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Displaying 451–460 of 578 for “Retinitis pigmentosa”
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Foundation News
My Retina Tracker Program is the highest volume IRD genetic testing program in the U.S.
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Foundation News
Known as Pro-EYS, the study will help researchers design clinical trials for potential therapies
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Foundation News
The program will offer patients with inherited retinal disease no-cost genetic testing and genetic counseling in the United States. Look for updated information on how to participate to be posted in mid-October, with program registration starting shortly thereafter.
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Foundation News
Three-day conference in San Diego will feature retinal science’s leading researchers and clinicians, and focus on the year’s top science and emerging treatments
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Foundation News
The free, online event on March 20, 2024, will feature presentations from Rachel Huckfeldt, MD, PhD, Mass Eye and Ear, and Rachelle Lin, OD, Ketchum University.
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Foundation News
The May 11th gala will raise awareness and fund research leading to treatments and cures for blinding retinal diseases.
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Foundation News
Uni-Rare Study will improve clinical understanding of more IRDs and boost development of potential therapies.
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My name is Christy Johnson, I have Retinitis Pigmentosa, a degenerative, progressive disease that will eventually rob me of my sight. Having been diagnosed only 2 years ago, I learned that I now have 38 degrees of periphery, suffer from severe night blindness, and I am having difficulty being able to see certain colors.
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Foundation News
Initiatives to increase engagement and awareness around blinding retinal diseases.
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Foundation Fighting Blindness Makes Key Appointments to Leadership Team
Foundation NewsSeveral executives promoted to continue the advancement of the Foundation’s notable research and philanthropic efforts.
