Fundraising Feature: Alison invites you to help her mark a grim anniversary | 06 August 2018
Alison Woodland decided to celebrate the strength it has taken to endure 10 years with M.E. by hosting a virtual tea part for the ME Association.
2018
NICE ME/CFS Clinical Guideline Review: ME Association Submission re: Scoping Report | 02 August 2018
In our submission, we highlight the issues we believe NICE should either include or omit from the new clinical guideline on ME/CFS.
ME Association July Summary of ME/CFS Published Research | 02 August 2018
ME Association July Summary of ME/CFS Published Research | 02 August 2018 Read More »
This monthly summary lists all ME/CFS research published in the previous month and also provides a free download of all research ever published on the disease.
Fundraising Feature: A close shave for Katie… | 25 July 2018
Fundraising Feature: A close shave for Katie… | 25 July 2018 Read More »
“Beauty does not come from what you look like, what your clothes look like, or what your hair looks like. Beauty comes from the heart.”
America calls for a cultural shift in the way care is offered to ME/CFS patients | 13 July 2018
The world-leading Centers for Disease Control and Prevention has upped the stakes in the fight to get better care for people with ME/CFS.
ME Association June Summary of ME/CFS Published Research | 04 July 2018
ME Association June Summary of ME/CFS Published Research | 04 July 2018 Read More »
The latest M.E. research abstracts for June 2018, and a newly updated and free-to-download M.E. Research Index.
Fundraising Feature: A Fond Farewell to Foggy | 03 July 2018
Fundraising Feature: A Fond Farewell to Foggy | 03 July 2018 Read More »
Foggy’s exploits are coming to an end. He’s helped raised over £10,000 for M.E. research and will be pawly-missed.
Fundraising Feature: A Vintage Day for M.E. | 02 July 2018
Fundraising Feature: A Vintage Day for M.E. | 02 July 2018 Read More »
Karen and Hannah Radenkova will be throwing a 1920s ‘Gatsby-themed’ tea party on 11th August.
MEA Summary Review: ME/CFS and the Biopsychosocial Model – By Dr Keith Geraghty | 29 June 2018
In a guest review, Dr Geraghty summarises his most recent study examining the BPS model in ME/CFS
BBC News: MP Carol Monaghan leads campaign for new ME treatment | 25 June 2018
BBC News: MP Carol Monaghan leads campaign for new ME treatment | 25 June 2018 Read More »
M.E. is incorrectly treated, lacks sufficient funding and is poorly understood by many in the medical profession.
NICE ME/CFS Clinical Guideline: Final scope consultation and lay member recruitment | 25 June 2018
The deadline for the NICE Scope Consultation and for Committee Recruitment is 26 July 2018.
Daily Mirror: Tory minister demands comedian Ricky Gervais apologises for branding M.E. sufferers ‘lazy’ | 23 June 2018
Comedian Ricky Gervais was called out for an old joke that epitomised and lent credence to the stigma surrounding M.E..
Rochdale News: MP calls for ‘much more to be done to tackle M.E.’ | 23 June 2018
Rochdale News: MP calls for ‘much more to be done to tackle M.E.’ | 23 June 2018 Read More »
“ME is such a misunderstood illness, as the sad case of Merryn Crofts from Norden demonstrates.”
MPs demand more biomedical research for cruel ‘death sentence’ disease | 22 June 2018
MPs demand more biomedical research for cruel ‘death sentence’ disease | 22 June 2018 Read More »
This MEA press release summarises some of the main points from the Parliamentary debate on M.E.
The complete Ministerial response from the Parliamentary debate on M.E. treatment and research in Westminster Hall | 22 June 2018
A full transcript of the Ministerial response to the three-hour landmark debate on M.E. in Parliament.
Fundraising Feature: Sarah’s Big Shave for M.E. | 20 June 2018
Fundraising Feature: Sarah’s Big Shave for M.E. | 20 June 2018 Read More »
Sarah Summers is taking on an extreme challenge – a head shave – to raise awareness and funds for M.E.
Rochdale News: For years dismissed as ‘laziness’, but now cruel disease is finally getting attention it deserves | 20 June 2018
A devastating disease is to be discussed in a landmark three-hour parliamentary debate.
The ME Association to fund six student bursaries for 2018 CMRC research conference | 19 June 2018
The ME Association is especially keen to help medical students develop or extend their interest in M.E.
The House: Carol Monaghan: We must change perceptions of the debilitating illness M.E. | 19 June 2018
Carol Monaghan, MP, is leading the debate on M.E. in Westminster Hall on Thursday, 21st June, 2018.
Let’s Talk Social Care Services: For people with M.E. and those who take care of them | 15 June 2018
We explain what is meant by social care and the various benefits that are available to you.