• 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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    Public perceptions towards ME/CFS and its sufferers

    "Oh my AndyPR, Thank you for helping me me With a mind to learn and two typing hands." Thanks, got it changed :)
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    Public perceptions towards ME/CFS and its sufferers

    I didn't even notice that. I'll put that typo down to cognitive dysfunction o_O
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    Public perceptions towards ME/CFS and its sufferers

    Thanks A.B. I have emailed him, hopefully he can point me towards something :)
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    Public perceptions towards ME/CFS and its sufferers

    Hello, This is my first post on the forum, apologies if I have posted it in the wrong thread. I am a 4th year psychology student preparing a research dissertation into public attitudes towards (and perceptions of) ME/CFS and those who suffer from it. I have searched through multiple journals...