

Imagine if the songs The KKK Took My Baby Away and Fire of Unknown Origin (took my baby away) are talking about one really unfortunate baby that keeps on being taken away by random stuff.
Imagine if the songs The KKK Took My Baby Away and Fire of Unknown Origin (took my baby away) are talking about one really unfortunate baby that keeps on being taken away by random stuff.
But in all seriousness, we would probably ask them what they think about reddit’s working environment and a few questions like that, and then everybody would move along
Pretty much like this:
Some people fake it with children to fake appeareances (they may not care about the child, but they do care about the opinion of the parents or anyone watching), I find it way more telling when looking how they treat animals and pets, since those are often percieved as “inferior beings” and its harder to fake it.
I personally trust my dog’s opinion on people upon meeting them.
Maybe not in real life, but I would love a sims 4 update that includes death by submarine
Sorry for the long ass answer. I happened to study this for a while.
Paul Ekman had this “theory of basic emotions” that were supposedly universal for humans and had their set of “innate” gestures for each one.
For his original works, he travelled to some secluded communities and registered that the expressions for “happiness / fear / anger / disgust / sadness / surprise” were supposedly shared among human kind.
Why do I say supposedly? Because a lot of Ekman’s theory was disproved (for example, he claimed each emotion had an area of the brain dedicated to it, or at least some unique structure, which fMRI studies are not finding to be true, even if there is a lot we still don’t know on human emotion). There’s also claims that he contamined his data when he went to these secluded communities, and influenced (probably unknowingly) his results to make everyone’s expressions match the ones he expected for each emotion.
So… are there universal expresions of emotion? Not an easy answer. The physical responses more linked to survival probably are (say fight/ flight in response to fear, startle in response to surprise). The more social ones? don’t know, some may be heavily influenced by culture. You would have to make a study on very young, blind babies from different cultures or something of the sort which would not be easy. Also there’s the thing that babies cannot tell you what emotion they are experimenting, even if you can asume some (loud noise and baby is crying probably equals fear, BUT the baby can’t confirm it, which is a methodological problem for some Scientists).
If this interests you, Ledoux has some great approachable work on the “survival circuits” of the brain that explain emotion in a way comparable to animals and linked to their evolutional value.
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You can do it!
I had a hard time at first (I always do adapting to new technology things, technology is scary for me and it takes me more time than most). But Im guetting the hang of it and having fun.
I found it helpful to just start posting and commenting where I normally would not, just to get familiar with things (first posts required a couple tries, it happens). It helps build content here and it helps me figure thing out.
And Ive been using https://browse.feddit.de/ to find communities that interest me.
Yesterday and the day before I was intimidated by (lemmy /kbin / the fediverse) today Im already more comfortable. Anyone feeling the same, I advice to just mess around commenting and posting, people in here are nice, you’ll get the hang of it if you try.
Haven’t gone on reddit since the blackout and probably won’t go back.
Hope more of us join, so far its been fun.
Although some of the communities I liked to browse on reddit are not yet here, its helping me expand and diversify a bit on the content I usually read, so I ain’t complaining.
Hello there!
Yesterday I was intimidated by (lemmy /kbin / the fediverse) today Im already more comfortable. Anyone feeling the same, I advice to just mess around commenting and posting, people in here are nice, you’ll get the hang of it if you try.
Haven’t gone on reddit since the blackout and probably won’t go back.
Hope more of us join, so far its been fun.
Although some of the communities I liked to browse on reddit are not yet here, its helping me expand and diversify a bit on the content I usually read, so I ain’t complaining.
Oh yeah, Back on reddit I never checked the notifications on my comments. I liked giving the advice but got terrible anxiety when someone answered because I knew there was a fifty-fifty chance of someone flying off the handle. Making it even harder, english ain’t my native language and from time to time if Im tired I mess up.
In here people have been so nice, even as Im learning and messing up how to work this platform.
I dont get it either, Ive been browsing different instances(? and when I find some community I like I search it up in kbin (which Im trying to make my main account I guess) by copying that little bit that comes up that says “copy and paste in your node’s search bar”, If I cant join from kbin I make a new account and join from there.
Its whatever, Ill figure it out eventually.
It depends A LOT on your country and health system / coverage among many other things. But here’s my two cents based on a country with public healthcare.
It is a common cathegory in neuropsicological evaluations when a person starts refering to cognitive difficulties that may or may not be quantifiable as of yet. We put this group under “cognitive complain”, sometimes their evaluation reveals actual changes in cognitive performance, sometimes it doesn’t. This group sometimes progresses throughout the years into dementia, but not always, since many factors can impair your cognitive habilities (stress, depression, anxiety, other conditions like MS, etc.).
The laboratory could benefit then from providing a bunch of hospitals that perform these evaluations with the tests to diagnose the profile they need for the medicine to work (as Ive seen done in my country with many conditions, including rarer types of cancer and rare genetical disseases). The lab benefits cause otherwise, no one would buy the drug and no coverage would approve it without proof its going to work. This works becuase anyone, money or not, can schedule an evaluation and these hospitals when they have cognitive complaints.
There´s also clinical trials and or other research projects usually in place in these kinds of hospitals, already studying and performing various tests on dementia patients. Elly lilly just has to find and support a PHD project that studies amyloid buildup and then everyone participating gets tested (and then referred somewhere for treatment with the drug). I dont wanna reveal too much of my life on the internet but Ive seen something awfully similar to this first hand in my own country, a bunch of families got genetical testing for dementia for free, then everyone positive to certain genes got referred for treatment.
As research progresses, some other laboratory may come up with a drug that works for a different type of dementia profile, and then it gets easier because they often strike up deals between the two laboratories. They both eat up the cost of testing, since one of them is likely to benefit from it. It is already done this way for genetical testing for rare disseases (again, we are talking a country where the patient does not need to pay or just pays their monthly fee for private coverage but no extra for these things cause they are covered by law).
Then all they need is to get their medication approved and included in the lists of medicines that are covered by law. There’s health coverages specifically for older people that often get deals with the laboratories of medications their patients are more likely to need. you get the ball rolling, probably a patient support program that can help with adherence and provide guidance to the patients and their families as to which documents to submit and where to get their medication covered.
What I mean is, its going to be different in different places, but there are already plenty of medications that require prior testing (sometimes really expensive testing) so the pipeline is already in place. I know nothing of amyloid buildup, but if there’s any chance its genetic, then the easier it will be (cause then you take current dementia patients and test their families).