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    Leber Congenital Amaurosis Leber Congenital Amaurosis Leber Congenital Amaurosis Leber Congenital Amaurosis
    • About
      • Our Story
      • Our Vision/Mission
      • Our Team
      • Hope in Focus Ambassadors
      • Pressroom
    • Living with LCA
      • What is LCA?
      • ID Your Gene
      • Clinical Trials
      • Family Connections
    • Community
      • Community News
      • Resources
      • Rare Retinal Disease Glossary
    • Events
      • LCA Conference 2025
      • Party for Sight
      • Dinner in the Dark
      • Photo Gallery
    • Contact
      • Get in Touch
      • Newsletter
    • DONATE

    Archives

    Monthly Archive for: "July, 2018"
    0
    By Sofia Sees Hope
    In Blog
    Posted July 17, 2018

    Tell Us Your Story: ‘Do Not Limit Yourself’

    By Angélica Bretón Morán I am 22 years old and I have LCA. My name is Angélica Bretón Morán, I am from Mexico, I am 22 years old and I […]

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    0
    By Rosanne Smyle
    In Blog
    Posted July 8, 2018

    An Amazing Year

    This is the seventh in a series following the progress of Creed Pettit, a 9-year-old Florida third-grader, who completed treatment in March with the breakthrough gene-therapy drug called [...]

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    0
    By Eissa Bass
    In News
    Posted July 5, 2018

    Sofia Sees Hope Receives Grant From Sanofi Genzyme

    Sofia Sees Hope, a nonprofit dedicated to assisting those with Leber congenital amaurosis (LCA) and other rare inherited retinal diseases (IRDs), has received a $22,000 grant from Sanofi Genzyme, [...]

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