nm + / - 30nm, to be transmitted from the light source.[000423] The lighted border can comprise wavelengths within the range of at least one of:480nm + / - 30nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, 500nm + / - 30nm, or 650nm + / - 30nm, or 700nm + / - 30nm. The ocular photo- bio-stimulation effect targeted can be one or more of (by way of example only), increased dopamine in the eye; prevention of myopia; slowing or stopping myopia; healing myopia; improving myopia diagnosis; increasing one or more of dopamine, serotonin or norepinephrine in the brain; increasing alertness; and / or reducing depression severity.[000424] The lighted border can comprise wavelengths within the range of at least one of:480nm + / - 30nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, 500nm + / - 30nm, or 650nm + / - 30nm, or 700nm + / - 30nm. The ocular photo-bio-stimulation effect targeted can be one or more of (by way of example only), reduced pain severity, reduced frequency of headaches, and / or reduced frequency of migraines.[000425] The same can be provided for a red-light border within the wavelengths 630nm + / -20nm or 650nm + / - 30nm, or 650nm – 700nm, or 700nm + / - 30nm. The ocular photo-bio- stimulation effect targeted can be one or more of (by way of example only), increased mitochondrial health or mitochondrial numbers within the retina of the eye for the purposes of reducing the severity or improving a retinal disease / disorder such as one or more (by way of example only), dry AMD, retinitis pigmentosa, and / or diabetic retinopathy. In certain cases, the red wavelength border light can also be of help with dry eye conditions whereby the tear layer evaporates too quickly by way of stimulating the lids meibomian glands.[000426] In certain embodiments the range of wavelength band includes the peaks of themost sensitive spectral points of rhodopsin (500nm) and melanopsin (480nm). This way both rhodopsin and melanopsin can be stimulated or excited. By way of example, by utilizing a filteredoptic or lens that predominantly transmits within the wavelength range of at least one of 460nm – 520nm or 470nm to 520nm, or by utilizing a light source or light emitter that predominately transmits within the wavelength range of at least one of 460nm to 520nm or 470nm to 520nm. This would include blue, bluish green and green wavelengths. This can be most beneficial when stimulating the production of increased dopamine in the retina of an eye. This can be most beneficial when stimulating the production of increased one or more of dopamine, serotonin or norepinephrine, in the brain by way of stimulating the retina of an eye.[000427] An embodiment can be of an electronic display screen, wherein the electronicdisplay screen comprises a programable ocular photo-bio-stimulation light border within the display screen, wherein the programable ocular photo-bio-stimulation light border provides one or more light wavelengths within the range of at least one of: 480nm + / - 30nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, 500nm + / - 30nm, 650nm + / - 30nm, or 700nm + / - 30nm, wherein the plurality of light emitters that generate the programable ocular photo-bio-stimulation light border are controllable, manually or automatically, with regards to one of intensity, on and / or off time, and / or wavelength band, and wherein one of the intensity of the ocular photo-bio-stimulation light border, or size of the ocular photo-bio- stimulation light border can be automatically adjusted depending upon one of distance from the face of the user or ambient light of the room or space. Further the programable border can be of any shape and can partially or fully surround a central area of the electronic display. The ocular photo-bio-stimulation light can comprise a timer to provide the appropriate level of ocular photo- bio-stimulation therapy.[000428] Another embodiment can be that of an lighted electronic display screen frame,wherein the electronic display screen frame comprises an ocular photo-bio-stimulation light border around the display screen, wherein the programable ocular photo-bio-stimulation light border provides one or more light wavelengths within the range of at least one of: 480nm + / - 30nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, 500nm + / - 30nm, 650nm + / - 30nm, or 700nm + / - 30nm, wherein the plurality of light emitters that generate the programable ocular photo-bio-stimulation light border are controllable, manually or automatically, with regards to one or more of intensity, on and / or off time, and / or wavelengthband, and wherein the intensity of the ocular photo-bio-stimulation light border is automatically adjusted depending upon one of distance from the face of the user or ambient light of the room or space. Further the programable border can be of any shape and can partially or fully surround a central area of the electronic display. The ocular photo-bio-stimulation light border can be one or more of, attachable to the display screen frame, attachable and detachable to the display screen frame, or built into and integral with the display screen frame.[000429] The light border can have an intensity of 300 lux or greater. The light border canhave an intensity of 400 lux or greater. The light can have an intensity of 1,000 lux or greater. The light can have an intensity of 5,000 lux or greater. The time of ocular photo-bio-stimulation treatment can be 5 minutes – 10 minutes. The time of ocular photo-bio-stimulation treatment can be 10 minutes to 30 minutes. The time of ocular photo-bio-stimulation treatment can be 30 minutes to 1 hour. The time of ocular photo-bio-stimulation treatment can be 30 minutes or more.[000430] Ocular Photo-Bio-Stimulation Electronic Display Screen with Fixed LightedBorder Edge[000431] In certain embodiments a lighted border can comprise wavelengths of light withinthe range of 440nm to 700nm. The lighted border can be a white lighted border. The white light can comprise peaks of light wavelengths of; 460nm + / - 10nm, 525nm + / - 10nm, and / or 620nm + / - 10nm. The transmission peak of 460nm + / - 10nm can be greater than 80%. The transmission peak of 525nm + / - 10nm can be greater than 70%. The transmission peak of 620nm + / - 10nm can be greater than 60%. Such a white lighted border can provide ocular photo-bio-stimulation. The light intensity of lux given off from the ocular photo-bio-stimulation light source can be one of, 500 lux or more, 1,000 lux or more, or 2,000 lux or more. When considering the light radiating in a cone light manner from the ocular photo-bio-stimulation light source to strike the eye and face of the user or subject, the number of lumens given off from the ocular photo-bio-stimulation light source can be one of, 25 lumens or more, 50 lumens or more, 100 lumens or more, or 200 lumens or more.[000432] In certain embodiments an electronic display can comprise wavelengths of lightwithin the range of 440nm to 700nm. The lighted border can be a white lighted border. The white light can comprise peaks of light wavelengths of; 460nm + / - 10nm, 525nm + / - 10nm, and / or 620nm + / - 10nm. The transmission peak of 460nm + / - 10nm can be greater than 80%. The transmission peak of 525nm + / - 10nm can be greater than 70%. The transmission peak of 620nm+ / - 10nm can be greater than 60%. Such a white lighted electronic display can provide ocular photo-bio-stimulation. The light intensity of lux given off from the ocular photo-bio-stimulation light source can be one of, 500 lux or more, 1,000 lux or more, or 2,000 lux or more. When considering the light radiating in a cone light manner from the ocular photo-bio-stimulation light source to strike the eye and face of the user or subject, the number of lumens given off from the ocular photo-bio-stimulation light source can be one of, 25 lumens or more, 50 lumens or more, 100 lumens or more, or 200 lumens or more.[000433] In certain embodiments an ocular photo-bio-stimulation light source can comprisewavelengths of light within the range of 440nm to 700nm. The lighted border can be a white lighted border. The white light can comprise peaks of light wavelengths of; 460nm + / - 10nm, 525nm + / - 10nm, and / or 620nm + / - 10nm. The transmission peak of 460nm + / - 10nm can be greater than 80%. The transmission peak of 525nm + / - 10nm can be greater than 70%. The transmission peak of 620nm + / - 10nm can be greater than 60%. Such a white lighted ocular photo- bio-stimulation light source can provide ocular photo-bio-stimulation. The light intensity of lux given off from the ocular photo-bio-stimulation light source can be one of, 500 lux or more, 1,000 lux or more, or 2,000 lux or more. When considering the light radiating in a cone light manner from the ocular photo-bio-stimulation light source to strike the eye and face of the user or subject, the number of lumens given off from the ocular photo-bio-stimulation light source can be one of, 25 lumens or more, 50 lumens or more, 100 lumens or more, or 200 lumens or more.[000434] In reference to FIG. 15, in certain embodiments, the border of any electronicdisplay provides a lighted ocular photo-bio-stimulation therapy border. The embodiment can be a normal viewing screen with programable content that can be shrunk down to allow for an ocular photo-bio-stimulation border to be provided. By way of example only, an embodiment can be a blue light border comprising light wavelengths within the wavelength range of 480nm + / - 30nm, with the media content being displayed centrally. Said another way the blue light border was fully or partially around the central media that was being displayed. The lighting provided can be automatic and timed to occur for certain periods of usage time or manually set by the user. It can be programed to provide desired light wavelength and intensity for providing ocular photo-bio- stimulation therapy. Such an electronic display can be, by way of example only, a cell phone display screen, tablet display screen, laptop computer display screen, desktop computer display screen, or television display screen. Such a lighted border can be that of a lighted frame itself thathouses the display, or a light that attaches to the display screen’s outer frame. The photo-bio- stimulation border light can be programable with regards to one or more of: light intensity, wavelength, modulation or flicker, start time, and / or end time. If the border light is fixed to the frame of the electronic display or built into the frame of the electronic display, the size of the border light will be of a fixed size. The ocular photo-bio-stimulation light can comprise a timer to provide the appropriate time for photo-bio-stimulation therapy [000435] In embodiments when light wavelengths are generated by way of filtered optics orfiltered lenses, the transmission peak of the wavelength range that strike the eye’s retina falls within the wavelength range of at least one of: 480nm + / - 30nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, 500nm + / - 30nm, 650nm + / - 30nm, or 700nm + / - 30nm. [000436] In embodiments when light wavelengths are generated by a light emitter(s) ifambient lighting is present (including that of artificial light or sun light), the blended light wavelengths of the light emitter(s) and also the ambient light comprise wavelengths of light that strike the eye’s retina, which fall within the wavelength ranges of at least one of: 480nm + / - 30nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / -edge or a frame that goes around the outer edge. In certain embodiments a diffuser can be placed over the light emitters. In certain embodiments a filter or filters are used so to permit a higher concentration of wavelengths within the range of one of 480nm + / - 30nm, 530nm + / - 20nm, or 650nm + / - 30nm, to be transmitted from the light source. The photo-bio-stimulation light can modulate. The photo-bio-stimulation light can be comprised of a plurality of light emitters. [000438] The lighted border can comprise wavelengths within the range of at least one of:441nm or greater, or 480nm + / - 30nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, 500nm + / - 30nm, 650nm + / - 30nm, or 700nm + / - 30nm. The ocular photo-bio-stimulation effect targeted can be one or more of (by way of example only),increased dopamine in the eye, prevention of myopia, slowing or stopping myopia, increasing dopamine in the brain, increasing alertness, and / or reducing depression severity.[000439] The lighted border can comprise wavelengths within the range of at least one of:480nm + / - 30nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, or 500nm + / - 30nm. The ocular photo-bio-stimulation effect targeted can be one or more of (by way of example only), reduced pain severity, reduced frequency of headaches, and / or reduced frequency of migraines.[000440] The same can be provided for a red-light border within the wavelengths 630nm + / -20nm or 650nm + / - 30nm, or 650nm – 700nm. The ocular photo-bio-stimulation effect targeted can be one or more of (by way of example only), increased mitochondrial health or mitochondrial numbers within the retina of the eye for the purposes of reducing the severity or improving a retinal disease / disorder such as one or more (by way of example only), dry AMD, retinitis pigmentosa, and / or diabetic retinopathy. In certain cases, the red wavelength border light can also be of help with dry eye conditions whereby the tear layer evaporates too quickly.[000441] In certain embodiments the range of wavelength band includes the peaks of themost sensitive spectral points of rhodopsin (500nm) and melanopsin (480nm). This way both rhodopsin and melanopsin can be stimulated or excited. By way of example, by utilizing a filtered optic or lens, that predominantly transmits within the wavelength range of 460nm – 520nm or 470nm to 520nm, or by utilizing a light source or light emitter that predominately transmits within the wavelength range of 460nm to 520nm, 470nm to 520nm, or 480nm – 520nm. This would include blue, bluish green and green wavelengths. This can be most beneficial when stimulating the production of increased dopamine in the retina of an eye. This can be most beneficial when stimulating the production of increased dopamine in a brain by way of stimulating the retina of an eye.[000442] In embodiments, to stimulate the production of serotonin and / or dopamine in thebrain, light wavelengths within the range of 700nm + / - 30nm can be utilized. Wavelengths of 710nm LED light has been shown to not have any detrimental effect on dopamine neurons in substantia nigra of the brain.[000443] By way of example only, utilizing a 2024 iPhone 16 the following would apply indetermining the border size needed to stimulate dopamine in the eye of the user and / or one or moreof dopamine, serotonin or norepinephrine in the brain. This assumes the iPhone is held 11 inches from the eye of a 12-year-old user, that the user is wearing clear glasses (no filter), and that the user’s eye is attenuating the blue light at a rate of 30% before striking the child’s retina, and upon striking the retina of the child’s eye the light does so with an intensity of 400 lux. The iPhone 16 maximum brightness of white light is 2,000 nits, thus 186 lumens. The size of iPhone 16 pro screen measures 66mm X 144mm or 9,504 square mm. That is ~0.02 lumens per square mm. Therefore, if 60 lumens of light intensity are needed to impart 400 lux or more on the retina of an eye. The need is for a minimum of 3,000 square mm of lumens coming off of the cell phone display. Therefore, to have a peripheral zone of the cell phone display, around text messages of 8mm X 144mm X 2 or two sides of screen = 2,304 square mm (vertically) and 8mm X (66m – 16mm or 50mm) X 2 for two sides of screen = 800mm (horizontally). The total square mm of a peripheral zone around the cell phone display of an iPhone 16 that is approximately 8mm wide would equal approximately 3,104 square mm. Thus, having an 8mm peripheral border of white light around the image or text on an iPhone 16 would appear to be sufficient for providing 60 + lumens of light, in this particular example only. That would leave 66mm – 16mm or 50mm by 144m – 16mm or 128mm. Thus, the screen size would be 50mm X 128mm for text, email, or games when the border appeared to provide light therapy.[000444] The time of stimulation of the retina can affect the retina sensitivity (which includesmelanopsin, rhodopsin, and cones’ opsin). The longer the time of ocular photo-bio-stimulation exposure the less sensitive the retina, which causes a shift of sensitivity to lower light wavelengths of light. By way of example, 1 second of exposure is most sensitive by the retina at 510nm; 10 seconds of exposure at 500nm; and / or 100 seconds of exposure at 480nm. In certain embodiments the color of the ocular photo-bio-stimulation light can be alternated in a sequence. By way of example only green wavelengths, then blue green wavelengths, then blue wavelengths. In other embodiments, green wavelengths, then blue green wavelengths, then blue wavelengths, then white light. This can be done to maximize the stimulation effect of light wavelength versus time on retinal excitation. Said another way, first (for a short period of time) have the green light wavelengths excite the retina, then the bluish green wavelengths, and the longer the time period have the blue light wavelengths excite the retina. Thus, sequencing strong light intensity of green light wavelengths, then bluish green light wavelengths, and then blue light wavelengths provides for the maximum retinal stimulation. By way of example only, green for 1 – 5 seconds, bluishgreen for 10 – 60 seconds, then blue for 60 seconds, and so on, until the ocular photo-bio- stimulation is ceased. While time of stimulation shifts the retinal sensitivity to the left and lower wavelengths, age shifts the sensitivity of melanopsin to the right.