As grandparents of a handicapped child, one is often at a loss to know just how much you can help. The 'Angel Bear' is the concept of my husband – David Thomas – to produce a fund raising source for the future research of the syndrome.

Hi ! - My name is Anthony, and I have Angelman Syndrome.

Kirstie Webster lives in NSW, Australia, was diagnosed with Angeleman Syndrome at 18 months of age.

The Australian Angelman Syndrome Association was founded on March 20,1993 at a meeting held at the St. George Hospital, Kogarah, NSW. The meeting was organised by a group of three interested parents, two leading medical professionals and fourteen families attended.