#stargardt vision

[robynjones59]

Vision Training Software

A vision training software focuses on enhancing the eyesight of patient’s post-cataract surgery through strategic eye muscle exercises and vision therapy. We have the best vision improvement solution that allows for personalized treatment. Speak to our eye specialists to learn more about the eyesight problems that typically occur after surgery.

[grantminor98]

Fuzzy Vision After Cataract Surgery

Experiencing fuzzy vision after cataract surgery among other symptoms is very common in patients. Expert eye specialists may let the patients undergo certain innovative brain training programs or sessions that assist in normalizing their vision. It is crucial to deal with this issue correctly with the help of expert guidance.

[majimassqueaktoy]

Just thinking. Trying to maybe write later...

[dear-indies]

Disabled actors with ungiffed roles (of course any roles are welcomed) for disability pride month:

Michael J. Fox (1961) - has Parkinson's Disease - Designated Survivor (2018), See You Yesterday (2019).

Mat Fraser (1962) - has thalidomide-induced phocomelia - Loudermilk (2017-2020).

Daryl Mitchell (1965) African-American - is paraplegic - Fear the Walking Dead (2018-2023).

Warwick Davis (1970) - has spondyloepiphyseal dysplasia congenita - Willow (2022-2023).

Selene Luna (1971) Mexican - has dwarfism - Mayans M.C (2022-2023).

Cherylee Houston (1974) - has Hypermobility Ehlers-Danlos syndrome - Coronation Street (2010-2023).

Callan Mulvey (1975) ¼ Maori, ¾ Scottish - is blind in one eye - has been in a lot of things including Last King of the Cross (2023), Firebite (2021-2022), Till Death (2021), and Mystery Road (2020).

Shannon Murray (1976) - is paraplegic - Viewpoint (2021), Get Even (2020).

Kurt Yaeger (1977) - is a leg amputee - Another Life (2021).

Katy Sullivan (1979) - is a double leg amputee - Dexter: New Blood (2021-2022).

Jamie-Lynn Sigler (1981) Cuban / Ashkenazi Jewish, Romaniote Jewish, Sephardi - has multiple sclerosis - Big Sky (2021-2023).

Prince Amponsah (1985 or 1986) Ghanaian - is a double arm amputee, with his right arm amputated above the elbow and his left arm amputated below the elbow - Avacado Toast the series (2022) and Station Eleven (2021-2022).

Rana Daggubati (1984) Telugu Indian - is blind in one eye - Rana Naidu (2023).

Rick Glassman (1984) Jewish / Italian - is autistic - As We See It (2022), Not Dead Yet (2023).

Ali Stroker (1987) - is paraplegic and bisexual - Echos (2022), Only Murders in the Building (2021-2022), Ozark (2022).

Josh Thomas (1987) - is autistic, has ADHD, and is gay - Everything’s Gonna Be Okay (2020-2021).

Jillian Mercado (1987) Domincian - has spastic muscular dystrophy - The L Word: Generation Q. (2019-2023).

Ruth Madeley (1987) - has spina bifida - The Almond and the Seahorse (2022).

Tim Renkow (1989) Mexican Jewish - has cerebral palsy - Jerk (2019-2021).

Melissa Johns (1990) - is an arm amputee - Grantchester (2021-2022).

Steve Way (1990) - has muscular dystrophy - Ramy (2019-2022).

James Moore (1992) - has cerebral palsy - Emmerdale (2018-2023).

Arthur Hughes (1992) - has an upper limb indifference - The Innocents (2018).

Madison Ferris (1992) - has muscular dystrophy - Panic (2021).

RJ Mitte (1992) - has cerebral palsy - The Unseen (2023).

Mei Kayama (1994) Japanese - has cerebral palsy - 37 Seconds (2019).

Ryan J. Haddad (1995) Lebanese - has cerebral palsy - The Politian (2019-2020).

Lauren Spencer / Sitting Pretty Lolo (1996) African-American - has Lou-Gehrig’s disease - The Sex Lives of College Girls (Season 2).

Annabelle Davis (1997) - has dwarfism - Hollyoaks (2023).

Kayla Cromer (1998) - is autistic - Everything’s Gonna Be Okay (2020-2021).

Micah Fowler (1998) - has cerebral palsy - Speechless (the latter seasons!)

Daniel Monks (?) - is quadriplegic - Sissy (2022).

Matthew Jeffers (?) - has dwarfism - New Amsterdam (2018-2023).

Ben Mehl (?) - has macular degeneration called Stargardt's disease, which causes one to lose central vision- You (2021).

