Successful launch night of Jeremy Jeff’s photography exhibition, ‘Lives we cannot Live’, at London’s Oxo Tower Wharf
Last night (Wednesday 24th September), the ME Association held a […]
News
APPG on ME – 10th September meeting minutes now available
APPG on ME – 10th September meeting minutes now available Read More »
The minutes from the 10 September APPG meeting are now
Living Magazine: Herts Woman Features in Photography Exhibition highlighting ME/CFS
Living Magazine: Herts Woman Features in Photography Exhibition highlighting ME/CFS Read More »
The experiences of Hertfordshire woman, Maureen Kinnear (72), who has
Andrew Jackson and Jeremy Jeffs interviewed about new exhibition on ITV Border News!
Andrew Jackson and Jeremy Jeffs interviewed about new exhibition on ITV Border News! Read More »
This morning (19/09/2025) Andrew Jackson, a Cumbrian farmer with ME/CFS
Survey: Your feedback on Diabetes medication
Survey: Your feedback on Diabetes medication Read More »
Do you have non insulin requiring diabetes in addition to
The Lancet: Autoantibodies in long COVID
The Lancet: Autoantibodies in long COVID Read More »
On the 8th September 2025, The Lancet Infectious Diseases published
The Journal of Nuclear Medicine: Varying Levels of Inflammatory Activity in Patients with Persistent Fatigue and Difficulty Concentrating After COVID-19
The results of this new study, ‘Varying Levels of Inflammatory
Lincolnshire World: Lincolnshire photographer exhibits striking photography collection highlighting living with ME/CFS
Documentary film-maker and photographer, Jeremy Jeffs from Lincolnshire, is exhibiting
Research: New Study to Harmonise Research Definitions in ME/CFS
Research: New Study to Harmonise Research Definitions in ME/CFS Read More »
The ME Association is delighted to announce that it has
The ME Association categorically disagrees with the opinions expressed in Science Norway article
***Sharing for information – not a recommendation*** Today, an opinion
Parliamentary questions surrounding the DHSC Delivery Plan on ME/CFS
Parliamentary questions surrounding the DHSC Delivery Plan on ME/CFS Read More »
Ashley Dalton, Parliamentary Under-Secretary of State for Public Health and Prevention
Research: Second-Phase Funding to Advance the Development of a Diagnostic Test for ME/CFS
The ME Association and ME Research UK are excited to
Farming Life: Cumbrian farmer features in unique photography exhibition highlighting ME/CFS
The experiences of Cumbrian farmer, Andrew Jackson (58), who has
Ask your MP to sign the Early Day Motion!
Ask your MP to sign the Early Day Motion! Read More »
Ask your MP to sign the Early Day Motion (EDM)
Have Your Say on Disability And Employment/Volunteering
Have Your Say on Disability And Employment/Volunteering Read More »
We first ran this survey in 2022; we are updating
Disabled people call for an independent PIP review; add your name
Disabled people call for an independent PIP review; add your name Read More »
Disabled people’s organisations have published an open letter calling for
Journal of Clinical Medicine: Autonomic Dysfunction in ME/CFS
Journal of Clinical Medicine: Autonomic Dysfunction in ME/CFS Read More »
ME/CFS patients exhibit a substantial autonomic symptom burden that correlates
MP John Milne writes to Wes Streeting
MP John Milne writes to Wes Streeting Read More »
Under a heading “Concerns regarding ME/CFS Strategy in the Final
Metro: I thought I had food poisoning – it was far worse
Metro: I thought I had food poisoning – it was far worse Read More »
I couldn’t get out of bed. I felt drained, constantly.
Parliamentary questions on ME/CFS and Long Covid research funding, and the Epsom and St Helier NHS Foundation Trust service
MP Tom Morrison, Liberal Democrats asked Ashley Dalton, Parliamentary Under-Secretary