NICE announces next steps for ME/CFS guideline
NICE announces next steps for ME/CFS guideline Read More »
Forward-ME response to the statement from NICE: “Forward-ME have now […]
NICE announces next steps for ME/CFS guideline Read More »
Forward-ME response to the statement from NICE: “Forward-ME have now […]
Why Deciphering the Symptoms of Long COVID-19 Is Slow, Painstaking Work Read More »
The Wire has an article written by Allison Navis, assistant
What we’re not being told about ME Read More »
There is an excellent article on the unherd site about
BBC Radio 4: Woman’s Hour – Dr Nina Muirhead and Dr David Strain Read More »
This morning (August 24) on BBC Radio 4 Woman’s Hour
We need to stop quibbling over guidelines and treat patients
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
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.
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
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 Read More »
A further report on the resignations appears in the Times