#but i think a lot of times people struggle with existing as a disabled person in society

[3liza]

everyone arguing with material analysis/assertion about how art is a "luxury" has rarely if ever spent rent or food money on art, if they even pay rent or buy their own food, and if they did that would be considered extremely dysfunctional, and thats what i/we mean. artists are not providing a necessary service.

our plane crashes in the Andes and you are not particularly excited about my "can draw that Playboy centerfold of Marge Simpson from memory" like that is not an essential survival skill. lots of extremely skilled workers work in luxury artisan and craft jobs, it's not an insult to say even a very famous and very talented and influential artist is not producing a commodity necessary for the furtherance of human life. none of us are doing that, no matter how we stretch and strain the definitions of "essential" or even things like "morale" or "group identity". i will burn my copy of Finnegan's Wake to stay warm and thats what it comes down to.

i get foamy crazy snarling and biting about the idolization and obfuscation of what artists actually do because it is a labor issue! the public conception of artists as people possessed of a divine talent they dont consciously work to develop like any other skill, and the public idea that we are simply pleased and privileged to make art all day and "not work", something people say to my face every time i get asked "what i do", is largely responsible for the absolute dogshit reality of how subsistence and working class artists have to survive. we usually dont have health insurance unless we're so poor we qualify for medicaid AND live in a state that will enroll us. most of us are too disabled or crazy to go to a real job every day. most of us have tried, over and over, to enter the normal workforce, and have failed, and been forced to develop alternate skills that allow us to make rent in the ten hours per month we're actually functional. many of the artists i know work from bed because standing up is dicey. this has been turned into a charming eccentricity of famous artists and writers instead of people wondering why a person would need to stay in bed all day and take the enormous bother of bringing their stupid pens and paper and writing board or typewriter or whatever to their bed instead of just getting up and getting dressed and going to work. ive done this, i spilled ink in my sheets. its a huge hassle.

and artists play along with this mystique because people dont want to buy paintings from sadlords! they want to buy paintings and books and marge simpson nudes from cool guys who get a lot of chicks and wear rockstar outfits and party a lot, because of the transitive properties! of course!!! this is basic marketing!!!!! and if the artist doesnt play along they turn into Sad Story Artist where they're doing emergency commissions and posting about how sick they are all the time. this is not cool or fun or sexy. it's a sand trap and its very hard to recover from. im struggling with this right now!

famous and successful artists and writers are constantly ending up 60-90 years old with cancer and multiple sclerosis and dementia, being the subject of some sort of public, last-ditch, humiliating GoFundMe because painting paperback covers fr 60 years means you dont get a pension, you often dont even have kids who can take care of you, you dont have life insurance, you dont have health insurance. 'died penniless and alone' is one of the stereotypical artist endings for a reason, that is not fiction. this happened to more artists than i can list on two hands. look up what happened to Peter S. beagle, the guy who wrote The Last Unicorn. you write a book like that you should be set for life, right? NO. thats not how it works

i'm not saying 'all artists are disabled and working class or poor' because that isnt true, observably. nepo babies and trust fund artists exist, obviously. but they take an outsized portion of the spotlight when the public thinks of the concept of "artist". they are not actually the norm. the average artist is probably making under 40k and living in extremely precarious circumstances and has had periods of homelessness, illness, extreme debt and/or bankruptcy.

