The Real ME: A Stock Photography Resource for the Media
We’ve all seen them in the news stories about ME/CFS: the guy in a suit at the office, yawning; the beautiful woman sitting at her desk with her immaculate make-up and elegantly coiffed hair, hand to her head and looking slightly pained.
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new article empowher.com "Lyme Disease: To Eradicate It, We Must Fully Identify It"

Discussion in 'Lyme Disease and Co-Infections' started by Jody, Aug 27, 2010.

  1. Jody

    Jody Senior Member

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  2. Lesley

    Lesley Senior Member

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    I look forward to reading this. My daughter and I were recently diagnosed with Lyme after years of CFS. I wish it had been properly investigated years ago.

    Thanks Jody!
     
  3. Jody

    Jody Senior Member

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    Hi Lesley,

    It would make so much difference -- with Lyme, with CFS, and so many other conditions -- if information was made available and treated like a priority instead of being dismissed.

    Our chronic communities are doing a great job of getting information out to each other, I think. Especially since ... we're sick, for heaven's sake. :rolleyes:

    Having each others' backs makes a huge difference.
     
  4. Frickly

    Frickly Senior Member

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    Thanks Jody! I have been sick for 9 years and was diagnosed with CFS a couple of years back and, finally, lyme about a month ago. My sister was also recently diagnosed with lyme. This is an excellent article and love that you mentioned autism! I am trying to get my son tested for lyme now. Keep writing!
     
  5. Jody

    Jody Senior Member

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    Holy cow, Frickly. Your poor family.

    Thanks for the feedback. I'll do my best to keep getting stuff out there.
     

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