America: Distinct immune and hormone responses shed light on Long Covid
America: Distinct immune and hormone responses shed light on Long Covid Read More »
People with Long Covid exhibit different immune and hormonal responses to the Covid-19 virus.
The ME Association Responds to Government Consultation: Interim Delivery Plan on ME/CFS
The ME Association Responds to Government Consultation: Interim Delivery Plan on ME/CFS Read More »
We would like the Final Delivery Plan on ME/CFS to be more encompassing and representative.
Independent: DecodeME: Major study hopes to tackle ME stigma
Independent: DecodeME: Major study hopes to tackle ME stigma Read More »
DecodeME is aiming to find a genetic cause of the condition which is estimated to affect 250,000 people in the UK
ME/CFS and Long Covid Research: 12 – 18 September 2023
ME/CFS and Long Covid Research: 12 – 18 September 2023 Read More »
The weekly research round-up includes recent publications about ME/CFS and Long Covid.
Protestors in Cambridge call for doctors to receive ‘better training’ about ME
Protestors in Cambridge call for doctors to receive ‘better training’ about ME Read More »
People with ME are protesting in Cambridge and want doctors to have better knowledge and training in ME.
ME/CFS and Long Covid Research: 05 – 11 September 2023
ME/CFS and Long Covid Research: 05 – 11 September 2023 Read More »
The weekly research round-up includes recent publications about ME/CFS and Long Covid.
The ME Association: A Very Successful Count ME In Campaign!
The ME Association: A Very Successful Count ME In Campaign! Read More »
THANK YOU for supporting the ME Association’s recent Count ME In campaign.
British Medical Journal: How can I support my colleague returning to work with Long Covid?
“Remember that no two people with Long Covid will be
America: Post-Acute Infection Syndromes will be the Focus of New Center at Yale School of Medicine
The new centre will investigate Long Covid, ME/CFS, and post-treatment Lyme disease.
Advertising Standards: Chrysalis Effect cannot claim ME/CFS recovery!
Advertising Standards: Chrysalis Effect cannot claim ME/CFS recovery! Read More »
The ME Association had made a complaint to the Advertising
Research: Developing a Blood Cell-Based Diagnostic Test for ME/CFS Using Peripheral Blood Mononuclear Cells
The following research was funded by the ME Association Ramsay
ME/CFS and Long Covid Research: 22 – 28 August 2023
ME/CFS and Long Covid Research: 22 – 28 August 2023 Read More »
The weekly research round-up includes recent publications about ME/CFS and Long Covid.
Guardian: UK scientists find link between proteins related to blood clots and Long Covid
Guardian: UK scientists find link between proteins related to blood clots and Long Covid Read More »
ME Association Comment: “Interesting new research from the University of
TIME: Long COVID Recovery Remains Rare
TIME: Long COVID Recovery Remains Rare Read More »
Since August 2020, David Putrino, director of rehabilitation innovation at
ME/CFS and Long Covid Research: 15 – 21 August 2023
ME/CFS and Long Covid Research: 15 – 21 August 2023 Read More »
The weekly research round-up includes recent publications about ME/CFS and Long Covid.
Research: Potential abnormalities found in home-based testing of everyday activities in ME/CFS
The following research was funded by the ME Association Ramsay
Research: A protein that disrupts a cell’s energy structure may be a culprit in ME/CFS (& Long Covid)
Researchers have identified a protein that’s present at unusually high levels in
Severe ME Week 2023: A parent’s perspective
Severe ME Week 2023: A parent’s perspective Read More »
Given the vast numbers of patients throughout the U.K. with
Severe ME Week 2023: Katie’s thoughts on relative improvements
Severe ME Week 2023: Katie’s thoughts on relative improvements Read More »
Living this life and deteriorating is hard beyond belief to