However, the main points to bear in mind are: - is someone checking how ill and what these individuals were doing before they were cured. There...
Indeed I think the added explanations include: - there is a massive added disability/ people sticking their foot out to trip out disabled people...
I note that the GP stuff gets targeted in the UK, particularly more so in recent decades, because they are independent from NHS (but not from the...
To me it struck me as a groundhog day repeat of the utter push to 'not investigate' that was secretly happenning with those who got dumped into...
I thought I would confirm whether the whole thing was utter bad advice first before I commented as I'm no expert, and I couldn't tell whether...
the second question is the following section from the article, particularly the middle paragraph. Where it says don't do all the tests for...
I have a few questions the first is that this post suggestions the major difference in what doctors are being told is an emphasis on increasing...
The article is: If It Feels Like Fibromyalgia? 'It Probably Is' (medscape.co.uk) The MEA facebook post is: ME Association - What are doctors...
Just posted this as it has come up on my facebook feed. I've had a squizz through the first page, but as the questions at the bottom are...
From the solve me/cfs initiative on facebook: Short Provider Survey on ME/CFS and LC (SPS-ML) (umassmed.edu) Please share with your provider!...
Problem is the way the Facebook threads are working for these - because of the way the project is being sent via email so it doesn’t have a big...
This a massive impact one the way it could be used is the issue. Ie a tool that could be used to undermine the progress made - and tbf was...
Indeed it’s 50% less than before - so a lot of very fit or able people often g eg hidden under that ‘but you still pass the tests so you can’t be...
Yep there’s the issue with most of the ME/CFs stuff - not just juniors, yet you’d hope the fresh blood might have spotted it or have been keen to...
Spot on
This
well.... I use ME/CFS because the new Nice Guideline is ME/CFS (where the old one is CFS/ME) if the HCP I'm meeting is going to google it etc....
I've got the following from the news item on AfME webpage: So was he the consultant for the Devon ME/CFS specialist service for a long time...
SO you'd think he'd had a good lot of involvement with ME/CFS for a while before then? @Cinders66 I'm guessing the research or 'working on' CFS...
It might be my memory vs a lot has happenned over the last few years, or just I've missed it but can I ask the question of why David Strain is...
Separate names with a comma.
