yeah me neither. the way I’ve described it is that 99% of my RAM capacity is gone, but my CPU is generally nearly as good as before I was sick. (I...
On more severe ends we sometimes have brain fog that never goes away. So if you want some sort of ability to understand things you just got to try...
That’s kind of ridiculous it took that long to get published.
I agree. From what I was trying to say the difference would be that a locally run open source LLM is being directly processed on the machine, so...
hopefully it would only be done with a locally run open source LLM. Like Llama or Mistral. because no one new is reading your data in that case....
if I recall correctly this study used the UK biobank which has pretty loose diagnostic criteria for ME that likely include a lot of "chronic...
Switzerland doesn't keep statistics. in fact as far as I'm aware ME has no official recognition as an illness or disease. 99% sure France doesn't...
oh yeah sorry never meant we should actually discuss that. just adding an example to your example of how one topic can lead to multiple quite...
Probably would have a third discussion about if you can truly call western neoliberal states democracies ie. rule by the people…
I think I’ve said this before — but I think the current model of peer review serves more to ensure ideological compliance, than to ensure quality....
I don’t know where to post this. But I read this the other day and it made me think of this thread. Apparently human manual labour (like digging...
Yeah honestly many people may look at me weird, but I’d rather a drug that makes me more tired than less tired. I’m triggering PEM all the time...
I actually think the vast majority of ME/CFS researchers assume PESE and PEM are the same thing. (PESE = Post Exertional Symptom Exacerbation)....
The "long COVID" being in quotes in the title makes me feel a bit icky.
I agree that it wouldn't suprise me that suicide is linked with ME. Not only have a bunch of studies looked at the link and found significant...
I kind of disagree, even though I think my onset was progressive as well. I think it's unlikely that we find a treatment that works for everyone...
Yay!
Yes have experienced decently often. When in PEM it feels like I have to exert far more mental exertion to get my body to do things. Like my...
1) Yes 2) Yes For me it felt more like the PEM came from sensory overexertion of having someone touch me than my legs being gently moved. (And...
I think Wessely wrote something about choppy seas but glorious voyage or something like that when describing PACE
Separate names with a comma.
