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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
  • Understanding SPS
    • SPS 101
      • Symptoms of SPS
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Recent Posts
  • The SPSRF Newsletter: May 2023
  • Remember the Zebras 🦓 Doggone It!
  • My SPS Story: Annie M.
  • My SPS Story: Chelsea L.
  • My SPS Story: L.K.
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    EIN 84-2291780


    Our mission is to raise awareness of Stiff Person Syndrome (SPS), to support research for better treatments and a cure for SPS, while strengthening our community through education and collaboration.


    2022 Platinum Member of the National Organization of Rare Diseases
    2022 Member of the Global Genes Advocacy Alliance
    The Stiff Person Syndrome Research Foundation is a Top-Rated Great Nonprofit in 2022

     

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    8621 Burdette Road
    Bethesda, MD 20817
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    Yujie Wang, M.D. reviewed this content for medical accuracy.Medically reviewed by Yujie Wang, M.D. 10/18/21
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