Not sure what your circumstances are @youngscum cant see your original post. If you’re working or off sick you might find it helps with your employer taking the illness a bit more seriously if you get a referral from your GP. Don’t expect that much from the clinic you might well not get any...
This is a great idea
Is there some kind of royalty system for use of such questionnaires or are they free to use? I hope there’s no money being made off this claptrap.
i don’t know how helpful this comment is but I think is important to distinguish between needing to sleep more and feeling bad and needing to lie down. I think often people get the two mixed up and both get described as fatigue.
For me flu like symptoms - feeling bad (dare I use the word...
Im miffed with the Liverpool questionnaire because I didn’t spot wording at the beginning that said you should fill it in with reference to when you were last well and in the questionnaire itself it definitely said by reference to a month ago because I was filling it in on that basis and put no...
If people only criticised and advocated against things that have not yet been implemented we wouldn’t be having the current NICE guidelines review so I don’t understand that argument. Nor that we should only advocate against things that specifically target people with ME - many issues that...
its a loophole - if you don’t have clarity it will be exploited. Slightly less bad is still bad and worth objecting to. British establishment are masters of fudging to get their own way. BPS crowd are masters of fudging and appropriating terms to avoid rejection by patients. This BDD...
As they ask for peoples age in the demographics surely they would then just sort it into different age groups if there’s any need to do that for analysis once they’ve collected the data so they should never need to put age limits. But given they’ve put together a rubbish set of questions it’s...
I decided to give it a go to see the questions got part way through filling it out then got dumped maybe it didn’t like my answers :whistle:
It was all HADS type stuff. Does worrying help you cope. What % of time do you spend focusing on your symptoms.
The first questions were hilarious...
Shows total lack of understanding of the ME community not expecting it would be shared widely. Shows what the agenda is that they didn’t in fact set it up in the first place to be shared widely. Presumably expecting recent attendees to be more under the impression that the CFS clinics are “a...
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