1. Patients launch $1.27 million crowdfunding campaign for ME/CFS gut microbiome study.
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ME/CFS: A disease at war with itself
We can all agree that ME/CFS is a nasty disease, particularly in its severe form, but there are abundant nasty diseases in the world. What is unique and particularly confounding about our disease is that so much controversy surrounds it, and not only surrounds it, but invades it too.
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About com.. Trisha Torrey

Discussion in 'Action Alerts and Advocacy' started by taniaaust1, Jul 15, 2010.

  1. taniaaust1

    taniaaust1 Senior Member

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    http://patients.about.com/gi/o.htm?...&tt=17&bt=0&bts=1&zu=http://trishatorrey.com/

    "In the five years I’ve been working on patient empowerment and patient advocacy, I’ve been thrilled to have been quoted in the likes of the Wall Street Journal, US News & World Report, Forbes, Fox, NPR, PBS and others…"

    She writes a lot about medical stories and horror issues with the medical system etc so Im wondering if anyone has written to her about the CFS, XMRV and the CDC affair yet?? Has she done any articles on it?? (i couldnt see any) . It would be up her alley.

    (I'll write to her within next few days or so if no one else has, if she hasnt done a story on all that yet. Feel free anyone else who wants to write to her too).

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