What is Angelman Syndrome?

In Episode 1 of the ASF Podcast, Amanda Moore, CEO of Angelman Syndrome Foundation, shares her family’s diagnosis journey. Amanda’s son, Jackson, is 7 years old and was diagnosed at a young age with AS. Amanda shares her personal experience working with doctors on the diagnosis and which ongoing resources have helped her family most.

Amanda also defines AS, what causes it and some overall characteristics of the syndrome.