1. Patients launch $1.27 million crowdfunding campaign for ME/CFS gut microbiome study.
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Knitting Equals Pleasure, Despite ME/CFS
Jody Smith loves knitting. Again. She thought her days of knitting and purling were long over but ... she's back ...
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The Conversation Shifts: Gov't Policy Harming Patients

Discussion in 'General ME/CFS News' started by leela, Nov 22, 2013.

  1. leela

    leela Slow But Hopeful

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    Couchland, USA
    http://www.americanbankingnews.com/...-fatigue-sydrome-patients-new-research-finds/

    Excerpt:
    PRESS RELEASE: NEW YORK, NY (11/20/2013) An untold number of New Yorkers, perhaps well over 100,000, who have been diagnosed with Myalgic Encephalomyelitis and Chronic Fatigue Syndrome (ME/CFS) could be at risk of relapsing and exacerbating their condition due to a course of a treatment suggested to them by the federal government, according to groundbreaking new research.
     
    ahimsa, Snowdrop, Iquitos and 10 others like this.
  2. anciendaze

    anciendaze Senior Member

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    Iquitos, Wayne, leela and 5 others like this.
  3. Little Bluestem

    Little Bluestem Senescent on the Illinois prairie, USA

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    Midwest, USA
    So the banking business can understand it, but the medical business cannot.
     
    ahimsa and leela like this.
  4. anciendaze

    anciendaze Senior Member

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    "It is difficult to get a man to understand something, when his salary depends upon his not understanding it!" Upton Sinclair
     
  5. Iquitos

    Iquitos Senior Member

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    Colorado
    It's a very educational piece and hopefully whoever reads it will learn something. Every little bit helps when it comes to educating the public.

    I'd like to encourage patients to comment favorably on this coverage so they know it's being read and appreciated. You can comment as a guest -- don't have to register. It could affect whether they "print" more on the subject, or not.
     
    ahimsa and leela like this.

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