Chronic Illness Support: That Chronic Thing
Hey there, I'm Cathy! Living with chronic illness isn't easy, and I'm here to talk about the ups, downs, and everything in between. Whether it's navigating relationships, work, or simply trying to make it through the day, I’m sharing my personal experiences and insights to offer support, humor, and connection for those walking (and rolling) the same path.
From dating while sick to finding small joys amidst the challenges, we’ll laugh, cry, and figure this chronic illness life out together. Join me as we create a space where you don’t have to go through it alone.
Chronic Illness Support: That Chronic Thing
ME/CFS is #notjustfatigue, featuring Founder Elizabeth Ansell
"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 includes your host and guest!)
→ There are no FDA approved treatments, biomarkers, or diagnostic tests.
→ There are over 60 symptoms, it's #notjustfatigue.
→ 45% of the Long COVID community fit the case definition for ME/CFS.
The multimedia website is a wonderful destination for those wanting to learn more about ME/CFS past, present, and future. It is a great resource for those with ME/CFS who are wanting to educate their friends and family when they say, "so you're basically tired all the time?" No, it's #notjustfatigue.
See it all at notjustfatigue Instagram TikTok X
Follow Elizabeth Instagram TikTok X
[Recorded April 1, 2025]
💌 Stay in touch with me at @indoorcathy on Instagram.
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"Glitter Blast" Kevin MacLeod (incompetech.com) Licensed under Creative Commons: By Attribution 4.0 License http://creativecommons.org/licenses/by/4.0/