this is true even for the 'successful' artists. having one or two or ten good projects and being a household name does not save you from just not having the safety net provided by a normal career path. i was very close with a major, famous 2000s network television creator and team that you have heard of. they won awards, they changed culture entirely, they were a big deal. one of them was turned down for a half dozen projects by the same network that made millions or bilions on their franchise over several years (each pitch is completely unpaid btw, imagine carefully preparing a PowerPoint for morons for months at a time for no reimbursement and thent he morons ask you if you can put a teenage witch looking for her lost cat in the alps in it and you're like, haha, well, it's a 4 part hard sci fi miniseries set on Europa and takes place entirely inside a pressurized lander settlement, i mean Ridley Scot said he was interested already and he pitched a bottle episode about a carbon monoxide poisoning, soooooo....and the executives look at each other and they're like "it's jst not really what we're looking for right now, thanks for coming in" and you go to coffee bean and tea leaf and kill yourself and thats sort of what its like. i made that example up it didn't actually happen i'm using an illustrative example), worked on a canceled film, and just. gradually ran out of money. thats what happens. that guy ended up slowly selling off all his belongings, getting roommates in a one bedroom apartment, and then eventually having to just live on a friend's couch for years. famous guy. you probably know his name. another major member of that same team ended up in GoFundMe/commission hell for years (might still be there) because they had to take care of their two dying, dementia patient parents by themselves. these are people who go to GenCon and sign autographs for four hours at a time. THE PUBLIC IS NOT AWARE OF THIS SHIT and i'm sick of it. im sick of going to a gallery opening night ("vernissage") and drinking bad wine and having a guy with an email job that pays six figures and benefits tell me being able to push "undo" on the computer is cheating. that's a real example, that has actually happened to me. more than once.

artists currently have zero labor protections whatsoever. all of us are undercutting each other in an unregulated market and relying on welfare and private insurance and not having families or buying houses. zero security until we get so old all our illnesses and dysfunction finally ground us permanently and then we get turned into a charity case by fans (humiliating) or just fade away into ghosts and die

whats my punchline? idk i dont have one. it's possible and likely that any given artist you meet is permanently in precarity and will be until they die, even the famous ones. the culture of selling art demands that artists do not admit to this in public unless shit gets really really bad. i guess my point is you should know this, as a person who looks at or listens to or reads things that people have made for your amusement, not for your survival

[girlcowboy1]

I think gen z ultimately lost the war against mental illness when they decided to adapt the older generations rhetoric of "mentally ill ppl who have noticeable symptoms are bad and evil and must be avoided at all costs, they deserve to be alone and die alone" which... most people are not saying that outright, but that IS what they're saying, whether they realize it or not, when they choose to discuss these issues based on personal concepts of morality and punishment instead of approaching it with a mix of empathy and an understanding of science, and how the brain operates.

"Having a mental illness isn't an excuse" is true to a certain extent, but I think a lot of people don't understand that to an extent, it also IS an excuse. The only reason people like to believe that it isn't in any capacity is because mental illness is an invisible disability, and if there's one thing that people love to dismiss the impact of, it's invisible disabilities. Because we can't see what's going on beneath the surface, we struggle to understand the issue, we struggle to empathize with the affected person, whom we may prefer to instead write off as being lazy or malicious, when in reality they are in pain and/or are missing an important tool that helps them function the way they'd like to.

Before getting on medication, I felt and (still sometimes feel) as though I existed behind an invisible glass that separated me from everyone else. I could not understand the point of a lot of mundane things, I couldn't relate to those around me, I felt like my existence was a mistake that should have never happened and the universe was attempting to expunge me by making my life so hard I would kill myself.

And then I got on medication, and suddenly I was able to see things that I had never seen before but had existed in front of me the whole time. I was able to be kinder to people, to be more patient, to talk myself out of bad thoughts I would previously ruminate about for days and weeks. I was able to communicate more coherently, to express my feelings in a way I couldn't before. I wanted to do things again. I wanted to dress up, look nice. I wanted to BE nice.

Of course, these are all still things I struggle with. Like with most tools for disability, medication is helpful in giving me the ability to function in a way that makes life more enjoyable— but it doesn't completely cure the issue. The point is. I tried so hard, time and time again, to change on my own. I tried taking supplements, I tried mindfulness, I tried changing the way I eat, I tried self-help videos/books. But I was a deeply depressed, deeply agitated person whose brain was not wired the way it should have been. So none of what I tried would stick. I would act out in ways I KNEW was wrong, but when you get into a certain state of mind, it's difficult to speak to yourself, to talk yourself down from doing or saying things you know you probably shouldn't. Especially when you feel so isolated from others, and struggle to see the point in anything.

It was only after medication that I made long-term improvements. It was only after my brain chemistry was physically altered in a positive way that my brain could begin to function better, and that my outward behavior improved.

