Kate Ahern discusses strategies for fostering a supportive community among users of Augmentative and Alternative Communication (AAC) devices. She emphasizes the importance of creating environments where AAC users can connect, share experiences, and support each other’s communication journeys. The presentation provides insights into building inclusive communities that empower AAC users to express themselves fully.
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.