We’ve been testing therapy like it’s a pill – and some patients are paying the price
Why the NHS keeps offering you the same therapy. And why the science behind that decision is shakier than you think.
theconversation.com
This isn't about ME/CFS and I have placed it here because this is where the IAPT (now 'talking therapies' or something like that) thread is located and because it is implicitly referenced in this and in the fb post a lot of comments mention IAPT
For those not on fb the only text with the link is:
Why the NHS keeps offering you the same therapy. And why the science behind that decision is shakier than you think.
But I think it is really worth us having here because it doesn't necessarily exclude ME/CFS and noting other threads some seem to be caught up in this bigger fallacy of 'these things must work' etc.
The author is:
Sahanika Ratnayake
Postdoctoral Researcher, Evidence Synthesis, University of Manchester
And here is where I want to make my point which is that the argument taken is that the issue is that they have been doing randomised controlled trials - I'm pretty sure the standards used in other conditions for CBT 'trials' are little better than what we see as an ongoing treadmill gravy train here. SO someone might want to get in touch with the conversation or the author (and maybe some commenters)....?
PLus also..... please do discuss the article itself and why it has been written too of course! - because I think it might be interesting to see what comes up in this from the perspective of other angles