How the anatomy of the brain effects a person is a crucial part of mental health that gets left out of relating discussions too often, I think, and its where I believe gen z unfortunately tends to overlap with gen x and boomers. The brain is an organ like any other, and if it is damaged, or sick, or lacking somewhere in its anatomy.... it will not function properly. The person whose body it inhabits will not function properly.

[gardenstateofmind]

i'm kind of pedantic about the words normal and common just bc i think it really often leads to misconceptions about disabilities and chronic illnesses, bc like, in my experience, it is incredibly common to have problems with your body, in fact i think Not having any issues is more uncommon. as amazing as human bodies are, there is so much that can go wrong. and most of the time, for most people, they can still get by. and that's just life.

so like yes it is common to struggle. it should also be common to receive help for these struggles. and if this kind of help is more normalized and accessible, then hopefully people with higher support needs won't have to jump through hoops just to have their basic fucking needs met.

i think many people see it like you either are or are not disabled. and if you don't meet their arbitrary standard for what counts as disabled, then you need to just suck it up and deal with it. bc that is the attitude they apply in their own life. but like it obviously does not work that way. everything exists on a spectrum. getting help in life should be standard, some people will need more help, some people might not need much at all.

[rowenablade]

Okay. I’m going to wait to do a second watch before I articulate most of my other feelings here, but I want to address one thing.

I’m seeing a lot of posts like, “I related to Izzy because I am also queer and older/disabled/depressed. By killing him off, the writers are saying that I deserve to die.”

Guys.

I’m not saying your feelings aren’t valid. I totally understand grieving a character that you relate to. But speaking as a writer, I just want to point out that trying to write with the shadow of “what is the absolute worst and most harmful way a reader can interpret this” will smother your ability to create. Twisting yourself in knots, trying to think up the worst-faith takes possible and scotch-guarding all your writing decisions against them is exhausting to the point of making you just not want to write anymore.

And we’ve seen the writers deliberately choose not to do this in Season 1. Remember all those terrible “Izzy is racist” takes that the writers and cast seemed completely blindsided by? That happened because the writers and directors and actors weren’t going over every scene with a fine tooth comb, ferreting out every shot or line of dialogue or micro expression that could possibly be interpreted as racist, and scrubbing it off. Because there comes a point where your story is what it needs to be, and you have to accept that some people will interpret it in ways you didn’t intend them to. And if you can’t accept that, you’ll never find the courage to put your work out there.

The point of diverse casts and writing teams isn’t to achieve a state of, “Nothing bad ever happens to a character from a marginalized demographic ever again.” It’s to achieve a status quo of these types of characters just being people in the world of the story. Not symbols, not representation boxes to tick, not tokens that you can point to so that you can say, “Here, we acknowledged this type of person exists, now where’s our woke points?”

OFMD is full of characters of color, queer characters, older characters, characters of differing body types. And in stories, things happen to characters. Some fall in love. Some make the same mistakes over and over. Some turn into birds. Some die.

Izzy’s character represents a lot of things, but he does not represent every older, disabled fan or fan who has struggled with suicide, any more than Jim represents all genderqueer fans, or Olu represents all black fans. That’s not how the writers were handling him. They were handling him like a character, because that’s what you have to do.

Again, I understand being sad. I am so, so fucking sad. But this idea of, “Any time something bad happens to a character I relate to means that the writer thinks I deserve these bad things to happen to me,” will poison everything you engage with eventually. Because stories are full of things happening to characters, and they won’t all be good things. And the more representation we get, the more often bad things will happen to characters we relate to.

But good things will happen too.

Queer couples get married. Disabled women run off with their favorite husbands. Middle-aged characters change careers. A multiracial polycule finds a home at sea. A fat man covered in tattoos stars in a drag show and all his friends cheer. All these things happened in the same show as Izzy’s death. This is what this world is.

Anyway. I know emotions are running high and I’ll probably get blocked or unfollowed by a few people for this. But I’m just trying to find my peace where I can, and if anyone else finds this useful, cheers.

