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Displaying 31–40 of 1139 results
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Sep 22, 2025
Agnes Gund – Renowned Philanthropist, Social Justice Champion, and Art Patron – Passes Away
The documentary “Aggie: An Incredible Story of Art and Justice” chronicles her story.
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Sep 22, 2025
A Family United: Thomas’ Hero’s Journey with CRB1
When Becky’s son Thomas was diagnosed with a rare CRB1-associated disease, their family’s world changed. But today, Becky and Thomas are embracing advocacy, community, and research as they work to raise awareness and fuel progress toward treatments and cures.
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Sep 18, 2025
What to Expect from a Therapy Consultation
Therapy consultations can help you find the right fit before committing. Learn what to expect, key questions to ask, and how to make the most of your time.
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The United in Vision 2026 conference unites two prestigious events—the Foundation Fighting Blindness VISIONS conference and the Retina International World Congress—into one extraordinary global gathering.
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Sep 17, 2025
Letter to House Energy & Commerce Committee regarding H.R.1262, the Give Kids a Chance Act.
On behalf of the Foundation Fighting Blindness and the millions of Americans impacted by inherited retinal diseases (IRDs), we urge you to advance H.R.1262, the Give Kids a Chance Act, and reauthorize the Rare Pediatric Disease Priority Review Voucher (PRV) Program.
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Sep 17, 2025
Give Kids a Chance: Reauthorizing a Lifeline for Children’s Vision
The House Energy & Commerce Committee is considering H.R.1262, the Give Kids a Chance Act, which would reauthorize the Rare Pediatric Disease Priority Review Voucher (PRV) Program.
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Funded Foundation Fighting Blindness Grants and Awards for Fiscal Year 2024 (July 1, 2024 – June 30, 2025)
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Sep 12, 2025
Nacuity’s Antioxidative Therapy NACA Performs Encouragingly in Phase 1/2 Clinical Trial
NACA is a gene-agnostic, oral medication designed to preserve vision in people with retinitis pigmentosa and Usher syndrome.
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Sep 11, 2025
Recording Available: Insights Forum | Wednesday, August 27, 2025
The 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 August 27, 2025.
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Sep 8, 2025
Maverick, a determined and adventurous 11-year-old, was diagnosed with X-linked retinoschisis (XLRS) at age six, which led his family to find support and resources through the Foundation Fighting Blindness. Since his diagnosis, Mav continues to pursue his passions in sports and outdoor activities, inspiring his family with his resilience and positive attitude.