Hospital Care for people with severe and very severe ME
This article, also printed in the Summer Newsletter 2024, provides useful resources, including the relevant NICE Guidance, for…
Response to the Interim Delivery Plan from 25% ME Group
Response to the Interim Delivery Plan from 25% ME Group, a national charity which supports people with severe…
ME/CFS CPD | Module
ME/CFS CPD | Module https://www.studyprn.com/p/chronic-fatigue-syndrome A message from course author, Dr Nina Muirhead BA (Oxon), BMBCh (Oxon), MRCS…
#DecodeME Matters
#DecodeME Matters As many of you are aware our advocacy worker, Helen Baxter, has been assisting people with…
25% ME Group at The Malnutrition Task Force Sharing Practice Day
Our advocacy worker, Helen Baxter, did a talk on preventing avoidable malnutrition in severe ME at The Malnutrition…
Feedback on survey
Many of you took part in the surveys put together by the James Lind Alliance ME/CFS Priority Setting…
The IACFSME conference
The IACFSME conference was covered by journalist, Miriam Tucker, who chose to focus an article on our advocacy…
25% ME Group at IACFSME Conference
25% ME Group at IACFSME Conference Advocacy worker, Helen Baxter attended the International Association for Chronic Fatigue Syndrome/Myalgic…
Ensuring the Voice of the Very Severely Affected Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Patient Is Heard in Research—A Research Model.
Abstract Most of the research about Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) has focused on ambulant patients who are…
The 25% ME Group’s Season’s greetings video
E D I T . The video has been viewed over 250 times in the last 24 hours!…