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Nursing Times: People with chronic fatigue 'lacking support', claims charity

Discussion in 'General ME/CFS News' started by Firestormm, May 12, 2014.

  1. Little Bluestem

    Little Bluestem All Good Things Must Come to an End

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    I assume that is why half of the patients have had the sense to avoid them.
     
  2. maryb

    maryb iherb code TAK122

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    quote

    “We know that there are many brilliant and supportive professionals working with people with ME/CFS out there"
    :rofl::rofl::rofl:
    its either that or cry.............
     
    Little Bluestem, Valentijn and Min like this.
  3. Min

    Min Guest

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    The only brilliant and supportive professional I have met in nearly 30 years of severe M.E was hauled before the GMC and banned from working with ME patients for daring to treat our physical illness aa a physical illness.
     
    Wildcat, Valentijn, Sidereal and 2 others like this.
  4. maryb

    maryb iherb code TAK122

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    Yes I was just talking about that person to a friend in an e-mail - she called the GMC bastards......I agreed
     
    Min, Wildcat and peggy-sue like this.
  5. Min

    Min Guest

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    The good doctor came far too near to uncovering the cause of myalgic encephalomyelitis for the GMC's comfort, and so was silenced and stopped.
     
    maryb and peggy-sue like this.
  6. Firestormm

    Firestormm

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  7. maryb

    maryb iherb code TAK122

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    Sorry to go off thread but the issue of blood culturing is something that's been on my mind over the past 2 weeks, now that doctor did this, if only the NHS would do something like a 7 day blood culture on ME patients, be interesting to see what they'd find, you could actually call that research!!!
     

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