Home care is the theme for Severe ME Day on August 8th
Why should home care be the theme on Understanding and Remembrance Day for Severe ME on August 8? Helen Brownlie of the 25% ME Group has written an explanation for Phoenix Rising ...
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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 Senescent on the Illinois Prairie ❀❤✿Ƹ̵̡Ӝ̵̨̄Ʒ✿❤❀

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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.
     
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  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
     
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  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 Guest

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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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