The session from the 2017 ASF Family Conference emphasizes the importance of building a supportive network for individuals with Angelman syndrome and their families. The discussion covers strategies for fostering community connections, accessing resources, and collaborating with professionals to enhance the quality of life for those affected by Angelman syndrome. The session highlights the collective strength and shared experiences within the Angelman community.
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.