Dr. Bateman answers IOM questions from the community: Part 1
Clark Ellis brings us Part 1 of an interview with Dr. Lucinda Bateman, where she answered questions posed by the patient community ...
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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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