• Welcome to Phoenix Rising!

    Created in 2008, Phoenix Rising is the largest and oldest forum dedicated to furthering the understanding of, and finding treatments for, complex chronic illnesses such as chronic fatigue syndrome (ME/CFS), fibromyalgia, long COVID, postural orthostatic tachycardia syndrome (POTS), mast cell activation syndrome (MCAS), and allied diseases.

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cfsme

  1. JasonPerth

    The moderator of Reddit r/cfsme & r/mecfs pushes CBT and brain retraining and GET and bans you if you say something about it.

    Stay away from r/cfsme & r/mecfs It's full of misinformation & harmful treatments. (Like brain retraining)(CBT) The moderator deletes all comments negative about his/her beliefs so you will only find positive one sided opinions. This is what brain retraining pages do. Remove anything negative...
  2. C

    Tick-borne illnesses that look like ME

    There’s an article in the current Atlantic by Meghan O’Rourke, a writer I’ve been following for some time because for years she believed she had ME, and was writing a book about it. Here’s the link: https://www.theatlantic.com/magazine/archive/2019/09/life-with-lyme/594736/ It seems that she’s...