M.E. Support Northern Ireland – Upcoming Talks with Dr Charles Shepherd and Dr. Night Speight
M.E. Support Northern Ireland are hosting two upcoming online talks […]
BBC News: Sister of bedbound ME sufferer urges more funding
BBC News: Sister of bedbound ME sufferer urges more funding Read More »
The sister of a woman with severe myalgic encephalomyelitis (ME)
Parliamentary Questions regarding the DHSC delivery plan on ME/CFS
Parliamentary Questions regarding the DHSC delivery plan on ME/CFS Read More »
Recently, a few MPs have asked parliamentary questions surrounding the
Update: UK ME/CFS Biobank Steering Group
Update: UK ME/CFS Biobank Steering Group Read More »
The ME Association (MEA) has invested £850,000 in the UK
DWP Replies to Dr Charles Shepherd’s Letter Regarding Welfare Cuts
DWP Replies to Dr Charles Shepherd’s Letter Regarding Welfare Cuts Read More »
On the 15th of March, 2025, Dr Charles Shepherd, MEA
BMJ published paper highlights key findings from The MEA’s Count ME In survey
BMJ published paper highlights key findings from The MEA’s Count ME In survey Read More »
A fully independent research paper by The University of Exeter,
Technology Network: Pregnant Women Less Likely to Develop Long COVID
Technology Network: Pregnant Women Less Likely to Develop Long COVID Read More »
“About 16% of pregnant individuals developed symptoms consistent with Long
Press Release: Leading UK Charity invests in Canadian trial of drug treatment for ME/CFS and Long Covid
The ME Association, a leading UK charity for people with
Cornish and Devon Post: Russell Fleming (MEA) shares his experience of ME/CFS and journey from banker to ME advocate
“My life experience dictated that infections were short-lived and resulted
Department of Health and Social Care have issued an update on the delivery plan
Department of Health and Social Care have issued an update on the delivery plan Read More »
The statement outlines the departments plans to publish the Delivery
The MEA attended the Clinical Post Covid Society Conference in Birmingham on Wednesday
The MEA attended the Clinical Post Covid Society Conference in Birmingham on Wednesday Read More »
The MEA were pleased to be at the Clinical Post
NIHR evidence review and map of research activity involving ME/CFS
NIHR evidence review and map of research activity involving ME/CFS Read More »
An ME/CFS evidence review and associated interactive map has now
University of Surrey: Study finds long Covid patients feel pressure to prove their illness is real
People living with Long Covid often feel dismissed, disbelieved and
Survey Results: ME/CFS Diagnosis Pre & Post 2021 NICE Guideline
Survey Results: ME/CFS Diagnosis Pre & Post 2021 NICE Guideline Read More »
At the beginning of this year, the ME Association asked
MEA Signs Long Covid Kids Open Letter to The Rt Hon Wes Streeting and Ashley Dalton MP
MEA Signs Long Covid Kids Open Letter to The Rt Hon Wes Streeting and Ashley Dalton MP Read More »
Summary The ME Association has signed an open letter to
Science Norway: Almost no ME/CFS patients return to work
Science Norway: Almost no ME/CFS patients return to work Read More »
A new Norwegian study shows that very few ME/CFS patients
Irish ME/CFS Association: 3,600 information packs to be sent to Irish GPs
Irish ME/CFS Association: 3,600 information packs to be sent to Irish GPs Read More »
The Irish ME/CFS Association has been working hard to organise
The ME Association fervently refutes the psychosomatic model of causation applies to ME/CFS or indeed Long Covid
Professor Paul Garner and Dr Charles Shepherd, have spoken to
Guardian: Councils and NHS could face millions in extra costs due to disability benefit cuts
Government plans for Pip cuts will drive up costs for
Student Research: To what extent do Long Covid patients perceive the treatment available appropriate?
The ME Association is sharing this survey with the community