Angelman Syndrome Foundation Podcast

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.

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Avsnitt(42)

We Are Single Caregivers

We Are Single Caregivers

Share Your Feedback or Recommend New TopicsTwo single mothers of children with Angelman syndrome discuss what help looks like for them.+ + +Learn more about Angelman Syndrome Foundation at Angelman.or...

15 Maj 202334min

AS Clinical Experts Panel

AS Clinical Experts Panel

Share Your Feedback or Recommend New TopicsIn this previously recorded webinar, listen to an "ask all, tell all" session with four Angelman syndrome clinical experts.+ + +Learn more about Angelman Syn...

1 Maj 20231h 22min

How Diet Therapy Saved My Son

How Diet Therapy Saved My Son

Share Your Feedback or Recommend New TopicsParent Lizzie Sordia describes how the ketogenic diet eventually stopped her son's seizures. Learn more about Diet Therapy: Angelman.org/articles/diet-therap...

1 Dec 202210min

Newly Diagnosed 101

Newly Diagnosed 101

Share Your Feedback or Recommend New TopicsTwo mothers join Amanda to discuss their newly diagnosed journey and early signs of Angelman syndrome in their children.+ + + Learn more about Angelman Syndr...

31 Okt 202248min

Understanding Episodes of Myoclonus

Understanding Episodes of Myoclonus

Share Your Feedback or Recommend New TopicsASF Clinician Dr. Robert Carson discuss non-epileptic myoclonus, a movement disorder that presents itself with sudden, brief, shock-like jerks in individuals...

20 Okt 20221h 3min

Understanding Adults with AS

Understanding Adults with AS

Share Your Feedback or Recommend New TopicsASF CEO Amanda Moore interviews Robin Wilkerson, parent of Paige, a 29-year-old with AS. Diagnosed at age 5, Robin discusses her family's journey and the uni...

11 Okt 202232min

Understanding The UBE3A Gene

Understanding The UBE3A Gene

Share Your Feedback or Recommend New TopicsASF Clinic Director Christian Hommes and Matt Judson from The Philpot Lab at UNC explain the complexities of UBE3A.* * *Learn more about Angelman Syndrome Fo...

3 Okt 202246min

Sibling Spotlight: Baden Moore

Sibling Spotlight: Baden Moore

Share Your Feedback or Recommend New TopicsIn Episode 3, ASF CEO Amanda Moore interviews a special guest! Her 7-year-old son Baden explains first-hand what it's like being a twin sibling to his brothe...

26 Sep 202220min

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