BMJ Rapid Response: Long-Covid & ME/CFS by Dr Nina Muirhead
BMJ Rapid Response: Long-Covid & ME/CFS by Dr Nina Muirhead Read More »
Nina Muirhead, SAS Doctor Dermatology Surgery, Buckinghamshire Healthcare NHS Trust, […]
treatment
The ME Association ME/CFS Research Round-up
The ME Association ME/CFS Research Round-up Read More »
In the last week, 5 new studies have been published. We look at the prevalence of perineural cysts and multi-omics revelations in ME/CFS.
Scottish Government Issue Caution Notice for Graded Exercise Therapy in ME/CFS & Post/Long-Covid
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.
News & Comment: The Long-Covid Crisis and £10 million on NHS Specialist Clinics for Post-Covid Sufferers
The ME Association appeared in several media publications at the weekend sharing opinion about Long-Covid and the proposed new specialist clinics.
The ME Association Pneumonia and the Pneumococcal vaccine – do you need this protection?
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.
New Free Leaflet: The ME Association Guide to Post-Covid Fatigue Syndromes and Post-Covid ME/CFS
The information in this new guide should be of help to people when managing post-Covid fatigue syndrome and post-Covid ME/CFS.
Early Day Motion: Researching and supporting people with long Covid-19 symptoms
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.
Medscape: Small-Fiber Polyneuropathy May Underlie Dysautonomia in ME/CFS
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.
How it feels to have Very Severe M.E. by Ruth Braham
How it feels to have Very Severe M.E. by Ruth Braham Read More »
“It is incessant, inescapable torture. You are trapped. Completely powerless. You’re in agony with countless unbearable symptoms…”
Meet The Scientist: Professor Chris Ponting – DecodeME
Meet The Scientist: Professor Chris Ponting – DecodeME Read More »
Chris Ponting talks about the DecodeME study that seeks to understand the causes of M.E. and could help advance the discovery of effective treatments.
The DecodeME Genetics Study: Letters to The Times
The DecodeME Genetics Study: Letters to The Times Read More »
Published letters in response to the DecodeME research announcement and recent articles. With Jeremy Hunt and Carol Monaghan.
ME Awareness: “GP’s have not been given any training to recognise a patient with ME,” by Smita Dutta | 13 May 2020
“The GP’s I have seen treat everyone based on symptoms rather than the whole illness itself…”
ME Awareness: The Lost Years by Smita Dutta | 06 May 2020
ME Awareness: The Lost Years by Smita Dutta | 06 May 2020 Read More »
“While writing this I am again thinking, “Why me?” I do not know when I am going to stop thinking about his question, maybe I never will.”
ME Awareness: What you need to know about M.E. | 01 May 2020
ME Awareness: What you need to know about M.E. | 01 May 2020 Read More »
This free download provides information to help in the understanding of Myalgic Encephalopathy.
ME Association Weekly Update: Coronavirus and ME/CFS – Free Leaflet and Vulnerability Letter | 24 April 2020
Dr Shepherd has updated the weekly bulletin on covid-19 and ME/CFS.
ME Association Weekly Update: Coronavirus and ME/CFS – New Leaflet and Letter | 17 April 2020
We provide a weekly update on Covid-19 in a new free leaflet and a letter about vulnerability to be used when required.
Share Your Stories for ME Awareness Week: The Lost Years and a Focus on Symptoms| 06 March 2020
Sharing your story is one of the best ways we have of improving understanding and awareness of M.E.
MEA Website Survey: Physiotherapy and ME | 02 July 2019
MEA Website Survey: Physiotherapy and ME | 02 July 2019 Read More »
A new group of health professionals – Physios For ME – are seeking your feedback in this month’s MEA website survey.