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Ah, I suggested 1st year rather than 3rd year (when students in the UK are generally doing their honours project) because that is when most students start aligning themselves with their favoured lecturers and are often easily influenced and manipulated (unless very critically minded)!

I anticipate that this may be used to close the 'specialist CFS/ME' services and replace them with the IAPT MUS-CFS ones, since every CCG must now commission these (whereas many do not even have any specialist 'CFS/ME' services) and the IAPT model has been built on 'monitoring outcomes'. I know...

So is it a first year undergrad project?

Thanks for asking that question - this is really useful information to have readily available.

It's the insiduous way that IAPT is taking over that I worry about. It still seems to be expanding 'under the radar' as far as I can tell. It's only being on this forum that enabled me to see what's happening in this area. Where are all the ME charities on this? Not only is it GET type CBT, but...

Given the rollout of the IAPT Medically Unexplained Symtoms 'management services', with the CFS category using the Chaldler Fatigue Scale and giving all these patients a 'somatising' ICD code, if anyone is able (unfortunately beyond me with my current circumstances) it would be good to submit...

There is a current discussion on this questionnaire on this thread: https://www.s4me.info/threads/bristol-cfs-me-clinic-researching-patients-problems-with-chalder-fatigue-questionnaire.10683/#post-196078 IAPT 'CFS' services must surely be an important consideration for the NICE guidelines...

And the really worrying bit from the same Appendix:

Nice short (2 page) article that can be printed and handed to your GP if they seem uncomfortable about your request to record the consultantion or if they try to refuse it (UK based, but possibly applicable in other countries): https://www.bmj.com/content/bmj/364/bmj.l1101.full.pdf Edit: Or...

Merged thread I can't see an existing thread so am starting one to discuss a patient's right to record their medical consultations with GPs, Consultants and other health professionals. I thought many members may not be aware of their legal rights around this issue and that doing so may help...

I read the Boss ear pads wear out (not the actual headphones) but these can be replaced. I believe they are easy to find on Ebay.

I'll start a thread when I am able (soon hopefully). The lenses can be made up either with no prescription or with a prescription, then fitted to any standard eye glass frames by your own optician.

This is what the authors of the book argue.

I see a paper that is a follow-on of this book/website has been discussed previously on the forum: https://www.s4me.info/threads/key-concepts-for-informed-health-choices-a-framework-for-helping-people-learn-how-to-assess-treatment-claims-and-make-informed-choices.2128/ In the paper they do...

Apologies too - I'm autistic, so not good at softening my responses with social niceties. I just didn't want members to be put off trying to challenge negative responses by GPs or hospital consultants/administrators.

Long Term Conditions. Its the Medically Unexplained Symptoms which CFS/ME falls under, as well as things like Irritable Bowel Syndrome, Fibromyalgia etc.

Your post was written in 2017. I have posted the most up to date legislation (2018) and the link that provides information to whom and how to complain if your request is refused. It is up to individuals members if they wish to use this information and if they want to expend the necessary energy...

Well, at least we have David Tuller on our side, thanks to the M.E. community! Sorry, that should be - at least we have a man called David Tuller on our side...

But the MUS and LTC part is still being rolled out. Additionally, in the pilot areas many of the projects were quite different from the form it is going to take now. My CCG are actually putting off implementing it as long as they can, but it is being imposed on them from NHS England (I was...

There is a drive for GPs iin England to create a 'Summary Care Record' for all their patients. This can be shared with other care services outside the NHS. You do have the option to 'opt out' of having one or giving consent for sharing health information outside the NHS...