[yeehawtist]

i think a lot of people miss out on this but spending time with diverse groups of disabled people makes you realize that people's needs will constantly contradict each other. if one person stims, tics, speaks, breathes, etc. loudly, then there will be at least one other person who can’t stand the sound of it. they need to be able to leave if they need it. the loud person cannot be forced to stop being loud but the one who is sensitive to loudness cannot be forced to tolerate something they can’t either. maybe there’s a person who needs aromatherapy to cope with or reduce problems that their disability causes them. but there may also be a person who gets seizures or migraines from strong scents. you cannot deny that coping skill but you cannot let it trigger someone either. someone who struggles to sit might need a standing desk, someone who needs to sit will need a chair, some people might need alternative seating or flexible seating, and all of those options need to be available. one standing desk in the corner isn’t going to cut it most of the time and people need to be able to accept that and do better.

i could give endless examples of times when people's needs will contradict each other. most of which i’ve seen happen in real life spaces. physical, processing, communicating, everything can be contradictory to someone else's need. everything. a truly accessible space will try to accommodate to all those who exist within it.

[nightmaretour]

I feel like there's a pretty significant issue with a not insignificant portion of people on this site assuming that every physically disabled person they talk to on here is ambulatory, invisibly disabled, has low support needs or is generally at the same severity of disability as them. I think that's where we get a lot of this "nobody is more disabled than anyone else" and "physical disability and neurodivergence is ALWAYS the same because it's the same in MY experience" stuff from. It's easy to broadly apply your own experiences to people you've never met in person and haven't witnessed the real everyday life of.

But I really urge everyone to make a conscious effort to NOT do that. There are people who use this site who are bed bound, cannot breathe or eat without assistance, experience varying degrees of paralysis, rely on full time care, have high grade neurological/cognitive disabilities, have a terminal illness, have undergone very extensive surgeries just to survive, etc. and are OBJECTIVELY more disabled than you. There are tons of people on here who are OBJECTIVELY more disabled than me. Those aren't obscure hypotheticals, these are real people who you and I have interacted with in this community.

That doesn't mean your disability isn't real or that you aren't struggling, it's just a fact. If you feel invalidated by that, perhaps that's an issue you have to work on yourself rather than outright denying and ignoring other people's experiences and silencing them to feel better. Literally none of this whole validity competition stuff matters in the real world, where the REAL PEOPLE you are talking to exist.

[hiiragi7]

Things I've experienced post-Final Fusion:

All of a sudden, the days felt really... really... really long. I never really felt like there was any time in the day prior to final fusion; living my life in parts, I had never experienced such continuous flow of time before. It's long.

It feels like I now have a lot more time to do things in the day, and I have to be careful not to push myself too hard. I've found myself being online less and less and getting a lot more involved in my offline hobbies and reading. I have a lot more time to work towards things I want to do.

I can actually think about and plan for the future now, and it's incredibly exciting. I talk to my partner constantly about it. I am very excited about the future.

I can remember so much more of my childhood, things I never thought I would ever remember I now do. That being said, there are still things I don't remember, likely tied to other memory issues, and I've made my peace with that.

While my memory certainly got significantly better in many ways, I've realized I struggle with non-dissociative memory issues as well, and I will live with those issues for the rest of my life; it's just how my brain developed, and that's okay.

Speaking of memory, I can remember things freely that before were limited to the memory banks of my individual parts. I no longer have to worry about what parts hold which memories and go about tracking them down; I as a whole either remember something or I don't, and of my memories, I can remember any of them whenever I want.

I feel a sense of ownership over my life, over my memories and my sense of self and my body. I can look at it all and very confidently say "that's me", and I feel and know it to be 100% true. A long way away from not being able to recognize myself in the mirror.

I can't dissociatively "take a break" from life the way I used to (ie switching out and letting another part handle it), and while it took a long adjustment period to get used to this, I'm okay with that; I have other ways to take breaks while still being present, I can listen to music or watch videos. If I really just need to be unconscious, I take a nap.

