Developing a clinical assessment toolkit for people with ME/CFS and clinical services Participant Information Sheet
You are being invited to take part in a research study to develop a clinical assessment toolkit for…
WCA consultation support for organisations
The DWP are proposing to make the WCA much harder to pass and this is going to have…
The woman being denied the NHS care she needs to treat her ME
This is the inpatient experience of a patient with very severe ME, whose father Michael Gordon gave an…
DecodeME: the largest study into the causes of ME/CFS – Add your voice!
DecodeME: the largest study into the causes of ME/CFS – Add your voice! DecodeME launched in September 2022, and…
We Live With A Monster A Myalgic Encephalomyelitis (M.E.) Story
Sharon Tiday said on Twitter: For a while now people have told me that I should get this…
A life cut short by medical neglect
A life cut short by medical neglect: interview with Sarah Boothby, whose daughter Maeve died at 27 of…
Thousands of ME patients ‘failed by shockingly poor NHS care’
National treatment guidelines published two years ago are still not widely implemented, says charity Kat Lay, Health Editor…
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…
Having Severe ME/CFS: A Report From Norway
In 2018, the Norwegian ME Association undertook a large survey of severely ill ME patients. We wanted to…