Invisible Illness Awareness Week 2016: Our Voices Need to Be Heard
Never heard of Invisible Illness Awareness Week? You're not alone. Jody Smith sheds a little light to make it more visible
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what we have to put up with!

Discussion in 'General ME/CFS News' started by justy, Dec 17, 2010.

  1. justy

    justy Senior Member

    Hi all, i dont normally take any interest in the NHS (for obvious reasons) but just found myself looking at the NHS website info on "cfs". I thought the UK government agreed it was M.E and that they have adopted the WHO listing of it as a neurological diease - not so the NHS, which just writes any old crap! no wonder we dont get taken seriously by anyone- including the medical proffession.

    Check out their info here:

    I find it spectacularly offensive. Who writes this? and can we get it changed?
  2. free at last

    free at last Senior Member

    Hi Justy, trust me,untill science proves a testable consistent test, or biomarker,many will never be convinced. Its sad i know. Not surprising some put all there faith in a retro virus is it.

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