I had to come to terms with the fact I couldn't push myself past my limits anymore in the way that I used to, and that this is in fact an expression of self-care for me. I used to be able to push far past what I should have been able to, especially with regards to physical pain, and to some extent I can still do this under specific circumstances, but it is no longer something that I will do in my day-to-day life living with disability and chronic pain.

Actually existing in my body now, I have come to realize just how much chronic pain I have been in. It's made me a lot more alert to my needs and how to care for myself, what makes it better and what makes it worse.

When people say "there's always a chance you'll split again", it doesn't scare me; it comforts me to know my brain would still know how to cope if such an extreme situation occured that I needed to split again. I've worked through dissociative barriers, I could do it again. I know what lies at the end of that path is love.

No part of me has ever gone away. Even fully fused, we are all still here. I can even still communicate with myself as parts if I choose to. I still have parts, they just look different now. There are no barriers between us.

My parts held a lot of different aspects of my identity to them, aspects I'm still to this day sorting out. I've had a lot of realizations about who I am as a person post-final fusion, especially with regards to gender and disability. A lot of things about myself were formerly very heavily fragmented and dissociated which no longer are, and I'm still making sense of them.

I no longer experience flashbacks and nightmares. This is a major thing for me I sometimes still am in disbelief about, my nightmares used to be so severe that I would refuse to sleep because of them, and my flashbacks were horrible and caused very intense physical sensations. I no longer have them, and that's incredible.

Life is so much more vivid and colorful than I ever realized. I never realized how dull everything felt and looked before final fusion. It feels like a complete perspective shift that is hard to grasp in words.

I can feel my body so much more now physically than I ever could before. I feel each of my limbs, I feel changes in temperature, I feel my own breath, I feel different textures and sensations, everything I hear and see and feel and taste has so much more depth to it now.

I have emotions! A whole lot of them, and I can feel all of them. I can feel emotions that might be percieved as "contradictory" at the same time, I can feel emotions over little things and big things and just about anything at all. I'm no longer limited to feeling my emotions in parts, and it's incredibly freeing.

On that note, I have so much more emotional capacity now for feeling all of the love I have for myself and others. It's wonderful. I can't shut up about it.

[copperbadge]

how did u psych urself up to go to therapy? my executive function has been awol for like 2 years and it's gotten to the point where it's wrecking my ability to do anything. i'm scared to waste a bunch of time and money going and getting told i'm just lazy or that the problem is just me

Happy to talk about that! But this is really two issues, so I gotta do a fly-by real first on "scared of getting told I'm just lazy". :D

It sounds to me like you're aware intellectually that laziness isn't the issue. You know this is an executive function issue and not a personal flaw, but I definitely get that it's hard to internalize that. So I'm going to drop links here to some discussion of "laziness":

How do you know you're not just lazy? (ask sent to me -- it's long, but you can skim for the laziness bits if you want.)

Lack of motivation means you are avoiding pain (second ask in response to the first)

Laziness Does Not Exist by Devon Price

These are essentially my proofs when I want to remind you that laziness is a label that stigmatizes an innate behavior -- inability to act is real, laziness is not. If a therapist tells you that you are lazy, and ESPECIALLY that you are the problem, you should fire that therapist. Don't even stay the rest of the session if you don't want to, just say "I see we are not compatible," and bounce. I don't think the odds are high that you'll encounter that, but on the off-chance that you do, that's a bright neon sign that they're a bad therapist.

In fact I would open with that pitch: "I'm struggling with executive function and the self-perception that I'm really just lazy. I need help with the actual executive function issues but also with how I view myself because of them." The therapist's response will tell you a lot about whether they'd be a good fit.

So with that out of the way...

I eased myself into therapy with the speed of a small child entering an extremely cold lake. It helped a lot that all of my therapy has been virtual via Zoom, so a lot of stuff that would have been a barrier, like going to the physical appointments, discomfort in a strange space, etc. were swept away.

