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Displaying 591–600 of 830 for “retinal diseases”
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Feb 5, 2024
Foundation’s Reach Inspires Partnership for Nixon Family
After Janine’s diagnosis of an IRD caused by a mutation of the PRPH2 gene, she and her husband set out to learn and help all they could. So they started working with the Foundation Fighting Blindness and have launched the ‘PRPH2 and Associated Retinal Degenerations Program.’
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Jun 27, 2024
Grab your friends for a fun night out to support Foundation Fighting Blindness and our mission to fund research to prevent, treat, and cure blinding retinal diseases.
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Jun 17, 2024
You are invited to join us at the inaugural Fountain Cup for a day of golf to support the urgent mission of the Foundation Fighting Blindness to find treatments and cures for blinding retinal diseases.
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May 30, 2024 (PST)
We invite you to join us at the Seattle Taste for Sight event to enjoy a selection of wine, beer, specialty craft cocktails, and delicious bites in support of the urgent mission of the Foundation Fighting Blindness to find treatments and cures for blinding retinal diseases.
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May 9, 2024
We invite you to join us for our annual Night for Sight event at The Lighthouse. This event will support the Foundation Fighting Blindness’ mission to find treatments and cures for blinding retinal diseases and macular degeneration.
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VISIONS 2024, the national conference of the Foundation Fighting Blindness, is a one-of-a-kind event in which individuals who are visually impaired, and their families, have the opportunity to hear about exciting advancements in blindness research.
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May 12, 2023
Eye on the Cure Podcast – Transcripts
The Eye on the Cure Podcast from the Foundation Fighting Blindness provides science information, news, and insights from the world of vision and retinal diseases. The podcasts are hosted by Ben Shaberman, vice president, science communications, and often include conversations with guests from the research and vision communities.
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The Foundation Fighting Blindness Peer Guide Program brings people who share common life experiences and goals together. Whether you live with a blinding retinal disease or have a family member or friend, the benefits are empowering. While working with a Peer Guide, they will direct you to some of the various resources
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Nov 18, 2022
Eye on the Cure Podcast – Episode 35: Kenji Fujita, MD
November 18, 2022. Ben Shaberman talks with Kenji Fujita, MD.
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Colin was born in the small Western New York Community of Jamestown. His emersion into the arts started naturally, his mother was a designer and his father an art and antiques collector.