Facebook: https://www.facebook.com/AngelmanSyndromeFoundation

Angelman syndrome (AS) is a rare neuro-genetic disorder that occurs in one in 15,000 live births or 500,000 people worldwide. It is caused by a loss of function of the UBE3A gene in the 15th chromosome derived from the mother.

Angelman syndrome shares symptoms and characteristics with other disorders including autism, cerebral palsy and Prader-Willi syndrome. Due to the common characteristics, misdiagnosis occurs often. People with Angelman syndrome have developmental problems that become noticeable by the age of 6 – 12 months.

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. Program provides financial assistance to help improve quality of life for those with AS, including safety supports, adaptive supports and communication devices.

Send Care Package
Complete the form here: https://angelman.org/send-sunshine and the ASF Care Committee will send a “little sunshine” in the form of a card or package. This service is available in the U.S. only.