I note it says he will be making the Adolf Meyer memorial lecture in San Francisco in May.
When doing something outside the house setting off I walk normally & on good days don’t need the walking stick. After doing the thing coming home...
No but ME Association have a track record of taking complaints to ASA notably LP.
Yep. I couldn’t bring myself to pursue any details. So no idea of where diagnosed and by whom.
I met someone on Facebook a young woman who had MECFS and POTS I think was the other diagnosis but also had been tagged with FND and told it was...
Oh right so he thinks cognitive disfunction has never been seen before. Wow.
Even if they would do it just for one sounds useful. Facebook is pretty hopeless for getting to people in my experience.
Ok thanks not a term used in the UK
MVP? (The only acronym I’m familiar with is minimum viable product which seems inappropriate)
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...
Spot on.
Spread your bug to the whole workforce - increased overall sick absence- creating unnecessary staffing shortfalls affecting productivity risks...
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...
Isn’t using freedom of information requests one of the things Crawley etc were arguing amounted to harassment.
Separate names with a comma.
