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The ME Association
We're here for you…
The ME Association has been providing expert help since 1980. We understand the challenges faced by people with ME/CFS and Long Covid and believe that nobody should struggle alone.
Health Crisis
We estimate that at least 404,000 people in the UK have ME/CFS. In addition, 950,000 people unable to recover from a Covid infection could meet the diagnostic criteria for ME/CFS. This could mean that 1,350,000 adults and children in the UK are affected by ME/CFS. It represents a very real health crisis, and we are determined to improve the healthcare that people receive.
Changing attitudes and improving lives…
Membership
We put our member's interest at the forefront of all that we do. In return for your support you will receive ME Essential magazine.
Get Involved
There are so many ways to help including fundraising, campaigning, legacies, and joining as a member.
Support
At ME Connect we listen and we understand. If you need help or want to talk, we’re here, 6 days a week.
Research
We make prudent investments in medical research to increase our knowledge in the hope it will lead to effective treatments.
Healthcare4ME
We are committed to working with the NHS and social care providers to improve healthcare for people with ME/CFS and Long Covid.
Literature
We have an extensive range of free literature written by Dr Charles Shepherd, other advisers, and topic experts.
Medical Matters
Do you have a question about symptoms, treatments, or other health-related topics? See our specialist advisers' Q&A.
The Latest News
Welfare Benefits: Face-to-face and telephone health assessments to be audio recorded from June 29
Research: Does poor oxygenation and a delay in muscle energy recovery contribute to fatigue and PEM in ME/CFS? Now Recruiting!
Preprint Research: Mapping the Symptom Profile and Burden of ME/CFS: Insights from the TIMES Survey
Scottish Parliament: Helen McDade Question on ME and Long Covid Specialist Clinics
Research Review: tVNS for Post-COVID-19 Condition: A Systematic Review and Critical Appraisal of Clinical Evidence
The ME Association is joining Scope to call for Work Without Barriers: Sign the Open Letter
House of Lords Debate: Treatment and research into severe myalgic encephalomyelitis (ME) – 18 June 2026
Research: Long term health outcomes in Q-fever: a non-viral infection that can cause an ME/CFS like illness
Carers Week 2026: Jayne's Story
ME Association Job Vacancy: ME Connect Officer
Carers Week 2026: Suzie's Story
Representing the ME/CFS Community at Westminster for Carers Week 2026
Petition: Caroline Roberts: Inpatient Leicester Royal Infirmary Hospital with very severe ME
Caring for someone with Severe ME: Myfanwy’s story
Carers Week 2026: Yvette's Story
The ME Association joins other organisations to sign an open letter to the Royal College of Psychiatrists
Carers Week 2026: Dave's Story
Carers Week 2026 Press Release: Nearly half of unpaid carers feel their role goes unrecognised in their community
ME Awareness Week: ME/CFS Friendship Group organise an information stand at Gloucestershire Hospitals NHS Foundation Trust
ME Association provides information for BBC Morning Live interview with Dr Ranj on ME/CFS
More News >>
ME Association Testimonials
Terminology
PVFS = Post-Viral Fatigue Syndrome
ME = Myalgic Encephalomyelitis/Encephalopathy
CFS = Chronic Fatigue Syndrome
Long Covid = Post-Covid Syndrome











