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
Adults & Caregiver Support
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Angelman Syndrome Foundation
Parent of an 28-year-old daughter with Angelman syndrome, Robin Wilkerson discuss the importance of community and how to support adults.
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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.