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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
      • Hope in Focus Podcast
      • Resources
      • Rare Retinal Disease Glossary
    • Events
      • Chef’s Menu at Cedars
      • Holiday Shop
      • Photo Gallery
    • Contact
      • Get in Touch
      • Newsletter
    • DONATE

    Blog

    0
    By Sofia Sees Hope
    In Blog
    Posted May 15, 2017

    Flexibility, Growth and Drive Cure This Rare Disease

    Being blind, or living with someone who is, requires all sorts of adaptation and flexibility. Creating a nonprofit to cure blindness caused by rare inherited retinal diseases like Leber [...]

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    0
    By Sofia Sees Hope
    In Blog
    Posted April 20, 2017

    What’s for Dinner?

    Wondering what has been served at Dinner in the Dark over the years? Here are the menus!   Dinner in the Dark 2025 This year marked our 10th Dinner in […]

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    0
    By Sofia Sees Hope
    In Blog
    Posted April 12, 2017

    To Test or Not To Test: 5 reasons we think you can and should get a genetic diagnosis for your IRD

    Hey LCA or IRD family, does any of this sound familiar? You or your child has received a clinical diagnosis of LCA (leber congenital amaurosis), RP (retinitis pigmentosa), cone-rod dystrophy, [...]

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    0
    By Sofia Sees Hope
    In Blog
    Posted April 1, 2017

    It’s April Fool’s Day, and we’ve got a great post to share with you!

    “We can all make our lives much happier if we choose to laugh, live our lives more intentionally and find joy in the little things.” The quote above is from […]

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