[000445] In certain embodiments, the ocular photo-bio-stimulation light can modulatewithin the range of at least one of: 5 Hz to 15 Hz, 10Hz to 20Hz, and / or 40Hz + / - 20Hz. In other embodiments the ocular photo-bio-stimulation light source cannot modulate and thus has zero Hz. In certain embodiments an invisible white light spectral flickering can occur. In certain embodiments by using blue light within the wavelength range of 480nm + / - 30nm and modulating at 40Hz + / - 10 Hz, the invention can result in a significant improvement in the subject’s improving one or more of: depression, cognitive ability, alertness, and decision making. However, visually 40Hz + / - 10Hz can be annoying and distracting for a user. In certain embodiments an invisible spectral flickering can occur. In certain other embodiments which reduce visual unpleasantness for the driver or user, the ocular photo-bio-modulation light source can be modulated within the ranges between blue (450nm – 495nm) and bluish green / cyan (495nm – 520nm). In still other embodiments which reduce visual unpleasantness, the ocular photo-bio- modulation light source can be modulated within the ranges between blue (450nm – 495nm) and green (495nm- 570nm). The ocular photo-bio-stimulation light can then stimulate, one or more of dopamine, serotonin, and / or norepinephrine in the brain. In certain embodiments by using blue light within the wavelength range of 480nm + / - 30nm and modulation or flickering between 5Hz and 15Hz, or between 10Hz and 12Hz, the invention can be used to stimulate production or increase the production of dopamine in the eye’s retina of the user.[000446] Ocular Photo-Bio-Stimulation Steering Wheel, dashboard, or instrument panelof a Vehicle.[000447] Ocular photo-bio-stimulation while driving, flying, or navigating a vehicle on land,sea, or air, can be used to increase alertness, improve cognitive ability, and speed decision-making. Ocular photo-bio-stimulation has been shown to increase one or more of dopamine, serotonin or norepinephrine in the brain. Biofeedback involving one or more of, pupil size increase, lid blink increase, heart rate increase, and / or blood oxygen level increase, can be an indication of increased production or stimulation of dopamine or norepinephrine in the brain and in some cases serotonin.[000448] The amount of required light intensity given off by an ocular photo-bio-stimulationartificial light source (not the sun) is dependent upon the distance of the light source from the eyeof the subject receiving ocular photo-bio-stimulation treatment, the age of the subject, and whether or not the subject is wearing an eyeglass that either filters or refracts light. In most, but not all cases, for light sources that give off ocular photo-bio-stimulation which are 12 inches away from the eye of the subject, the light intensity needs to be at least one of: 60 lumens of more, 80 lumens or more, or 100 lumens or more, leaving the ocular photo-bio-stimulation light source. By way of example only, if the ocular photo-bio-stimulation light source is located on or in the steering wheel, the number of lumens required of the light source would be less than if the ocular photo- bio-stimulation light source was located on or in the dashboard. The preference is for 400 lux of ocular photo-bio-stimulation light or more to strike the retina of the eye of the subject for a period of time in order for the subject to have the desired physiological response.[000449] Additionally, in certain embodiments, the ocular photo-bio-stimulation light canmodulate within the range of at least one of: 5 Hz to 15 Hz, 10Hz to 20Hz, or 40Hz + / - 20Hz. In other embodiments the light cannot modulate and thus has Zero Hz. By using blue light within the wavelength range of 480nm + / - 30nm and modulating at 40Hz + / - 10 Hz, the invention can result in a significant improvement in one or more of the subject’s mood, cognitive ability, alertness, and decision making. However, visually 40Hz + / - 10Hz can be annoying and distracting for a user or driver. In certain embodiments an invisible spectral flickering can occur. In certain other embodiments which reduces visual unpleasantness for the driver or user, the ocular photo-bio- modulation light source can be modulated within the ranges between blue (450nm – 495nm) and bluish green / cyan (495nm – 520nm). In still other embodiments which reduce visual unpleasantness, the ocular photo-bio-modulation light source can be modulated within the ranges between blue (450nm – 495nm) and green (495nm- 570nm). The ocular photo-bio-stimulation light can stimulate, one or more of dopamine, serotonin, or norepinephrine in the brain.[000450] In still other embodiments when the ocular photo-bio-stimulation light sourcecomes on it remains with a lower level of modulation (including zero modulation), however the steering wheel can vibrate at a modulation rate of 40 Hz+ / - 10Hz during the time of which ocular photo-bio-stimulation is occurring. The ocular photo-bio-stimulation light and vibration can then stimulate one or more of dopamine, or serotonin, norepinephrine in the brain. In certain embodiments the grip portion of the steering wheel is what vibrates, and in other embodiments the hub and the grip section vibrate. In other embodiments the steering wheel and the seat vibrate at 40 Hz + / - 10 Hz. In still other embodiments only the steering wheel vibrates at a modulation rate of40 Hz + / - 10 Hz without any ocular photo-bio-modulation for the purposes of one or more of, improving mood, increasing alertness, increasing cognitive ability, and speeding decision-making. And in still other embodiments the steering wheel and the seat vibrate at 40 Hz + / - 10Hz without any ocular photo-bio-stimulation.[000451] In still other embodiments when the ocular photo-bio-stimulation light sourcecomes on it remains with a lower level of modulation (including zero modulation), however the driver’s seat can vibrate at a modulation rate of 40 Hz + / - 10Hz during the time of which ocular photo-bio-stimulation is occurring. The ocular photo-bio-stimulation light and vibration can then stimulate, one or more of dopamine, serotonin, or norepinephrine in the brain. In certain embodiments the bottom of the seat (which the driver sits on) is what vibrates, and in other embodiments the bottom of the seat (which the driver sits on) and the seat back section vibrate. In other embodiments the driver’s seat vibrates, and the ocular photo-bio-stimulation occurs at 40 Hz + / - 10 Hz. In still other embodiments only the driver’s seat vibrates at a modulation rate of 40 Hz + / - 10 Hz without any ocular photo-bio-modulation for the purposes of one or more of increasing alertness, increasing cognitive ability, and speeding decision-making. And in still other embodiments the driver’s seat and the steering wheel vibrate at 40 Hz + / - 10Hz without any ocular photo-bio-stimulation.[000452] In certain embodiments an ocular photo-bio-stimulation light source can comprisewavelengths of light within the range of 440nm to 700nm. The white light can comprise peaks of light wavelengths of; 460nm + / - 10nm, 525nm + / - 10nm, and / or 620nm + / - 10nm. The transmission peak of 460nm + / - 10nm can be greater than 80%. The transmission peak of 525nm + / - 10nm can be greater than 70%. The transmission peak of 620nm + / - 10nm can be greater than 60%. Such a white lighted ocular photo-bio-stimulation light source can provide ocular photo-bio- stimulation. The light intensity of lux given off from the ocular photo-bio-stimulation light source can be one of, 500 lux or more, 1,000 lux or more, or 2,000 lux or more. When considering the light radiating in a cone light manner from the ocular photo-bio-stimulation light source to strike the eye and face of the user or subject, the number of lumens given off from the ocular photo-bio- stimulation light source can be one of, 50 lumens or more, 100 lumens or more, or 200 lumens or more. The light emitter(s) can be covered by a diffuser. The light emitters can be without a diffuser.[000453] In reference to FIG. 16, embodiments include an ocular photo-bio-stimulationapproach that can be implemented to keep a driver of a vehicle alert when driving day or night.The embodiment can be that of a system that comprises an ocular photo-bio-stimulation light source, a steering wheel or a portion of a steering wheel, one or more sensors, electronics, and optional artificial intelligence (AI). In certain other embodiments the system can also include vibration of the steering wheel, use of the radio, and an optional personal assistant.[000454] An ocular photo-bio-stimulation light source can be attached to or incorporated witha portion of the steering wheel having wavelengths of light within the wavelength range of one or more of, 480nm + / - 30nm (blue and blue green), 530nm + / - 20 nm (green), and / or 650nm + / - 30nm (red). The ocular photo-bio-stimulation light source can provide a light intensity of 250 lux or more, 500 lux or more, 1,000 lux or more, or 2,000 lux or more. The ocular photo-bio- stimulation light source can provide a light intensity of 50 lumens or more, 100 lumens or more, 250 lumens or more, or 500 lumens or more. The light striking the retina of the eye of the driver can be 300 lux or more, 400 lux or more, or 500 lux or more. Ocular photo-bio-stimulation has been shown to stimulate one or more of dopamine, serotonin or norepinephrine in the brain.[000455] The ocular photo-bio-stimulation light source can be attachable, detachable, orpermanently built into a steering wheel. The ocular photo-bio-stimulation light source can be built into the rim or grip section of a steering wheel. The ocular photo-bio-stimulation light source can be attached to the rim or grip section of a steering wheel. The ocular photo-bio-stimulation light source can be built into a portion of the central or hub portion of a steering wheel. The ocular photo-bio-stimulation light source can be attached to the central or hub portion of a steering wheel. The ocular photo-bio-stimulation light source can be built into a portion of the dashboard of a vehicle. The ocular photo-bio-stimulation light source can be attached to portion of the dashboard of a vehicle. The system can comprise its own power source. The system can utilize the electrical power of the automobile.[000456] The ocular photo-bio-stimulation light source or its light emitter(s) can be manuallyor automatically adjustable so as to be pointed or angled upward such that an imaginary straight line can be drawn from the center of a light emitter directly entering the pupil of the driver’s eye. It is important that the light rays from ocular photo-bio-stimulation light source are not blocked by the upper lids of the driver.[000457] The ocular photo-bio-stimulation light source can be programed to come on after atimed period of driving. It can be timed to remain on for a timed period. The control can be automatic or manual. The light can be modulated or flicker when being used if desired. The ocularphoto-bio-stimulation effect targeted is, in aspects, increased alertness of the driver, improved cognitive ability, faster decision making and faster reaction time. The ocular photo-bio-stimulation light source can comprise a sensor to measure the distance from a user to the ocular photo-bio- stimulation light source and the light intensity can be automatically or manually adjusted to provide that appropriate level of light intensity required for the ocular photo-bio-stimulation effect based upon at any given time the distance of the driver’s eyes from the ocular photo-bio- stimulation light source.[000458] The steering wheel can comprise sensors to determine if the driver is becoming lessalert. The dashboard can comprise sensors to determine if the driver is becoming less alert. The automobile or vehicle can comprise sensors to determine if the driver is becoming less alert. Should the sensors detect that the driver is becoming less alert or falling asleep, the sensors can cause the ocular photo-bio-stimulation light source to automatically turn on or change. In some embodiments the sensors can also cause the steering wheel to vibrate. In still other embodiments the sensors can also cause the horn to sound.[000459] In still other embodiments the sensors can also cause a personal assistant to orallyby way of the radio, in aspects, to wake up and / or pull over. In certain embodiments facial recognition within the automobile or vehicle can learn and identify the driver’s identity and sense the amount of drive time when the specific driver becomes less alert. Thus, in this embodiment, the automobile or vehicle will know in advance certain driving habits of the driver and will then turn on and off the ocular photo-bio-stimulation light source in accordance with those learned driving habits or experiences of the driver. Artificial intelligence (AI) and ML can be incorporated within the embodiment to optimize the desired physiological effect for the driver.[000460] Biofeedback or diagnostics involving one or more of, pupil size increase, lid blinkrate increase, heart rate increase, and / or blood oxygen level increase, can be an indication of increase production or stimulation of dopamine or norepinephrine in the brain and in some cases serotonin. An increase in contrast sensitivity, B wave amplitude of an ERG, scleral thickening, and / or slowing of axial length eye growth indicates an increase in the production of dopamine in the retina.[000461] Such an ocular photo-bio-stimulation approach can be that of utilizing a blue, bluishgreen, or green light emitter(s), having one or more blue wavelengths within the range of 480nm + / - 30nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm,495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, or 500nm + / - 30nm. Such a light can be built into, by way of example only, the steeringor instrument panel of the vehicle, such as directly in front of the steering wheel. In embodiments a sensor can identify the distance from the eye of the user and can automatically adjust the intensity of the blue light to be appropriate for such a distance. [000462] In embodiments when light wavelengths are generated by way of filtered optics orfiltered lenses, the transmission peak of the wavelength range that strike the eye’s retina falls within the wavelength range of at least one of: 480nm + / - 30nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, 500nm + / - 30nm, 650nm + / - 30nm, or 700nm + / - 30nm. [000463] In embodiments when light wavelengths are generated by a light emitter(s) ifambient lighting is present (including that of artificial light or sun light), the blended light wavelengths of the light emitter(s) and also the ambient light comprises wavelengths of light that strike the eye’s retina fall within one of the wavelength ranges of at least one of: 480nm + / - 30nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / -500nm + / - 30nm, 650nm + / - 30nm, or 700nm + / - 30nm. [000464] In addition, the blue light intensity can be automatically or manually adjusteddepending upon the ambient lighting available within the vehicle (or outside the vehicle). Further, the time for the lighted ocular photo-bio-stimulation stimulation can be set manually or automatically for the driver of the car. In certain embodiments facial recognition can be utilized. By way of example only, the blue light can be programmed to turn on after a driver has driven for one hour and can remain on for 30 minutes. It further can be programmed (by way of example only) to come on every hour and off every hour. The light can also be programmed to modulate or flicker. In addition, vibration and or sound can be programmed to occur at certain intervals when the blue light is either on or off. The light can be further programmed to turn on if the car senses the driver is not alert. In certain embodiments a diffuser can be placed over the light emitters. In certain embodiments a filter or filters are used to permit a higher concentration of wavelengths within the range of 480nm + / - 30nm to be transmitted from the light source. Artificial intelligence(AI) and ML can be incorporated within the embodiment to optimize the desired physiological effect for the driver.[000465] The light can have an intensity of 300 lux or greater. The light can have an intensityof 400 lux or greater. The light can have an intensity of 1,000 lux or greater. The light can have an intensity of 5,000 lux or greater. The time of ocular photo-bio-stimulation treatment can be 5 minutes – 10 minutes. The time of ocular photo-bio-stimulation treatment can be 10 minutes to 30 minutes. The time of ocular photo-bio-stimulation treatment can be 30 minutes to 1 hour. The time of ocular photo-bio-stimulation treatment can be 30 minutes or more. The light can modulate. The light can flicker. The light can modulate within the range of one of 5 Hz to 15 Hz, 10Hz to 20Hz, or 40Hz + / - 20Hz.[000466] An embodiment can be that of an ocular photo-bio-stimulation light within avehicle, wherein the ocular photo-bio-stimulation light provides blue wavelengths of light predominantly within the wavelength range of 480nm + / - 30nm, and wherein one of, the intensity of the ocular photo-bio-stimulation light, or the size or location of the ocular photo-bio-stimulation light, is automatically adjusted depending upon one of distance from the face of the user or ambient light of the vehicle (and / or outside the vehicle). The ocular photo-bio-stimulation light can comprise a timer to provide the appropriate level of ocular photo-bio-stimulation therapy.