Gloria May Eshkibok (?) Mohawk, Ottawa, Irish, French - is Two-Spirit (she/her) and has one eye - OChiSkwaCho (2018).

Zack Weinstein (?) - is quadriplegic - Sing It! (2016).

Angel Giuffria (?) - is a congenital arm amputee - To the Dust (2022), Good Trouble (2022), Impulse (2019).

Joci Scott (?) - is paraplegic - Smash or Pass (2023).

Jacob Mundell (?) - congenital hand amputee - The Expanse (2021-2022).

+ HERE'S MY DISABLED FC MASTERLIST FOR MORE!

+ let me know if you have suggestions!

+ let me know if anybody wants suggestions with youtube content!

[twinkl22004]

“Fundus Flavimaculatus”, Victor McKusick, Mendelian Inheritance in Man, 1966.

Here I present: “Fundus Flavimaculatus”, Victor McKusick, Mendelian Inheritance in Man’, 1966. INTRODUCTION. Stargardt macular degeneration is a genetic eye disorder that causes progressive vision loss.  Fundus flavimaculatus (FFM) is an allelic subtype of Stargardt disease that has been associated with mutation in the ABCA4 gene.  FFM has a later age of onset. If loss of visual acuity begins in…

[amliflatiron]

Apartments Near Atlanta Financial Center

Living in an apartment near Atlanta Financial Center gives plenty of benefits, especially for those working in the area or enjoying the urban core lifestyle. Also, commuting to work is a breeze, as it can be done by walking, biking, or using public transportation. The area is the heart of Atlanta's business district, surrounded by skyscrapers, vibrant energy, and diverse restaurants, bars, and shops. Living near the Financial Center provides easy access to career opportunities, especially for professionals in finance, banking, insurance, or related fields. Besides, the Downtown Atlanta have a variety of cultural attractions, museums, art galleries, theaters, sporting events, concerts, and nightlife venues for you to enjoy. If you're looking for an apartment near Atlanta Financial Center, visit the AMLI Flatiron because this is an excellent choice. Schedule your appointment, contact (866) 478-0109.

Atlanta, GA, Job Market

Atlanta is known for its stable labor market, so largely thanks to the high concentration of Fortune 500 corporations within the city. There are 16 of them, so you can find jobs immediately if you're looking for a job. The major businesses in Atlanta span various sectors such as healthcare, education, and infrastructure, providing a wide array of professional opportunities. There are also notable companies like Delta Air Lines, The Home Depot, and Coca-Cola, which consistently offer exciting career prospects. Also, Atlanta's growing IT and entertainment industries contribute to the diverse job market, creating even more opportunities for job seekers.

Atlanta History Center

The Atlanta History Center is a museum that showcases Atlanta's rich past, showcasing its evolution and people's stories. The visitors can explore permanent exhibits like Atlanta in Five Acts, Civil War Atlanta, Making Atlanta Modern, and Beyond the Ballot: Black Suffrage and Voting Rights in Georgia. This center also houses historical houses like Swan House, Smith Family Farm, and Wood Family Cabin, showcasing the lives of past residents. You can also look at Margaret Mitchell House & Museum which provides insight into the world of Margaret Mitchell, the author of Pulitzer Prize-winning novel "Gone With the Wind." The center also houses the Kenan Research Center, a vast archive with historical documents, photographs, and artifacts, for researchers and genealogists. There are also special events like lectures, workshops, film screenings, and family-friendly programs.

Team USA Shines Bright in Paralympics Games

Atlanta native Gia Pergolini won the 100m backstroke S13 at the 2024 Paris Paralympic Games. I'm proud of her for helping the Team USA retain its back-to-back title. Pergolini, a 20-year-old from Atlanta, won gold in the same event in 2021 at the Tokyo Paralympic Games. She also won gold in the same event at the 2022 World Championships and added a gold in the 100m freestyle S13. Her 100m backstroke time of 1:04.64 in the final at the Tokyo Games set a world record that everyone admires. According to his bio, Pergolini began focusing on swimming after being diagnosed with Stargardt disease. It's a degenerative muscular condition of the eyes that causes vision loss during childhood or adolescence. He proved that he could do more regardless of what condition he had.

