fbpx
Skip to content
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
      • Diagnosing SPS
      • Types of SPS
      • Treatments for SPS
    • Patient Stories
      • 2022
      • 2021
      • 2020
      • Share Your SPS Story
    • Patient Advocacy
      • 5 Things to Help Deal with a Rare Disease
      • How to Prepare for Doctor Appointments
      • Face Sheet for Doctor Appointments
      • NORD Rare Action Network
    • Additional Resources
      • SPS Q&A For Medical Professionals
      • Ask the Neurologist
      • Ask a Primary Care Physician
      • Support for Patients and Caregivers
      • Medical Institutions
      • Research Articles
Sign Up
  • About the Foundation
    • News
      • RArE Moments
      • Our Newsletters
      • Media Coverage of the SPSRF
    • Events
      • Ultra 4 Isla
      • #Move4Rare
      • SPS Awareness Day
        SomoBreathe Soundbath
      • Share Your Power With Power Train Rockville
      • Traversing Tassie 2020
    • About
      • Our Founder’s Story
      • Board of Directors
      • Medical Advisory Board
      • Organization Financials
      • Work with The SPSRF
DONATEDONATE NOW
  • ❤️ DONATE TODAY
  • 💻 Create A Facebook Fundraiser
  • 📰 Sign Up For Newsletter
  • Resources
  • Patient Advocacy
  • Patient Stories
  • News
    • Our Newsletters
    • RArE Moments
  • Events
    • Ultra 4 Isla
    • #Move4Rare
  • About Us
    • Work with The SPSRF
    • Medical Advisory Board

Voices of SPS: Michael Weiss

https://stiffperson.org/wp-content/uploads/2022/03/voices_of_sps__michael_weiss-720p.mp4

Voices of SPS: Michael Weiss

Share this Article
Share on FacebookShare on Facebook TweetShare on Twitter Share on LinkedInShare on LinkedIn Share on WhatsAppShare on WhatsApp
  • Privacy Policy
Necessaries

2020 © The Stiff Person Syndrome Research Foundation

Go to Top