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.
Website Survey September 2023: Autumn Covid Booster and Flu Vaccinations
Website Survey September 2023: Autumn Covid Booster and Flu Vaccinations Read More »
Please take part in the online survey to record your decisions and experiences with the 2 vaccinations.
Lee’s swim will turn into a tour de force for The ME Association
Lee’s swim will turn into a tour de force for The ME Association Read More »
Talk about determination! Illness in the family which “knocked us
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
Research recruitment: Are you the parent of an adult child with ME/CFS?
Research recruitment: Are you the parent of an adult child with ME/CFS? Read More »
Could I interview you about your experience as a parent
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.
The ME Association: Covid Autumn Booster Vaccine Information (2023)
The ME Association: Covid Autumn Booster Vaccine Information (2023) Read More »
We have reviewed the Covid Booster so you can make an informed decision about whether to have this latest vaccination.
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
Tony Wimpenny takes on the toughest Kilimanjaro challenge
Tony Wimpenny takes on the toughest Kilimanjaro challenge Read More »
Tony Wimpenny is about to do the stuff that dreams
The ME Association writes to Lancashire and South Cumbria NHS Foundation Trust about ‘discriminatory’ and ‘offensive’ wording in a job advert
Dr Shepherd has written to Lancashire and South Cumbria NHS
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
Our Christmas Challenge – pledging now happily wrapped up!
Our Christmas Challenge – pledging now happily wrapped up! Read More »
THANK YOU ALL, WE REACHED OUR CHRISTMAS CHALLENGE PLEDGE TARGET
‘I miss that my Mum isn’t able to do so much any more!’
‘I miss that my Mum isn’t able to do so much any more!’ Read More »
A 12-year-old girl from Norfolk is going to throw herself
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
May 2023 survey – Household income and benefits
May 2023 survey – Household income and benefits Read More »
We ran a survey asking people about state benefits and
TIME: Long COVID Recovery Remains Rare
TIME: Long COVID Recovery Remains Rare Read More »
Since August 2020, David Putrino, director of rehabilitation innovation at
Please help us power up our Christmas Challenge
Please help us power up our Christmas Challenge Read More »
Please pledge at least £100 now (or whatever you can
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.