[000467] An embodiment of the invention which can be utilized to improve the alertness ofany pilot, driver, or steerer of a vehicle, and can be a system that employs blue, bluish green or green light of the wavelengths predominantly within the range of 480nm + / - 30nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, or 500nm + / - 30nm, and wherein the blue light strikes the retina of the eye(s) of the pilot, driver, or steerer of the vehicle, is hereby disclosed. Such a vehicle can be that of any vehicle, for example only, car, automobile, truck, bus, subway, trolley, tram, train, aircraft, spaceship, boat, ocean liner, cargo ship, or ship. The blue light can be releasably attachable and detachable to the steering wheel or integrated into the steering wheel. The blue light can paint the retinas of the wearer’s eyes as the steering wheel is rotated or turned while driving. The blue light can be releasably attachable and detachable to the dashboard or integrated into the dashboard. The blue light emitter can be any light emitter that emits blue light predominantly within the wavelength range of 450nm to 510nm or 480nm + / - 30nm. The blue lights can be programed to turn on automatically when the pilot,driver, or steerer of the vehicle shows signs of fatigue. The blue lights can be turned on manually when the pilot, driver, or steerer of the vehicle feels signs of fatigue. The blue lights can be modulated to turn on for X period of time and turn off for Y period of time. The lights can be set to turn on for, by way of example, only 2 minutes every 2 hours of driving time and then turned off until it is time for them to be turned on. This timing sequence can be set manually by the driver or automatically programmed. The intensity of the blue lights can become brighter during daytime and less bright during nighttime. The lights can be controlled by a dimmer or programed to maintain a certain intensity depending upon ambient light in the vehicle. The blue lights can be manually adjusted towards the eyes of pilot, driver, or steerer of the vehicle. Artificial intelligence (AI) can be incorporated within the embodiment to optimize the desired physiological effect for the driver.[000468] While the above discusses using blue light predominantly within the wavelengthrange of 450nm – 510nm, red light within the wavelength range of 650nm + / - 30nm or 700nm + / - 30nm.can be used in place of the blue light, or a combination of blue light and red-light wavelengths predominantly within the range of 450nm – 510nm and of 650nm + / - 30nm can be utilized. This is due to the fact that the light wavelengths predominantly within the ranges of450nm – 500nm, of 650nm – 700nm, or of 700nm + / - 30nm, produce dopamine and increasealertness. In certain cases, for morning hours the blue light of wavelengths predominantly within the range of 450nm to 500nm are used and for afternoon hours red light predominantly within the wavelength ranges of 620nm – 700nm or of 700nm + / - 30nm are used.[000469] The steering wheel can comprise one or more pressure sensor(s) such that when thepilot, driver, or steerer feels tired or desires to manually set such a hand pressure sensitive system, it can be set to the pressure threshold as desired by the pilot, driver, or steerer. So long as the pilot, driver, or steerer exerts the set hand pressure, the system (within certain limits) will function as if it is dormant, however, should the pressure become relaxed, and an established relaxed pressure threshold become met, an alert system within the car can cause the driver to become more awake or alert. Such a system can use, by way of example only, sound, light, electrical shock, and / or vibration to increase the alertness of the pilot, driver, or steerer. In certain embodiments for use with blue lighting of the wavelengths within the range of 450nm – 510nm for a vehicle as disclosed above, or for the steering wheel pressure system disclosed, a vision system can also be utilized to further identify the lack of alertness on the part of the pilot, driver, or steerer. In certainother embodiments for use with red lighting of the wavelengths within the range of 650nm + / - 30nm for a vehicle as disclosed herein, or for the steering wheel pressure system disclosed, a vision system can also be utilized to further identify the lack of alertness on the part of the pilot, driver, or steerer. Artificial intelligence (AI) can be incorporated within the embodiment to optimize the desired physiological effect for the driver.[000470] Ocular Photo-Bio-Stimulation Light, Lamp or Light Box[000471] In certain embodiments an ocular photo-bio-stimulation light source can comprisewavelengths of light within the range of 440nm to 700nm. The lighted border can be a white lighted border. The white light can comprise peaks of light wavelengths of 460nm + / - 10nm, 525nm + / - 10nm, and / or 620nm + / - 10nm. The transmission peak of 460nm + / - 10nm can be greater than 80%. The transmission peak of 525nm + / - 10nm can be greater than 70%. The transmission peak of 620nm + / - 10nm can be greater than 60%. Such a white lighted ocular photo- bio-stimulation light source can provide ocular photo-bio-stimulation. The light intensity of lux given off from the ocular photo-bio-stimulation light source can be one of, 500 lux or more, 1,000 lux or more, 2,000 lux or more, 5,000 lux or more, or 10,000 lux or more. When considering the light radiating in a cone light manner from the ocular photo-bio-stimulation light source to strike the eye and face of the user or subject, the number of lumens given off from the ocular photo-bio- stimulation light source can be one of, 10 lumens or more, 25 lumens or more, 50 lumens or more, 100 lumens or more, or 200 lumens or more.[000472] In reference to FIG. 17, embodiments include an ocular photo-bio-stimulationtherapy lamp, wherein the ocular photo-bio-stimulation therapy lamp comprises an ocular photo- bio-stimulation light(s), wherein the lamp can be programable, wherein the lamp can provide one or more light wavelengths within the range of at least one of: 480nm + / - 30nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, 500nm + / - 30nm, 650nm + / - 30nm, or 700nm + / - 30nm, wherein one or a plurality of light emitters that generate the programable ocular photo-bio-stimulation light or lamp can be controllable, manually or automatically, with regards to one or more of intensity, on and / or off time, and / or wavelength band, and wherein the intensity of the ocular photo-bio-stimulation therapy lamp’s light or lamp can be automatically adjusted depending on distance from the face of the user or ambient light of the room or space. The light or lamp can comprise a distance sensor. The ocular photo-bio-stimulation light or lamp can be comprised of one light emitter or a plurality of light emitters. The ocular photo-bio-stimulation light source can increase the production of dopamine in the eye and / or one or more of dopamine, serotonin or norepinephrine in the brain. [000473] Embodiments when light wavelengths are generated by way of filtered optics orfiltered lenses the transmission peak of the wavelength range that strike the eye’s retina falls within the wavelength range of at least one of 480nm + / - 30nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, 500nm + / - 30nm, or 650nm + / - 30nm, orare aambient lighting is present (including that of artificial light or sun light), the blended light wavelengths of the light emitter(s) and also the ambient light comprises wavelengths of light that strike the eye’s retina fall within wavelength ranges of at least one of: 480nm + / - 30nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, 500nm + / - 30nm, or 650nm + / - 30nm, or 700nm + / - 30nm. [000475] In certain embodiments the range of wavelength band includes the peaks of themost sensitive spectral points of rhodopsin (500nm) and melanopsin (480nm). This way both rhodopsin and melanopsin can be stimulated or excited. By way of example, this can be accomplished by utilizing a filtered optic or lens, which predominantly transmits within the wavelength range of at least one of 460nm – 520nm or 470nm to 520nm, and / or by utilizing a light source or light emitter that predominately transmits within the wavelength range of at least one of 460nm- 520nm, 470nm to 520nm, or 480nm to 520nm. This would include blue, bluish green and green wavelengths. This can be most beneficial when stimulating the production of increased dopamine in the retina of an eye. This can be most beneficial when stimulating the production of or increasing one or more of dopamine, serotonin or norepinephrine in the brain, by way of stimulating the retina of an eye. [000476] The light or lamp can have an intensity of 300 lux or greater. The light or lamp canhave an intensity of 400 lux or greater. The light can have an intensity of 1,000 lux or greater. The light can have an intensity of 5,000 lux or greater. The time of ocular photo-bio-stimulation treatment can be 1minute – 5 minutes, 5 minutes – 10 minutes. The time of ocular photo-bio-stimulation treatment can be 10 minutes to 30 minutes. The time of ocular photo-bio-stimulation treatment can be 30 minutes to 1 hour. The time of ocular photo-bio-stimulation treatment can be 30 minutes or more. The light can flicker. The light can modulate. The light can modulate, by way of example only, within the range of one of 5Hz and 15Hz, 10Hz to 20Hz, or 40Hz + / - 20Hz. In certain embodiments the light source has zero Hz (no modulation).[000477] In embodiments, the ocular photo-bio-stimulation light or lamp can identify thedistance from the eye of the user and can automatically adjust the intensity of the blue, green, or red-light to be appropriate for such a distance. In a certain embodiment the ocular photo-bio- stimulation light or lamp comprises a distance sensor and optionally facial recognition. In addition, the light intensity can be adjusted automatically or manually depending upon the ambient lighting available in the room or space. In certain embodiments a diffuser can be placed over the light emitters. In certain embodiments a filter or filters are used so as to permit a higher concentration of wavelengths within the range of at least one of: 480nm + / - 30nm, 480nm + / - 20nm, 500nm + / - 30nm, 500nm + / - 20nm, 510nm + / - 30nm, 510nm + / - 20nm, 530nm + / - 20nm, 650nm + / - 30nm490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, 500nm + / - 30nm, or 650nm + / - 30nm, or 700nm + / - 30nm, to be transmitted from the light source. The ocular photo-bio-stimulation light or lamp can modulate or flicker. The ocular photo-bio-stimulation light or lamp can comprise a timer to provide the appropriate level of ocular photo-bio-stimulation therapy.[000478] The ocular photo-bio-stimulation light or lamp can comprise wavelengths withinthe range of 441nm or greater, or 480nm + / - 30nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, 500nm + / - 30nm, or 650nm + / - 30nm, or 700nm + / - 30nm. The ocular photo-bio-stimulation effect targeted can be one or more of (by way of example only), increased dopamine in the eye, prevention of myopia, slowing or stopping myopia, increasing or one or more of dopamine, serotonin or norepinephrine in the brain, increasing alertness, and / or reducing depression severity.[000479] The ocular photo-bio-stimulation light or lamp can comprise wavelengths withinthe range of 530nm + / - 10nm, or 530nm + / - 15nm, or 530nm + / - 20nm, or 500nm to 550nm. Theocular photo-bio-stimulation effect targeted can be one or more of (by way of example only), reduced pain severity, reduced frequency of headaches, and / or reduced frequency of migraines.[000480] The ocular photo-bio-stimulation light or lamp can comprise wavelengths withinthe range of 630nm + / - 20nm or 650nm + / - 30nm, or 650nm – 700n or 700nm + / - 30nm. Theocular photo-bio-stimulation effect targeted can be one or more of (by way of example only), increased mitochondrial health or mitochondrial numbers within the retina of the eye for the purposes of reducing the severity or improving a retinal disease / disorder such as one or more (by way of example only), dry AMD, retinitis pigmentosa, and / or diabetic retinopathy. In certain cases, the ocular photo-bio-stimulation light or lamp can also be of help with dry eye conditions whereby the tear layer evaporates too quickly.[000481] In certain embodiments the ocular photo-bio-stimulation light can modulate withinthe range of, one of: 5 Hz to 15 Hz, 10Hz to 20Hz, or 40Hz + / - 20Hz. In other embodiments the ocular photo-bio-stimulation light source cannot modulate and thus has zero Hz. In certain embodiments an invisible white light spectral flickering can occur. In certain embodiments by using blue light within the wavelength range of 480nm + / - 30nm and modulating at 40Hz + / - 10 Hz, the invention can result in a significant improvement of one or more of: depression, cognitive ability, alertness, and decision making of the user. However, visually 40Hz + / - 10Hz can be annoying and distracting for a user. In certain embodiments an invisible spectral flickering can occur. In certain other embodiments which reduce visual unpleasantness for the user the ocular photo-bio-modulation light source can be modulated within the ranges between blue (450nm – 495nm) and bluish green / cyan (495nm – 520nm). In still other embodiments which reduce visual unpleasantness the ocular photo-bio-modulation light source can be modulated within the ranges between blue (450nm – 495nm) and green (495nm- 570nm). The ocular photo-bio- stimulation light can then stimulate, one or more of dopamine, serotonin, or norepinephrine in the brain. In certain embodiments by using blue light within the wavelength range of 480nm + / - 30nm and modulation or flickering between 5Hz and 15Hz, or between 10Hz and 12Hz, the invention can be used to stimulate production or increase the production of dopamine in the eye’s retina of the user.[000482] Eyewear and Optics for Providing Ocular Photo-Bio-Stimulation[000483] In certain embodiments, an ocular photo-bio-stimulation light source can comprisewavelengths of light within the range of 440nm to 700nm. The lighted border can be a whitelighted border. The white light can comprise peaks of light wavelengths of 460nm + / - 10nm, 525nm + / - 10nm, and / or 620nm + / - 10nm. The transmission peak of 460nm + / - 10nm can be greater than 80%. The transmission peak of 525nm + / - 10nm can be greater than 70%. The transmission peak of 620nm + / - 10nm can be greater than 60%. Such a white lighted ocular photo- bio-stimulation light source can provide ocular photo-bio-stimulation. The light intensity of lux given off from the ocular photo-bio-stimulation light source can be one of, 250 lux or more, 500 lux or more, 1,000 lux or more, or 2,000 lux or more. When considering the light radiating in a cone light manner from the ocular photo-bio-stimulation light source to strike the eye and face of the user or subject, the number of lumens given off from the ocular photo-bio-stimulation light source can be one of, 10 lumens or more, 25 lumens or more 50 lumens or more, or 100 lumens or more.[000484] Eyewear embodiments for ocular photo-bio-stimulation can comprise a lens or opticthat permits a wearer to view an image, wherein certain light wavelengths that pass from the eyewear or the optic stimulates dopamine or serotonin of the wearer, wherein certain of the light wavelengths are of the blue light, and wherein the highest concentration of blue, bluish green, or green light, that reach the eye of the wearer falls within the wavelengths range of 480nm + / - 30nm, 450nm – 520nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, or 500nm + / - 30nm, and wherein light wavelengths are filtered or blocked so to cause the overall light transmission of the lens or optic to be less than 50%. Blue, bluish green, green light radiation wavelengths can be within the range of 480nm + / - 30nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, or 500nm + / - 30nm, and can increase alertness and concentration, by way of example, upon waking in the morning or during the day when tired and less alert. This occurs by way of increasing dopamine production. In other embodiments wavelengths within the range of 650nm + / - 30nm or 650nm - 700nm, or 700nm + / - 30nm, can be used. It is further known that low levels of dopamine can be associated, by way of example only, with ADHD, myopia and Parkinson disease. The ocular photo-bio-stimulation light source can increase the production of dopamine in the eye and / or one or more of dopamine, serotonin or norepinephrine in the brain.[000485] Embodiments providing ocular photo-bio-stimulation can filter or block damaginghigh energy blue light, UV, and reduce bright light visual discomfort.[000486] Embodiments when light wavelengths are generated by way of filtered optics orfiltered lenses the transmission peak of the wavelength range that strike the eye’s retina falls within the wavelength range of at least one of: 480nm + / - 30nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, 500nm + / - 30nm, or 650nm + / - 30nm, or 700nm + / - 30nm.[000487] Embodiments when light wavelengths are generated by a light emitter(s) if ambientlighting is present (including that of artificial light or sun light) the blended light wavelengths of the light emitter(s) and also the ambient light comprises wavelengths of light that strike the eye’s retina fall within one of the wavelength ranges of 480nm + / - 30nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, 500nm + / - 30nm, or 650nm + / - 30nm, or 700nm + / - 30nm.[000488] In other embodiments for ocular photo-bio-stimulation, the eyewear or optic cancomprise green light within the range of 480nm + / - 30nm, 450nm – 520nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, or 500nm + / - 30nm. Green light wavelengths can, in aspects, reduce the sensation of pain. In still other embodiments the eyewear or an optic can comprise red light within the range of 660nm + / - 20nm, 650nm + / - 30nm, or 600nm to 700nm. Red light wavelengths within the range of 660nm + / - 20nm, 600nm to 700nm, or 700nm + / - 30nm, can be soothing, calming and relaxing to the brain, thereby assisting with (by way of example) going to sleep. The eyewear and / or optic can be any type of eyewear or optic known to one of ordinary skill in the art. The eyewear and / or optic can be disposable. The eyewear and / or optic can be an insert that can be inserted or attached to existing eyewear. In most, but not all cases, the insert is positioned behind the corrective eyeglass lenses and is supported by the eye glass frame (see FIGs.18, 19A, 19B, 19C, 19E, and 19F). The eyewear and / or optic can be a component that is removable or permanently attached to existing eyewear. As used herein an optic can be a lens. A lens can be an optic. A lens or optic can comprise optical power. A lens or optic can comprise no optical power. As used herein an optic can be any item that transmits light, such as a lens, flat sheetof transparent plastic or glass, film, light diffuser, window, etc., as would be understood by one of ordinary skill in the art.