August 8th, 2016: Understanding and Remembrance Day for Severe Myalgic Encephalomyelitis
Jody Smith joins with other ME voices in honor of Understanding and Remembrance Day for Severe Myalgic Encephalomyelitis.
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How to Get Funding for CFS/ME Research

Discussion in 'General ME/CFS Discussion' started by Wishful, May 19, 2017.

  1. Wishful

    Wishful Senior Member

    Dr. Davis' new test for CFS biomarkers should help (once independently verified), but there will probably still be people denying that CFS is a valid physical condition. Dr. Davis' finding that it's caused by something carried in plasma makes the solution quite simple: offer to do a serum swap with a CFS patient. Then the deniers can feel the symptoms themselves. ;)
    belize44 and deleder2k like this.
  2. Demepivo

    Demepivo Dolores Abernathy

    I don't think Dr Davis and colleaggues are quite there with a biomarker but they are doing fantastic work.

    The latest OMF new letetr said they had raised $1 million in April.

    Look out for a paper from Robert Naviaux, the metabolomics/mitochondria expert at UCSD, later this week plus his CDC talk on Thursday.

    Much to look forward to :)

    Anything else you are allowed to share @Ben Howell ?

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