Moved from the thread on the government consultation on ME/CFS
I've just come across the following from Headway (brain charity):https://www.headway.org.uk/about-brain-injury/professionals/approved-provider-scheme/
It got me thinking regarding perhaps one strand of how to tackle the conundrum of people making their various fortunes 'in the name of' whilst the desperate essential needs of those wih ME/CFS are ignored. As well as of course the issues for those who end up seriously unwell and currently I don't think we have a network that could even advise someone where to turn at the various levels of the systems to find safety etc.
I haven't set this up as a separate thread but I think the general concept and the how and who (and wha might also need to go alongside it) is perhaps worthy of it.
At this point perhaps having charities - be they ones that exist [in this form] yet or not - actually taking on assessing whether anywhere is indeed good enough and being blunt in that way as to whether somewhere meets basics might perhaps need to be the interim whilst we have a lot of 'do what they wants but expect to get funding in the name ofs' etc?
I've just come across the following from Headway (brain charity):https://www.headway.org.uk/about-brain-injury/professionals/approved-provider-scheme/
Headway has developed the Approved Provider scheme, an accreditation scheme open to residential care settings. This includes NHS and independent hospitals, neuro-rehabilitation units, residential and nursing homes and respite facilities, specialising in acquired brain injury (ABI).
The scheme utilises standards developed to reflect the specific needs of people with ABI, using these to evaluate a range of facilities including hospitals and neuro-rehabilitation units, residential and nursing homes and respite facilities.
The process involves units signing off a statement of compliance against each required standard and undergoing a robust on-site assessment, within an inspection system that also involves unannounced interim reviews.
This process ensures that units gaining Approved Provider status can demonstrate their provision of appropriate specialist care for those with complex, physical and/or cognitive impairment due to acquired brain injury. Key aspects of the process include ensuring staff working in the unit are aware of and responsive to issues associated with ABI, and that the unit gives consideration to the information and other needs of the service user, their family and carers.
It got me thinking regarding perhaps one strand of how to tackle the conundrum of people making their various fortunes 'in the name of' whilst the desperate essential needs of those wih ME/CFS are ignored. As well as of course the issues for those who end up seriously unwell and currently I don't think we have a network that could even advise someone where to turn at the various levels of the systems to find safety etc.
I haven't set this up as a separate thread but I think the general concept and the how and who (and wha might also need to go alongside it) is perhaps worthy of it.
At this point perhaps having charities - be they ones that exist [in this form] yet or not - actually taking on assessing whether anywhere is indeed good enough and being blunt in that way as to whether somewhere meets basics might perhaps need to be the interim whilst we have a lot of 'do what they wants but expect to get funding in the name ofs' etc?
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