This session focuses on strategies for building a supportive network and planning future steps for individuals with Angelman syndrome. It offers insights into collaborating with various stakeholders, including healthcare providers, educators, and community members, to enhance the quality of life for those affected by Angelman syndrome. The presentation also discusses practical approaches to advocacy and resource development.
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.