Nature Article: The four most urgent questions about long COVID
Nature Article: The four most urgent questions about long COVID Read More »
Scientists are starting to get insights into the lingering disorder […]
Nature Article: The four most urgent questions about long COVID Read More »
Scientists are starting to get insights into the lingering disorder […]
The ME Association ME/CFS (& Long Covid) Weekly Research Round-up Read More »
The weekly research round-up now includes recent publications about ME/CFS
Dr Shepherd on Treating Long Covid with Histamine Receptor Antagonists Read More »
Earlier this year I attended a medical webinar where we
Research: Medical School Education on Myalgic Encephalomyelitis by Dr Nina Muirhead Read More »
Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) is a complex multi-system disease with a significant impact on the quality of life of patients and their families, yet the majority of ME/CFS patients go unrecognised or undiagnosed.
The ME Association ME/CFS (& Long Covid) Weekly Research Round-up Read More »
Note: The round-up should have been published on Friday 04
Orthodoxy on trial: the pathogenesis of a diagnosis Read More »
David J Black looks at the shameful treatment of ME/CFS
Open Letters to Healthcare Professionals from people with ME/CFS – Part 4 Lianne Read More »
Against the background of a new NICE Clinical Guideline for
MEA Monthly Poll: DWP Benefits during Covid-19 Read More »
Background Dr Shepherd will be attending one of his regular
Against the background of a new NICE Clinical Guideline for
Against the background of a new NICE Clinical Guideline for
Against the background of a new NICE Clinical Guideline for
The ME Association ME/CFS (& Long Covid) Weekly Research Round-up Read More »
The weekly research round-up now includes recent publications about ME/CFS
For me this is hard. Putting down in words how
Early Day Motion on the Retirement of Countess of Mar as Chair of Forward-ME Read More »
Carol Monaghan MP (Chair of the All-Party Parliamentary Group on
Mail Online: My canine carer can even tell when I’m about to faint Read More »
After years of ill health nearly destroyed her, Libbi Mattick
ME Association Statement: Aripiprazole (Abilify) & ME/CFS Read More »
We received reports that a small number of people with
The ME Association Champion Bloggers Read More »
The ME Association is incredibly lucky to have a wonderful group of people who write honest and emotive blogs about ME/CFS and we call then the ‘Champion Bloggers.’
Isle of Man Minister savaged for delays in setting up specialist M.E. service Read More »
The Minister for Health and Social Care on the Isle
Mark started getting symptoms of ME when he was in
New Leaflet: Personal Relationships – Intimacy in ME/CFS Read More »
All humans have a fundamental need to feel connected to and build intimate relationships with others. The diagnosis of a chronic health condition can severely impact the way we view ourselves as well as how we relate to our partners and loved ones…