Phoenix Rising tells QMUL: release the PACE trial data
Mark Berry, Acting CEO of Phoenix Rising, presents the Board of Directors’ open letter to Queen Mary University of London (QMUL) urging them to release the PACE trial data, and hopes that other non-UK organisations will join British charities in the same request...
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ME, CFS and current treatments

Discussion in 'General ME/CFS Discussion' started by Skippa, Dec 16, 2015.

  1. Skippa

    Skippa Anti-BS

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    Say, I'm really curious now.

    Lately there have been patients that respond to Rituximab (but not everyone).

    Patients that respond to LDN (but not everyone).

    Even a group of opiate responders (including myself) but even more interestingly not all opiate responders respond to LDN.

    So, are there patients out there who consider they have ME that have found benefit from any of these treatments I just mentioned?

    Likewise, are there any patients who consider they have CFS (or perhaps lets call it "not ME") that have found benefit from any of these treatments?
     
  2. ahmo

    ahmo Senior Member

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    Northcoast NSW, Australia
    ME, LDN increased my stamina.
     

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