The KCNA2 & Rare Epilepsy’s Podcast

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Episodes: 16

Description

Welcome to KCNA2 & Rare Epilepsy Podcast, a podcast created for the people living this journey and the people working to understand it.

Each episode, hosted by Dr. Nancy Musarra, invites listeners into honest, generous, and sometimes vulnerable conversations with parents, researchers, clinicians, and board members to discuss the daily experiences of living with KCNA2, seizures, and other rare forms of epilepsy. You’ll hear stories, questions, and hopes from people who understand and are living with this disease. Our mission is to raise awareness, build connections and foster hope.

This isn’t a science podcast (though you’ll learn a lot), our focus is on belonging and education. Together, we can move towards better treatments, clinical trials and ultimately, a cure. 


Episode Date
Living With KCNA2 Epilepsy: One Father’s Story of Seizures, Strength & Hope with Jeffrey Gomez
Jun 11, 2026
Genetic Testing in Rare Epilepsy: What Families Need to Know with Gillian Prinzing & Nancy Musarra
Jun 04, 2026
How Genomics Can Inform Medication Decisions in Rare Epilepsies with Drs. Gray & Musarra - Part 2
May 28, 2026
Epilepsy & Mental Health Are More Connected Than People Realize with Monica Lopez Morales
May 21, 2026
Rare Epilepsy and Genomic Testing Explained with Dr. Erika Gray and Dr. Nancy Musarra
May 14, 2026
Epilepsy Is More Than Seizures with Monica Lopez Morales and Dr. Nancy Musarra
May 07, 2026
Understanding KCNA2 Epilepsy with Researcher Dr. Ulrike (Uli') Hedrich-Klimosch & Dr. Nancy Musarra
Apr 30, 2026
What Does a Seizure Feel Like? Real Stories from Monica Lopez Morales and Dr. Nancy Musarra
Apr 23, 2026
What KCNA2 Parents Should Know About Neurologically Focused Chiropractic Care with Dr. Nate DeJong
Apr 16, 2026
One Family's Journey After Receiving A New KCNA2 Diagnosis with Alysha Applebaum and Nancy Musarra
Apr 09, 2026
“It’s More Than Just a Seizure” Living With KCNA2 Epilepsy Day to Day
Apr 02, 2026
From Diagnosis to Advocacy: Inside the Rare Epilepsy Network (REN)
Mar 26, 2026
A Mother’s 23-Year Journey with KCNA2 Epilepsy
Mar 19, 2026
From the NICU to a KCNA2 Diagnosis: A Parent’s Early Warning Signs
Mar 12, 2026
What Happens in the ER After a Seizure? Emergency Doctors Share Their Insights With Dr Nancy Musarra
Mar 05, 2026
The KCNA2 and Rare Epilepsy Podcast Trailer
Jan 09, 2026