Severe ME Awareness Week: Forest’s story
Severe ME Awareness Week: Forest’s story Read More »
My name is Forest Lewis, I’m 35 and 3 years ago […]
2021
Severe M.E Awareness Week: Sally Doherty
Severe M.E Awareness Week: Sally Doherty Read More »
I’ve been ill with ME for over fifteen years now
Severe M.E Awareness Week: My Story
Severe M.E Awareness Week: My Story Read More »
My name is Phil, and I’m 42. Four years ago, I would have described
Experts quit over call to drop exercise as treatment for ME
Experts quit over call to drop exercise as treatment for ME Read More »
A further report on the resignations appears in the Times
BMJ ARTICLE ABOUT NICE COMMITTEE RESIGNATIONS
BMJ ARTICLE ABOUT NICE COMMITTEE RESIGNATIONS Read More »
The BMJ reports 3 members of the NICE guideline committee
CHRONIC FATIGUE SYNDROME PATIENTS — IT’S TIME TO RECONSIDER OUR ATTITUDES
CHRONIC FATIGUE SYNDROME PATIENTS — IT’S TIME TO RECONSIDER OUR ATTITUDES Read More »
Sooyoung Lee, a recent medical graduate, writes in the British Journal
Severe ME Awareness Week 2021: How I feel … I’m Tired
Severe ME Awareness Week 2021: How I feel … I’m Tired Read More »
Olivia (15) has kindly provided an account of her experiences
Dr Charles Shepherd stands down from the NICE guideline committee with immediate effect
Dr Charles Shepherd stands down from the NICE guideline committee with immediate effect Read More »
MEA statement re the development of the new NICE guideline
British Medical Journal: Working together to find the cause & effective treatments for ME/CFS by Dr Charles Shepherd
As a charity that funds biomedical research into myalgic encephalomyelitis/chronic
Research Summary – Passive transfer of fibromyalgia symptoms from patients to mice – July 2021
A recent publication by Goebel et al. with research carried
Scientists raise hopes of blood test for long Covid
Scientists raise hopes of blood test for long Covid Read More »
Extracts of an article in The Medical Device Network. Long
Announcing the Launch of Doctors with M.E.
Announcing the Launch of Doctors with M.E. Read More »
Mission and Values To improve patient outcomes worldwide by empowering
Announcing The Howes Goudsmit Prize for Severe ME Research
Announcing The Howes Goudsmit Prize for Severe ME Research Read More »
The ME Association is pleased to announce the establishment of
But you did it before… Explaining M.E. by Mahli Quinn
But you did it before… Explaining M.E. by Mahli Quinn Read More »
Members of the ME Association will already have seen Mahli
Open Letters to Healthcare Professionals from people with ME/CFS – Part 10: Teri
Open Letters to Healthcare Professionals from people with ME/CFS – Part 10: Teri Read More »
Seeing what’s happened with Long Covid has been awful. It is also frustrating watching the scientific effort now to find a cure when M.E. has been ignored for so long…
BMJ Rapid Response Re: ME/CFS and Long Covid: Moving beyond the controversy – by Dr Charles Shepherd
An article by Melanie Newman was published in the British
The Telegraph: Everything we know about long Covid
The Telegraph: Everything we know about long Covid Read More »
A new study reveals that a third of Covid sufferers
Open Letters to Healthcare Professionals from people with ME/CFS – Part 9 Gaynor
Open Letters to Healthcare Professionals from people with ME/CFS – Part 9 Gaynor Read More »
The new NICE Clinical Guideline for ME/CFS due to be published on
Emotions of carers who care for people with ME/CFS
Emotions of carers who care for people with ME/CFS Read More »
Knowing how to care I wish I knew how to