I didn't even want to see a psychiatrist for my Adderall prescription, but I knew I needed help and medication seemed to be my best option, so with the assurances of several people that it wasn't therapy so much as mental health maintenance, I saw a psychiatrist. And he was lovely! (I just met with him yesterday to go over my next few months of scrip.) For a while that was all I did: talked every month to a kind person who asked specific and measurable questions about my mental health -- mood, sleep patterns, ability to work, hobbies -- without getting especially personal. I thought, okay, I can handle this, I can probably handle more, so I asked him for a recommendation for a therapist.

He looked at the network of independent practitioners he belonged to (Clarity Clinic Chicago, if you want an example of a good network) and found me a couple of options. I got extremely lucky to find someone I felt was appropriate for me right out of the gate, though some of that was also knowing what criteria I had: I wanted someone who explicitly stated they specialized in adult ADHD and disability, and who seemed like they were interested in addressing a whole person and not a single issue. When we met she seemed nice, wasn't pushy or judgey, was familiar with spoon theory and disability activism because she also has ADHD, and didn't blink (or ask overly invasive questions) when I said I was very uneasy about therapy because of past experience. She was comfortable with the ambiguity I brought -- I basically said "Look, I think this is something I need but I'm not entirely sure what my goals are yet, it's just I only recently found out I have ADHD and I am rethinking a lot of stuff," and she was like fine, let's rethink it together.

It still took me a long time to start talking about anything meaningful, but she handled the non-meaningful stuff as if it was serious and important, which helped. Admittedly I have really good insurance so I pay $20 a session for therapy, which also helps; it's pretty negligible in terms of health costs for me. I can afford to dawdle.

So, all that said...my path may not be an option for you, but I think it indicates the kinds of options you have. You don't have to jump into serious and heavily emotional processing first thing if you don't want to. You can shop around for therapists and you can drop any bad ones you encounter speedily, or if you find one you immediately like you can still spend time getting comfortable before dropping into the heavier stuff.

I would suggest that if you have a prescribing psych or doctor for any kind of mental health meds, ask them if they have a recommendation. If you don't have that, ask around people you know or believe have access to therapy and see what they think. If those aren't available to you or you're uncomfortable with that, I'd do a search for licensed therapist and your health insurance, or see if your workplace has an employee assistance program that can recommend you someone.

Good luck! I hope you get what you need. Lord knows I've been there.

[sweetestcaptainhughes]

What are you trying to say? - Trevor Zegras

Word Count - 3600

Author's Note - I 100 percent projected my own dysleixia hardcore into this. This was 100 percent written for the dyslexic girlies and learning disability girlies only. Also not me accidentally maybe becoming a Trevor girlie after writing this oh no. This one is by far my favorite segment.

Warnings - light angst but like it ends happy shocking for this page, who am I becoming???

Summary - In the talking stage with Trevor Zegras you're not sure how his joking personality will respond to your struggles that you have with being an adult with dyslexia, especially since it doesn't affect you how media expects it to.

Let me love you masterlist main masterlist

This isn’t something new to you, you’ve struggled your entire life with the fact that you're dyslexic. It’s a lot more complicated than people may recognize. Many people assume that it only comes up when you're trying to read something like a textbook or an article, and that when you’re finished with school it won’t really affect your daily life anymore but that’s far from the truth. In truth, being an adult with dyslexia affects you in little ways daily. From having difficulty knowing your left and right when given verbal directions, your spelling being terrible when texting others, mispronouncing certain words and being easily embarrassed when it gets pointed out, or worse sometimes the word is literally on the tip of your tongue you can even physically see in your brain but your mouth can’t form the proper sounds, how certain fonts you struggle to read vs others, or that black ink on white paper is the bane of your existence.  Although all of these are “little” things, it does impact the way you communicate with others. It does feel extremely frustrating sometimes feeling like people think that you're using your dyslexia as an “excuse” when in reality your brain is wired completely differently because of it. 

Since you first met Trevor and started talking to him, you had that fear you always do in the pit of your stomach, will he pick on you the first time that he truly can’t understand a text or the first time he hears you mispronounce a word despite years of speech therapy where you tried to but still you can’t pronounce correctly. Although, part of you knew that your fear was extremely irrational, part of you couldn’t shake the feeling that was until proven otherwise the jokester in Trevor would make a joke about something you truly couldn’t control. 

