That the symptoms and disability we experience are real. The cause or causes do not matter for the ‘realness’ of that.
IMO, we don’t need a test to prove that ME/CFS is real. But it would be very helpful to have one for a lot of reasons. So we definitely should...
This has already been done, it didn’t really show anything you wouldn’t be able to find by spending a bit of time in a Facebook group etc....
I also notice that my eating rythm gets messed up.
[IMG] I don’t understand the 15 day data point for blue (probiotics). And what happened to the error bars? Edit: it’s figure 2.
That’s a very important ethical consideration!
The product page: https://www.ab21probiotic.com/
[IMG] [IMG]
This is an interesting inclusion!
Or that enough people have tried it in the same time period as a natural positive fluctuation of their illness. Or that people report that it...
We know that people with ME/CFS can experience substantial placebo effects based on the trials by Fluge and Mella. So I don’t see anecdotes as a...
I really wish we could stop using generic LLMs for medical info.
One objection to this approach is that we have a limited amount of resources and drug trials are expensive as heck.
To understand the policy changes and their implications - absolutely. And I appreciate your effort to educate myself and others. To understand...
I imagine she probably knows someone involved and said she’s interested to be a part of it.
Just to be clear, neither do I.
And it should be the other way around?
Are there any discussions here about it? I’m wonder how they’ve tried to falsify it.
The fact that people get better doesn’t mean that the treatments caused the improvement. This is the same issue as with LC or PVF. And what’s...
As long as we don’t just look for the keys under the street lamps. Bringing a torch is probably wise.
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