[000489] The optic can comprise a single bandpass filter to provide for the transmission ofthe desired light wavelengths. The optic can comprise a double bandpass filter to provide for the transmission of the desired light wavelengths. The level of transmission of light to the eye’s retina used in the various embodiments disclosed herein can be provided at one of scotopic, mesopic, and / or photopic light levels. In embodiments the light level is above 400 lux and is in the higher end of mesopic and most of the time photopic.[000490] In embodiments, ambient light can be filtered or engineered by the design of theoptic or lens to spread or focus over the retina, including that of the optic nerve head. In certain embodiments the blue wavelength band of chromatic aberration is engineered by way of the optic design or optic power to focus on or within the retina peripheral to the macula. The optic can be an ophthalmic lens. The optic can be a thin plastic or glass section or part having no optical power that transmits light. An optic can be a window. An optic can be a light diffuser. An optic can be a film. The optic can comprise optical power. The optic can comprise prescription optical power. The optic can comprise no optical power. The optic can be a spectacle lens. The optic can be a contact lens. The optic can be an intra ocular lens.[000491] In some embodiments the highest concentration of blue light radiation or bluewavelengths falls within the range of 460nm + / - 20 nm or 470nm + / - 20nm or 480nm + / - 30nm or 450nm – 520nm. In some embodiments the highest concentration of blue light radiation or blue wavelengths falls within 460nm + / - 35 nm. In some embodiments the highest concentration of blue light radiation or blue wavelengths falls within the range of 460nm + / - 20 nm. In some embodiments the highest concentration of blue light radiation falls within the range of 470nm + / - 15 nm. In some embodiments the highest concentration of blue light radiation or blue wavelengths falls within the range of 470nm + / - 20 nm. In some embodiments the highest concentration of blue light radiation or blue wavelengths falls within the range of 470nm + / - 25nm. In some embodiments the highest concentration of blue light radiation falls within the range of 480nm + / - 10 nm. In some embodiments the highest concentration of blue light radiation falls within the range of 480nm + / - 15nm. In some embodiments the highest concentration of blue light radiation or blue wavelengths falls within the range of 480nm + / - 20 nm. In some embodiments the highest concentration of blue light radiation or blue wavelengths falls within the range of 480nm + / - 30nm. In some embodiments the highest concentration of blue light radiation or blue wavelengths falls above 449nm. In some embodiments the highest concentration of blue light radiation or blue wavelengths falls above 454nm. In some embodiments the highest concentration of blue light radiation or blue wavelengths falls above 459nm.[000492] The eyewear or optic can cause the wearer to be, by way of example only, morealert and / or have better concentration. In aspects, light wavelengths within the range 460nm + / - 10nm or 470nm + / - 20nm, more specifically within the range of 480nm + / -30nm, are known to produce dopamine within the human eyes’ retina and brain. In other embodiments wavelengths within the range of 650nm – 700nm can be used to increase alertness by increasing dopamine production. Light wavelengths within the wavelength range of 480nm + / - 30nm and 650nm + / - 30nm can excite the melanopsin containing ipRGC and / or rods so as to cause an increase in dopamine and / or serotonin production in the retina of an eye. Light wavelengths within the wavelength range of 480nm + / - 30nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm,500nm + / - 10nm, 500nm + / - 20nm, 500nm + / - 30nm, or 650nm + / - 30nm, or 700nm + / - 30nm, canexcite the melanopsin containing ipRGC and / or rods so as to cause an increase in dopamine and / or serotonin production in the eye, eye’s retina, and / or one or more of dopamine, serotonin or norepinephrine in the brain.[000493] In some embodiments, blue light wavelengths below 450nm are blocked or filtered.In certain embodiments the blue light wavelengths below 450nm and above 490nm are blocked or filtered. In certain embodiments all light wavelengths below 450nm and above 490nm are blocked or filtered. In certain embodiments the blue light wavelengths below 450nm and above 480nm are blocked or filtered. In certain embodiments all light wavelengths below 450nm and above 480nm are blocked or filtered. In certain embodiments all light wavelengths below 450nm and above 510nm are blocked or filtered. As used herein a filter is intended to filter light and affect the transmission thereof. In embodiments, a filter can affect / block or reduce the transmission of certain ranges of light wavelengths. In certain embodiments the filter blocks and / or filters certain light wavelengths while transmitting others.[000494] The optic can be an ophthalmic lens. The optic can be a thin plastic, film, or glasssection or part having non-optical power that transmits light. An optic can be a light diffuser. The optic can be antireflection coated. The optic can be slightly tinted. The optic can be without a coloror tint. The optic can be mostly clear of color. The optic can be scratch resistant coated. The optic can be surface treated like any ophthalmic lens. In certain embodiments the optic can be an electrochromic lens.[000495] In certain embodiments the lens or optic can be a chromatic aberration focused lens.The design can include one or more of refractive or diffractive, or a combination of refractive and diffractive. An example of a refractive / diffractive design is one of a lens or optic that comprises a central optic zone having refractive curves (comprising a spherical power or plano / no power) and a zone that is outside of the central zone that comprises Fresnel optical prismatic elements. In other embodiments the lens can be completely a Fresnel diffractive lens in the central zone and the peripheral zone. The peripheral zone can be of an optical power that is more minus or less plus optical power than the central zone. By way of example only, the central zone can be plano and the peripheral zone can be within the range of -0.75D to – 5.00D or in certain embodiments having an optical power within the range of -1.00 D - -2.00D. Such a lens or optic can be worn or utilized when providing ocular photo-bio-stimulation therapy to an eye. This lens or optic can be worn in addition to the wearer’s conventional eyeglasses when the ocular photo-bio-stimulation therapy is being provided or applied. And it can be removed for normal daily use when the ocular photo-bio- stimulation therapy is no longer being provided or applied. In certain embodiments it is worn in front of and in optical communication with the wearer’s conventional eyeglasses. In other embodiments it is worn behind but in optical communication with the wearer’s conventional eyeglasses.[000496] In certain embodiments, the lens or optic can be of a design that can include one ormore of refractive, or diffractive, or a combination of refractive and diffractive. An example of a refractive / diffractive design is one of a lens or optic that comprises a central optic zone having refractive curves (comprising a spherical power or plano / no power) and a zone that is outside of the central zone that comprises Fresnel optical prismatic elements. In other embodiments the lens can be completely a Fresnel diffractive lens in the central zone and the peripheral zone. The peripheral zone can be of an optical power that is more plus or less minus optical power than the central zone. By way of example only, the central zone can be plano and the peripheral zone can be within the range of +0.75D to + 5.00D or in certain embodiments having an optical power within the range of +1.00 D to +2.00D. Such a lens or optic can be worn or utilized when providing ocular photo-bio-stimulation therapy to an eye. This lens or optic can be worn in addition to thewearer’s conventional eyeglasses when the ocular photo-bio-stimulation therapy is being provided or applied. And it can be removed for normal daily use when the ocular photo-bio-stimulation therapy is no longer being provided or applied. In certain embodiments it is worn in front of and in optical communication with the wearer’s conventional eyeglasses. In other embodiments it is worn behind but in optical communication with the wearer’s conventional eyeglasses.[000497] Eyewear can be of any type of eyewear worn around or in the eye. Eyewear as usedherein can comprise any eyewear, by way of example only: spectacles, sunglasses, disposable eyewear, goggles, dress eyewear, safety eyewear, sports eyewear, clip-on eyewear, fit-over eyewear, military eyewear, smart eyewear, XR eyewear, AR eyewear, VR eyewear, MR eyewear, contact lens, intra-ocular lenses, or corneal implant. When required the eyewear can comprise a power source and the appropriate electronics needed. Non-prescription can mean non optical power. Plano means no optical power. Optical power can mean all optical powers. The optic can be made of plastic or glass. The use of the word filter means in most cases reducing, but not fully eliminating. However, in some cases, filtering can mean eliminating. The use of the word blocking means eliminating. Diffusing means to spread out. Defocus means not focusing on the retina of the eye of the user. The eyewear or optic can comprise one or more of: a notch filter, bandpass filter, selective blue light filter, absorptive filter, interference filter, a plurality of filters, or a combination of any one or more.[000498] A bandpass filter can be a type of interference filter. An interference filter can be abandpass filter. The filter can be used in association with one or more lenses, lens blank, optic, and / or optical blank. The filter can be in optical communication with one or more of: a lens, lens blank, optic, optical blank, or another filter. The filter can be applied to one or more of: the concave surface, convex surface, or buried or embedded within the lens, lens blank, optic, or optical blank. The filter can be separated and / or distance separated and in optical communication with one or more of: the lens, lens blank, optic, and / or optical blank. A filter can be used in combination with another filter. A filter can be used in optical communication with a distance separated filter.[000499] A filtered optic or filtered lens can be that of an optic or lens that comprises one ormore of: an interference filter, bandpass filter, neutral density filter, notch filter, absorption filter, absorber(s), dyes, and / or selective blue light filter.[000500] In certain embodiments when a filtered optic or filtered lens is used the overall lighttransmission through the filtered optic or filtered lens can be 50% of less, while the light transmission within the predominant transmitted filtered wavelength range being transmitted to the eye can be 50% or more. In certain cases, the pupil of the eye enlarges when looking through the filtered optic or filtered lens and constricts when looking absent of the filtered optic or filtered lens.[000501] In certain embodiments when a filtered optic or filtered lens is used the overall lighttransmission through the filtered optic or filtered lens can be 40% of less or 30% or less, while the light transmission within the predominant transmitted filtered wavelength range being transmitted to the eye can be 40% or more. In certain cases, the pupil of the eye enlarges when looking through the filtered optic or filtered lens and constricts when looking absent of the filtered optic or filtered lens.[000502] The eyewear or optic can comprise one or more of blue light emitter(s), green lightemitter(s), and / or red-light emitter(s). Examples of light emitters can be, by way of example only, LEDs, OLEDs, micro-OLEDs, micro-LEDs, quantum dots, iLEDs, fluorescent, incandescent, and / or the sun. As used herein a light emitter and be any light source that gives off light radiation. By way of example only: an LED, OLEDs, micro-OLED, micro-LED, quantum dots, diode, or the sun. In certain embodiments a light ring is utilized to minimize pupil constriction. This occurs as the eye being treated can fixate on a distant object through the center of the light ring while the light of the light ring is stimulating the photoreceptors of the eye. This further allows for providing light exposure to the peripheral retina of the eye. When an electrical light emitter is utilized, the light can flicker. The light can modulate. The light can modulate within the modulation range of 5 Hz and 15 Hz. Depending upon the type of light source, the light intensity utilized can be 300 lux or greater, 400 lux or greater, 1000 lux or greater, or 10,000 lux or greater.[000503] In certain embodiments, eyewear can comprise blue or red-light emitters facingtowards the eye of the wearer, facing inward and reflecting off the optic supported by the eyewear, and / or facing towards the wearer’s pupil(s). In other embodiments a band of blue, green, or red- light wavelengths can be varied in intensification of light radiation. The highest concentration of blue, green, or red-light radiation being transmitted can be varied in terms of light radiation. The blue, bluish green or green light emitters can comprise a wavelength within 480nm + / - 30nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / -10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, or 500nm + / - 30nm. The blue light emitters can comprise a wavelength greater than 449nm but less than 510nm. The eyewear or optic can comprise a diffuser for the purposes of diffusing light. The green light emitters can comprise wavelengths within the range of 480nm + / - 30nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, or 500nm + / - 30nm.The redlight emitters can comprise wavelengths within the range of 630nm + / - 20nm, 650nm + / -30nm, or 600nm to 700nm, or 700nm + / - 30nm. In embodiments disclosed herein, the light emitters can (optionally) be pulsed or modulated on and off to permit the pupil of the wearer / user to open more (enlarge) before it reduces in diameter. In cases, by using red light, the pupils of the eye will constrict less. Also, by causing the eye to focus on a distant object as opposed to a near object, the pupil of the eye will constrict less. In embodiments disclosed herein, a filter can be utilized to reduce the transmission of non-essential light wavelengths so as to cause the pupil diameter to enlarge compared to what the diameter would have been if all the light was permitted to enter the eye.[000504] Embodiments when light wavelengths are generated by way of filtered optics orfiltered lenses the transmission peak of the wavelength range that strike the eye’s retina falls within the wavelength range of at least one of: 480nm + / - 30nm, 450nm – 520nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, 500nm + / - 30nm, or 650nm + / - 30nm, or 700nm + / - 30nm.[000505] In embodiments when light wavelengths are generated by a light emitter(s) ifambient lighting is present (including that of artificial light or sun light), the blended light wavelengths of the light emitter(s) and also the ambient light comprises wavelengths of light that strike the eye’s retina can fall within one of the wavelength ranges of at least one of: 480nm + / - 30nm, 450nm – 520nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, 500nm + / - 30nm, or 650nm + / - 30nm, or 700nm + / - 30nm.[000506] In certain embodiments the range of wavelength band includes the peaks of themost sensitive spectral points of rhodopsin (500nm) and melanopsin (480nm). This way both rhodopsin and melanopsin can be stimulated or excited. By way of example, this can be accomplished by utilizing a filtered optic or lens that predominantly transmits within thewavelength range of 460nm – 520nm or 470nm to 520nm or by utilizing a light source or light emitter that predominately transmits within the wavelength range of 460nm- 520nm, 470nm to 520nm, or 480nm + / - 30nm. This would include blue, bluish green and green wavelengths. This can be most beneficial when stimulating the production of increased dopamine in the retina of an eye. This can be most beneficial when stimulating the production of one or more of dopamine, serotonin or norepinephrine in the brain by way of stimulating the retina of an eye.[000507] In embodiments, the blue or green or red-light emitters can be located around theperiphery of a clear or lightly tinted optic permitting the center of the optic to be free of most, but not all, blue or green or red light. In embodiments the blue or green or red-light light emitters can be located around the periphery of a clear or lightly tinted optic permitting the center of the optic to be free of all blue or green or red-light light. The blue or green or red-light light emitters can be located around the backside of the eye-wire of an eyeglass frame closest to the eye of the wearer, thereby permitting the center of the optic to be free of most, but not all, blue or green or red-light light. The blue or green or red-light light emitters can be covered by a diffuser.