The Adult Taskforce was created in 2019 after a survey was completed where the Angelman community overwhelmingly voiced the need for information and resources for adults with Angelman syndrome.Â
The Adult Taskforce is made up of parents, siblings and caregivers of adults with AS. The group develops ideas, educational pieces and materials that support adult individuals with Angelman syndrome and their caregivers.
See the Resources page for resources specifically for adults that were created and cultivated by the Adult Task Force.
This committee is lead by Lesley McCallister and Robin Wilkerson.
Open to new 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.