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Displaying 21–30 of 217 diseases results
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May 30, 2025
Legacy Donor Spotlight: Dr. Debora Elliott Ward
Dr. Debora Elliott Ward, a clinical psychologist living with retinitis pigmentosa, shares her journey of resilience, professional success, and commitment to supporting the Foundation Fighting Blindness by naming it a beneficiary in her estate plans.
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May 29, 2025
I find it difficult to explain my eyesight to people. I have retinitis pigmentosa (RP), which is a condition that progressively causes vision loss. I am legally blind, my peripheral vision is very limited, and most of what I see is blurry.
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May 23, 2025
Eye on the Cure Podcast | Episode 86: Lenore von Krusenstiern, MD, PhD
Dr. Lenore von Krusenstiern talks about Bluerock’s clinical trial for a photoreceptor replacement therapy for people with inherited retinal conditions such as retinitis pigmentosa and cone-rod dystrophy.
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May 15, 2025
ARVO 2025 Highlight: J&J’s XLRP Gene Therapy Didn’t Meet Primary Endpoint in Phase 3 Clinical Trial
Despite missing the primary endpoint, the treatment improved vision for some patients.
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May 13, 2025
The company is planning a Phase 2/3 clinical trial for the therapy in late 2025.
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May 12, 2025
Part B of the trial will enroll nine adult patients as well as three pediatric patients.
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May 9, 2025
The company is currently enrolling patients in its Phase 2/3 VISTA Clinical Trial.
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May 8, 2025
Eye on the Cure Podcast | Episode 85: Cindy Elden
Cindy 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.
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May 5, 2025
Rob Howden’s journey with AMD and GA truly shows that individuals can take control of their vision loss journey and find strength within their community. His story emphasizes the importance of proactive treatment, taking care of your mental health, and the invaluable support of friends and neighbors.
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May 2, 2025
Living With Usher Syndrome: Practicing, Prioritizing, and Protecting Your Mental Health
In this deeply personal reflection, Rebecca Alexander, LCSW-R, MPH, RYT, shares the emotional journey of living with Usher syndrome—not as a single moment of diagnosis, but as an ongoing evolution of identity, loss, and resilience. Drawing from her experience as a psychotherapist, she offers powerful insights and coping tools for navigating grief, preserving connection, and embracing the full complexity of the human experience.