Review: 'Through the Shadowlands’ describes Julie Rehmeyer's ME/CFS Odyssey
I should note at the outset that this review is based on an audio version of the galleys and the epilogue from the finished work. Julie Rehmeyer sent me the final version as a PDF, but for some reason my text to voice software (Kurzweil) had issues with it. I understand that it is...
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Rituximab story in Huffington Post

Discussion in 'Rituximab: News and Research' started by Sasha, Oct 27, 2011.

  1. Sasha

    Sasha Fine, thank you

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    Here's the link (please do visit the site - the more traffic they get, the more they'll keep reporting on us). It's a sympathetic piece - it starts:


    "Chronic fatigue syndrome wrecks people's lives. It does so physicially, socially and economically. Appearing "normal" yet not being able to think or work causes enormous hardship compounded by many doctors who think the illness does not really exist -- a position health and disability insurance companies are more than happy to endorse. "​


    Comments are allowed - there are 13 already. I've added a couple. This is a good platform - let's have meaty, heartfelt, non-ranty stuff on there! Let's give them some facts we want out there. I've mentioned the Norwegian govt apology and called for NIH funding.
     
  2. Roy S

    Roy S former DC ME/CFS lobbyist

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    Illinois, USA
    From the perspective of a 41 year patient and early activist, I think the Huffington Post article is one the best I've ever seen. An M.D. hitting these points over and over is great advocacy.

    "Chronic fatigue syndrome wrecks people's lives. It does so physicially, socially and economically. Appearing "normal" yet not being able to think or work causes enormous hardship compounded by many doctors who think the illness does not really exist http://www.huffingtonpost.com/john-falk/chronic-fatigue-syndrome-_b_829651.html-- a position health and disability insurance companies are more than happy to endorse."


    "Second, this study goes a fair way to knocking off the strong belief in the medical community that CFS is "only in people's heads.""


    "The biggest change may occur with public acceptance and awareness. It's one thing to live with a chronic disease that controls much of your life; it's another to live with an illness many do not believe exists."
     
  3. justinreilly

    justinreilly Senior Member

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    nice article!
     
  4. SOC

    SOC Senior Member

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    Wonderful article! We need many more articles like this in front of the public -- well thought out, frank, informative.
     
  5. maddietod

    maddietod Senior Member

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    East Coast, USA
    Great article; thanks for posting, Sasha.
     
  6. Battery Muncher

    Battery Muncher Senior Member

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    Yes - thank you for posting this excellent piece of journalism.
     

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