Agree strongly with this. I’m hoping she will pursue this.
I posted here about her intervention and the impact on DHSc https://www.s4me.info/threads/house-of-lords-govt-discussions-with-nice-on-me-cfs-main-chamber-tuesday-12-october-2021.22424/page-2#post-380744
disagree it was a waste of time that Minister now has ME/CFS guidelines embedded as an issue in his memory due to the mauling he got from the Baronesses
I’d like to big up these Baronesses for standing up. Unlike previous experiences in the Lords when Wessely got his mates to speak against us.
ETA just watched it on BBC iplayer so it’s available if anyone missed it
I would hope that if the minister has anything about him he will understand how poor his briefing and line to take has been and will be kicking ass back in the department
Excellent intervention from Baroness Finlay of Glandaff.
ETA that will be causing some thought in the relevant Department of Health policy team and whoever in NHS is responsible for liaison with them. if they are doing their job properly they will be researching what her issue about reporting...
I think people with ME who may have had some elements of supportive care from individuals within the current structure make that known. The charities also have contact with NHS people and see them as doing their best. Shuffling deckchairs will not get us to a functioning service for PWME
Good on them for coming up with the idea. As ever it’s easy to comment from the sidelines but I think it would be a lot more effective in communication if it focused on top priorities - MEAction call to action for MillionsMissing springs to mind
- end to GET
- end to FII cases against families...
I agree the handling of someone’s post about their negative experience by reposting someone’s positive experience is an extremely poor approach in terms of how to deal with any type negative feedback. Almost a textbook example of how not to do it.
And given the content of the experiences...
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