The National Guardianship Association’s website provides an interactive map detailing state-specific guardianship associations across the United States. By selecting individual states, users can access information about local guardianship organizations, resources, and contact details, facilitating connections with state-specific support and guidance.
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.