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
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
Health Expectations: Under-Served Groups and Myalgic Encephalomyelitis Research Workshop; Multiple Barriers to Effective Healthcare, Research and Public Participation
This research article discusses the barriers faced by under-served groups
The ME Association signs Scope’s open letter to the chancellor regarding welfare cuts
The ME Association signs Scope’s open letter to the chancellor regarding welfare cuts Read More »
The ME Association has joined over 50 (EDIT19.05.25 now 120
Frontiers: Dysregulation of lipid metabolism, energy production, and oxidative stress in ME/CFS, Gulf War Syndrome and fibromyalgia
Comprehensive metabolomic and proteomic analyses are crucial for advancing the
MEA writes to the Rt Hon Liz Kendall, Secretary of State for Work and Pensions
MEA writes to the Rt Hon Liz Kendall, Secretary of State for Work and Pensions Read More »
Summary The MEA has written to Liz Kendall to express