Free. Know someone who could use some encouragement? Fill out the request form below and the Care Committee will send a “little sunshine” in the form of a card or package.
Due to high shipping costs, this service is open to those in the US only.
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.