Medical Research Council

From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history
(Redirected from MRC)
Jump to: navigation, search

The Medical Research Council (MRC) is a British government organization that funds medical research. The MRC states its research priorities publicly.[1]

Funding[edit | edit source]

CFS/ME Expert Group[edit | edit source]

(updated Mar 2019)

Research funded[edit | edit source]

Criticism[edit | edit source]

The charity ME Research UK has criticized the MRC.[3] 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.[4] 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.[5]

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% ME Group

Announcements[edit | edit source]

See also[edit | edit source]

Learn more[edit | edit source]

References[edit | edit source]

  1. Chronic Fatigue Syndrome/Myalgic Encephalomyelitis (CFS/ME)
  2. Medical Research Council (Jul 12, 2018). "CFS/ME". Medical Research Council. Retrieved Mar 4, 2019. 
  3. The Medical Research Council: a case to answer?
  4. MRC Funding of Research into ME/CFS
  5. 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 

Oxford University - a prestigious university located in Oxford, England renowned for its teaching and research in health and medicine

myalgic encephalomyelitis (ME) - A disease often marked by neurological symptoms, but fatigue is sometimes a symptom as well. Some diagnostic criteria distinguish it from chronic fatigue syndrome, while other diagnostic criteria consider it to be a synonym for chronic fatigue syndrome. A defining characteristic of ME is post-exertional malaise (PEM), or post-exertional neuroimmune exhaustion (PENE), which is a notable exacerbation of symptoms brought on by small exertions. PEM can last for days or weeks. Symptoms can include cognitive impairments, muscle pain (myalgia), trouble remaining upright (orthostatic intolerance), sleep abnormalities, and gastro-intestinal impairments, among others. An estimated 25% of those suffering from ME are housebound or bedbound. The World Health Organization (WHO) classifies ME as a neurological disease.

The information provided at this site is not intended to diagnose or treat any illness.
From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history.