MEF2Cast

MEF2Cast

Haley and Eli, parents of a child with MEF2C Haploinsufficiency Syndrome (MCHS), speak to both other parents and scientific experts to educate, support, and build community around MCHS

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Avsnitt(48)

Episode 8: Pathways to Hope with James Kelly & Lorena García Fernández

Episode 8: Pathways to Hope with James Kelly & Lorena García Fernández

In today’s episode, we are joined by James Kelly and Lorena In today’s episode, we are joined by James Kelly and Lorena García Fernández, founders of the MEF2C Foundation and parents to Elijah. James ...

23 Maj 20251h 37min

Episode 7: From Diagnosis to Advocacy with Chris & Erin: MEF2C Family Foundation Cofounders

Episode 7: From Diagnosis to Advocacy with Chris & Erin: MEF2C Family Foundation Cofounders

In today’s episode, we are joined by Erin Kindrachuk and Chris Kninitski, co-founders of the MEF2C Family Foundation and parents to Sam.Erin and Chris join us to discuss Sam’s journey to diagnosis, wh...

16 Maj 20251h 34min

Episode 6: The Inner Workings of MCHS with Dr. Christopher Cowan

Episode 6: The Inner Workings of MCHS with Dr. Christopher Cowan

In today’s episode of the MEF2Cast, we interviewed Dr. Christopher Cowan, a neuroscientist studying neurodevelopmental conditions like MCHS. Dr Cowan joins us to discuss the role of MEF2C in the brain...

10 Maj 202547min

Episode 5: Exploring MEF2C with Dr. Wendy Chung

Episode 5: Exploring MEF2C with Dr. Wendy Chung

In today’s episode of the MEF2Cast, we interviewed Dr. Wendy Chung, a medical geneticist and Chair of Pediatrics at Boston Children’s Hospital and a researcher studying neurogenetic conditions like MC...

2 Maj 202532min

Episode 4: An Everyday Perspective: Life with MCHS with Becky and Brandon

Episode 4: An Everyday Perspective: Life with MCHS with Becky and Brandon

In this episode, we speak with Becky and Brandon, from Canada, about their son Bodie. We discuss Bodie's story, their journey with MCHS, and what everyday life looks like for their family. We hope you...

24 Apr 202543min

Episode 3: Finding Andrew's Voice with Susan Simmons

Episode 3: Finding Andrew's Voice with Susan Simmons

This conversation explores the journey of Susan Simmons and her son Andrew, who has autism and MEF2C. Susan shares insights into Andrew's early development, the challenges of his diagnoses, and the em...

17 Apr 20251h 20min

Episode 2: From Diagnosis to Action: The MEF2C Family Foundation with Meredith and Aleah

Episode 2: From Diagnosis to Action: The MEF2C Family Foundation with Meredith and Aleah

In this conversation, Meredith and Aleah share their experiences navigating the challenges of diagnosis, early intervention, and the emotional impact of raising children with unique needs. They discus...

10 Apr 20251h 24min

Episode 1: Get to Know Us and MCHS Explained

Episode 1: Get to Know Us and MCHS Explained

Enjoy this introduction for our new podcast where we explain who we are, why we started the podcast, how it will work, and give a brief overview of MEF2C Haploinsufficiency Syndrome. Key takeaways inc...

8 Apr 202529min

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