John Peters

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Revision as of 22:49, February 28, 2019 by Notjusttired (talk | contribs) (Rapid response in letters, FOIA requests)

John Peters is a British person with myalgic encephalomyelitis and an advocate for people with ME/CFS. He is from Swansea, Wales, UK.[1]

Talks, letters and interviews

Freedom of information act

John Peters requested the minutes from the PACE trial's Trial Steering Committee (TSC) and Trial Management Group (TMG) meetings, which discuss some of the protocol and other changes made during the trial. Queen Mary University of London initially refused this request, but it was granted after an appeal to the Information Commissioner's Office, with the names redacted.[3]

Online presence

See also

Learn more

References

  1. ↑ Peters, John. "johnthejack". Retrieved February 28, 2019. Cite has empty unknown parameter: |dead-url= (help)
  2. ↑ Peters, John (July 31, 2016). "Rapid Response - Chronic fatigue syndrome: is the biopsychosocial model responsible for patient dissatisfaction and harm?". British Journal of General Practice.
  3. ↑ WAMES (March 26, 2018). "PACE Trial Committee & Team Minutes available online". WAMES (Working for ME in Wales). Retrieved February 28, 2019. Cite has empty unknown parameter: |dead-url= (help)
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