This group helps plan and make decisions about the next ASF Family Conference to ensure that it is as fun as it is educational and transformational.
This committee is lead by Lesley McCallister.
This group is not currently looking for members.
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.