このポッドキャストについて 🔗

更新頻度:
biweekly
平均音声長:
17 minutes
英語
アメリカ合衆国
5 エピソード
2026年7月5日から
episodic

最新エピソード 🔗

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.

過去のエピソードを検索

Pull Up a Chair Let's Talk LEMSの以前のエピソードを検索します。

以前のエピソード

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.
このポッドキャストのエピソードはすべて視聴済みです
免責: このページに埋め込まれているポッドキャストとアートワークは The LEMS Family Association からのものであり、その所有者の所有物であり、Listen Notes, Inc. と提携または承認されていません。