I think you can get it more or less anywhere. One of mine was between my neck and shoulder and the other on my lower back, and my friend got it...
I guess, but it's probably more unusual nowadays? You'd need to be both diagnosed badly and unable to see online information about ME/CFS. There...
Yep, and the only way you can do this is to ask them. Maybe two straightforward questions: Are you currently experiencing PEM symptoms? No Yes...
Yes, these prompted some eye-rolling. In particular, publicly allowing an association to personality type is so absurd and so flagrantly...
I think it would be more helpful to use FUNCAP scores. They take into account that some people have more severe impairments in one domain than it...
Absolutely. 1) Unfit for any kind of work: tick. Unable to stand for more than a minute: tick. Always need a wheelchair outdoors, and sometimes...
Ahh, sorry – misunderstood why you wanted it.
The file might be too big to upload? I never download videos but sometimes rip sound-only files from YouTube to help with music practice. Even...
The contrary side of my brain thinks it might be better to have a note saying it's outdated and unreliable than allowing Cochrane to save face...
Where on earth does he get that from, I wonder. Tried to list with my headphones on, but I can't work out where in the presentation it is. It's...
I wonder how much if this is coming from government. A lot of financial, political and ideological capital has been invested in the...
Sorry, I wasn't very clear, was I! What I meant was, how many are joint replacements are done in people with ME/CFS? The frequency could be...
It is, but I wonder how many are done? Several friends and close relatives of my age (mid-60s) have already had hip and knee replacements. Mine...
Maybe it should be equity? Tackling barriers faced by groups of people should be prioritised according to potential for harm and budgeted in line...
Thanks, Jonathan, that looks great. Couple of minor suggestions sharpening up—disregard if they change any of the meaning, they're not intended...
Trouble is, the theories don't seem to get tested. It appears to be more about weaving stories than doing science. If an idea's speculative,...
What I meant was that most people with ME/CFS have little or no spare money to give. They'd need to share the appeal on social media to people...
It's never that simple. For a start, you have to make absolutely sure you're not misrepresenting what they're currently doing or raising false...
Thinking more about this, another option is collaborating with Action for ME on it as a specific project. Chris probably hasn't got time for the...
Someone has to be legally responsible for the money raised, though. Even if it's done via a platform like GoFundMe, there will have to be an...
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