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#is at a DISADVANTAGE. bc of the AUTISM. can you believe it
bloodsbane · 11 days
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what i love about laios is that he's actually very good at putting puzzle pieces together BUT HERE'S THE THING 1) he needs to HAVE the information, and 2) (this is important) he needs to KNOW it is information he should care about
and i think this could be said of anyone but the thing with laios is that people tend to view his lack of awareness wrt social etiquette and memory problems as pure indifference and/or obliviousness; sometimes they misinterpret his motives based on their inaccurate expectations of him and therefore don't give his thoughts on a subject the credit he deserves
one of the most obvious examples of this happens at least twice in the manga as i remember it, but the most recent incident was when they were trying to resurrect falin. there's a moment where laios mentions reconstructing both of the warg skeletons, as their bones are mixed in with hers. both chilchuck and senshi balk at this, with chilchuck complaining aloud, questioning laios' priorities,
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and laios quickly, angrily retorts. his reason for making the suggestion is perfectly logical and practical, but because his friends are used to his interest in monsters influencing his judgement, often in ways they see as frivolous or dangerous, they don't come to the same conclusion. one which i'd argue is kind of obvious considering the situation
we see it again during his fight with toshiro, where toshiro demands to know what laios plans to do to save falin. laios takes a minute to answer, but he DOES answer, following the logic that if falin is a chimera because of (and controlled by) the mad mage, then the logical next step is to confront/defeat/usurp them
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then in the following episode, when chilchuck brings it up again, laios explains what he (now) knows about thistle, mentioning that he's the same elf that laios saw in the living paintings, which is why he knows thistle's connection to delgal. the party reacts like this:
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i'd say this is an example of them feeling frustration over laios' habit of having 'bad timing', not knowing when or how to speak at appropriate moments. theyre judging him for not saying something earlier, as if he already knew all this but didn't think to mention it when it was relevant, when the reality is that laios only just now had all the pieces he needed to understand the full picture
and i mention this bit specifically because i think it's a great way to explain what i mean by point 2: laios needs to know when information is important and worth considering
which, again, feels fucking obvious. but as someone who ALSO has debilitating issues with remembering important shit, i find this particular element of it pretty relatable and critical to my overall point. it's not laios' fault that he didn't know who thistle was or his significance - why the hell would he assume that a person he met in a living painting, presumably long since dead in reality, should be someone who's face, name, or motives he keeps in mind?
ultimately, i guess what i'm trying to say with all this is that the way others treat laios' intelligence is not congruent to how actually smart he is. one of the things i love most about laios, what is possibly his biggest strength and the reason he is such a great protagonist, is that laios is willing to think things through and find the most logical conclusion to a problem, no matter how outlandish or dangerous or seemingly impossible that conclusion may be. sister got eaten? race back down to go get her. can't afford food? fight, defeat, and eat dangerous monsters. sister's fully digested? use black magic to bring her back. now she's a chimera? defeat the mage controlling her and use that power to fix it.
anyways. what was even my point with this post? i guess it is that laios is smart, at least as smart as anyone else in the cast, arguably smarter than some. he is intelligent and utilizes that intelligence in many ways, not JUST when it comes to monster info (though that is his best and sexiest brand of knowledge)
and also please be nice to your friends with memory problems. it's rough out here for forgetful bitches
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steponmepinkjun · 3 years
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Sara I hope you dont mind me dropping this kind of ask, I just dont have anyone to talk abt this topic in particular and i have seen you open up about being neurodivergent multiple times.
All this time I believe that im neurotypical and always have to progress through life the way neurotypical people do, but from like 2 years ago i'm starting to question if i really am one bcs when I read about neurodivergency I slowly began to see myself in the description. How does one get um.. Diagnosed? I feel like theres sth abt myself that i havent figured out yet and I just want to know and love myself better.
Also forgive me for not being articulate enough, this is something im working out on.
Okay so I am obviously not a doctor or expert on neurodivergency, but I've gleaned a bit of knowledge from the nearly three decades I've spent being ND. So heres my advise.
First, I would begin with identifying why you'd like to seek an official diagnosis. Depending on what it is you're trying to diagnose, there are advantages and disadvantages.