Link to map

Atlanta History Center 130 W Paces Ferry Rd NW, Atlanta, GA 30305, United States Take W Paces Ferry Rd NW to Peachtree Rd NE 4 min (0.6 mi) Turn right onto Peachtree Rd NE 5 min (1.2 mi) Continue on Lenox Rd NE to your destination 2 min (0.4 mi) AMLI Flatiron 3480 Lakeside Dr NE, Atlanta, GA 30326, United States

[retinography]

Stargardt disease

Stargardt disease, associated with mutations in the ABCA4 gene, is the most common form of inherited juvenile macular degeneration. It is characterized by progressive loss of central vision, often beginning in childhood or adolescence. The disease leads to the accumulation of lipofuscin in the retinal pigment epithelium, visible as yellowish flecks on imaging studies, predominantly affecting the…

[marjaystuff]

Interview with Tarrie Marie

Blaque Pearle

Creed Family Book 1

Tarris Marie

Black Odyssey Media

Sept 26th, 2023

Blaque Pearle by Tarris Marie intertwines crime, romance, and the ‘90s era. Much like her characters, the author also took a powerful journey, having to overcome Stargardt Disease, a genetic condition that caused her legal blindness and cost her a corporate job. 

The plot has deeply flawed but relatable characters who risk everything for love and family.  The main female lead, Pearle Brown was an aspiring actress that got caught up in her brother’s scheme.  She decides to use her beauty and acting skills to swindle money and expensive jewels from unsuspecting people. When she and her brother are hired to steal a priceless Basquiat from the debonair kingpin and art collector, Blaque, her talents might not be enough to keep her from falling into a trap she never saw coming, falling in love with him. Although he is from two powerful crime families he also falls in love with Pearle and will do anything to keep her safe.  Together they use their skills to battle their enemies and help those in need.

The book has vivid descriptions, captivating characters, and a complex storyline. It is not only riveting but informative as well.

Elise Cooper: Why become a writer?

Tarris Marie: I decided to write after I lost my central vision.  I had come from the corporate world and after losing some of my vision I became depressed and was on a downward spiral. When I was on the floor, I heard a voice telling me to get up.  I asked God what to do and heard, write a book. This was in 2020 when I decided to write a series, a total of four novels.

EC:  Do you want to talk about your disease?

TM:  Stargardt Disease is a hereditary disease of the retina, affecting the central sight.  It is a juvenile form of Macular Degeneration. For me, I got it my late thirties.  Now I am legally blind.  It does not affect my peripheral vision, but I could not see anything I directly look at. My support system is my husband, children, family, friends, and the best doctors. I use technology to help me become independent. 

EC:  Is the story related to your life?

TM:  I wrote about the decade in which I grew up. I was trying to find myself, so I went back in time. This book is the first book to come out, taking place in the 1990s.  I grew up in an urban environment in Gary Indiana, America’s murder capitol.  I grew up in a loving home.  I lived the 1990s culture, the hip-hop music, and the hairstyles. I met a lot of people, learned a lot, and grew a lot. 

EC:  Why did you make your hero and heroine “bad guys?”

TM:  They start off as “bad.”  But there was redemption, and the characters were relatable considering the decisions made was to survive. I was also able to relate to these characters because I do know what it feels like to be in a place where you must do what is necessary to survive. 

EC:  Why not end the story with Part I?

TM:  Part I was more about the drug aspect, while Part II concentrated on human trafficking. In the late 1990s it used the Internet, a lot of traps for young girls.  

EC:  How would you describe Pearle?

TM:  Low-key, greedy, quiet, protective, and loyal. I named her Pearle, symbolic because it has a lot of layers.  Like the gemstone, the character has a hard exterior, but has layers. 

EC: How would you describe Blaque?

TM:  Gentle but could be rough and powerful.  A listener, honest, funny, open-minded, adventurous, mysterious, and serious. I named him Blaque to represent the black male that I knew. He loved the women in his life and respected them. The color black is mysterious and sexy. Putting his name along with Pearle, the gemstone Black Pearl is unique, created in a different type of oyster. It represents healing of broken hearts. Like me, I needed to heal because I was broken. I hope to take any reader on that journey as well.

EC: Next book?

TM:  The title is Empress Creed, out in February 2024.  It is a prequel with a hindsight into the family. It takes place in the 1930s in the Midwest and shows how the crime family got started. 

THANK YOU!!

[nexuseyecare]

Inherited retinal diseases (IRD)

Inherited retinal diseases (IRD) are a group of rare genetic conditions that affect the retina, the delicate tissue at the back of the eye responsible for vision. These conditions are typically caused by mutations in specific genes responsible for maintaining the health and function of the retina. IRD can result in varying degrees of visual impairment, and in some cases, lead to blindness. They can be inherited in several ways, such as dominant, recessive and sex-linked. 

