Young Carers
It was Carers week last week and we don’t often […]
2021
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
The ME Association ME/CFS (& Long Covid) Weekly Research Round-up
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
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
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
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
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
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
Open Letters to Healthcare Professionals from people with ME/CFS – Part 3 Anne and Maryjane
Against the background of a new NICE Clinical Guideline for
Open Letters to Healthcare Professionals from people with ME/CFS – Part 2 Nicola and Jules
Against the background of a new NICE Clinical Guideline for
Open Letters to Healthcare Professionals from people with ME/CFS – Part 1 Kate and Margaret
Against the background of a new NICE Clinical Guideline for
The ME Association ME/CFS (& Long Covid) Weekly Research Round-up
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
Guest blog: “I’m learning to use the word ‘fatigue’ as tiredness doesn’t leave you collapsing on the floor and crying like a baby.”
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
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
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
ME Association Statement: Aripiprazole (Abilify) & ME/CFS Read More »
We received reports that a small number of people with
New Leaflet: Personal Relationships – Intimacy in ME/CFS
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…
The ME Association ME/CFS (& Long Covid) Weekly Research Round-up
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
Video: Long Covid, PVFS, & ME/CFS with leading experts including Dr Charles Shepherd
Video: Long Covid, PVFS, & ME/CFS with leading experts including Dr Charles Shepherd Read More »
This is an excellent new video, and we commend Broken