Angelman Syndrome Foundation

Angelman Syndrome Foundation Podcast

Health EN ↓ Επεισόδια: 39

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.

Μην παραλείψεις να επισκεφτείς τη σελίδα του podcast και να στηρίξεις τον δημιουργό: angelmansyndromefoundation.buzzsprout.com

Δημιουργός

Angelman Syndrome Foundation

Κατηγορία

Health

Ιστοσελίδα του podcast

angelmansyndromefoundation.buzzsprout.com

Τελευταίο επεισόδιο

30 Σεπ 2026

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Επεισόδια

All Things Seizures 11.07.2023

Share Your Feedback or Recommend New Topics Dr. Ron Thibert, ASF Clinician at Massachusetts General Hospital, discusses everything families need to know about seizures in Angelman syndrome. + + + 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 .

AS Medical Care For All Ages 26.06.2023

Share Your Feedback or Recommend New Topics In this previously recorded conversation, listen to medical experts answer commonly asked questions about medical care. + + + 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 .

Angelman Dads 12.06.2023

Share Your Feedback or Recommend New Topics Fathers discuss everything there is to know about being a dad to a child with Angelman syndrome. + + + 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 .

Clinical Trials in AS 30.05.2023

Share Your Feedback or Recommend New Topics In this previously recorded conversation, listen to a Q&A moderated by Dr. Elizabeth Jalazo about exciting clinical trial news. + + + 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 .

We Are Single Caregivers 15.05.2023

Share Your Feedback or Recommend New Topics Two single mothers of children with Angelman syndrome discuss what help looks like for them. + + + 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 .

AS Clinical Experts Panel 01.05.2023

Share Your Feedback or Recommend New Topics In this previously recorded webinar, listen to an "ask all, tell all" session with four Angelman syndrome clinical experts. + + + 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 .

How Diet Therapy Saved My Son 01.12.2022

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

Newly Diagnosed 101 31.10.2022

Share Your Feedback or Recommend New Topics Two mothers join Amanda to discuss their newly diagnosed journey and early signs of Angelman syndrome in their children. + + + 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 .

Understanding Episodes of Myoclonus 20.10.2022

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

Understanding Adults with AS 11.10.2022

Share Your Feedback or Recommend New Topics ASF 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 unique challenges of AS in adulthood. + + +  Learn more about Angelman Syndrome Foundation at Angelman.org. Follow us on Facebook and Instagram and connect with our community. Find an Angelman Synd...

Understanding The UBE3A Gene 03.10.2022

Share Your Feedback or Recommend New Topics ASF Clinic Director Christian Hommes and Matt Judson from The Philpot Lab at UNC explain the complexities of UBE3A. * * * 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.

Sibling Spotlight: Baden Moore 26.09.2022

Share Your Feedback or Recommend New Topics In 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 brother Jackson, who has AS. * * * Learn more about Angelman Syndrome Foundation at Angelman.org. Follow us on Facebook and Instagram and connect with our community. Find an Angelman Syndrome Foundati...

Ladder Learning Network 18.09.2022

Share Your Feedback or Recommend New Topics In Episode 2, ASF CEO Amanda Moore and ASF Chief Medical Officer Liz Jalazo discuss the importance of clinical care and introduce the LADDER Learning Network. A perfect listen for newly-diagnosed families as well as those who are further along in their journey, learn how to get a plan for clinical care for your loved one with AS. * * * Learn more about A...

What is Angelman syndrome? 30.08.2022

Share Your Feedback or Recommend New Topics In Episode 1 of the ASF Podcast, Amanda Moore, CEO of Angelman Syndrome Foundation, shares her family's diagnosis journey. Amanda's son, Jackson, is 7 years old and was diagnosed at a young age with AS. Amanda shares her personal experience working with doctors on the diagnosis and which ongoing resources have helped her family most. Amanda als...

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