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 […]
News
The ME Association is joining Scope to call for Work Without Barriers: Sign the Open Letter
On Friday 19th June, Scope launched a new campaign called
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
Research: Long term health outcomes in Q-fever: a non-viral infection that can cause an ME/CFS like illness
A new research paper, titled “Health-related quality of life changes
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
Representing the ME/CFS Community at Westminster for Carers Week 2026
Representing the ME/CFS Community at Westminster for Carers Week 2026 Read More »
As part of Carers Week 2026, The ME Association was
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
ME Association provides information for BBC Morning Live interview with Dr Ranj on ME/CFS
On June 2nd 2026, BBC Morning Live featured an interview
Eight-year-old Chester school boy takes on 50 mile bike ride for ME/CFS in honour of his mum
Eight-year-old Harvey Capewell from Chester is embarking on a 50
BBC Morning Live covers ME/CFS – ME Association Response
BBC Morning Live covers ME/CFS – ME Association Response Read More »
UPDATE (2nd Jun 2026): As a result of the correspondence
Gordon family issue an update on Karen’s health and emails from NHS ESHT solicitors
Gordon family issue an update on Karen’s health and emails from NHS ESHT solicitors Read More »
The Gordon family has provided an update on Karen’s condition
Oxford ME/CFS Research: Highlights and Final Report (2019–2026)
Oxford ME/CFS Research: Highlights and Final Report (2019–2026) Read More »
Over the past seven years, the ME Association has funded
Research: Effect of Vagus Nerve Stimulation on fatigue in people with Long Covid
Research: Effect of Vagus Nerve Stimulation on fatigue in people with Long Covid Read More »
A new research paper, still awaiting peer review, has been