Medical Research Council
Funding[edit | edit source]
CFS/ME Expert Group[edit | edit source]
- Professor Stephen Holgate - University of Southampton (Chairman)
- Professor Jill Belch - University of Dundee
- Dr Esther Crawley - University of Bristol
- Professor Philip Cowen - University of Oxford
- Professor Malcolm Jackson - University of Liverpool
- Dr Jonathan Kerr - St George’s University of London
- Professor Ian Kimber - University of Manchester
- Professor Hugh Perry - University of Southampton
- Dr Derek Pheby - National CFS/ME Observatory
- Professor Anthony Pinching - Peninsula Medical School
- Dr Charles Shepherd - ME Association
- Sir Peter Spencer - Action for ME
- Professor Peter White - Bart’s and the London School of Medicine and Dentistry, Queen Mary University of London
(updated Mar 2019)
Research funded[edit | edit source]
Criticism[edit | edit source]
The charity ME Research UK has criticized the MRC. The charity Invest in ME Research has also been critical of its support for research into the "behavioral model" of M.E., the amount of ME/CFS funding allocated to the "psychiatric lobby" and the lack of funding allocated to biomedical research by the Medical Research Council. The ME Association, including Dr Charles Shepherd, a member of the MRC CFS/ME Experts Group, have campaigned against several research projects funded by the MRC, including the PACE trial, and the FINE trial.
Announcements[edit | edit source]
- 2011, Medical Research Council announces further details on research funding for ME/CFS
- 2014, Encouraging new ideas for CFS/ME research
See also[edit | edit source]
Learn more[edit | edit source]
References[edit | edit source]
- Chronic Fatigue Syndrome/Myalgic Encephalomyelitis (CFS/ME)
- Medical Research Council (Jul 12, 2018). "CFS/ME". Medical Research Council. Retrieved Mar 4, 2019.
- The Medical Research Council: a case to answer?
- MRC Funding of Research into ME/CFS
- ME Association (Jun 2007). "MEA support statement on wasteful research". ME Association. Retrieved Mar 4, 2019.
"Public money is being wasted on research that will be of little benefit and may actually be harmful to ME patients. It is about time serious money was spent on the pathology of this devastating illness." - Simon Lawrence, 25 Percent ME Group
Myalgic encephalomyelitis or chronic fatigue syndrome