Angelman Syndrome: Support Groups and Organizations

New Horizons Un-limited is not endorsing and assumes no responsibility in guaranteeing the products, services, programs or conditions as described. If you are interested in a resource listed below, call or contact the resource to verify the current situation. Evaluate the information, analyze your unique circumstances, use your best judgment and make your own decisions when using the information. Before making any change, consult your health care professional.

National

Angelman Syndrome Foundation, Inc. is available to provide information, education and support to those affected by this relatively rare condition. Their website provides Angelman Syndrome facts and information to families and doctors. The foundation offers Angelman Syndrome from A to Z, a terrific resource developed by family members. For more information, call (800) 432-6435 or e-mail info@angelman.org.

New Sign K12 Academics: Angelman Syndrome is a website devoted to providing resourceful information for a number of topics in education and disorders. The section for Angelman Syndrome includes history, Pathopysiology, features, diagnosis, treatment, prognosis, books, videos, organizations, support services & mailing lists for the disorder.

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