ME Awareness week 12th-18th May
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 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.
Based on past epidemiological research evidence we estimated that at least 250,000 people had ME/CFS in the UK. This figure is likely to be a significant under-estimate as a result of some people having remained undiagnosed or misdiagnosed, and more recently with people developing ME/CFS after catching Covid-19.
Research evidence also indicates that around 50% of people with some form of Long Covid (currently around 2 million in the UK) meet diagnostic criteria for ME/CFS. We are currently reviewing all the research evidence with a view to producing a new estimate that is still evidence-based and would be accepted by organisations such as NHS England.
More information
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
MedicalXpress: Long COVID biomarkers found in blood associated with respiratory problems
Parliamentary Questions regarding Long Covid treatment and research
Help the ME Association secure £5,000 from Benefact Group
MSP tables Motion to mark International ME Awareness Day at Holyrood
Back from injury, Jack's all set for a second stunning marathon
The Times: Scientists call for research hubs to solve mystery of ME
News Medical: Global clinical trial tests two anti-inflammatory medicines for long COVID
Deputy CEO of ESHT responds to Dr Charles Shepherd's Letter
Three of the best – our runners in the London Marathon!
Ask your MP to join the joint meeting of the APPG on ME and APPG on Long Covid
New collaborative campaign launched calling for an ME/CFS, Long Covid and Post-Infectious Disease research platform
The Times: ME sufferers ‘feel invisible and ignored’ amid lottery of NHS care
Join us for Anna's Blue Sunday Tea Party on 18th May
BMJ: Hyperbaric oxygen therapy compared to sham treatment for Long Covid
First-time marathon runner was a French Canadian hockey star!
Nature: Identifying commonalities and differences between representations of Long Covid and ME/CFS in Electronic Health Records
Play highlighting the invisibility of ME debuts this May
M.E. Support Northern Ireland – Upcoming Talks with Dr Charles Shepherd and Dr. Night Speight
BBC News: Sister of bedbound ME sufferer urges more funding
Parliamentary Questions regarding the DHSC delivery plan on ME/CFS
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!





