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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 Senior Member

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    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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