1. Patients launch a $1.27 million crowdfunding campaign for ME/CFS gut microbiome study.
    Check out the website, Facebook and Twitter. Join in donate and spread the word!
Never Ask Us if We're Hungry -- The Answer's Always No
There are three of us here and for many years, none of us ever got hungry. When our brains would turn to mush, when our faces would go numb, and we would start the invisible vibration which is the signature dance of ME/CFS, we knew we needed to eat.
Discuss the article on the Forums.

About com.. Trisha Torrey

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

  1. taniaaust1

    taniaaust1 Senior Member

    Messages:
    7,404
    Likes:
    4,134
    Sth Australia
    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).

See more popular forum discussions.

Share This Page