Professor & patients' paper on the solvable biological challenge of ME/CFS: reader-friendly version
Simon McGrath provides a patient-friendly version of a peer-reviewed paper which highlights some of the most promising biomedical research on ME/CFS ...
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UK XMRV demo 1st November

Discussion in 'Action Alerts and Advocacy' started by Kate_UK, Oct 20, 2010.

  1. Min

    Min Guest

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  2. Sasha

    Sasha Fine, thank you

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  3. Tia

    Tia Senior Member

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    When will Sweden put a ban on it? Why doesn't anything happen over there? Noway at least have mobile teams for ME-patients. Sweden has NOTHING, they're like a poor old country that knows nothing about ME. They don't ecen know what ME is.. A friend over there said the doctors asked him if he didn't mean MS, when he said ME, and they said it in a tone as.. - Yes, u mean MS.. Moron doctors with no training in this! When will this stop? When will the doctors there be more educated then their paitents?
     
  4. Fibrobabes

    Fibrobabes

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    thanks everyone
    FB
     
  5. Sasha

    Sasha Fine, thank you

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    Nice picture, Fibrobabes, very glam & retro!
     

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