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.
September 2023
Oslo Chronic Fatigue Consortium ‘New Hope’ is “More Unhelpful Nonsense”!
Oslo Chronic Fatigue Consortium ‘New Hope’ is “More Unhelpful Nonsense”! Read More »
ME Association statement about Oslo Chronic Fatigue Consortium research.
America: How one woman’s quest to understand chronic fatigue sparked a scientific breakthrough
Researchers found that a protein was reducing cellular energy production.
Webinar: Long Covid Misconceptions with Dr Charles Shepherd and People with Lived Experience
Bournemouth University are hosting a public webinar about the myths,
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.
Janice Kent – a tower of strength for people with ME/CFS
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
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.
Adam’s cricket match will celebrate his successful Great North Run
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
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.
Information on ME/CFS for GPs in New Zealand – Definitely not recommended.
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
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 Association receive apology from Oxford NHS Trust regarding ‘inaccurate’ and ‘offensive’ job advert
We have now received an apology from the Oxford University
Kilimanjaro Marathon – They ran it. They won it!
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
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