https://www.meresearch.org.uk/nice-draft-guideline-on-pain-and-application-to-me-cfs/Concerns have been raised over the possible application of certain provisions within the draft NICE guideline for ‘Chronic Pain Assessment and Management’ to people whose diagnosis of ME/CFS has yet to been confirmed. The guideline is aimed primarily at those experiencing chronic primary pain – i.e. pain that is not linked to an underlying medical condition and so, in theory, ought not apply to pain in ME/CFS – which can be severe, difficult to treat, and involve nerves (neuropathic pain), muscles and joints.
Healthwatch have produced a survey to gather info on those with chronic pain to feed back to NICE.
WARNING: includes questions on suicidal thoughts and self harm.
https://docs.google.com/forms/d/e/1...JccgrcBtTwe0LuYd7Slq65mqbZ5pEVg_iX9CKt73GrhSg
I haven't taken the survey, so I don't know how good it is or not.
By physicians for physicians to garner a particular response ?Very poor questionnaire, frankly. I don't think the responses will be of much use.
Probably worth filling it but it's poorly worded and structured, very superficial. As is tradition with anything psychosocial. By physicians for physicians.
and also top of NICEs list of treatments is CBT, and ACT. This has got to stop.Please sign if you believe that people with unexplained pain need access to some meds other than antidepressants!
the link is wrong, thats a letter about brexit![]()
Letter says 150 more signatories online. From an article in Pulse and comments from doctorsnet, many GPs and other doctors are really anti this draft as well.Letter to the Editor in today's TIMES from six pain consultants: