Angelman Syndrome Foundation Podcast

Angelman Syndrome Foundation Podcast

Por: Angelman Syndrome Foundation
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.
36 episodios disponibles

Latest episodes of the podcast Angelman Syndrome Foundation Podcast

Advocacy Abby: Opening Doors to Resources and Relief 10/11/2025
Advocating for Access: How Policy Shapes the Future of Gene Therapy 30/10/2025
Rest Assured: Safe Sleep for Angelman Families 10/10/2025
Planning for the Future: ASF Housing Champions Share Their Journeys 08/09/2025
Inspired Careers: Siblings and Relatives Share Their Journeys 27/08/2025
Talking Toileting with Dr. Colin Muething 13/08/2025
The History of Disabilities with Hannah Oppenheim 26/02/2025
An Interview with "Out of My Mind" Director, Amber Sealey 11/02/2025
Genetics 101 22/01/2025
Intensive Therapy: Bryan LaScala and the NAPA Center 08/01/2025
Epilepsy in Angelman Syndrome 17/12/2024
Food is Medicine 10/12/2024
Decision Fatigue to Peace with Lisa Jamieson 26/11/2024
Travel Tips 13/11/2024
Top 10 Questions With Amanda Moore 30/10/2024
Behavior and Anxiety in Angelman Syndrome 16/10/2024
Miles For Smiles w Deanna McCurdy 03/10/2024
Genotypes: A Conversation with Parents 19/09/2024
Adults & Caregiver Support 18/09/2023
An Interview With Angie Kim, Best-Selling Author 29/08/2023
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