1. Patients launch a $1.27 million crowdfunding campaign for ME/CFS gut microbiome study.
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Patient Experience: "What Bronllys taught me about pacing."
In 2012, Maya, who had tried to cope with ME/CFS on her own for many years, attended a pain management centre in Wales, U.K., and is now able to achieve more through pacing and acceptance, than she had been able to before the course...
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There is a separate forum for retroviral research discussions:

Discussion in 'Latest ME/CFS Research' started by Dolphin, Sep 13, 2011.

  1. Dolphin

    Dolphin Senior Member

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    There is a separate forum for retroviral research discussions:
    http://forums.phoenixrising.me/forumdisplay.php?57-XMRV

    Also, if you don't want to put it there for some reason, but it's not a research study that involves ME/CFS patients (or very similar e.g. Gulf War Syndrome patients, etc), it should go into the following section:
    This is the description of the current forum:
    It is nice to have a forum like this that isn't too busy (in terms of the number of threads) so let's not spoil it.

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