Angelman Syndrome Foundation Podcast
Welcome to the Angelman Syndrome Foundation community! In each episode, Amanda Moore, CEO of Angelman Syndrome Foundation, will discuss Angelman syndrome with experts in their field to provide resources and education to families. From a deep dive into the genetics of Angelman syndrome, to understanding clinical treatments for treating seizures to discussions with IEP specialists and communication specialists, we are here to help as many families as possible on this journey. We are so glad you have joined us and look forward to connecting and supporting this community together.
Angelman Syndrome Foundation Podcast
Understanding Adults with AS
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Angelman Syndrome Foundation
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Season 1
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Episode 5
ASF CEO Amanda Moore interviews Robin Wilkerson, parent of Paige, a 29-year-old with AS. Diagnosed at age 5, Robin discusses her family's journey and the unique challenges of AS in adulthood.
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Learn more about Angelman Syndrome Foundation at Angelman.org.
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Find an Angelman Syndrome Foundation Clinic at Angelman.org/as-clinics.