The most common types of IRD include Retinitis Pigmentosa (RP), Stargardt disease, Bests Juvenile Dystrophy and others.

Symptoms of IRD

The symptoms of IRD can vary widely, even among individuals with the same condition. According to retina specialists, night blindness, tunnel vision, and difficulty distinguishing colours are common early signs. Vision loss is usually slow-progressing. In later stages, central vision may also be affected, impacting simple daily activities like reading and recognising faces. Living with IRD often requires adapting to a changing visual landscape.

Diagnosis of IRD

Early and accurate diagnosis is pivotal in managing IRD. Electrophysiology testing often helps clarify if IRD is present or not, and genetic testing can help identify specific mutations for an accurate diagnosis and management plan.

Treatment

Regular visits to an ophthalmologist or retinal specialist, to monitor the progression of the disorder, manage symptoms, and provide support are important. Genetic counselling may also be recommended to understand the inheritance pattern and potential implications for children and family members. Additionally, emerging treatments and clinical trials may be discussed with retina specialists as part of ongoing care. 

While there is currently no cure for most IRD, ongoing research holds promise for future treatments. Gene therapy, stem cell therapy and retinal implants are among the innovative approaches being explored to slow or halt the progression of vision loss. Additionally, low vision aids, orientation and mobility training, and adaptive technologies play a crucial role in managing visual challenges and enhancing the quality of life for those affected by IRD.

Support groups and advocacy organizations are valuable resources to connect individuals and families affected by IRD. These communities provide a platform for sharing experiences, accessing resources, and participating in research initiatives that aim to unravel the mysteries of these complex disorders. 

IRDs are challenging and often difficult to predict and manage. As science continues to advance, there is hope for improved diagnostics and ground-breaking treatments. Through increased awareness, support networks, and ongoing research, vision loss due to IRD may one day be preventable or effectively managed. It is important for individuals with IRDs to work closely with their healthcare team and retina specialists to address their specific needs and stay informed about available options.

[spacenutspod]

5 min read NASA’s Modern History Makers: Maricela Lizcano Maricela Lizcano poses inside NASA Glenn Research Center’s Aerospace Communications Facility.Credit: NASA/Bridget Caswell >back to gallery Maricela Lizcano never dreamed of working for NASA. In fact, she wasn’t planning on furthering her education until she had a revelation in her late twenties. “I was watching one of those forensic shows, and I loved the way they caught the criminals with science,” said Lizcano, research materials engineer at NASA’s Glenn Research Center in Cleveland. “I wanted to be able to do that. I realized I should be studying science and engineering.” It took Lizcano about ten years to prepare mentally and financially to go back to school, and during that time, she received some startling news. “I found out that I was losing my sight, and it was very scary,” Lizcano said. “I think that was one of the things that tossed me off the rails. I had so many questions: ‘What am I going to do? How am I going to work or go to school? How quickly am I losing my vision?’ There were no answers.” Lizcano was diagnosed with Stargardt disease, a rare genetic eye disease that occurs when fatty material builds up on the macula — the small part of the retina needed for sharp, central vision. “My Stargardt disease started on the outer edges of my macula, and over time, it grew to the center,” Lizcano said. “By the time I was 45 years old, it had pretty much taken all of my central vision, and now I rely on my peripheral vision to see.” Eventually, Lizcano viewed this as another obstacle to hurdle, no different from any others she had experienced in her life. She attended the University of Texas–Pan American, now called the University of Texas Rio Grande Valley. She started during a second summer session, easing her way to full-time attendance while also holding a job. Because of her new disability, she couldn’t see what professors were writing on the board. She taught herself to listen intently to the topics being discussed in the lecture, then after class, she read the textbook and rewrote the lecture notes using special magnification tools. “It took that much longer, but you learn to adapt,” Lizcano said. “There are certain skills you develop because of the changes you have to make when you have a disability. I learned that I really have to listen.” After five years, Lizcano completed her mechanical engineering degree. She didn’t get a job right away after graduation, so she continued her education and earned master’s and doctorate degrees. “I can’t just look at my disability as some great thing that I really had to overcome,” Lizcano said. “I think a lot of people overcome many obstacles because we are driven by the desire to achieve things. You don’t see the challenges as challenges, you just see them as something to conquer to get to your goal.” In 2010, former President Barack Obama signed an executive order to increase federal employment of individuals with disabilities. The executive order directed executive departments and agencies to improve their efforts to employ workers with disabilities through increased recruitment, hiring, and retention of these individuals. “Through the Workforce Recruitment Program, I had the opportunity to interview with representatives from federal agencies,” Lizcano said. “I heard nothing for a long time, but then suddenly I got an email from NASA Glenn asking if I’d present my research.” She accepted a job as a research materials engineer and now leads a team working on high-voltage materials for electrified aircraft. She collaborates with various universities to develop composite insulation materials and lightweight conductors. Even now working at NASA, Lizcano faces challenges that she finds ways to overcome. She depends on her fellow colleagues to carpool to work and accessibility tools — like the magnifier app — to use her computer. “Understanding my needs allowed me to get over the fact that I lost my independence,” Lizcano said. “It was a mind shift to be all right with asking for help.” Lizcano’s recommends a science, technology, engineering, and mathematics career to anyone looking for a challenge or excitement. “We’re always solving problems. If you’re one of those people who really wants to make a difference in the world, STEM careers are a good place to start,” Lizcano said. “Any challenge that you may have in result of a disability is no different than the challenge you’re trying to solve, and it will give you the motivation and unique skills you need to be successful.” NASA is in a Golden Era of aeronautics and space exploration. In partnership with commercial and private businesses, NASA is currently making history with significant missions such as Artemis, Quesst, and electrified aviation. The NASA’s Modern History Makers series highlights members of NASA Glenn’s workforce who make these remarkable missions possible. Jacqueline MinerdNASA’s Glenn Research Center Explore More 6 min read Lynn Bassford Prioritizes Learning as a Hubble Mission Manager Lynn Bassford levels decades of experience and a desire for self-growth as she helps lead… Article 7 days ago 1 min read Dr. Guy Bluford Reflects on 40th Anniversary of Historic Shuttle Flight  Article 1 week ago 3 min read Glenn in the Community Article 1 week ago

