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Frecuencia de actualización:
biweekly
Duración media del audio:
17 minutes
Inglés
Estados Unidos
5 episodios
desde 5 de julio de 2026
episodic

ÚLTIMO EPISODIO 🔗

In this episode we visit with Devon, a husband, father, and teacher, who lives and works while dealing with Lambert-Eaton Myasthenic Syndrome (LEMS). We explore his life before diagnosis, how getting LEMS changed everything, and how he lives a full life now.

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Buscar episodios anteriores de Pull Up a Chair Let's Talk LEMS.

EPISODIOS ANTERIORES

We discuss the supplement, Creatine, with Dr. Stephen Meriney, Ph.D. Professor of Neuroscience at The University of Pittsburgh. Why is everyone talking about it? Who is using it? What is it, and how does it work? Dr. Meriney speaks about the clinical evidence for creatine, why it's interesting s…

Tracy Talks LEMS

We talk with Tracy Sharp from Kentucky about his early experiences and struggles from his LEMS diagnosis. He also discusses adapting his life to this new reality, living with a neuromuscular disorder, and his work advocating for LEMS patients with doctors for the LEMS Family Association. He also …

Meet Madeline

This episode we meet The LEMS Family Association's Executive Director, Madeline Miller. Get to know Madeline, her background in rare diseases, and her perspective on the ultra-rare disorder, LEMS, and her the challenges LEMS patients face.
Episode 1 Host introduction and the defining mission of the podcast and it's goals for the Lambert-Eaton myastenic disorder (LEMS) community of patients, caregivers and family.
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Descargo de responsabilidad: El podcast y el arte incluidos en esta página son de The LEMS Family Association, que es propiedad de su propietario y no está afiliado ni respaldado por Listen Notes, Inc.