Ian Lazonby was a vet and a lawyer before glandular fever as an adult led to M.E. He talks about his experience with the condition, how he has recovered to an extent, and has accepted M.E.
Tag: chronic fatigue syndrome
Sarah Elsby has begun her impressive walking challenge in support of her mother who has M.E. Please donate and help the ME Association do more for this vulnerable community.
The ME Association has given a cautious welcome to the BACME position statement, but still has a number of concerns and questions.
New medical education initiative launched in Scotland by collaboration of charities including the ME Association and the CMRC Medical Education Group.
Dr Charles Shepherd wrote a piece for The Virginia Waters Magazine where he shared his insights into Post-Long Covid-19.
In an announcement that was delayed due to the pandemic, Scotland has now issued a cautionary notice on the use of GET in ME/CFS.
In this statement we explain why we have been working to help people with Post/Long Covid and how these syndromes overlap with ME/CFS.
We have a new free leaflet on this year’s Flu Vaccination, and a Website Poll asking you about any reactions you might have had to the vaccine.
Dr Charles Shepherd comments on the decision in England and Scotland to produce a new guideline on Post/Long-Covid Management.
NICE has confirmed that the Chronic Pain Guideline and recommendations do not apply to people with a diagnosis of ME/CFS.
Dr Shepherd answers a question about the pneumonia vaccine and provides the information you need to make an informed decision.
The information in this new guide should be of help to people when managing post-Covid fatigue syndrome and post-Covid ME/CFS.
We will shortly be updating our free leaflet on the Flu Vaccine and M.E. But we hope this information proves helpful in the meantime.
This week 3 new research studies have been published and we highlight 2 of them.
The ME Biobank team with Dr William Weir are hoping to conduct research into Post-Covid and ME/CFS. Please register your interest in taking part.
Do you have a passion for M.E. research? We are seeking a suitable candidate to join our team and help report scientific advances to the patient community.
Paul Garner continues his BMJ Blog, explaining his experiences with Long-Covid and calls for appropriate guidance and support.
This letter is now available for anyone to download and share to help raise awareness of Post-Covid management and the similarities with M.E.
“The NHS is urging people to exercise at a time when many, just like people with post-viral ME, need to rest, recuperate and pace themselves,” Countess of Mar.
We have updated the central index of ME/CFS published research for July, and include 4 new studies published this week.