Robert Courtney

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Robert Courtney (d. March 7, 2018) was a patient advocate for myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) and an outspoken critic of the PACE trial and the biopsychosocial model (BPS) of chronic fatigue syndrome (CFS). He authored numerous published letters in medical journals regarding the PACE trial and, also, filed freedom of information requests in an attempt to get the authors of the PACE trial to release the full trial data to the public for scrutiny.

Robert Courtney passed away on March 7, 2018 at the age of 48.

Freedom of information requests[edit | edit source]

Letters[edit | edit source]

Responses[edit | edit source]

Comment: Submitted to... Cochrane Database of Systematic Reviews[edit | edit source]

Formal complaint to Dr. David Tovey, Editor in Chief of the Cochrane Library[edit | edit source]

Publications on ME/CFS[edit | edit source]

  • 2018, Rethinking the treatment of chronic fatigue syndrome—A reanalysis and evaluation of findings from a recent major trial of graded exercise and CBT[1] (Full Text)

See also[edit | edit source]

Learn more[edit | edit source]

References[edit | edit source]