Angelman Syndrome Foundation

The mission of the Angelman Syndrome Foundation 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. We exist to give all of them a reason to smile, with the ultimate goal of finding a cure. 

The ASF Board of Directors has developed a strategic plan to help the ASF achieve its goals and objectives for the future. The ASF strategic plan is centered around three areas: Support for Angelman families, Commitment to Research and Supporting the ASF AS Clinics. Focusing funding and energies in these 3 areas will not only improve the lives of those living with Angelman syndrome now and in the future.