[vaidyaeyehospital]

What are some unusual or rare eye conditions that most people are not aware of?

There are several unusual and rare eye conditions that many people may not be aware of. These conditions often affect a small percentage of the population and can vary in terms of symptoms and severity. Here are a few uncommon eye conditions:

1. Aniridia: Aniridia is a congenital condition characterized by the absence of the iris (the colored part of the eye). People with aniridia often have sensitivity to light and visual impairments.

2. Achromatopsia: Achromatopsia, also known as "total color blindness," is a rare genetic condition in which individuals cannot perceive any colors and see the world in shades of black, white, and gray. They also often have extreme light sensitivity.

3. Ocular Albinism: Ocular albinism is a genetic condition that affects the pigmentation of the eyes, resulting in reduced visual acuity and nystagmus (involuntary eye movements). People with ocular albinism may have pale blue or gray irises.

4. Stargardt Disease: Stargardt disease is an inherited form of macular degeneration that typically affects children and young adults. It leads to central vision loss and can cause difficulty with reading and recognizing faces.

5. Iris Coloboma: Iris coloboma is a congenital condition in which there is a notch or gap in the iris. This can cause varying degrees of visual impairment and light sensitivity.

6. Keratoconus: Keratoconus is a progressive eye condition in which the cornea (the clear front surface of the eye) thins and bulges into a cone shape. This can result in distorted vision and may require specialized contact lenses or surgery for correction.

7. Retinitis Pigmentosa: Retinitis pigmentosa is a group of inherited disorders that affect the retina, leading to gradual vision loss. Symptoms often include night blindness and tunnel vision.

8. Charles Bonnet Syndrome: This condition occurs in people with significant vision loss, such as those with macular degeneration or glaucoma. They experience vivid and complex visual hallucinations, which can be unsettling.

9. Visual Snow Syndrome: Visual snow is a neurological condition in which individuals perceive constant, static-like visual disturbances, similar to "visual noise." It can be accompanied by other visual symptoms.

10. Birdshot Chorioretinopathy: This is a rare inflammatory eye disease that primarily affects the retina and choroid. It can lead to vision loss, floaters, and difficulty adapting to changes in lighting.

These are just a few examples of rare eye conditions. While these conditions are uncommon, they can have a significant impact on an individual's vision and quality of life. If you or someone you know experiences unusual or concerning eye symptoms,

It's important to consult an eye care professional Dr. Vaidya one of the Best Eye Doctors in Mumbai for a proper diagnosis and management. know more information visit our hospital at Dr. Vaidya Eye Hospital.

