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.
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 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 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! Read More »
THANK YOU for supporting the ME Association’s recent Count ME In campaign.
“Remember that no two people with Long Covid will be
The new centre will investigate Long Covid, ME/CFS, and post-treatment Lyme disease.
Advertising Standards: Chrysalis Effect cannot claim ME/CFS recovery! Read More »
The ME Association had made a complaint to the Advertising
The following research was funded by the ME Association Ramsay
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 Read More »
ME Association Comment: “Interesting new research from the University of
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 Read More »
The weekly research round-up includes recent publications about ME/CFS and Long Covid.
The following research was funded by the ME Association Ramsay
Researchers have identified a protein that’s present at unusually high levels in
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 Read More »
Living this life and deteriorating is hard beyond belief to
Severe ME Week 2023: John’s Story Read More »
Conditions on the ward, similar to the other wards he
Severe ME Week 2023: Leanne’s Story Read More »
But the hardest symptoms to explain to people are how
Severe ME Week 2023: Sylvia’s Story Read More »
The brain fog overwhelms my ability to comprehend the multiple