25% M.E. Group - Supporting Those With Severe M.E.

Help us make a difference for severe M.E. sufferers

The 25% M.E. Group is a nationwide charity. We campaign to raise awareness of M.E and provide services to people affected by severe M.E. (Myalgic Encephalomyelitis). Your support is vital to our success. Join us to become a member, donate or get involved in our campaigning.

Another nail in the coffin of those who claim that ME is psychosomatic

Simon Lawrence 28/12/2020

Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: Organic Disease or Psychosomatic Illness? A Re-Examination of the Royal Free Epidemic of 1955 https://www.mdpi.com/1010-660X/57/1/12/htm?fbclid=IwAR1oGKAoMHD3enIA-hvYxdDtaOI6NC1op1P_gEhwoHzP7Uvv5otp70z4Kxg

The long march by patients to prove that the official treatment for ME/CFS was wrong and damaging

Simon Lawrence 24/12/2020

A long-running battle between patients and therapists over the best way to treat debilitating chronic fatigue was won by the patients back at the beginning of November. In a dramatic…

GET This! NICE Pulls the Plug on Graded Exercise Therapy and CBT asTreatments for ME/CFS

Simon Lawrence 14/11/2020

Who would have thought? We knew that National Institute for Health and Care Excellence (NICE) – the executive branch in the U. responsible for producing treatment guidelines – was reconsidering…

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Another nail in the coffin of those who claim that ME is psychosomatic

The long march by patients to prove that the official treatment for ME/CFS was wrong and damaging

GET This! NICE Pulls the Plug on Graded Exercise Therapy and CBT asTreatments for ME/CFS