ME/CFS quality of life impact research project
We are excited to announce a new international research study looking at the impact of ME/CFS on the…
ME Charities Joint statement of covid 19 vaccination
M.E. charity statement on the Covid vaccine We are receiving a very high number of enquiries from people…
25% ME Group NICE guidelines Draft feedback
Charity response to the NICE draft guidelines December 2020 https://25megroup.org/download/2302/?v=3673
To Vaccinate or Not – with ME/CFS
Veterans with concerns related to Gulf War illness have a lot in common with ME/CFS patients, so my…
Charity COVID-19 vaccine statement
STATEMENT ON VACCINATION CHOICE BY MEDICAL ADVISORS 25% Group members are naturally asking for advice as to whether…
Another nail in the coffin of those who claim that ME is psychosomatic
Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: Organic Disease or Psychosomatic Illness? A Re-Examination of the Royal Free Epidemic of 1955…
The long march by patients to prove that the official treatment for ME/CFS was wrong and damaging
A long-running battle between patients and therapists over the best way to treat debilitating chronic fatigue was won…
GET This! NICE Pulls the Plug on Graded Exercise Therapy and CBT asTreatments for ME/CFS
Who would have thought? We knew that National Institute for Health and Care Excellence (NICE) – the executive…
Research on severe ME
“Profile of circulating microRNAs in myalgic encephalomyelitis and their relation to symptom severity, and disease pathophysiology https://www.nature.com/articles/s41598-020-76438-y?fbclid=IwAR3LphYMqzLHxrPpSoxFwYqs15J8x8LSTKvspThsTjiy8v6orYWKmtkgfFw
The Long Hauler Tragedy: More Frightening than Halloween Nightmares
For the past 30 years, still another group has suffered from the trauma of an illness and then…