Invisible Illness Awareness Week 2016: Our Voices Need to Be Heard
Never heard of Invisible Illness Awareness Week? You're not alone. Jody Smith sheds a little light to make it more visible
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comments needed on this article that includes ME/CFS story

Discussion in 'Action Alerts and Advocacy' started by RivkaRivka, Aug 25, 2011.

  1. RivkaRivka

    RivkaRivka Senior Member

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    comments needed on this press article in the online newspaper, the Examiner.com (see link below). the article includes me discussing my life with ME/CFS, along with my work for women's rights. i am not sure why the columnist (a very nice man) did not state the name of my illness in the article, and only described it (but without a name). if you comment on the story, please feel free to do just that: state the name of the illness! anyway, i was told that if we get a lot of comments on this story, it could jump from online to being published in the hard copy newspaper. i was also told that they get 5 million hits per day on this Examiner.com website. so if anyone wants to comment on the article, i'd welcome that. thanks -- rivka

    http://www.examiner.com/film-institute-in-los-angeles/that-takes-ovaries-to-play-los-angeles-review
     
  2. *GG*

    *GG* Senior Member

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    Concord, NH
    A few comments have been added. FYI

    GG
     

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