ME Association New Free Leaflet – The Importance of Early & Accurate Diagnosis in ME/CFS Read More »
A new FREE 6-page leaflet that helps determine what is required to make an early and accurate diagnosis of ME/CFS.
Join our team in next year’s London Landmarks Half Marathon! Read More »
We have places available for the London Landmark’s Half-Marathon in 2021. Contact us if you would like to take part and help us to do more for people with M.E.!
The ME Association Research Round-up Read More »
This week we review 4 new research studies that have been published about ME/CFS.
NICE has confirmed that the Chronic Pain Guideline and recommendations do not apply to people with a diagnosis of ME/CFS.
The ME Association Pneumonia and the Pneumococcal vaccine – do you need this protection? Read More »
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.
The ME Association Flu Vaccine Information and Guidance for 2020 – 2021 Read More »
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.
The ME Association Research Round-up Read More »
This week we feature a new study that examines acute Epstein Barr as a trigger and another that reports on use of IV Saline as a potential treatment.
“We’ve got this tsunami of people that were previously strong adults who are just not getting better and general practice is just not equipped for these people”. – Dr Shepherd
IACFS/ME New York Research Conference Report Read More »
The ME Association has produced a summary report of the recent M.E. research conference which took place in New York.
“I was infected with coronavirus in March, six months on I’m still unwell,” Read More »
Charlie Russell, 27, is one of an estimated 600,000 people with post-Covid illness, a condition that may give an insight into ME – with Dr Charles Shepherd.
The ME Association Research Round-up Read More »
This week 3 new research studies have been published and we highlight 2 of them.
Early Day Motion: Researching and supporting people with long Covid-19 symptoms Read More »
Carol Monaghan has tabled an Early Day Motion that we would like you to encourage your own MPs to support. A template email is included for you to use.
MEA Monthly Poll: How has M.E. affected your ability to access education? Read More »
This month’s website poll is part of our focus on education. Please vote and join the discussion on MEA social media.
Potential research into Long-Covid and ME/CFS at the ME Biobank Read More »
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.
The ME Association: We are seeking a research correspondent to join our team! Read More »
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 on long haul covid-19—Don’t try to dominate this virus, accommodate it! Read More »
Paul Garner continues his BMJ Blog, explaining his experiences with Long-Covid and calls for appropriate guidance and support.
Medscape: Small-Fiber Polyneuropathy May Underlie Dysautonomia in ME/CFS Read More »
These potentially important findings were presented by Ryan Whelan from the Simmaron Research Institute at the recent IACFS/ME virtual conference.
The ME Association Research Round-up Read More »
This week 5 new studies were published. We highlight 3 that include neuroimaging reviews, hypermobility and intracranial hypertension, and the economic cost of ME/CFS in Australia.
Having a consultant physician as part of a ME/CFS clinical team is essential. This is a fantastic opportunity to join one of the best NHS services in the country.
