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The Stiff Person Syndrome Research Foundation
Breaking through barriers to find a cure.
The Stiff Person Syndrome Research FoundationThe Stiff Person Syndrome Research Foundation
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    November 4, 2021

    7,000 rare diseases, one community fighting for cures. We’re excited to be part of the @ChanZuckerbergInitiative’s #RareAsOne Network

    🏆 Championing SPS 🏆

    Autoimmune disease, Fundraiser, Newsletters, Stiff Person SyndromeBy Tara ZierNovember 4, 2021

    SPSRF Newsletter November 2021 It’s not a trophy but it sure feels like one! The Chan Zuckerberg Initiative selected 20 patient-driven rare disease groups to receive a grant to boost networking, organizational, and funding opportunities. 🎥 Please watch this message and let us know the next steps you’d like to see from The SPSRF. “Focus…

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