ME/CFS Final Delivery Plan. (A national healthcare policy document)
My PA who has been a professional carer for 25 years will not be able to access the 3rd eLearning Module on severe and very severe ME/CFS, due to be available later this year because she does not have the required email account. For those who do not know the 'IDP' is the 'My Reality: Interim Delivery Plan' attached to the public consultation which took place in Sept/Oct 2023. Below are what I believe are the reasons why.
The following quotes are from the Final Delivery Plan
This feeds in to a problem with informed consent because of Montgomery v. Lanarkshire Healthcare Board [2015] Supreme Court decision.
Below is from a review of the legal aspects surrounding the principle of informed consent. It includes a discussion about the 'therapeutic exception' formerly known as 'therapeutic privilege'.
Author Emma Cave Professor of Healthcare Law, published 29 June 2017
https://journals.sagepub.com/doi/10.1177/1473779517709452#fn90-1473779517709452
Long read - mostly for medico-legal people - but includes this on therapeutic exception i.e. withholding of information:
GMC guidance on consent:
This guidance came into effect on 9 November 2020.
The guidance was updated on 13 December 2024 when regulation of physician associates and anaesthesia associates by the GMC came into effect.
https://www.gmc-uk.org/professional-standards/the-professional-standards/decision-making-and-consent
In this BMJ article written 2 years after the Montgomery decision, whose authors include a QC - 12 May 2017
https://www.bmj.com/content/357/bmj.j2224
It could be argued that the ME/CFS Final Delivery Plan, as a cross government healthcare policy document, tells doctors it's OK to carry on as before regarding severe and very severe patients, in particular.
ETA: The Montgomery case involved a pregnant woman with diabetes.