ME/CFS

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A community for people with Myalgic Encephalomyelitis (ME), sometimes called Chronic Fatigue Syndrome (CFS).

No quackery or denialism. Empathy first, is a must to participate. No unsolicited advice.

founded 3 weeks ago
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Five reasons why the NIH should retract the “effort preference” claims in their intramural ME/CFS paper (thesicktimes.org)
submitted 2 weeks ago by [email protected] to c/[email protected]
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Crowdfunding for David Tuller's Trial by Error Spring 2024 (crowdfund.berkeley.edu)
submitted 2 weeks ago by [email protected] to c/[email protected]
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Not a single bed set aside to treat ME in any UK hospital, says NHS director (www.theguardian.com)
submitted 2 weeks ago by [email protected] to c/[email protected]
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Medical Education on Post-Exertional Malaise and Pacing in ME and Long COVID patients (Video) Dr Brayden Yellman et al. (youtube.com)
submitted 2 weeks ago by [email protected] to c/[email protected]
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cross-posted from: https://mander.xyz/post/18748327

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Well-done sky news segment on Long COVID and ME (youtu.be)
submitted 2 weeks ago by [email protected] to c/[email protected]
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Tribute to Sarah-Jayne Lewis, 1974 - 2024 (sarah-jaynelewis.muchloved.com)
submitted 3 weeks ago by [email protected] to c/[email protected]
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