Science + Love = CURE
The STXBP1 Foundation is a parent-led advocacy organization. We are Leading the Charge for a Cure to epileptic encephalopathies and related neurodevelopmental disorders caused by changes in the STXBP1 gene. We are comprised of a diverse team of families and their supports, scientists and medical professionals dedicated to ending STXBP1 Disorders. In fostering partnerships with physicians, researchers, and other foundations, we share learnings and efficiencies to increase awareness of this rare, genetic disorder and identify therapeutic strategies. We believe that through our work, we are accelerating development of improved therapies and ultimately ending STXBP1 Encephalopathy.