The Call for Opposition: Challenging the P2P and IOM Processes
In our second article on how to react to the publication of the draft P2P report, Gabby Klein provides her view of why she and a large group of advocates and patients are continuing their protest of the government’s ongoing control and manipulation of our disease via their processes...
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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

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    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: http://www.nhs.uk/conditions/chronic-fatigue-syndrome/Pages/Introduction.aspx

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

    free at last Senior Member

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    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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