[000508] The emitted light wavelengths can strike or mostly strike the non-macular area ofthe retina, while mostly visible light wavelengths that pass through the center of the optic can strike or mostly strike the macular area of the retina. The optic can be tinted, by way of example only, blue, and blue light emitters can shine through the blue tinted optic. The wavelengths range being transmitted to the eye of the wearer can be within the range of 480nm + / - 30nm, 450nm – 520nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, 500nm + / - 30nm, or 650nm + / - 30nm, or 700nm + / - 30nm. The blue, bluish green, or green light emitters can excite one or more of, the retinal cones, rods and melanopsin containing ipRGCs. In a preferred case the blue light emitters excite the rods and melanopsin containing ganglion cells. The green light emitters can excite one or more of, the macula cones, retinal rods and melanopsin containing ipRGCs. Certain green light emitters within the wavelength range 500nm and 530nm can excite rhodopsin and melanopsin. Certain green light emitters within the wavelength range 500nm and 530nm can increase dopamine in the eye. Certain green light emitters within the wavelength range 500nm and 530nm can increase dopamine in the brain. The red-light emitters can excite one or more of, the macula cones, retinal rods and melanopsin containing ipRGCs. Certain blue light wavelengths increase alertness, focus, and cause thegeneration of dopamine in the eye and the brain. Certain blue light wavelengths can slow or stop myopia progression. Certain blue light wavelengths can prevent myopia from occurring in the first place. Certain green light wavelengths decrease pain. Certain red-light wavelengths increase calmness and relaxation. Certain red-light wavelengths increase dopamine production and increase alertness. Certain red-light wavelengths of 650nm + / - 30nm or 700nm + / - 30nm can improve the health of mitochondria.[000509] In certain embodiments the range of wavelength band includes the peaks of themost sensitive points from rhodopsin (500nm) and melanopsin (480nm). This way both rhodopsin and melanopsin can be stimulated or excited. By way of example, the range of 460nm – 520nm or 470nm – 520nm, or 480nm – 520nm, can be used. This would include blue, bluish green and green wavelengths.[000510] The intensity of the light intensity of the ocular photo-bio-stimulation light can bein certain cases, by way of example only, 300 lux or greater. In other cases, by way of example it is less than 500 lux. In still other cases it can be greater than 500lux. In still other cases it can be 1,000 lux or greater. In certain cases, by way of example, the time of light exposure is within the range of 1 -5 minutes. In other cases, by way of example, it is 10 minutes or less. In still other cases, by way of example, it is greater than 10 minutes.[000511] In embodiments for eyewear, the light emitter can have blue light wavelengthswithin the range of 460nm + / -20nm or 470nm + / - 20nm or 450nm to 510nm and can be blended with white light such as providing a blue wavelength enhanced or enriched by or with white light. By way of example only, certain fluorescent light that provides indoor warm white lighting can provide blue light wavelengths within the range of 460nm + / -20nm or 470nm + / - 20nm or 450nm to 510nm. In examples a white florescent light can be used with a blue light emitter. In other examples, certain incandescent light that provides indoor lighting can also provide blue light wavelengths within the range of 460nm + / -20nm or 470nm + / - 20nm or 450nm to 510nm. In other examples, certain incandescent light that florescent light that provides indoor lighting can be used with an LED having blue light wavelengths within the range of 460nm + / -20nm or 470nm + / - 20nm or 450nm to 510nm. And in still other embodiments, by way of example only, a white LED can be provided in combination with a blue LED having wavelengths within the range of 480nm+ / - 30nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm,495nm + / - 10nm, 495nm + / - 20nm, or 495nm + / - 30nm. And in still other embodiments, by way ofexample only, a white light emitter can be provided in combination with a blue light emitter having wavelengths within the range of 460nm + / -20nm or 470nm + / - 20nm or 450nm to 510nm. And in still other embodiments, by way of example only, a blue LED can provide a level of blue light within the wavelength range of 460nm + / -20nm or 470nm + / - 20nm or 450nm to 510nm. The ocular photo-bio-stimulation light source can increase the production of dopamine in the eye and / or one or more of dopamine, serotonin or norepinephrine in the brain.[000512] In embodiments for eyewear, the light emitter can have green wavelengths withinthe range of 500nm – 520nm, 510nm to 540nm, or 530nm + / - 20nm, and be blended with white light such as providing a green wavelength enhanced or enriched by or with white light. By way of example only, certain fluorescent light that provides indoor warm white lighting can also provide green wavelengths within the range of 500nm to 540nm. In examples a white florescent light can be used with a green light emitter. In other examples, certain incandescent light that provides indoor lighting can also provide green light wavelengths within the range 510nm to 540nm. In other examples, certain incandescent light that florescent light that provides indoor lighting can be used with by way of example, an LED having green light wavelengths within the range of 500nm – 520nm, 520nm + / - 10nm, 530nm + / -20nm, or 510nm to 540nm. And in still other embodiments, by way of example only, a white LED can be provided in combination with a green LED having wavelengths within the range of 530nm + / - 20nm, 530nm + / - 20nm, or 510nm to 540nm. And in still other embodiments, by way of example only, a white light emitter can be provided in combination with a green light emitter having wavelengths within the range of 500nm + / - 10nm, 520nm + / - 10nm, 530nm + / - 20nm, or 510nm to 540nm.[000513] In embodiments for eyewear, the light emitter can have red wavelengths within therange of 630nm + / - 20nm, 650nm + / - 30nm, or 600nm to 700nm, and be blended with white light such to provide a red wavelength enhanced or enriched white light. By way of example only, certain fluorescent light that provides indoor warm white lighting can also provide red wavelengths within the range of range of 630nm + / - 20nm, 650nm + / -30n, or 600nm to 700nm. In examples a white florescent light can be used with a red-light emitter. In other examples, certain incandescent light that provides indoor lighting can also provide red-light wavelengths within the range of 630nm + / - 20nm, 650nm + / -30nm, or 600nm to 700nm. In other examples, certain incandescent light that florescent light that provides indoor lighting can be used with an LED having red-light wavelengths within the range of range of 660nm + / - 20nm, 650nm+ / -30nm, or 600nm to 700nm.And in still other embodiments, by way of example only, a white LED can be provided in combination with a red LED having wavelengths within the range of range of 630nm + / - 20nm, 650nm + / -30nm, or 600nm to 700nm. And in still other embodiments, by way of example only, a white light emitter can be provided in combination with a red-light emitter having wavelengths within the range of range of 630nm + / - 20nm, 650nm + / - 30nm or 600nm to 700nm, or 700nm + / - 30nm.[000514] In embodiments, the blue light emitters can be located around the periphery of aclear or lightly tinted optic permitting the center of the optic to be free of most, but not all, blue light. In embodiments the blue light emitters can be located around the periphery of a clear or lightly tinted optic permitting the center of the optic to be free of all blue light. The blue light emitters can be located around the backside of the eye-wire of an eyeglass frame closest to the eye of the wearer permitting the center of the optic to be free of most, but not all, blue light. The blue light emitters can be covered by a diffuser. The blue light wavelengths can strike or mostly strike the non-macular area of the retina, while mostly visible light wavelengths that pass through the center of the optic can strike or mostly strike the macular area of the retina. The optic can be tinted blue and blue light emitters can shine through the tinted optic. The optic can be tinted blue and blue light emitters can reflect off the surface of the optic. The optic can be tinted blue and white light emitters can shine through the blue tinted optic. In certain embodiments the blue light emitters which are located on the backside of the eyewear can be pointed towards the pupil of the eye of the wearer. In other embodiments the blue light emitters are perpendicular to the backside of the eyewear and can point towards the face of the wearer.[000515] In embodiments the green light emitters can be located around the periphery of aclear or lightly tinted optic permitting the center of the optic to be free of most, but not all, green light. In embodiments the green light emitters can be located around the periphery of a clear or lightly tinted optic permitting the center of the optic to be free of all green light. The green light emitters can be located around the backside of the eye-wire of an eyeglass frame closest to the eye of the wearer permitting the center of the optic to be free of most, but not all, green light. The green light emitters can be covered by a diffuser. The green light wavelengths can strike or mostly strike the macular and non-macular area of the retina, while mostly visible light wavelengths that pass through the center of the optic can strike or mostly strike the macular area of the retina. The optic can be tinted green and green light emitters can shine through the green tinted optic. Theoptic can be tinted green and green light emitters can reflect off one of the surfaces of the optic. The optic can be tinted green and white light emitters can shine through the green tinted optic. In certain embodiments the green light emitters which are located on the backside of the eyewear can be pointed towards the pupil of the eye of the wearer. In other embodiments the green light emitters are perpendicular to the backside of the eyewear and can point towards the face of the wearer.[000516] In embodiments, the red-light emitters can be located around the periphery of aclear or lightly tinted optic permitting the center of the optic to be free of most, but not all, red light. In embodiments the red-light emitters can be located around the periphery of a clear or lightly tinted optic permitting the center of the optic to be free of all red light. The red-light emitters can be located around the backside of the eye-wire of an eyeglass frame closest to the eye of the wearer permitting the center of the optic to be free of most, but not all, red light. The red- light emitters can be covered by a diffuser. The red-light wavelengths can strike or mostly strike the macular and non-macular area of the retina, while mostly visible light wavelengths that pass through the center of the optic can strike or mostly strike the macular area of the retina. The optic can be tinted red and red-light emitters can shine through the red tinted optic. The optic can be tinted red and red-light emitters can reflect off of one of the surfaces of the optic. The optic can be tinted red and white light emitters can shine through the red tinted optic. In certain embodiments the red-light emitters which are located on the backside of the eyewear can be pointed towards the pupil of the eye of the wearer. In other embodiments the red-light emitters are perpendicular to the backside of the eyewear and can point towards the face of the wearer.[000517] In embodiments, the eyewear houses or supports an optic which can compriseoptical power. A defocusing lens can be utilized with the eyewear or optic. Such a defocusing lens can be housed within the eyewear, attached to the eyewear or optic, or worn behind the eyewear or optic. In cases, the defocusing lens is on the backside of a Bandpass Filter between the filter and the eye of the wearer or user. In certain embodiments the eyewear houses or supports an optic which can comprise non-optical power. In certain embodiments the eyewear houses or supports an optic which can comprise an eyeglass prescription. In certain embodiments the eyewear houses or supports an optic which can comprise an eyeglass lens that is non-prescription. In certain embodiments, by way of example, the eyewear can be disposable, comprising a colored optic such that when viewing a bright light source transmits light wavelengths within the range of 480nm + / -30nm, 450nm – 520nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, 500nm + / - 30nm, or 650nm + / - 30nm or 700nm + / - 30nm, to the eye of the wearer. In certain embodiments the can be a colored optic suchof 500nm – 520nm or 530nm + / - 20nm to the eye of the wearer. In certain embodiments the eyewear can be disposable, comprising a colored optic such that when viewing a distant separated bright light source transmits light wavelengths within the range of 630nm + / - 20nm, 650nm + / - 30nm, or 600nm to 700nm, or 700nm + / - 30nm, to the eye of the wearer. [000518] In certain embodiments the eyewear houses or supports an optic that comprises bluelight emitters having blue light wavelengths within the range of 441nm to 500nm, or 460nm + / - 20nm or 470nm + / - 20nm or 480nm + / -30nm. In certain embodiments, by way of example only, the eyewear houses or supports an optic that comprises a blue color having blue wavelength within the range of 441nm to 500nm, or 460nm + / - 20nm or 470nm + / - 20nm or 480nm + / -30nm, while, in aspects, filtering or blocking blue light wavelengths of 440nm or below. In certain embodiments the eyewear houses or supports an optic that comprises a blue color having blue light wavelengths within the range of 441nm to 500nm, or 460nm + / - 20nm or 470nm + / - 20nm or 480nm + / -30nm, and wherein the blue light wavelengths transmitted below 441nm have been reduced in number or intensity. In still other embodiments a bandpass filter transmits wavelengths within the range of 480nm + / - 30nm, 450nm – 520nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, 500nm + / - 30nm, or 650nm + / - 30nm, or 700nm + / - 30nm. Inhaving green light wavelengths within the range of 510nm – 540nm or 530nm + / - 20nm or 520nm + / - 10nm. In certain embodiments the eyewear houses or supports an optic that comprises a green color having green light wavelengths within the range of 510nm – 540nm or 530nm + / - 20nm. [000519] In some embodiments the eyewear or optic can comprise red-light emitters. Incertain other embodiments the eyewear or optic can comprise blue, bluish green, green, and / or red- light emitters. In such cases the light emitters are used for improving, by way of example only, increased alertness and cognitive ability. The light emitters can emit wavelengths within the range of 480nm + / - 30nm, 450nm – 520nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm+ / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, 500nm + / - 30nm, or 650nm + / - 30nm, or 700nm + / - 30nm. The optic can comprise a double bandpass filter that can be used to provide for these ranges of transmission.[000520] The eyewear can comprise blue or red light provided by an electronic display, andwherein the electronic display is located within an optic, in front of an optic, behind an optic, on the surface of an optic, on the eyewear and transmitted or projected to an optic, and / or on the eyewear and transmitted or projected to or on the human eye(s). Such an electronic display used with eyewear can be for XR (extended reality), VR (virtual reality), AR (augmented reality), MR (mixed reality), Modified Reality and in some cases just to provide blue, or green, or red-light to or from an optic. The red-light can be of a red-light within the wavelength range of 660nm + / - 30nm or 650nm + / - 30nm or 660 nm + / - 20nm. The blue light can have wavelengths within the range of 441nm to 500nm, or 460nm + / - 20nm or 470nm + / - 20nm or 480nm + / -30nm, while if needed filtering or blocking within the range of 420nm + / - 20nm. The green light can have wavelengths within the range of 510nm – 540nm or 530nm + / - 20nm. The red-light wavelengths can be within the range of 630nm + / - 20nm, or 650nm + / - 30nm, or 660nm + / - 30nm, or 600nm to 700nm, or 700nm + / - 30nm. A plurality of light emitters can be utilized to provide one or more of the preceding wavelength bands.[000521] In certain embodiments the eyewear or optic can comprise white light emitters thatshine on a blue colored lens or optic, or a green colored lens or optic, or a red colored lens or optic. Examples of light emitters can be, by way of example only: LEDs, OLEDs, micro-OLEDs, micro- LEDs, iLEDs, and / or quantum dots. A plurality of light emitters can be utilized. A clip-on optic or flip-up or down optic can attach to the eyewear (see, FIG.21A-D). The eyewear can comprise a prescription lens or non-prescription lens. The eyewear can comprise a lens having optical power or having non-optical power (plano power).[000522] In reference to FIG. 19, in embodiments, one or more lens housed or supported bythe eyewear can comprise a blue color having blue wavelengths within the range 450nm to 500nm or 460nm + / - 20nm, or 470nm + / - 20nm, or 480nm + / - 30nm, and can filter or block blue wavelengths below 450nm. A lens having a green color can have wavelength transmission within the range of 510nm – 550nm, or 530nm + / - 20nm, or 520nm + / - 10nm. A lens having a red colorcan have wavelength transmission within the range of 650nm + / - 30nm, or 660nm + / - 20nm or 600nm to 700nm, or 700nm + / - 30nm.