A distinguished and diverse group of community leaders serve in a volunteer capacity on ASF’s Board of Directors.
Demographics: 37% Female, 63% Male. Race/Ethnicity: 16% Black, 5% Hispanic, 79% White or other ethnicities. All members are US citizens, with one member having dual citizenship in the US and Germany.
The mission of 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.