This is a long document clearly written. You can scan through and see how many failures are recorded against the UKs own guidelines and statements.
A briefer document has also been produced by a group of ME charities, probably most easily viewed on the MEAssociation website. I prefer this one as it judges action against their own statements and concludes failure in every area that accurately sums up our experiences.
Daughter diagnosed CFS-ME, struggling with professionals different views and attitudes.
Possible M.E.
New and need help
What's the story on the brain fog?
Who diagnoses ME/CFS?