The power and pitfalls of omics part 2: epigenomics, transcriptomics and ME/CFS
Simon McGrath concludes his blog about the remarkable Prof George Davey Smith's smart ideas for understanding diseases, which may soon be applied to ME/CFS.
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By Nov 1st: We Are the 300,000+

Discussion in 'Advocacy Projects' started by leela, Oct 31, 2013.

  1. leela

    leela Slow But Hopeful

    Couchland, USA
    Lymies, have you sent your photo in for this campaign?
    Actress Jane Alexander sent in hers in solidarity!

    The "We Are The 300,000" LYME MEDIA CAMPAIGN

    United Lyme Action (ULA) is launching a photo campaign to get more
    media attention for Lyme disease.

    Our goal is to raise awareness about the fact that the CDC and HMOs
    are ignoring the Lyme disease epidemic.

    Here's How You Can Be Part of the Campaign

    We're asking people to take a photo of themselves holding a sign
    saying, "I am one of the 300,000 plus annual Lyme patients being
    ignored by the CDC and HMOs."

    We plan to develop the photos, connect them into banners, and send
    them to 4 major news networks.

    You can learn everything about the campaign here:

    You can make your own sign or print one out here:

    You can email your photos to:

    Check out some photos already sent in:


    Photos need to be sent in by NOVEMBER 1st
    SickOfSickness likes this.
  2. SickOfSickness

    SickOfSickness Senior Member

    Would like to see an M.E. version of this.
    Ruthie24, shannah and leela like this.

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