[000523] In still other embodiments the lens housed by eyewear can be clear of color. Theclip-on optic or flip-up or down optic can comprise a prescription lens or non-prescription lens. The housing of the clip-on optic or flip-up and down optic can attach to the eyewear, by way of example only, magnetically, mechanically, and / or by a tension mount. (See, FIGs.21A-D and FIG. 22.) In certain other embodiments the optic can be attached to the lens housed by the eyewear by way of example only, with magnets, removable adhesive, and / or through static energy.[000524] Other embodiments, by way of example, may include a ring, a band, or a section ofblue or green or red-light emitters, which can be adhered to the lens or optic surface, attached to the lens or optic surface, or embedded within the lens or optic surface, wherein the lens or optic is supported or housed by an eyeglass frame or eyewear. In certain other embodiments by way of example only, a ring, band, or a section of blue or green or red-light emitters, can be adhered to the lens or optic surface, attached to the lens or optic surface, or embedded within the lens or optic surface, such that it can be inserted or such that it is supported or stabilized on an eyeglass frame or eyewear. In aspects, the filters and / or emitters and related embodiments can be removeable inserts, such as attached to a lens, attached to eyewear, inserted into a lens, or embedded in a lens. (See, FIG.19A-F.)[000525] In reference to FIG. 20, in embodiments, the blue, or green, or red-light, or whitelight emitters, can provide light covering a central portion of the lens or optic. In other cases, the blue, green, or red-light, or white light emitters, can provide light covering a peripheral portion of the lens or optic leaving the center of the lens or optic mostly clear of blue, green, red, or white light. In still other embodiments the blue, green, red or white light emitters can provide light covering a portion of the lens or optic. (See, FIGs.20A-C.)[000526] In still other embodiments, the blue, or green, or red-light, or white light emitters,can be distance separated from the optic. The light emitters can be covered by a diffuser to spread and soften the light. The light can be directed towards the eye of the wearer. The light can be directed towards the pupils of the eyes of the wearer. In certain embodiments the light source or emitter can modulate for example, within the range of one of 5 Hz – 15 Hz, 10Hz to 20Hz, or 40Hz + / - 20Hz. In certain embodiments the light source or emitter can modulate, for example 10 times per second or less. In certain embodiments the light source or emitter can modulate (on andoff), for example, 20 times per second or less. In other embodiments the light source or emitter can modulate, for example, 50 times per second or less. And in still other embodiments the light emitter or emitter can modulate, for example, 100 times per second or less. In still other embodiments the light does not modulate or flicker.[000527] In embodiments utilizing blue light as the light source (wavelengths within therange of at least one of 480nm + / - 30nm, 450nm – 520nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, or 500nm + / - 20nm), can be of an intensity of 300 lux or more. In other embodiments the intensity can be of 500 lux or more. In other embodiments the intensity can be of 1,000 lux or more. In certain embodiments utilizing a blue light source, the time of treatment with the light source can be 1 hour or less. In other embodiments the time of treatment can be 30 minutes or less. In still other embodiments it can be 10 minutes or less. And in still other embodiments it can be 5 minutes or less.[000528] In certain embodiments utilizing a green light source (e.g., wavelengths within therange of 530nm + / - 20nm), the green light source can have an intensity of 250 lux or more. In other embodiments the intensity can be 500 lux or more. In other embodiments the intensity can be 1,000 lux or more. In certain embodiments, when utilizing a green light source, the time of treatment with the light source can be 1 hour or less. In other embodiments the time of treatment can be 30 minutes or less. In still other embodiments it can be 10 minutes or less. And in still other embodiments it can be 5 minutes or less.[000529] In embodiments utilizing a red- light source (wavelengths within the range of650nm + / - 30nm or 700nm + / - 30nm), the red-light source can have an intensity of 400 lux or more. In other embodiments the intensity can be of 500 lux or more. In other embodiments the intensity can be of 1,000 lux or more. In other embodiments the intensity can be of 5,000 lux or more. In certain embodiments utilizing a red-light source the time of treatment with the light source can be 1 hour or less. In other embodiments the time of treatment can be 30 minutes or less. In still other embodiments it can be 10 minutes or less. And in still other embodiments it can be 5 minutes or less. In reference to FIG.21, an embodiment can include a clip-on optic or flip-up or down optic comprising a lens having optical power or having non-optical power (plano power). In embodiments the clip-on optic or flip-up or down optic can transmit blue wavelengths within the range of 441nm – 500nm, or 460nm + / - 20nm, or 470nm + / - 20nm, or 480nm + / -30nm, such as, incases, using a bandpass filter. (See, e.g., 2101 in FIG.21a.) In still other embodiments the clip-on optic or flip-up or down optic can be clear of color and comprise blue light emitters having blue wavelengths predominately or solely within the range of 441nm – 500nm, or 460nm + / - 20nm, or 470nm + / - 20nm, or 480nm + / -30nm, around its periphery of that of the housing that supports the optic. (See, e.g., FIG.20A-C.) Such a housing can be a frame or an eyewear frame. In certain embodiments the clip-on optic or flip-up or down optic can transmit blue light (e.g., using one or more light emitter 2102) wavelengths within the range of 441nm – 500nm, or 460nm + / - 20nm, or 470nm + / - 20nm, or 480nm + / -30nm, and the lens housed by the eyewear can filter or block blue wavelengths 440nm or below. In certain embodiments the forward optic farthest away from the eye of the wearer can provide or emit a blue color having wavelengths within the range of 441nm – 500nm, or 460nm + / - 20nm, or 470nm + / - 20nm, or 480nm + / -30nm. In certain embodiments the forward optic is that of the clip-on or flip down optic and the optic located behind the clip-on or flip down optic is that of the eyewear optic. In certain other embodiments the optic housed in the eyewear can be a stack of two optics with the forward optic comprising a blue color having wavelengths predominately or solely within the range of 441nm – 500nm, or 460nm + / - 20nm, or 470nm + / - 20nm, or 480nm + / -30nm, and the optic closest to the eye of the wearer being the optic that either filters or blocks blue light wavelengths. The optic can be a clip on or flip down filter. The filter can be a bandpass filter. The filter can be an interference filter. The filter can be an absorption filter. Any of the clip-on optics or flip-up or down optics can be attachable and detachable to the eyewear, eyewear frame, or optic / lens; in other words, any of the clip-on optics or flip-up or down optics can be attachable and detachable to a frame, or any of the clip-on optics or flip-up or down optics can be integral with or embedded within the frame.[000530] The clip-on optic or flip-up or down optic can comprise a lens having optical poweror having non-optical power (plano power). In certain embodiments the clip-on optic or flip-up or down optic can comprise transmission of green light wavelengths predominately or solely within the range of 480nm + / - 30nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, or 500nm + / - 30nm. In still other embodiments the clip-on optic or flip-up or down optic can be clear of color and comprise green light emitters having wavelengths within the range of 500nm – 550nm, or 530nm + / - 20nm, around its periphery of that of the housing that supports the optic. Such a housing can be a frame or an eyewear frame. In certain embodiments the forward opticfurthest away from the eye of the wearer can provide or emit green wavelengths within the range of 480nm + / - 30nm, 450nm – 520nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, or 500nm + / - 30nm. In certain embodiments the forward optic is that of the clip-on or flip down optic and the optic located behind the clip-on or flip down optic is that of the eyewear optic comprising an optical power. The optic can be a clip on or flip down filter. The filter can be a bandpass filter. The filter can be an interference filter. The filter can be an absorption filter.[000531] The clip-on optic or flip-up or down optic can comprise a lens having optical poweror having non-optical power (plano power). In certain embodiments the clip-on optic or flip-up or down optic can comprise transmission of red-light wavelengths predominately or solely within the range of 630nm + / - 20nm, 650nm + / - 30nm, or 600nm – 700nm. In still other embodiments the clip-on optic or flip-up or down optic can be clear of color and comprise red light emitters having wavelengths within the range of 630nm + / - 20nm, 650nm + / - 30nm, or 600nm – 700nm, or 700nm + / - 30nm, around its periphery of that of the housing that supports the optic. Such a housing can be a frame or an eyewear frame. In certain embodiments the forward optic farthest away from the eye of the wearer can provide or emit red wavelengths within the range of 630nm + / - 20nm, 650nm + / - 30nm, or 600nm – 700nm, or 700nm + / - 30nm. In certain embodiments the forward optic is that of the clip-on or flip down optic and the optic located behind the clip-on or flip down optic is that of the eyewear optic comprising an optical power. The optic can be a clip on or flip down filter. The filter can be a bandpass filter. The filter can be an interference filter. The filter can be an absorption filter.[000532] As shown in FIG. 21D, an embodiment can include white light emitters (with orwithout a diffuser) 2103. The clip-on optic or flip-up or down optic can be prescription, or not. The lenses can be tinted, or not 2104. The lenses can include one or more filter. In embodiments, white LEDs are pointed towards the eye of the wearer, and they can transmit trough a filter 2105 (e.g., blue lens comprising notch filter or bandpass filter while transmitting especially between 480 + / - 30nm).[000533] With all embodiments requiring electronics provided herein the appropriateenabling electronics to drive, power, control, modulate, dim or brighten the light emitters are part of or in association with the embodiments even if not identified within the illustrations. With any of the embodiments disclosed herein when appropriate, by way of example only, one or more of abandpass filter, notch filter, interference filter, dye absorption filter, specialized filter, coating, and / or dye, can be utilized to achieve the desired wavelengths transmission results. In certain embodiments a plurality of filters is used such that each is in optical alignment with the other. The optic can be a clip on or flip down filter. The filter can be a bandpass filter. The filter can be an interference filter. The filter can be an absorption filter.[000534] In reference to FIG. 22, in embodiments, the eyewear and / or optic can be comprisedof a non-prescription optic that can by way of example only, one or more of: disposable, repeatably rolled up when not in use and extends back out when in use such that it utilizes pressure to attach to and eyewear frame, rests by way of arms on existing eyewear that is being worn, fits over existing eyewear, and / or clips or snaps on to existing eyewear. The non-prescription eyewear or optic can further be comprised of either a light wavelength filtered material or a light wavelength bandpass material. The eyewear or optic can be largely darkened, only allowing the transmission of 20% or less of the light through. The eyewear or optic can be largely darkened, only allowing the transmission of 15% or less of the light through. The eyewear or optic can be largely darkened, only allowing the transmission of 10% or less of the light through.[000535] Such a transmission will cause the pupil of the eye(s) to enlarge fully or slightly.This increase in the size of the pupil(s) then permits a larger area of the retina to be exposed to the light wavelengths that are being transmitted to the eye(s). In certain cases, light wavelengths within the range of 480nm + / - 30nm, 490nm + / - 5nm, 490nm + / - 10nm, 490nm + / - 20nm, 490nm + / - 30nm, 495nm + / - 5nm, 495nm + / - 10nm, 495nm + / - 20nm, 495nm + / - 30nm, 500nm + / - 5nm, 500nm + / - 10nm, 500nm + / - 20nm, 500nm + / - 30nm, or 650nm + / - 30nm, or 700nm + / - 30nm arelens can be housed within the eyewear, attached to the eyewear or optic, or worn behind the eyewear or optic. In most, but not all cases, the defocusing lens is on the backside of the bandpass filter between the filter and the eye of the wearer or user.[000536] In reference to FIG. 23, by largely acting as very dark sunglasses, embodiments cancause the pupil to partially or fully enlarge, thus allowing more of the retina to become exposed to the transmitted light wavelengths. This is especially helpful with blue light wavelengths of 460 nm or greater to 480nm or greater, or 510nm or less, where the blue light wavelength is intended to cause the wearer to become more alert or focused. This also is the case with red light within the range of 650nm + / - 30nm or 650nm -700nm. The very dark sunglass effect of the eyewear or opticcauses the pupil to partially or fully enlarge, which exposes more retinal rods and / or ipRGCs to the blue (or red) light wavelength being transmitted. This in turn increases dopamine production which then assists with making the wearer of the optic or eyewear more alert and focused. In addition, rods and cones are sensitive to green light wavelengths.[000537] Thus, by partially or fully dilating the eye it is possible to expose more of the retinalrods in addition to the cones. When an embodiment comprising a bright light is shined on the retina of a wearer the pupil of the eye constricts and reduces the amount of retina that is stimulated. It is one of the purposes of the invention to stimulate a larger amount of the retina, thus increasing the amount of dopamine produced. This can be accomplished by way of one or more of: defocused light, reducing or eliminating accommodative pupil constriction by fixating on a distant object, utilizing dim light, utilizing red light when possible, and / or utilizing a bandpass filter thus reducing the overall light transmission by way of allowing only the desired light wavelengths to be transmitted. The bandpass filter can be a single bandpass filter or a double bandpass filter. The filter can be a hybrid filter. A bandpass filter can be an interference filter.[000538] The degree of darkness of the sunglasses or treatment glasses can provide one of ormore of: scotopic condition, reduced mesopic conditions, and reduced photopic conditions. FIG. 23A shows examples of ocular photo-bio-stimulation disposable (or non-disposable) light wavelength filtered optic eyewear; the disposable eyewear can be made, by way of example only, a darkly tinted or near opaque colored plastic material having plastic or paper arms that are supported by the wearer’s ears, to wear over or around the user’s conventional eyeglasses, if needed. The wearer can look at a distance separated bright light source while wearing the disposable eyewear for a time. Such a bright light source can be one of LED, OLED, iLED, quantum dots, fluorescent, incandescent, sun light, laser, plasma display, TV display, tablet display, cell phone display, computer display, or electronic display. A defocusing lens can be utilized with the eyewear or optic. Such a defocusing lens can be housed within the eyewear, attached to the eyewear or optic, or worn behind the eyewear or optic. In most, but not all cases, the defocusing lens is on the backside of the filter between the filter and the eye of the wearer or user. FIG.23B shows examples of ocular photo-bio-stimulation disposable (or non-disposable) light wavelength filtered optic eyewear; the disposable eyewear can be made, by way of example only, a darkly tinted or near opaque colored plastic material having plastic or paper arms that are supported by the wearer’s ears, to wear over or around the user’s conventional eyeglasses, if needed. The wearercan look at a distance separated bright light source while wearing the disposable eyewear for a time. Such a bright light source can be one of LED, OLED, iLED, quantum dots, fluorescent, incandescent, sun light, laser, plasma display, TV display, tablet display, cell phone display, computer display, or electronic display. A defocusing lens can be utilized with the eyewear or optic. Such a defocusing lens can be housed within the eyewear, attached to the eyewear or optic, or worn behind the eyewear or optic. In most, but not all cases, the defocusing lens is on the backside of the filter between the filter and the eye of the wearer or user. [000539] If reference to FIG. 24, the embodiment can be eyewear comprising an optic,wherein the eyewear when worn causes the pupil of an eye to enlarge in diameter, wherein the optic transmits light radiation having wavelengths of light within the range of 450nm and 510nm and wherein the optic transmits 40% or less of visible light. Eyewear that comprises side shields can be used to assist in blocking light coming in from the periphery. The optic can comprise a filter or filters. The wavelengths of light that can be transmitted, by way of example only, are within the range of 460nm + / - 10nm or 480nm + / - 30nm or 450nm – 520nm. The optic can transmit 30% or less visible light. The optic can transmit 20% or less visible light. The optic can transmit 15% or less of ...

