Voices of SPS: Lea Jabre Fayad

Three things stand out immediately about Lea’s story. First, she has scoured the world to find a diagnosis and treatment. Second, her extensive personal videos of SPS spasms capture authentic moments of acute pain. Finally, and most profoundly for The SPSRF, Lea found life-changing resources on the foundation’s website, www.stiffperson.org, which is precisely our hope.