MP Julian Smith asks parliamentary questions regarding the lack healthcare provision for people with very severe ME
Last week, MP Julian Smith (Conservative, Skipton and Ripon) tabled three […]
Research: New Study provides first evidence of Dopamine System Injury in the brain of Long Covid patients
A new brain imaging study led by researchers at the Canadian
Research: Long-Term Follow-Up of Women with ME/CFS: A 16-Year Longitudinal Study
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
Article: Overcoming barriers in ME/CFS research: the CureME participatory model Read More »
A new article, written by Ella Abken from the CureME
The ME Association opposes the Closure of ME/CFS and Long Covid Services in Coventry and Warwickshire
Coventry and Warwickshire has lost its dedicated services for Myalgic
Long Covid Advocacy responds to Royal College of Psychiatrists regarding Open Letter
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
Welfare Benefits: Face-to-face and telephone health assessments to be audio recorded from June 29
Yesterday (29.06.26), GOV UK released a press release regarding ‘Health
Research: Does poor oxygenation and a delay in muscle energy recovery contribute to fatigue and PEM in ME/CFS? Now Recruiting!
The ME Association is pleased to confirm that Stage 1
Scottish Parliament: Helen McDade Question on ME and Long Covid Specialist Clinics
Scottish Parliament: Helen McDade Question on ME and Long Covid Specialist Clinics Read More »
Last Wednesday, Holyrood Health, Care and Sport Committee Convenor Helen
Research Review: tVNS for Post-COVID-19 Condition: A Systematic Review and Critical Appraisal of Clinical Evidence
MDPI published a research review (May 2026) entitled ‘Transcutaneous Auricular
House of Lords Debate: Treatment and research into severe myalgic encephalomyelitis (ME) – 18 June 2026
Today (18.06.26), Baroness Scott of Needham Market led a debate
Carers Week 2026: Jayne’s Story
Carers Week 2026: Jayne’s Story Read More »
*Pseudonyms and stock images have been used to share this
Carers Week 2026: Suzie’s Story
Carers Week 2026: Suzie’s Story Read More »
Suzie’s employer understands the realities, and the emotional and practical
Petition: Caroline Roberts: Inpatient Leicester Royal Infirmary Hospital with very severe ME
**Trigger Warning: Upsetting Content** Petition Introduction Caroline Roberts, once an
Caring for someone with Severe ME: Myfanwy’s story
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
Carers Week 2026: Yvette’s Story Read More »
“In the farming community, the ‘tough it out’ culture often
Carers Week 2026: Dave’s Story
Carers Week 2026: Dave’s Story Read More »
Dave does not see himself as a carer; instead, he
ME Awareness Week: ME/CFS Friendship Group organise an information stand at Gloucestershire Hospitals NHS Foundation Trust
Members of ME/CFS Friendship Group in Gloucestershire were invited by