ME/CFS and Long Covid Research: 19 – 25 September 2023
ME/CFS and Long Covid Research: 19 – 25 September 2023 Read More »
The weekly research round-up includes recent publications about ME/CFS and Long Covid.
ME/CFS and Long Covid Research: 19 – 25 September 2023 Read More »
The weekly research round-up includes recent publications about ME/CFS and Long Covid.
Oslo Chronic Fatigue Consortium ‘New Hope’ is “More Unhelpful Nonsense”! Read More »
ME Association statement about Oslo Chronic Fatigue Consortium research.
Researchers found that a protein was reducing cellular energy production.
Bournemouth University are hosting a public webinar about the myths,
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.
Janice Kent – a tower of strength for people with ME/CFS Read More »
We are very sorry to have to report that Janice
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.
Would you like one of our half marathon places in 2024? Read More »
This is just a brief note to let you know
Adam’s cricket match will celebrate his successful Great North Run Read More »
A teacher in the North East of England will be
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 Read More »
The weekly research round-up includes recent publications about ME/CFS and Long Covid.
Information on ME/CFS for GPs in New Zealand – Definitely not recommended. Read More »
New Zealand’s ME/CFS training for GPs is definitely not recommended by The ME Associations Medical Adviser.
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.
We have now received an apology from the Oxford University
Kilimanjaro Marathon – They ran it. They won it! Read More »
Swashbuckling brothers Tony and Ian Wimpenny did something extraordinary at
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.
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 Read More »
Talk about determination! Illness in the family which “knocked us
“Remember that no two people with Long Covid will be