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this post was submitted on 19 Jan 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.
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How did you figure out your allergies/intolerances? I've looked at testing but most look scammy.
By way of elimination, sorta like the fodmap diet but for environment factors. Symptoms that increase for everyone I have talked to are brain fog, neuropathy, lightheadedness. But yeah just remove the thing from your environment for some months then reintroduce it to see if you get worst. I highly suggest fragrance as a start as there are research studies showing it is common in people with post viral illnesses. You can also go an allergist and get a spot test done but it may not be conclusive.