The Times: ‘Doctors told me I needed to accept my fate but I continue to search for a silver bullet’
People with chronic fatigue syndrome have suffered more than just […]
People with chronic fatigue syndrome have suffered more than just […]
The Times: Link between long Covid and ME could transform the lives of sufferers Read More »
People with chronic fatigue syndrome have often complained they are
As new guidance on treating the condition is delayed, Hannah
SNP MP Carol Monaghan has slammed the National Institute for Health Care Excellence
The NICE Guideline ME/CFS: Personal Observations Dr Charles Shepherd Read More »
Good afternoon, We should have been welcoming the arrival of
Radio 4 Interview About NICE Guideline Read More »
The BBC Today programme interviewed Dr Alistair Miller and Sonya
BBC Health: Outrage at chronic fatigue syndrome advice update pause Read More »
A health watchdog has paused a final update to ME
Guardian: UK health watchdog delays new ME guidance in therapy row Read More »
Charities dismayed as move to stop recommending graded exercise therapy
Statement on the delay to publication of the NICE Guidelines
Hannah’s Instagram video fundraiser smashes target! Read More »
Hannah’s family and friends kindly helped make this Instagram video to go
ME/CFS Research Published 31 July to 6 August 2021 Read More »
The weekly research round-up includes recent publications about ME/CFS and
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 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.
Big Give Christmas Challenge – pledging phase is now complete! Read More »
Thank you everyone! Your exceptional generosity means that we now
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 Read More »
My name is Forest Lewis, I’m 35 and 3 years ago
Severe M.E Awareness Week: Sally Doherty Read More »
I’ve been ill with ME for over fifteen years now
The ME Association ME/CFS (& Long Covid) Weekly Research Round-up Read More »
The weekly research round-up includes recent publications about ME/CFS and
Severe M.E Awareness Week: My Story Read More »
My name is Phil, and I’m 42. Four years ago, I would have described
Severe M.E Awareness Week: Severe M.E and me….. Read More »
Severe M.E has taken so much away from me, my identity,