Claims

1. CLAIMS1. A device for applying ocular light therapy to an eye of a subject, the device comprising:one or more light sources applying ocular photo-bio-stimulation light to a retina of the subject’s eye, wherein light wavelengths of the ocular photo-bio-stimulation light are within a range of one or more of, 450nm - 500nm, 475nm + / -20nm, 530nm + / - 20nm, 575nm + / -30nm, 630nm - 700nm, or 830nm + / - 30nm; and a fixation target configured to form a fixation target image over part or all of a macula of the subject’s eye, and wherein the fixation target image protects part or all of the macula of the subject’s eye from harmful radiation from the ocular photo-bio-stimulation light.

2. The device of claim 1, wherein the fixation target one or more of, blocks, filters, or attenuates,some or all of the ocular photo-bio-stimulation light.

3. The device of claim 1, wherein the fixation target is configured to impart a full protectiveimage over part or all of the macula of the subject’s eye.

4. The device of claim 3, wherein the full protective image is partially or completely surroundedby a blended protective image, and wherein the blended protective image is partially or completely surrounded by the ocular photo-bio-stimulation light.

5. The device of claim 1, wherein the fixation target comprises or is in optical communicationwith a fine-tuned fixation target.

6. The device of claim 5, wherein the fine-tuned fixation target is a cross hair or a spot.

7. The device of claim 1, wherein the fixation target is between 3mm and 15mm in diameter.

8. The device of claim 1, wherein the device is one or more of, eyewear, eyewear housing a lensor optic, an augmented reality device, a mixed reality device, a virtual reality device, a modified reality device, an extended reality device, an instrument housing a lens or optic, a tabletop instrument, a handheld instrument, a handheld electronic display, a lens, or combinations thereof.

9. The device of claim 3, wherein the full protective image is one or more of, black, orange, cyan,grey, red, or a contrasting color compared to that of the ocular photo-bio-stimulation light.

10. The device of claim 4, wherein the blended protective image is one or more of, blackish-blueor dark blue transitioning to blue or a lighter shade of blue; orangish-blue; grey transitioning to blue; red, white, or grey transitioning to red or a lighter shade of red; greyish-blue; red transitioning to blue or a lighter shade of red; or reddish-blue or purple transitioning to blue.

11. The device of claim 3, wherein the full protective image is between 1.5mm and 5.5mm indiameter.

12. The device of claim 4, wherein the blended protective image including the full protectiveimage is between 1mm and 10mm in diameter.

13. The device of claim 4, wherein the blended protective image is, is generated by, or isconfigured by, a combination of the fixation target, rays of light outlining the fixation target that enter a pupil of the subject’s eye, and the ocular-photo-bio-stimulation light.

14. The device of claim 1, wherein a distance of the fixation target to the eye of the subject isadjustable along a Z axis or a subject’s line of sight.

