The MEA highlights the lack of sound and replicated scientific evidence to support CICT ‘brain training’
Researchers at the University of Alabama at Birmingham (UAB) have […]
Survey Results: Hypersensitivities, Sensitivities and Intolerances
Survey Results: Hypersensitivities, Sensitivities and Intolerances Read More »
Earlier in the year, the ME Association asked the ME/CFS
MSP tables Motion to mark International ME Awareness Day at Holyrood
MSP tables Motion to mark International ME Awareness Day at Holyrood Read More »
Liz Smith, Scottish Conservative and Unionist Party for Mid Scotland
News Medical: Global clinical trial tests two anti-inflammatory medicines for long COVID
News Medical: Global clinical trial tests two anti-inflammatory medicines for long COVID Read More »
Spanning four continents and enrolling hundreds of people, a new
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
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,
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
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
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
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
The ME Association signs Carers UK open letter regarding Carers Allowance Overpayments
The ME Association signs Carers UK open letter regarding Carers Allowance Overpayments Read More »
Together with Carers UK and 106 other organisations across the
Key Announcements: MP Liz Kendall, Secretary of State for DWP confirms the government plans on welfare reform
Yesterday (18.03.25), the government announced a series of significant changes