BBC Health: Outrage at chronic fatigue syndrome advice update pause
BBC Health: Outrage at chronic fatigue syndrome advice update pause Read More »
A health watchdog has paused a final update to ME […]
2021
Guardian: UK health watchdog delays new ME guidance in therapy row
Guardian: UK health watchdog delays new ME guidance in therapy row Read More »
Charities dismayed as move to stop recommending graded exercise therapy
M.E. charities ‘baffled by last-minute delay’ to NICE Guideline – Forward-ME announcement
Statement on the delay to publication of the NICE Guidelines
Disputed therapies for myalgic encephalomyelitis abandoned – Times Article
Disputed therapies for myalgic encephalomyelitis abandoned – Times Article Read More »
Sean O’Neill Tuesday, 17 August 2021 The Times has an
Meet the Scientist: Dr Mark Zinn: The Central Autonomic Network and ME/CFS
Meet the Scientist: Dr Mark Zinn: The Central Autonomic Network and ME/CFS Read More »
Dr Zinn’s ongoing research into the brain regions involved in the autonomic nervous system at DePaul University is an attempt to understand how brain dysregulation can result in the symptoms experienced by people with neurocognitive diseases. He is the author of numerous research papers in this field, and his latest research paper – co-authored with his late wife and Prof. Leonard Jason is the subject of the conversation below.
Meet the Scientists: Leonard Jason & Madeline Johnson: risk factors for suicide in people with ME/CFS
Several studies indicate that people with ME/CFS are at a higher risk of suicide than the general population. In 2020 you co-authored a study on the risk factors of suicide amongst people with ME/CFS
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
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