À PROPOS DE CE PODCAST 🔗

Fréquence de mise à jour:
biweekly
Durée audio moyenne:
17 minutes
Anglais
États-Unis
5 épisodes
depuis 5 juillet 2026
episodic

DERNIER ÉPISODE 🔗

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.

RECHERCHER LES ÉPISODES PASSÉS

Rechercher les épisodes précédents de Pull Up a Chair Let's Talk LEMS.

ÉPISODES PRÉCÉDENTS

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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Avertissement: Le podcast et les illustrations intégrés sur cette page proviennent de The LEMS Family Association, qui est la propriété de son propriétaire et n'est ni affilié ni approuvé par Listen Notes, Inc.