It wasn't that it was subtle - it was subtle as a brick - but I must have either forgotten what was normal or had the mindset that it was 'normal for illness' to feel worse the day after something than on the day and so hadn't bothered to think about it. It wasn't suggested to me - it was...
Even several years after I got sick, I wouldn't have been able to make it clear that I had PEM because I hadn't noticed it. I'd just got used to feeling rubbish for ages after extra activity but hadn't thought about it as a 'thing'. I never mentioned it to my GP because I'd forgotten what...
But isn't that the situation that we are in, in general practice, regarding ME/CFS? GPs don't know enough about it to be able to make a diagnosis.
I imagine this 'questionnaire' as consisting of only a couple of questions, that the GP wouldn't necessarily be reading off a cheat-sheet, and not...
Don't we currently have a huge cohort of PwME not getting diagnosed because GPs haven't heard about PEM? And not able to have a stab at diagnosing themselves with ME/CFS and seeking help for it because they haven't heard of it either?
That's interesting! But it would be easy to disabuse everyone of that notion.
@Jonathan Edwards, should that be in the factsheet for health professionals?
I hadn't thought about clinicians but I think we'd need people with experience in designing, testing and validating questionnaires.
Not necessarily. The critique could simply form the introduction to the paper about the new questionnaire. Or, if they were putting in for grant money, it could...
The Samms and Ponting paper show a ten-fold range of diagnosis across different regions of the UK, so certainly there's a bunch of places under- or over-diagnosing, but they say:
Lastly, we considered 6,113 English GP practices with at least 2,500 registered patients which each, given the...
Protests are relatively small because we're too sick to protest and the protests are basically an endless 'Give us more money for research', rather than 'There's a cure! Bring us back from the dead!' being delivered by now-fit PwME who are back from the dead.
It would make no sense at all to...
You're right, I've been assuming a 'daratumumab works' scenario in which there are full responders and non-responders, so you are basically 'back from the dead' or not. I think that's a good scenario to focus on for thinking purposes, though...
The diagnosis does exist. Loads of us have got it. GPs know they have patients who have it and who they are (otherwise, who have they been sending to the ME/CFS clinics?). There aren't specialists to drive the roll-out - hence the question of what happens. I don't see a sane world in which the...
If we did everything necessary and a brilliant paper was published showing our super new validated ultra-short PEM questionnaire, how would we get it widely adopted into clinical practice? Presumably when this kind of thing happens, people don't hang around for years waiting to get the new thing...
Thanks for putting this forward, @Simon M. I think this is genius. We've seen in the Samms and Ponting study that there was what, a ten-fold difference in ME/CFS getting diagnosis in different areas of the country? Doctors are leaving many thousands of PwME in the dark about their diagnosis and...
Any effective treatment for PwME is basically going to be like bringing people back from the dead. I'd expect the first severely ill PwMEs to recover to be plastered all over the news and a huge wave of public pressure on the NHS to rescue the rest of us.
That's an interesting comparison. But I can't see this as equivalent, since obesity has other available treatments (principally dietary, though I realise that a good diet is not available to everyone) and is not as disabling as ME/CFS.
According to Google AI::
You can get Ozempic on the NHS...
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