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    How FRAXA Research Foundation is keeping hope alive for a cure for Fragile X!

    How FRAXA Research Foundation is keeping hope alive for a cure for Fragile X!

    FromTalk Fragile X

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    How FRAXA Research Foundation is keeping hope alive for a cure for Fragile X!

    FromTalk Fragile X

    ratings:
    Length:
    50 minutes
    Released:
    Jan 18, 2022
    Format:
    Podcast episode

    Description

    Joining us for our second episode of 2022 is President & Co Founder of FRAXA Research Foundation; Katie Clapp! She shares with us the exciting research proposals coming up for FRAXA to support, the 2nd annual World Fragile X Day on July 22nd, 2022 and how you can be involved, and much more!
    Released:
    Jan 18, 2022
    Format:
    Podcast episode

    Titles in the series (67)

    Talk Fragile X Podcast exists to provide a platform for families and Fragile X experts to share their knowledge, resources, and experiences, all in the hopes of creating more awareness, advocacy, and support of Fragile X Syndrome! Even if you don’t know what Fragile X Syndrome is, this Podcast is for you! I want everyone to know what Fragile X is and understand it’s genetic prevalence in individuals lives.