Help Fund SPS Research in Jeanine Taylor's Name

Jeanine Taylor was diagnosed with Stiff Person Syndrome (SPS), a rare autoimmune neurological movement disorder that affects 4-5 people for every 1 million people. There is very little research, no known cause, and no known cure. Jeanine continued to fight SPS until she passed away on July 15, 2024.

In her honor, the family is setting up this GoFundMe to raise money for The Stiff Person Syndrome Research Foundation (SPSRF) so that they can continue to support the Johns Hopkins Stiff Person Syndrome Center led by Dr. Scott Newsome as well as support their efforts to establish The SPS Global Registry and Natural History to understand SPS further, develop better treatments, and get closer to a cure.