Angelman Syndrome Foundation Podcast

Author: 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.
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Genres: Health & Fitness

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Advocacy Abby: Opening Doors to Resources and Relief
Episode 7
Monday, 10 November, 2025

Share Your Feedback or Recommend New TopicsIn this episode, Amanda sits down with Abby Zachritz, better known as Advocacy Abby, the Director of Family Advocacy at Support Now and creator of the Connect grants database. Abby shares how her personal journey as a mom navigating the disability world inspired her to help other families access financial assistance for therapies, adaptive equipment, and more. Together, they discuss how Support Now’s all-in-one platform simplifies fundraising and connects families to thousands of verified grants, so no one has to face financial barriers alone. Whether you’re just beginning your journey or searching for better resources, this conversation is filled with encouragement, practical advice, and proof of the strength found in community.+ + +Learn more about Angelman Syndrome Foundation at Angelman.org.Follow us on Facebook and Instagram and connect with our community.Find an Angelman Syndrome Foundation Clinic at Angelman.org/as-clinics.