The ASF Parent Advisory Committee serves as a platform connecting the Angelman Syndrome Foundation to voices from the diverse members of the AS community. The committee members are engaged representatives of their geographic region, and provide input on the workings and direction of the ASF.
The mission of the committee is to advise and share feedback to ensure the ASF is effectively addressing the needs of the Angelman community.
The volunteer committee meets 4 times a year and makes a committment to serve for two years.
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.