1. Patients launch $1.27 million crowdfunding campaign for ME/CFS gut microbiome study.
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Hunting down the cause of ME/CFS & other challenging disorders - Lipkin in London
In a talk to patients in London on 3rd September, Dr. W. Ian Lipkin described the extraordinary lengths he and his team are prepared to go to in order to track down the source of an illness, with examples ranging from autism to the strange case of Kawasaki disease.
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PatientsLikeMe doing a CFS/FMS survey for Petrie (major psychobabbler)

Discussion in 'Action Alerts and Advocacy' started by Dolphin, Feb 1, 2011.

  1. leela

    leela Slow But Hopeful

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    Couchland, USA
    :confused:?!?!!?:headache:
     
  2. justinreilly

    justinreilly Stop the IoM & P2P! Adopt CCC!

    Messages:
    2,490
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    1,175
    NYC (& RI)
    In response to another patient's questions and comments i told them that PEM distinguishes ME and FM and that they shouldn't exercise until they are mostly better and that cortef helps by lowering inflammation.

    the site said i couldn't make recommendations based on the science, only my personal experiences.

    God help us!!
     

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