Driving discovery: The ME Association invests £1.1m into pioneering research programme!
Driving discovery: The ME Association invests £1.1m into pioneering research programme! Read More »
Today, we are incredibly proud to unveil news of our […]
Driving discovery: The ME Association invests £1.1m into pioneering research programme! Read More »
Today, we are incredibly proud to unveil news of our […]
Update: LDN clinical trial: Progress Report July-September 2025 Read More »
We are pleased to share the latest quarterly update on
Research Update: ME Research Case Definition Consensus Survey Read More »
Professor Leonard A. Jason provides an update on the survey,
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 and ME Research UK are excited to
Update: Low-dose naltrexone (LDN) clinical trial: Progress Report April-June 2025 Read More »
Following our initial announcement in April, we’re pleased to share
Dr Krista Clarke is a post-doctoral researcher at the University
Update: UK ME/CFS Biobank Steering Group Read More »
The ME Association (MEA) has invested £850,000 in the UK
The ME Association, a leading UK charity for people with
ME Biobank: New research into the immunology of ME/CFS Read More »
We are pleased to report that some important new research
Physios for ME: Now recruiting – vagus nerve stimulation study Read More »
**EDIT: Please Note: Due to a fantastic response, Physios for
Dr Krista Clarke is a post-doctoral researcher at the University
This jointly funded project by ME Research UK and the
We hope the protocol when implemented will bring relief to the hundreds of thousands of people who suffer from these very debilitating symptoms
Endorsed by UK CRC, DHSC, UKRI MRC, NIHR, and CSO in Scotland.
Research: Sex and disease severity‑based analysis of steroid hormones in ME/CFS Read More »
Study found that levels of steroid hormones in were significantly different in ME/CFS…
Prevalence: How many people have ME/CFS in the UK? Read More »
The honest answer is that we just don’t know how many people have ME/CFS in the UK.
Patient Reported Outcome Measures (PROMs) in ME/CFS Read More »
A welcome review of the Chalder Fatigue Scale has prompted a statement from Professor Tyson about the PROMs project she is leading…
The UK ME/CFS Biobank: People with severe form of illness needed for HHV-6 study! Read More »
The UKMEB is looking for people with severe ME/CFS for a ‘spit and post’ DNA study.