[sanjeevannetralaya]

Stargardt Disease Symptoms Type Causes & Treatment

Stargardt disease, also referred to as Stargardt macular dystrophy or juvenile macular degeneration, is an inherited disorder affecting the macula - the small central area at the back of each eye that provides sharp, detailed vision in straight lines.

Disease typically begins during childhood or adolescence and progresses over time to cause progressive vision loss, including central vision loss, difficulty reading, difficulties recognising faces and loss of color vision.

Stargardt disease is caused by mutations to the ABCA4 gene, which provides instructions for producing an ATP-binding cassette transporter A4 protein that transports lipofuscin away from retinal cells - in those suffering from Stargardt disease, lipofuscin accumulates and eventually kills macula cells, leading to vision loss over time.

Current treatments of Stargardt disease do not offer a permanent solution, but treatments may help manage symptoms and slow progression such as tinted glasses, vitamin supplements, or low-vision rehabilitation.

Stargardt disease is an inherited disorder caused by mutations to genes passed down from parent to child. More specifically, Stargardt disease stems from mutations to ABCA4 gene which provides instructions for making an ATP-binding cassette transporter A4 protein involved with transporting lipofuscin out of retina cells.

What are the causes of Stargardt Disease?

Stargardt disease is caused by mutations to the ABCA4 gene that lead to an accumulation of lipofuscin in cells of the macula, ultimately leading to their death and gradual vision loss. Stargardt is passed down autosomally recessively; meaning a person must inherit two copies from each parent in order to develop symptoms; those inheriting only one mutated copy from either parent are known as carriers who do not usually show signs or symptoms but can pass the gene onto future generations.

Stargardt disease can be caused by mutations to the ABCA4 gene, with severity and progression depending on which mutation has taken place.

What are the symptoms of Stargardt Disease?

Stargardt disease affects central vision, or your ability to see fine details and objects directly in front of you. Symptoms may differ depending on the person suffering, but may include:

· Blurry or distorted vision when looking directly at objects.

· Difficulties reading text that appears smudged, distorted, or blurry.

· Loss of color vision where colors appear washed-out or faded-out. And difficulty recognising faces or familiar objects as soon as they enter your field of vision.

· Sensitivity to bright light or difficulty adapting to changes in lighting.

· Visual hallucinations or illusions such as seeing patterns or shapes that do not actually exist. Progressive vision loss over time that could eventually lead to legal blindness.

Stargardt disease typically impacts both eyes equally, with symptoms often starting in childhood or adolescence; however, they can sometimes appear later in life. Not everyone experiencing Stargardt experiences all of its symptoms, as its severity and progression varies considerably among individuals.

Sanjeevan Netralaya has a customised treatment plan for each patient and treats Stargardt Disease effectively. There is no discomfort, pain or side effect from the treatments. You should have your eyes checked regularly, so make an appointment today!

[dear-indies]

hey! do you have any suggested faceclaims for daredevil/matt murdock? im not sure it’s appropriate to use charlie and would love to use a blind fc if possible

Stephen Wallem (1968) - is visually impaired.

Bruce Horak (1974)

Chris McCausland (1977)

Adam Morse (1983) - also did his own stunts in "See."

Blake Stadnik (?)

Melchior Beslon (?)

Ben Mehl (?) - has Stargardt's disease.

Non-actors:

Scott MacIntyre (1985) - only has 2% field of vision and has tunnel vision both due to Leber’s Congenital Amaurosis.

Justin Kauflin (1986) - blind due to retinopathy.

Vernon Barnard (1993) Afrikaner.

Mac Potts (?)

HOLLYWOOD HIRE ACTUAL DISABLED ACTORS CHALLENGE. Natalie and I made a blind/visually impaired masterlist over HERE but these are the people who (seem to!) have the most content but it'll be worth going over the list yourself too!

[crows-nest-system]

So I found out that I have Stargardts Disease. (An eye disease that causes central blindness and vision issues)

My mother is legally blind and has Stargardts, so this isn't new to me by any means at all. She's the type you will see with sunglasses and a cane due to the stage her stargadts is.

Mine is in the very early stages, known as stage one so I just see small blurry or hazy shapes and white speckles or floaties in my central vision. But it was surprising to find out as late as 26 that I have it.

The tiny dots and gold flecks is Stargardts.

[newstrendline]

Stargardt disease

Is Stargardt Disease the Cause of Your Loss of Vision? There are a number of questions people with Stargardt disease often ask, including whether the disease is curable and how fast it progresses. Other questions include whether you can drive if you have Stargardt, and whether the disease causes total blindness. To learn more, read on. Here are a few tips for determining if Stargardt is the cause…