The STXBP1 Foundation is a parent-led 501(c)3 non-profit dedicated to raising awareness and finding a cure for STXBP1-Related Disorder, a rare neurodevelopmental condition and genetic epilepsy. We work with families, physicians, scientists, and pharmaceutical innovators. The STXBP1 Foundation was created by a group of dedicated parents and our nonprofit is focused on advocacy, driving research, and providing our families and their physicians with information and resources.