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
Newly Diagnosed 101
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Angelman Syndrome Foundation
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Season 1
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Episode 7
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Two mothers join Amanda to discuss their newly diagnosed journey and early signs of Angelman syndrome in their children.
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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.