Review: 'Through the Shadowlands’ describes Julie Rehmeyer's ME/CFS Odyssey
I should note at the outset that this review is based on an audio version of the galleys and the epilogue from the finished work. Julie Rehmeyer sent me the final version as a PDF, but for some reason my text to voice software (Kurzweil) had issues with it. I understand that it is...
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WHO classification of ME/CFS (ICD10: G93:3) - House of Lords question

Discussion in 'General ME/CFS Discussion' started by charles shepherd, Nov 26, 2014.

  1. charles shepherd

    charles shepherd Senior Member

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  2. biophile

    biophile Places I'd rather be.

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    But, according to key members of the UK CFS/ME Research Collaborative, asking such questions is "harassment"?

    Behind the scenes: Setting up the UK CFS/ME Research Collaborative (UK CMRC)

    The Young ME Sufferers Trust (Tymes Trust)

    August 2014

    http://bit.ly/1vSRhOI

    https://www.dropbox.com/s/92m09l9tq55pihh/Behind the Scenes - Research Collaborative.pdf?dl=1

     
    Last edited: Nov 27, 2014
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  3. Kati

    Kati Patient in training

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    Last edited: Nov 26, 2014
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  4. Min

    Min Guest

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    UK
    So why has the UK defied the WHO classification for the past thirty years and treated our neurological illness as psychosomatic (harming tens of thousands of patients), and why do the charities in the Collaborative chose to work with the very doctors responsible for this outrage?
     
    Wildcat, RustyJ, Countrygirl and 2 others like this.

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