SPS Global Registry Announcement

We are pleased to announce the launch of the SPSD Global Registry! The SPSD Global Registry creates a platform for patients around the world to strengthen their voices and share information about Stiff Person Syndrome Spectrum Disorders (SPSD). SPSD is a rare disease that causes debilitating muscle spasms, rigidity, and chronic anxiety. Stiff Person Syndrome Spectrum Disorders currently has no cure. Designed with the input of scientists and patients, this global resource will provide data for researchers to use to advance drug development and treatment options to help improve SPSD patient care. Join now and let your data tell your story! Register at http://spsglobalregistry.iamrare.org/