UK Government ME/CFS Delivery Plan (includes Attitudes and Education Working Group and Living with ME Working Group) and consultation

MEA update on the new end-of-June publication timeline, which apparently "follows requests from the Task and Finish Group members to allow for more time to develop the Plan".
The department also state the extended publication timeline allows for the plan to be more closely aligned with related government strategies, such as the upcoming 10-Year Health Plan.
The Task and Finish Group, where both Action for ME and The ME Association are represented, will meet again to review “a more comprehensive set of actions for further discussion.”

We are pleased to see that the DHSC has taken concerns raised by members of the Task and Finish Group, regarding its lack of ambition, seriously. The increased timeline and further engagement present an opportunity to strengthen the plan, ensuring that associated actions are meaningful and impactful for people with ME/CFS.
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https://meassociation.org.uk/2025/0...e-have-issued-an-update-on-the-delivery-plan/
 
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Nightsong said:
MEA update on the new end-of-June publication timeline, which apparently "follows requests from the Task and Finish Group members to allow for more time to develop the Plan".
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Sadly, all this seems to do is confirm that the plan is empty. The government strategy is a disaster so things can only really get worse. Everything will be shunted to privatised health centres. Why can we not have an open public debate?
 
I did have some hope for this plan, have tried raising it with my MP, etc. But it’s not looking positive is it.

To be honest I wouldn’t mind if they closed all the specialist clinics. They’re a waste of time in my experience and used as somewhere to shuffle people off to, part of the mechanisms for avoiding responsibility for us. Of course I don’t have experience of the LC ones so maybe they have been of use to some.

What we really need is to be under a specialism as Jonathan and others have suggested in the past.
 
I think that this post on Action for ME sums up the position of many patients who've been waiting for progress a long time and met an unacceptably indifferent response:

Michael Van Zattern:
And of course, no matter how well written the delivery plan with regards to what needs to change, none of that change is possible without significant, ringfenced, funding. Why on earth do they think it is ok to NOT fund research into an illness with a prevalence of IBD, MS and Parkinsons combined, that also happens to have the worst health related quality of life of any serious illness it has ever been compared to, including stage 4 cancer and renal failure? https://pubmed.ncbi.nlm.nih.gov/26147503/
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