이 팟캐스트 소개 🔗

업데이트 빈도:
biweekly
평균 오디오 길이:
17 minutes
영어
미국
에피소드 5 개
2026년 7월 5일부터
episodic

최신 에피소드 🔗

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.

과거 에피소드 검색

Pull Up a Chair Let's Talk LEMS의 과거 에피소드를 검색하세요.

이전 에피소드

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.
이 팟캐스트의 모든 에피소드를 보셨습니다
면책 조항: 이 페이지에 포함된 팟캐스트와 작품은 The LEMS Family Association에서 가져온 것입니다. 이 팟캐스트는 소유자의 재산이며 Listen Notes, Inc.와 제휴하거나 보증하지 않습니다.