No future without funding
This site was created in June 2007 for the ME patient, carer and advocacy community and provides information, resources, commentary and archives on the political issues affecting the lives of UK Myalgic encephalomyelitis (ME) sufferers.
ME agenda is not an organisation. It has no affiliations with any national or regional ME or CFS patient organisation, support group, advocacy group or website or with any not-for-profit or commercial organisation. The publishing of material on this website originating from ME or CFS patient organisations or support groups or from other organisations does not imply endorsement or recommendation.
The site is owned and maintained by Suzy Chapman.
Before using this site please read the Disclaimer page.
WordPress sites can be utilised as either websites or blogs, with or without a comment facility enabled. In December 2008, the decision was taken to disable the pre-moderated comment facility on ME agenda site following issues arising out of the posting of material by individuals with professional and commercial interests.
To contact ME agenda please use the Contact page
Informing the UK ME patient, carer and advocacy community:
Archives for agendas, minutes, summaries and reports of meetings of the All Party Parliamentary Group on ME
Scottish Cross Party on ME notices
ME in Parliament: House of Lords debates; House of Commons Written Answers; EDMs; Adjournment debates
Countess of Mar’s Forward-ME group
ME Alliance activity
APPG on ME Inquiry into NHS service provision
RiME newsletters, notices and reports on APPG on ME meetings
Patient organisation press releases, position statements, summaries and reports of meetings
Updates on patient organisation activity in the areas of welfare reform, NHS service provision, DoH, DWP, NICE, MRC
Isssues around NHS CFS/ME Clinics and NHS service provision
Government reports, documents and guidelines
The NICE Guideline (CG53) on CFS/ME Judicial Review
MRC research; MRC Holgate multi-disciplinary CFS/ME panel
Information obtained under Freedom of Information Act
MSbP, social services intervention and child protection issues; Justice for Families reports (via John Hemming MP)
Selected research papers, reviews and reports
Demonstrations, protests, public meetings and events (also on Read ME UK Events)
Commentary, articles and papers by researcher Margaret Williams, sociologist Angela Kennedy and others
ME and related issues in medical and allied health professional journals
YouTube advocacy and activism videos
DSM-V and ICD-11 Revision Processes
Dx Revision Watch | Monitoring the DSM-5 and ICD-11 revison procesess
Twenty-six soldiers of lead | An extension site to ME agenda site
Read ME UK Events | Updates on demonstrations, protests and public meetings
To contact ME agenda please use the Contact page.
This page last updated | 11 January 2012
© 2012 Suzy Chapman