Advocacy partner: Angelman Syndrome Foundation
About the Angelman Syndrome Foundation
The mission of the Angelman Syndrome Foundation (ASF) is to advance the awareness and treatment of Angelman syndrome through education and information, research, and support for individuals with Angelman syndrome, their families and other concerned parties. ASF is equally committed to each of our four pillars: Family Support through resources and programs, Clinics that connect families with medical experts, Research to find treatments and ultimately a cure, and Community through events that bring people together.
Contact: Amanda Moore – CEO
Phone: 800-432-6435
Email: [email protected]
Upcoming events
About Advocacy Partners
The information above is provided by our partner. Learn more about our advocacy partners here.