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Or you could just put a bit of funding into patient support groups where people will get proper mutual support and stop trying to dictate what people should do. Saving a hell of a lot of time and money on so called research.

Spot on.

Spread your bug to the whole workforce - increased overall sick absence- creating unnecessary staffing shortfalls affecting productivity risks of individual errors by people working while ill - at simplest employers risk losing money through mistakes - at worst health and safety errors can...

LLM?

Really good to have this information recorded in a published study.

Wow does he realise/care who he will be rubbing shoulders with?

Yes I was given minor depression diagnosis for symptoms which were the gradual onset of ME & only got ME diagnosis 10 years later.

Reading the content thoroughly really isn’t the point of these online programmes, silly patients looking for something of value!

Yeah That’s just testing the look and feel of some web pages it’s not testing the whole user experience.

A R Burton (of Sydney ) has previously published with A Lloyd which presumably explains the use of CFS/ME. Fukuda is on the panel of editors for this research topic

Isn’t using freedom of information requests one of the things Crawley etc were arguing amounted to harassment.

You can actually get 25mg pregabalin tablets I know this because I couldn’t tolerate 75mg and asked for the lowest dose instead. (In the end I stopped taking it regularly then stopped altogether because even at 25mg am and pm I had side effect of tremor)

I only did the first few questions about ME/covid. Not the clearest & I couldn’t face trying to understand how to respond to multiple questions so abandoned. I am not making this criticism to be awkward, I had experience in my job of commissioning quantitative and qualitative staff and...

Or maybe not separate just immediate and delayed effects of the same process

Lille psychosomatic proponents need to learn from their colleagues https://www.s4me.info/threads/viruses-and-endocrine-diseases-2023-magloire-pandoua-nekoua-et-al.31824/

There’s organisations like Healthwatch that have local reach into NHS May be worth considering as well.

They are pathetic

This is the social enterprise organisation they worked with https://diversityandability.com/ the intervention is said to be based on the therapist being trained in Bridges approach https://www.bridgesselfmanagement.org.uk/ only very briefly skimmed on the face of it seems if you have to have...

Good to see the involvement of Professor Tyson. Hopefully she can help get the message out to her profession.

Presume this is the statement on behalf of the Scottish Government in closing the debate rather than an SNP policy statement.