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 […]
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 Read More »
The BMJ reports 3 members of the NICE guideline committee
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 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 Read More »
MEA statement re the development of the new NICE guideline
As a charity that funds biomedical research into myalgic encephalomyelitis/chronic
A recent publication by Goebel et al. with research carried
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. Read More »
Mission and Values To improve patient outcomes worldwide by empowering
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 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 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…
An article by Melanie Newman was published in the British
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 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 Read More »
Knowing how to care I wish I knew how to
The challenges carers face when caring for people with ME/CFS Read More »
Pretending everything is Normal It took seven months for John
Fiona Lowenstein writes in the Guardian of her experience of resting
Open Letters to Healthcare Professionals from people with ME/CFS – Part 8 Andrew Read More »
I’m Andrew and have had ME/CFS for over 20 years. It’s been a difficult road, but you have seen me over that time to try to help. Some of you have been helpful and some have been understanding, and I thank you for that.