this post was submitted on 27 Feb 2024
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Chronic Fatigue Syndrome / Myalgic Encephalomyelitis

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This is a new place for people coming from r/cfs.

For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). ME/CFS is a multi-systemic neurological disease, distinct from chronic fatigue as a symptom.

Icon based on the Lemmy logo by Andy Cuccaro licensed under the Creative Commons Attribution-Share Alike 4.0 International license. Eyes taken from the r/cfs logo.

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cross-posted from: https://lemmy.world/post/12465570

Clues to a better understanding of chronic fatigue syndrome emerge from a major study

Long before the world had heard of long COVID, Sanna Stella experienced firsthand how a simple respiratory infection can shape-shift into a chronic illness.

In 2014, a case of bronchitis left Stella, a therapist who lives in the Chicago area, with debilitating fatigue.

Within a month, she was barely able to walk from the couch to her kitchen table. Eventually, Stella learned she had chronic fatigue syndrome, now called myalgic encephalomyelitis/chronic fatigue syndrome, or simply ME/CFS.

Patients can suffer from a range of symptoms, including profound exhaustion, brain fog and post-exertional malaise, an escalation in symptoms following exertion. There is no FDA-approved treatment for the illness, which affects more than 4 million people in the U.S.

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