1. Patients launch $1.27 million crowdfunding campaign for ME/CFS gut microbiome study.
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Hunting down the cause of ME/CFS & other challenging disorders - Lipkin in London
In a talk to patients in London on 3rd September, Dr. W. Ian Lipkin described the extraordinary lengths he and his team are prepared to go to in order to track down the source of an illness, with examples ranging from autism to the strange case of Kawasaki disease.
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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 Senior Member

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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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