Research: Long-Term Follow-Up of Women with ME/CFS: A 16-Year Longitudinal Study Read More »
Last month, research entitled ‘Long-Term Follow-Up of Women with Myalgic […]
Article: Overcoming barriers in ME/CFS research: the CureME participatory model Read More »
A new article, written by Ella Abken from the CureME
Coventry and Warwickshire has lost its dedicated services for Myalgic
Long Covid Advocacy responds to Royal College of Psychiatrists regarding Open Letter Read More »
In May, The ME Association co-signed an open letter, written
Yesterday (29.06.26), GOV UK released a press release regarding ‘Health
The ME Association is pleased to confirm that Stage 1
Scottish Parliament: Helen McDade Question on ME and Long Covid Specialist Clinics Read More »
Last Wednesday, Holyrood Health, Care and Sport Committee Convenor Helen
MDPI published a research review (May 2026) entitled ‘Transcutaneous Auricular
On Friday 19th June, Scope launched a new campaign called
Today (18.06.26), Baroness Scott of Needham Market led a debate
A new research paper, titled “Health-related quality of life changes
Carers Week 2026: Jayne’s Story Read More »
*Pseudonyms and stock images have been used to share this
Carers Week 2026: Suzie’s Story Read More »
Suzie’s employer understands the realities, and the emotional and practical
Representing the ME/CFS Community at Westminster for Carers Week 2026 Read More »
As part of Carers Week 2026, The ME Association was
**Trigger Warning: Upsetting Content** Petition Introduction Caroline Roberts, once an
Caring for someone with Severe ME: Myfanwy’s story Read More »
One of Myfanwy’s greatest challenges is the widespread lack of
Carers Week 2026: Yvette’s Story Read More »
“In the farming community, the ‘tough it out’ culture often
Carers Week 2026: Dave’s Story Read More »
Dave does not see himself as a carer; instead, he
