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- Apr 25, 2026
- 10:00 a.m. - 12:00 p.m. (EDT)
- 221 Crescent St, Suite 103A, Waltham, MA 02453
Community EventJoin us for the New England Vision Connection
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Opus Genetics Reports Promising Early Results from BEST1 Gene Therapy Trial
Research NewsFirst patient shows vision improvements with a good safety profile.
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The Super-Sticky Shoes: Living With Retinitis Pigmentosa When the World Can’t See the Glue
Invisible DisabilityIn this deeply personal reflection, author Patti Brite Taylor shares what it feels like to live with retinitis pigmentosa—and how that experience inspired her mystery novel, The Vanishing Cactus, centered on a heroine with low vision.
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Eye on the Cure Podcast | Episode 91: Dr. George Magrath
Eye on the CureDr. George Magrath is the CEO of Opus Genetics, a clinical-stage biopharmaceutical company developing gene and small molecule therapies for vision-threatening eye diseases.
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Eye on the Cure Podcast | Episode 89: Dr. Christine Curcio
Eye on the CureDr. Curcio talks to host Ben about her epic career and recent Proctor Medal lecture with Dr. Cynthia Owsley at the 2025 ARVO conference.
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Eye on the Cure Podcast | Episode 88: Richard Small
Eye on the CureRichard Small, CEO of Neurotech, talks to host Ben Shaberman about ENCELTO™, the first and only FDA-approved treatment for adults with idiopathic Macular Telangiectasia Type 2 (MacTel).
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Want to support this historic event? Sponsorship and exhibitor opportunities are available for organizations, foundations, and industry partners dedicated to advancing retinal research and innovation. Learn more by sending an email to Partnerships@FightingBlindness.org.
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We are thrilled to announce Anastasia Pagonis will be the keynote speaker at United in Vision 2026!
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D.C. Metro Chapter Volunteer Opportunities
The DC Chapter is growing! Join our young professionals events for the Foundation Fighting Blindness, or become a part of the Young Professionals Committee.
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Eye on the Cure Podcast | Episode 85: Cindy Elden
Eye on the CureCindy Elden talks about her journey with Usher syndrome type 3 (USH3), the decades-long work and persistence of her non-profit, and the clinical trial it launched for an USH3 small molecule therapy.
