SOBRE ESTE PODCAST 🔗
Pull Up a Chair exists to provide information, encouragement, and community for people living with Lambert-Eaton Myasthenic Syndrome and those who care about them.
Frequência de atualização:
biweekly
Duração média do áudio:
17 minutes
Inglês
Estados Unidos da América
5 episódios
desde 5 de Julho de 2026
episodic
NESTE PODCAST 🔗
ÚLTIMO EPISÓDIO 🔗
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.
PESQUISAR EPISÓDIOS PASSADOS
Pesquisar episódios anteriores de Pull Up a Chair Let's Talk LEMS.
EPISÓDIOS 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…
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 …
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.
Já viu todos os episódios deste podcast
Aviso: O podcast e a arte incorporada nesta página são de The LEMS Family Association, que é propriedade de seu proprietário e não é afiliado ou endossado por Listen Notes, Inc.
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