1. Patients launch $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!
No Longer Naive in the Ways of The Beast
After having lived for years with ME/CFS, Jody Smith learned there's more to this beast of an illness than she realized, and that what might help one person may not help others ...
Discuss the article on the Forums.

GALWAY FIBRO ME/CFS & Chronic Pain Group

Discussion in 'General ME/CFS News' started by suzhannah, May 16, 2011.

  1. suzhannah


    Hello all,
    I am a Fibromyalgia sufferer. But looking at articals and taking to friends with ME lupus and CFS it is astounding how much we have in common.

    If you are from Ireland or even if you are not, feel free to talk about your day, the way you feel, good or bad. Or post events and info about any or all of the above.

    It is a safe and honest place to chat, make friends across the world that understand you because sometimes out family and loved ones just cannot grasp what we go through on any given day or night.

    I do not mean to take over this forum, i will be looking at many things now i am a memeber, but if you have facebook:
    FIBRO ME/CFS and Chronic Pain GALWAY GROUP
    is available to all (i only ask that you do not say anything abusive)

    Lots of love, have a good day for yourself i hope

    p.s. Sunday 22nd May there is the film 'INVISABLE' showing at the Marriot Hotel in Galway at 2pm, it is free - the hotel is near Dunnes and across from the Menlo Park Hotel, headford rd.

    Take care:angel:

See more popular forum discussions.

Share This Page