
ME/CFS is #notjustfatigue, featuring Founder Elizabeth Ansell
From Chronic Illness Support: That Chronic Thing by Cathy Beederman
September 25, 2025 · 25 min · Season 1 · Episode 48
About this episode
Cathy Beederman interviews Elizabeth Ansell about the realities of ME/CFS and its impact on daily life.
"So you're basically tired all the time?" No, it's #notjustfatigue. In this episode of That Chronic Thing, Cathy chats with Elizabeth Ansell (Founder, Executive Director) of notjustfatigue.org, a site dedicated to the education and advocacy of Myalgic Encephalomyelitis, or ME/CFS, an extremely debilitating illness. → 75% of those affected are unable to attend school or work (note: this includes your host and guest!) → 25% are completely homebound or bedbound (note: this also...
People in this episode
Host: Cathy Beederman
Guest: Elizabeth Ansell
Topics covered
- ME/CFS
- chronic illness
- advocacy
- education
- fatigue
- health
Keywords
- ME/CFS
- chronic fatigue
- health advocacy
- Myalgic Encephalomyelitis
- chronic illness
- education
- fatigue
Mentioned in this episode
Organizations: notjustfatigue.org, Myalgic Encephalomyelitis, ME/CFS
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