1. Patients launch a $1.27 million crowdfunding campaign for ME/CFS gut microbiome study.
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Lessons from ME/CFS: Finding Meaning in the Suffering
If you're aware of my previous articles here at Phoenix Rising then it's pretty clear that I don't generally spend my time musing upon the philosophy of the disease. I find it better to spend my time reading research and trying my best to break it down to its core elements and write...
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2 suggestions

Discussion in 'General Symptoms' started by mellster, Jul 23, 2011.

  1. mellster

    mellster Marco

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    1. Create a new poll listing all the new ME criteria just published and see what the prevalence of each one is (all in one poll).

    2. Seeing how valuable richvank's input has been, maybe try and find an immunologist/virologist/endocrinologist/neurologist who is willing to interpret lab results occasionally (without any guarantees of course) since we have a lot of questions along lab values that are not specifically of nutritional nature as well (e.g. NK/CD cells etc.) Maybe someone young and fresh with a new practice who could drive their name and recognition by helping us out.

    If I knew how to start a poll I'd start with 1.) when I find more interruption-free time (not easy with that kiddo) ;)

    cheers

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