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    • About
      • Our Story
      • Our Vision/Mission
      • Our Team
      • Pressroom
    • For Families
      • What is LCA?
      • ID Your Gene
      • Clinical Trials
      • Resources
      • Rare Retinal Disease Glossary
      • Family Connections
      • Sofia Sees Hope Ambassadors
      • Let’s Chat About…
    • Stories
      • Posts & Videos
      • Photo Gallery
    • Get Involved
      • Dinner in the Dark
      • LCA Family Conference
      • Event Calendar
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    Archives

    Monthly Archive for: "February, 2020"
    0
    By Rosanne Smyle
    In Blog
    Posted February 27, 2020

    Connecticut Rare Disease Day 2020

      The end of February signals the time to focus awareness on rare conditions by celebrating Rare Disease Day, a global event addressing the thousands of rare diseases that affect one in [...]

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    0
    By Eissa Bass
    In Blog
    Posted February 14, 2020

    Living with Leber Congenital Amaurosis: Dami’s Story

    By Damiana Harper I was born in 1976 in Spokane, Washington. By the time I was born, my parents’ relationship was basically over, so I was raised by a single mom. It was clear from a very young [...]

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    0
    By Eissa Bass
    In News
    Posted February 14, 2020

    Sofia Sees Hope Supports Research into Inherited Retinal Diseases Treatment

    Sofia Sees Hope donated more than $100,000 at the end of 2019 to support research into treatments for inherited retinal diseases (IRDs), including Leber congenital amaurosis (LCA), and to provide [...]

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