Causes: Birth Defects & Genetic Diseases, Epilepsy, Epilepsy Research, Health

Mission: 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. Our mission is to build awareness of STXBP1 disorders, and to accelerate development of therapies and hopefully a cure.