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this post was submitted on 27 Oct 2024
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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.
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Sadly, I'm not sure that human society will change without challenging the bleak aspects. This is a lot to ask for an individual.
Which is why people without ME should read it. I don’t know if you know anything about ME (if not then why haven’t you read the article?) but even reading an article like that can literally make someone with ME sick for a day or a week because of the emotional energy it costs to process it.