Angelman Syndrome Foundation Podcast
Angelman Syndrome Foundation
Welcome to the Angelman Syndrome Foundation community!In each podcast, Amanda Moore, CEO of Angelman Syndrome Foundation, will discuss Angelman syndrome with experts in the industry 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.
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