This is the story of one family’s 35 year experience with a profound developmental disability. This extraordinary journey has changed their view of the world, rearranged priorities and transformed their lives.
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.