The Angelman Syndrome Foundation is a U.S. nonprofit organization dedicated to advancing awareness, treatment, research, education, and family support for people affected by Angelman syndrome, a rare neurogenetic disorder.
Rare disease research funding, medical and scientific research support, patient and family services, disability and caregiver support, healthcare access and treatment awareness, and public education related to Angelman syndrome.
Primarily supported by charitable donations, fundraising, grants, and contributions from families, supporters, and philanthropic partners.
Angelman syndrome patients and families, clinicians and researchers in the Angelman syndrome community, and supporters involved in ASF programs and events.
Non-profit organization
