ME Connect helpline new freephone number is live!
0808 801 0484
Please save this new number.
We are providing a new and improved service from February 1st 2025.
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 250,000 people in the UK have ME/CFS. In addition, a significant but unknown number of people diagnosed with some form of Long Covid also meet diagnostic criteria for ME/CFS. It represents a very real health crisis.
PVFS = Post-Viral Fatigue Syndrome.
ME = Myalgic Encephalomyelitis/Encephalopathy.
CFS = Chronic Fatigue Syndrome.
Long Covid = Post-Covid Syndrome.
Changing attitudes and improving lives…
The Latest News
House of Lords Q&A on the DHSC Delivery Plan for ME/CFS
World Health Organisation (WHO): Post COVID-19 condition
House of Lords Q&A on ME/CFS Delivery Plan
Petitions to Westminster and Holyrood calling for better services for Autonomic Dysfunction and PoTS
Carers Week 2025: ‘Caring About Equality’
Publisher responds to petition to change ME/CFS definition in Kumar and Clark's Clinical Medicine Textbook
Nature: Plasma exchange therapy for the post COVID-19 condition
MDPI Article: Cognitive Dysfunction in ME/CFS – Aetiology and Potential Treatments
The Sunday Times: How a promising triathlete was left bedridden by cruel disease
News Medical: Interferon gamma persistence offers clues to Long COVID and potential therapies
Dr Charles Shepherd signs letter to Cochrane regarding the review ‘Exercise therapy for chronic fatigue syndrome'
Parliamentary Question: Employment: ME/CFS and Long Covid – Minister of State for DWP responds
Nature Communications: Dr Wüst and colleagues reply to a further letter misinterpreting research study
The Times: Plan to help ME sufferers will not include extra funding
Parliamentary Q&A on Funding for ME/CFS delivery plan and Centre of Excellence for chronic conditions
The Times: Plan to help ME sufferers has been delayed for too long
NHS Networks: Infographic guide available to support in the diagnosis of ME/CFS
Courageous run for the ME Association after Gem gets her cancer ‘all-clear'
Blog Survey: Hypersensitivities, Sensitivities and Intolerances
Nature Communications: Letters: Dr Wüst and colleagues refute a published letter that incorrectly interprets their research study
More News >>
The Real M.E. Campaign
People with M.E. and Long Covid are demonstrating they possess the confidence to be seen and are raising more awareness than ever before.
We began the campaign in 2018 and featuring images of ‘real' people has had a very positive impact!





