Science for ME

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Revision as of 13:27, May 10, 2019 by AndyPR (talk | contribs) (→‎Controversy: Removed heading as no content underneath)
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Science for ME (S4ME) is a British website that claims to be "an independent, patient-led, international forum for people with ME/CFS and the carers, clinicians, scientists and advocates who support us."[1]

S4ME reported that its forum had reached 400 members on 18th November 2017,[2] and 500 members on December 17th 2017.[3]


Notable Members[edit | edit source]

Researcher Interaction[edit | edit source]

Forum Member Advocacy Projects[edit | edit source]

  • Submission to the public review on common data elements for ME/CFS: Problems with the Chalder Fatigue Questionnaire [7]
  • Open letter to NICE concerning the Guideline Committee for ME/CFS [8]
  • Briefing document - The PACE Trial Controversy: A Summary [9]

Publicly Visible Forums[edit | edit source]

Online presence[edit | edit source]

References[edit | edit source]