15. The device of claim 1, further comprising a micro-lens or micro-lens array.

16. The device of claim 15, wherein the fixation target is in optical communication with a fined-tuned fixation target, and wherein the micro-lens or micro-lens array is distance separated and located between 1mm and 6mm in front of the fine-tuned fixation target.

17. The device of claim 1, wherein the ocular photo-bio-stimulation light has an intensity of 500lux or more, and wherein the ocular photo-bio-stimulation light has a light intensity of 400 lux or more when it is applied to and strikes the retina of the eye of the subject.

18. The device of claim 1, wherein the ocular photo-bio-stimulation light modulates or flickers.

19. The device of claim 1, wherein the fixation target is one or more of: an object devoid of light;an object providing light; a light source; a light source with an area devoid of light; an opticalfilter; a translucent optic; a lens; an opaque object; an object comprising a color; or an object devoid of a color.

20. The device of claim 1, wherein the fixation target is one or more of: fixed or stationary;continuously moving; or intermittently or periodically moving.

21. The device of claim 1, wherein the device is used in association with or in combination with anophthalmic lens or optic, wherein the ophthalmic lens or optic is one or more of, worn before the applied ocular light therapy, during the applied ocular light therapy, or after the applied ocular light therapy, and wherein the ophthalmic lens or optic is one or more of: a single vision lens; a multifocal lens; a lens or optic comprising a central zone for correcting a subject’s distance vision and a peripheral zone comprising or configured to provide defocused light; a refractive lens or optic; a diffractive lens or optic; a refractive or diffractive lens or optic; a myopia control lens or optic; a Fresnel lens or optic; a lens comprising a progressive zone ofdefocus; a lens or optic comprising a plurality of lenslets; a lens or optic comprising nanoparticles or micro structured materials; a lens or optic comprising optics that diffuse, disperse, or scatter light; or a lens or optic comprising rings of defocus or alternating rings of focus and defocus.

22. The device of claim 1, wherein the device is operative to treat an eye disorder or other disorderof the subject, including one or more of: myopia; diabetic retinopathy; wet macular degeneration; dry macular degeneration; glaucoma; cataract formation; retinitis pigmentosa; optic neuritis; optic atrophy; serous retinopathy; dry eye disease; meibomian glanddysfunction; Sjögren’s syndrome; vernal keratoconjunctivitis (VKC); atopic keratoconjunctivitis (AKC); amblyopia; or a neurological disorder, including one or more of, Parkinson’s disease, Alzheimer’s disease, alertness, mood, depression, attention deficit hyperactivity disorder (ADHD), seasonal affective disorder (SAD), alcoholism, addiction, a cognitive disorder, or anxiety.

23. The device of claim 3, wherein light generating and / or forming the full protective image strikesor covers part or all of the macula of the subject, and wherein the light generating and / or forming the full protective image is of a different light intensity of ocular photo-bio-stimulation light compared to the ocular photo-bio-stimulation light that is applied to the retina of the subject’s eye.

24. The device of claim 1, further comprising one or more of, a timer, biofeedback, an alarm,wireless communication, wired communication, an automatic timed switch, a controller, a computer processing unit, software, executable instructions, memory, or one or more sensors.

25. The device of claim 5, wherein the device is configured to turn down an intensity of the ocularphoto-bio-stimulation light or turn off the ocular photo-bio-stimulation light, if the eye of the subject looks away from the fixation target or the fine-tuned fixation target when the ocular light therapy is being applied to the eye of the user.

26. The device of claim 1, wherein the fixation target comprises or is in optical communicationwith a fine-tuned fixation target, and wherein the device further comprises and / or is controlled by a sensor in communication with a processor, the processor operative to identify a location of the eye of the subject relative to the fixation target or the fined-tuned fixation target.

27. The device of claim 1, wherein the one or more light sources include one or more of a fine-tuned fixation target light source or a fixation target light source, and wherein the one or morelight sources comprise one or more of, light-emitting diodes (LEDs), micro-LEDs, inorganic- LEDs (ILEDS), organic-LEDS (OLEDs), micro-OLEDs, quantum dots, fluorescent, incandescent, a laser, a plasma display, a television display, a cell phone display, a tablet computer display, a computer display, a watch display, or an electronic display.

28. The device of claim 5, wherein the device is configured to make the fine-tuned fixation targetappear in focus and at a distance relative to the subject.

29. The device of claim 1, wherein the fixation target is: located within or on a lens housed byeyewear; located in front of a lens housed by eyewear; located in front of the one or more light sources and closer to the eye of the subject than the one or more light sources; or located farther from the eye of the subject than the one or more light sources.

30. The device of claim 1, wherein the fixation target moves within a radius of an arc of the eye ofthe subject.

31. A method for slowing or stopping myopia progression of a subject’s eye, the methodcomprising: a. applying ocular photo-bio-stimulation light to a retina of the subject’s eye during anocular light therapy session while protecting all or part of a macula of the subject’s eye from the applied ocular photo-bio-stimulation light, wherein the ocular photo-bio-stimulation light is provided by one or more ocular photo-bio-stimulation light sources, wherein the ocular photo- bio-stimulation light is artificial light, and wherein the ocular photo-bio-stimulation light is provided to the subject’s eye for 60 minutes or less during the ocular light therapy session; b. providing a myopia control lens worn by the subject for more than 60 minutes perday one or more of, before the ocular light therapy session, during the ocular light therapy session, or after the ocular light therapy session; and c. causing, by the method as configured, the slowing or stopping of the myopiaprogression of the subject’s eye by way of one or more of, increasing choroidal thickness of the subject’s eye, slowing or stopping axial elongation of the subject’s eye, or slowing or stopping a subject’s need for an increase in an optical power correcting myopia.

32. The method of claim 31, the method further comprising: including a fixation target, whereinthe fixation target is located closer to the subject’s eye than the one or more ocular photo-bio- stimulation light sources.

33. The method of claim 32, the method further comprising: forming a fixation target image on theretina of the subject’s eye.

34. The method of claim 32, wherein the fixation target is one or more of, opaque; translucent;transparent; a light filter; an interference filter; a bandpass filter; an absorption filter; a notch filter; a selective wavelength(s) filter; a neutral density filter; an ultraviolet (“UV”) light filter; a High-Energy Visible (HEV) light filter; a light; a material that is black, devoid of color, or devoid of light; a grey color; a red color; a yellow color; a cyan color; or a contrasting color with the ocular photo-bio-stimulation light.

35. The method claim 31, wherein light wavelengths of the ocular photo-bio-stimulation light arewith a range of one or more of, 480nm + / - 30nm, 500nm – 550nm, or 600nm – 700nm.

36. The method of claim 32, wherein the fixation target comprises a fine-tuned fixation target,wherein the fine-tuned fixation target forms a fine-tuned fixation target image on one or more of, a fovea of the subject’s eye, the macula of the subject’s eye, or the retina of the subject’s eye.

37. The method of claim 36, wherein the fine-tuned fixation target image is in opticalcommunication with a micro-lens or micro-lens array before reaching the subject’s eye.

38. The method of claim 32, wherein the fixation target imparts or casts one or more of, a fullprotective image and / or a blended protective image, configured to cover part or all of the macula of the subject’s eye.

39. The method of claim 38, wherein the one or more of, the full protective image and / or theblended protective image, attenuates part or all of the ocular photo-bio-stimulation light.

40. The method of claim 31, the method further comprising: forming one or more of, a fullprotective image and / or a blended protective image, on the retina of the subject’s eye, configured to cover a fovea of the subject’s eye.

41. The method of claim 38, wherein the blended protective image is partially or completelysurrounded by the ocular photo-bio-stimulation light, and wherein the ocular photo-bio- stimulation light is configured to strike an optic nerve head of the subject’s eye and an additional area of the retina of the subject’s eye.

42. The method of claim 31, wherein the ocular photo-bio-stimulation light is applied when thesubject is wearing eyewear comprising the myopia control lens, such that the ocular bio-photo- stimulation light is transmitted through a front surface of the myopia control lens.

43. The method of claim 31, wherein the ocular photo-bio-stimulation light is applied when thesubject is not wearing eyewear comprising the myopia control lens.

44. The method of claim 31, wherein the provided myopia control lens is worn by the subjectoutdoors and in sunlight.

45. The method of claim 31, wherein the provided myopia control lens is worn by the subject aftera regiment of ocular light therapy sessions are completed.

46. The method of claim 32, wherein eyewear, spectacles, a headset, a face shield, a heads-updisplay, a helmet, a display screen, headwear, lens(es), optic(s), mobile equipment, hard-wired equipment, stationary equipment, or combinations thereof, comprise the one or more ocular photo-bio-stimulation light sources and / or the fixation target.

47. The method of claim 31, wherein the applied ocular photo-bio-stimulation light is defocused,and wherein the defocused applied ocular photo-bio-stimulation light strikes one or more peripheral areas of the retina of the subject’s eye.

48. The method of claim 31, wherein the ocular photo-bio-stimulation light applied to the retina ofthe subject’s eye is one or more of, diffuse light, collimated light, focused light, or defocused light.

49. The method of claim 31, wherein the one or more ocular photo-bio-stimulation light sourcesare one or more of, light-emitting diodes (“LEDs”), organic LEDs (“OLEDs”), transparent organic LEDs (“TOLEDs”), micro-organic LEDs, micro-OLEDs, micro-LEDs, ionic liquids for electrochemical devices (“iLEDs”), micro-iLEDSs, quantum dots, fluorescent nanoparticles, incandescent lights, fluorescent lights, one or more lasers, or plasma.

50. The method of claim 31, wherein the provided myopia control lens comprises a central zoneand a peripheral zone comprising or more of: light defocus; light dispersion; light diffusion; light scattering; lenslets; aspheric lenslets; a honeycomb array of lenslets; micro-structured materials; nanoparticles; alternating rings of focus and defocus; refractive optical power; diffractive optical power; a combination of diffractive and refractive optical power; a Fresnel lens; a micro-lens array; liquid crystal(s); electronic chromic material; zone(s) of progressive curvature changes; or chromatic aberration focused technology.

51. The method of claim 31, wherein the provided myopia control lens comprises one or more of,H.A.L.T. technology (Highly Aspheric Lenslet Target), D.I.M.S. technology (Defocus Incorporated Multiple Segments), C.A.R.E. technology (Cylindrical Annular RefractiveElements), DOT technology (diffusion optics technology), Focus Flow Technology, positive optical power defocus, negative optical power defocus, or chromatic aberration focused lens technology.

52. The method of claim 31, wherein the provided myopia control lens is housed within eyewear,spectacles, a headset, a face shield, a heads-up display, a helmet, a display screen, headwear, lens(es), optic(s), mobile equipment, hard-wired equipment, stationary equipment, or combinations thereof.

53. The method of claim 31, the method further comprising: including a fixation target, whereinthe fixation target is located within or on an optical lens or optic or incorporated within equipment.

54. The method of claim 31, wherein the one or more ocular photo-bio-stimulation light sourcesare supported by or attached to one or more of, eyewear, spectacles, one or more optical lenses, one or more optics, or mobile or stationary equipment.

55. The method of claim 31, wherein an intensity of the ocular photo-bio-stimulation light is500 lux or greater when measured at the one or more ocular photo-bio-stimulation light sources, and wherein the ocular photo-bio-stimulation light is 400 lux or greater when it strikes the retina of the subject’s eye.

56. The method of claim 31, the method further comprising: protecting the macula and / or fovea ofthe subject’s eye by way of imparting a fully protective image and / or a blended protective image that covers part or all of the macula and / or the fovea of the subject’s eye.

57. The method of claim 31, wherein the one or more ocular photo-bio-stimulation light sourcesmodulate within a range of one of: 5Hz to 15 Hz, 10Hz to 20Hz, or 40Hz + / - 20Hz.

58. The method of claim 31, the method further comprising: providing one or more of, an alarm,an automatic off, a timer, a capability to store in memory or communicate a time of applied ocular light therapy, wireless communication, wired communication, biofeedback, one or more sensor, or eye tracking.

59. The method of claim 36, the method further comprising: turning off the applied ocular photo-bio-stimulation light when the fine-tuned fixation target or the fixation target is not being seen by the subject, not in optical alignment with the macula of the subject’s eye, or both.

60. A method for slowing or stopping myopia progression of a subject’s eye, the methodcomprising:a. treating a subject with ocular photo-bio-stimulation light during an ocular lighttherapy session, wherein the ocular photo-bio-stimulation light is provided by one or more artificial ocular photo-bio-stimulation light sources, and wherein the ocular photo-bio- stimulation light treatment lasts for 60 minutes or less during an ocular light therapy session; b. protecting all or part of a macula of the subject’s eye from all or some of the ocularphoto-bio-stimulation light by using a fixation target located between the one or more artificial ocular photo-bio-stimulation light sources and the subject’s eye, and wherein the fixation target forms a protective image over part or all of the macula of the subject’s eye, such that the ocular photo-bio-stimulation light is configured to strike an optic nerve head of the subject’s eye, a portion of the retina of the subject’s eye peripheral to the optic nerve head, or both; and c. providing one or more myopia control lenses to be worn by the subject for at least60 minutes before the ocular light therapy session, during the ocular light therapy session, after the ocular light therapy session, or combinations thereof; and d. wherein the method is operative to (a) slow or stop the myopia progression of thesubject’s eye, and (b) reduce or eliminate damage or a potential for damage to part or all of the macula of the subject’s eye caused by the treating ocular photo-bio-stimulation light.

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