Officially being diagnosed with ADHD gave me a sense of understanding I never had, gave a name to the symptoms that had been, quite honestly, ruining my life, and most importantly gave me access to the medication that completely turned my life around and made me a functioning human being. Even though I was diagnosed late in life (ie after school/developing years), I was still very lucky—my psychiatrist saw what the six previous ones I'd seen didn't. Before that, I was in treatment for depression and anxiety since age 11, had seen 13 therapists, and been on over 15 medications, to no avail. I'm lucky because a lot of obtaining a diagnosis for ADHD relies on self-reporting and reports from your parents—which is fucking stupid considering adhd is genetic, so my adhd parent probably isn't going to see my behavior as abnormal, IF they can even remember my behavior or payed attention to it. Despite those things, I was able to finally get diagnosed at age 22, and it changed my life. However, despite the fact that I suspected since I was a teenager that I might be on the autism spectrum (my brother, father, and several members of his family are), I made the conscious decision not to seek an official diagnosis. The medical community at large is incredibly ignorant and biased in regards to diagnosing autism in women, getting a diagnosis is ridiculously expensive, and unfortunately where I live an autism diagnosis can put you at significant disadvantage in the court system (it's often used as proof that an individual isn't mentally competent enough to do things like stand trial or be given sole custody of their own children, among other things). Plus, autism itself isn't treatable, so in my eyes I saw no benefit to getting a piece of paper telling me what I already knew. That's a personal choice that no one can judge another for—your reasons for seeking diagnosis are entirely valid whatever they are, and you owe an explanation to no one. I only wish to point out that not all diagnosis carry the same cost/benefit.
Getting a diagnosis can be a huge uphill battle, and it usually takes stamina and mental fortitude to get there. But everyone needs and deserves to have a community, a sense of understanding, and a support network, and wanting that alone is a more than valid reason to pursue a diagnosis.
So here's what I'd do. Get yourself in to see a psychiatrist (a therapist will do IF they have the training to diagnose, not all do), and do some research beforehand. Things as simple as googling "I think I might have/be (insert neurodivergent term here, for me this would be ADHD or autistic)" can give you some good starting points for what traits/symptoms are common. And as you're doing your research, take notes! If you see something jump out at you that you super relate to or that puts a feeling you've always had into words, write it down, copy the phrase, include things like how often you feel that way and what age you were when you began experiencing that. If there are ND behaviors that your immediate family share, that is very relevant, and actually gives a lot of context as to if something is a ND trait, trauma response, or shared personality quirk. Bring those notes with you to your appointment, reference them, and take notes of your own with the Dr's feedback. If you feel like you're being dismissed, tell them that, if you feel dissatisfied with their assessment, say so, and ask what your options are going forward. You probably won't walk away with a solid answer in just one day, but it's a good place to start.
It usually doesn't hurt to seek out community online, either, provided you take it all with a grain of salt—I've found that doctors tend to minimize symptoms, while peers online tend to maximize them. Ie, the way ND tiktok has become a slew of "do you breathe oxygen? Here's why that might be a sign you have adhd" type vids. Get second and third and fourth opinions before you take something to heart, you know?
And (even though this may go without saying), while I am no doctor, I have amassed more knowledge of my own disorders (as well as cptsd, ho lawdy its a fuckin doozy) than perhaps any one person should, so if you're at all in my vein or neurodivergency then please feel free to reach out to me directly, I'm always open to offering advise or a friendly ear or a sounding board for thoughts and ideas.
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ghcstlight · 7 years
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hi hi so correct me if i'm wrong but i don't think they deleted their blog over being asked to make themes more accessible as much as many people on tumblr beginning to insult and degrade them as not even theme makers but as pEOPLE
Noah Fence, but you’re coming in here to defend ableists to me on the basis that they’re people? To someone who’s Autistic?
Listen to me, alright, because I’m gonna correct you because you’re wrong (can you believe I got on my PC just to correct you because you’re wrong wow). You can’t separate the ableism from the person as much as you can separate the autism from me, except they can learn and change their ways if they chose to, whereas people like me, or the people they’re unduly and (maybe unintentionally but not the point) disadvantaging cannot change the way we are. People cannot magically read 8px 9px or even 7px (yes I’ve seen it) posts that are in italic and probably also a serif font bc ya gotta go for that aesthetic. What can be changed is this ableist mindset that these people who cannot do these fucking weird arse aesthetic leaps should be ignored, alienated, and ostracised, bc who gives a fuck about them tbh?
I may not have super bad eye sight, and while reading a maximum of 9px fonts is a bit of a hassle for me, I know exactly what it’s like to be ignored, disregarded, or outright culled by a whole community/society. So I may be able to read 9px with a little effort, but that doesn’t mean that, any theme I make or use is going to have 9px fonts? Because there’s people out there in the world that I want to read what I wrote, I want them to be able to use and absorb my content, I want them to not feel like a burden because I know what it’s like to be in that position perpetually and pervasively.
Them making the themes as they did was a symptom of their ableism, not the source. The source is them as people who are ableist and don’t fucking care about anyone that is not them or like them specifically. Right? You coming here into my inbox defending them as people who are ableist at their source is like defending racists against POC because racists are just people too. You know what ableism leads to? The death of mentally and physically disabled people. Not calling out ableism when you see it, even when it doesn’t immediately result in death, is you being accessory to the death that does happen. It’s you being ableist because you feel shit like that can slide, and the people who die as a result of ableism aren’t people you know or care about, so it’s all okay.
They weren’t ultimately called out on their shit because their themes were ableist, but because they were, and I have 0 patience or sympathy for ableists ever. 
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