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
Miles For Smiles w Deanna McCurdy
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Angelman Syndrome Foundation
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Season 3
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Episode 2
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Inspiring mother, advocate and runner, Deanna McCurdy, talks with CEO Amanda Moore about uniting her passion and purpose to create Team Miles for Smiles.
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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.