New Technology Should Help Make Education More Accessible to People with Chronic Illnesses – by Anna Wood | 01 August 2019
Anna explores how technology can help to include more chronically ill students in education.
Anna explores how technology can help to include more chronically ill students in education.
John has never tackled anything quite like it before, but was inspired to do something to show support for his daughter Elaine.
The Guardian: ME and the perils of internet activism | 29 July 2019 Read More »
This latest article continues to shine an uncritical spotlight on an issue that we really don’t think stands up to scrutiny…
The Latest Leaflet from the ME Association: Blood Tests Explained | 13 July 2019 Read More »
Dr Shepherd talks about the kind of tests employed by researchers, what clinical tests should be taken to rule out misdiagnosis and what those tests can reveal.
MEA Summary Review: The Role of Mitochondria in ME/CFS | 13 July 2019 Read More »
This latest review looks at energy production, and the ongoing search for clues as to what might be causing problems in ME/CFS.
MEA Personal: Facing up to Mental Health Challenges | 11 July 2019 Read More »
We’ve been talking about mental health on social media. Russell explains how he’s faced up to these challenges over the years.
This new 35-page guide is intended for those making both new claims for ESA or for Universal Credit based on health grounds.
Raising Awareness of Severe ME – A Call for Case Studies | 10 July 2019 Read More »
Severe M.E. Day is approaching in August, and we are asking you to share your stories and experiences.
Turning a Passion for Wildlife into Prints for M.E. | 08 July 2019 Read More »
Jen Taylor is very kindly raising money for the ME Associaion by selling her fabulous limited edition animal prints.
Advances in Understanding the Pathophysiology of ME/CFS | 08 July 2019 Read More »
When does an illness become a disease? Dr Komaroff explores what we know about the biological abnormalities in ME/CFS.
The Emotional Impact of a Long-term Physical Illness by Anna Redshaw | 08 July 2019 Read More »
“No human being can endure what we endure as M.E. sufferers and come away unscathed.”
The Times – Baroness Blackwood: Why I fainted in the House of Lords | 08 July 2019 Read More »
Baroness Blackwood had been misdiagnosed with ME/CFS before it was determined she had Ehlers-Danlos Syndromes (EDS).
ME Association June Summary of ME/CFS Published Research | 05 July 2019 Read More »
We’ve updated our central Research Index and feature 17 ME/CFS research studies from June 2019.
MEA Website Survey: Physiotherapy and ME | 02 July 2019 Read More »
A new group of health professionals – Physios For ME – are seeking your feedback in this month’s MEA website survey.
CMRC researchers propose deep trawl of DNA to uncover causes of ME/CFS | 28 June 2019 Read More »
Simon McGrath has written an authoritative blog about potentially the largest study of ME/CFS in the world!
This is a report following the recent meeting with Justin Tomlinson. Thank you to everyone who responded to our request for information.
Forward ME: ‘People with ME do NOT have to undergo psychological therapy’ | 24 June 2019 Read More »
These are the minutes from the Forward ME meeting held in May 2019.
Sjogren’s has important pathological overlaps with M.E. These results provide further evidence of a potential mechanism for chronic fatigue.
Loneliness, ME and the benefit of local support groups by Bill Clayton | 21 June 2019 Read More »
Bill Clayton shares his experience of loneliness and how this aspect of M.E. affects him and others in the community.
ME Association May Summary of ME/CFS Published Research | 19 June 2019 Read More »
We’ve updated our central Research Index and feature 23 ME/CFS research studies from May 2019.