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Displaying 51–60 of 1175 results
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Living Life Through My Eyes: My Journey with XLRS
Invisible DisabilityThere are moments when I wish I could see the world the way everyone else does. But I’ve realized that focusing on what I’ve lost only takes away from what I still have. XLRS may affect my eyesight, but it doesn’t define who I am.
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Belite Bio Submits New Drug Application to FDA for its Stargardt Treatment
Research NewsTinlarebant becomes first Stargardt treatment submitted to FDA for approval
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Access United in Vision 2026 Recordings
United in Vision brought together the blind and low vision community for two days of groundbreaking science, inspiring patient stories, and expert-led discussions in Fort Worth this June. Whether you joined us in person, tuned in via livestream, or weren’t able to attend, you can now access the full library of session recordings.
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Eye on the Cure Podcast | Episode 101: Dr. Patrick Staropoli
Eye on the CureNew host Maddie Mossman interviews retinal surgeon Dr. Staropoli, the first medical doctor to win a NASCAR race.
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Invisible Disability
Life is inherently uncertain, but what happens if we embrace that? Trust yourself and your intuition. My strength is for me to define, no one else.
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Recording Available: Insights Forum | Wednesday, June 24, 2026
Foundation NewsThe Foundation Fighting Blindness is pleased to provide a recording and full transcript of the Insights Forum, our quarterly conference call providing updates to the blinding diseases community. The call took place on June 24, 2026.
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Foundation News
This two-day golf tournament at Sanctuary Golf Course will help accelerate research toward treatments and cures for blinding diseases.
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A Story About Losing Sight and Discovering the Power of Seeing Differently
Invisible DisabilityRead an excerpt from ‘I See You,’ where Meredith Kole shares her experience of being diagnosed with a blinding disease at age 13 and how art became a powerful form of self-expression, reflection, and resilience.
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Beacon Stories
Tamar Bresge is an artist, writer, and educator living with retinitis pigmentosa (RP) due to Usher syndrome. She reflects on her vision loss journey from hiding her diagnosis to embracing it as an inseparable part of her identity — and how her work in art, writing, and teaching has become a way to create the visibility and connection she once needed herself.
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Potential Oral Stargardt Treatment Advances to Phase 3 Clinical Trial
Research NewsPromising oral treatment moves closer for Stargardt patients.
