Severe ME Day of Understanding and Remembrance: Aug. 8, 2017
Determined to paper the Internet with articles about ME, Jody Smith brings some additional focus to Severe Myalgic Encephalomyelitis Day of Understanding and Remembrance on Aug. 8, 2017 ...
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New CFS Patient Advocate Blog

Discussion in 'Media, Interviews, Blogs, Talks, Events about XMRV' started by RustyJ, Jul 27, 2010.

  1. RustyJ

    RustyJ Contaminated Cell Line 'RustyJ'

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    Mackay, Aust
    New Blog by CFS Patient Advocate http://cfspatientadvocate.blogspot.com/

    He has some nice things to say about Harry Reid, opening of WPI building and upcoming NIH paper - all well written.

    Could moderator please fix title to maybe read 'New CFS Patient Advocate Blog'. I clicked wrong button. Sorry.
     
  2. Dorothy

    Dorothy

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    Thanks for posting this link!!! I like the optimistic tone of the blog entry. And I agree that it's important for patients in Nevada to support Harry Reid regardless of their political beliefs. He's really been one of our best friends in government, for as long as I can remember.
     
  3. Wasbeer

    Wasbeer

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    Amersfoort, Netherlands
    Great blog! Don't know if it's 100% realistic, but it sure is a possible scenario. Go Harry Go!
     

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