Skip to content
The Stiff Person Syndrome Research Foundation
Breaking through barriers to find a cure.
Understanding SPS
SPS 101
Symptoms of SPS
Diagnosing SPS
Types of SPS
Treatments for SPS
Patient Stories
Lea F.
2022
2021
2020
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
DONATE
DONATE NOW
❤️ DONATE TODAY
📰 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
Success
Thank you.
Take Action by Sharing
Share on Facebook
Share on Facebook
Tweet
Share on Twitter
Share on LinkedIn
Share on LinkedIn
Share on WhatsApp
Share on WhatsApp
Go to Top
