AVIVA Semi-Finals: National ME/FM Action Network is competing for $100,000
The National ME/FM Action Network in Canada is competing for $100,000 for biomedical research of ME and FM in the Aviva Community Fund contest. With thanks to all who helped, they made it through the first round of voting into the Semi-Finals.
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"Last Word on Nothing" Article - Part 2

Discussion in 'General ME/CFS News' started by slayadragon, Apr 24, 2014.

  1. slayadragon

    slayadragon Senior Member

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    twitpic.com/photos/SlayaDragon
    Here is the second half of Julie Rehmeyer's story in "Last Word on Nothing," which goes into the politics of the disease, the current issues with the definition, and her return to functioning via mold avoidance.

    I am really pleased that Ed Yong, one of the most influential science writers, has just tweeted a link to the story to his 51k+ followers. So a lot of science writers and people interested in science will end up seeing it.

    I am very happy with this story (and grateful for the enormous amount of work that Julie put into it), and hope that a lot of people connected to the M.E. community will end up reading it. Hits do matter, in terms of getting future coverage. So please share!

    http://www.lastwordonnothing.com/20...cal-unhelpful-about-chronic-fatigue-syndrome/
     
    allyb, Sparrowhawk, Bob and 2 others like this.
  2. Bob

    Bob

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    South of England
  3. caledonia

    caledonia

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    Does anybody know which large biomarker studies Klimas is referring to? And how can she be so sure that these particular studies are going to come up with a biomarker that's really going to help us out?
     

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