That is until today, when it happened it’s one of those rare days when you were driving and Trevor was in the passenger seat. His car was in the shop, and he needed a ride back from the arena to his apartment. Originally he was going to take an Uber but since you both already had plans after the morning skate you insisted on picking him up. 

“It’s easiest if you take this right up here to get back to my place.” He directs you without looking up from his phone,you tell him okay, turn on your left turn signal and get in the left lane. Trevor finally looks up from his phone while you're waiting at the red light for it to turn green to see you're in the wrong lane. 

“Sweetie?” asking in a questioning tone

“Hmmm” 

“This is the left lane. I told you to take a right.” Trevor says in a concerning tone as to how you were five traffic lanes away from where you needed to be. 

“sorry I thought you said ‘left’. I can make a u-turn?” Deciding in the moment you didn’t want to admit that you heard him correctly but processed the direction wrong, you offered as the traffic light finally turned green. 

“It’s alright we can just take the long way. Don’t worry about a u-turn.”  Not seeming to care at all that it will add an extra 10 minutes to the drive due to the mistake. 

As you continued driving you ended up making another wrong turn, Trevor put his left hand on your thigh and subconsiously rubbed small circles into skin to comfort your growing anxiety, he could feel this odd tension that was built up in the car. “Can you point please?” your voice barely over a whisper as you felt extremely embarrassed all of a sudden and started feeling overwhelmed all of a sudden. 

“Yeah Y/N/N I can do that, we could also switch places. I can drive you the rest of the way if you need it if you're feeling anxious all of a sudden.” Trevor was being really sweet, trying to fix the problem at hand thinking it was just some anxious thoughts and not your brain processing audible information incorrectly. 

“No, pointing is good.” Forcing yourself to look straight ahead because you don’t want to accidentally catch his eyes as he looks at you with a worried look. He squeezes your thigh in a comforting way and drops the topic. The rest of the ride felt quick as he pointed and said the direction you needed to go until you reached his apartment. Finding a parking spot in the garage you parked your car, as soon as you felt your foot on the brake, and your right hand pulled the gear in park, you leaned back automatically and sighed grateful you were done driving. Trevor still had his hand on your thigh, he turned his neck so that his head was also resting on the headrest. 

Trevor patiently waited until you opened your eyes, turning to him with a soft smile. “You ready?” you ask him, as you start to unbuckle your seatbelt. As you grab your purse from the back, your hand on the door handle. His hand that was on your thigh is gone and immediately pulls you by the wrist back into your seat. As he takes his other hand and gently places it on your cheek forcing you to look at him. 

“Can we talk about it?” His voice was steady, calm, confident but soft, almost as if he was scared of your reaction. 

Smiling a little wider now, in a split second you try to decide what you want to do. Do you want to tell a boy who you’ve only been casually talking to and hanging out with a handful of times - one of them being this current moment - about being dyslexic. Although it’s not that big of a deal in retrospect, it’s something that you can never take back once you said the words. Even though it’s something so simple and common no one ever looks at you the same again. Were you ready to tell Trevor, and see his face change permanently or did you want to live in ignorant bliss for a little longer. 

“I’m fine, it’s just when I drive somewhere new I like listening to the GPS and not a person telling me directions, it helps me focus better is all.” sheepishly you admit. 

Ignorant Bliss. That’s the choice you made. 

“Okay well next time, can you tell me that so I don’t have to watch you stress yourself out please?” His hand that was on your wrist, going down to your hand playing with your hand. Taking your hand that he was playing with, fully grasping his you squeeze his hand as a silent yes, and nod your head. He leans over the middle console and quickly peaks your lips as if it was a last minute impulse and he meant the cheek. “Thank you, let's go inside.” 

—-------------------------------

Living in ignorant bliss was great for a few weeks, until you started to actually like Trevor. Talking to a guy for a few months and it not going anywhere vs meeting someone and potentially seeing at least an exclusive relationship with them were two very different things. Knowing that you saw a relationship with him in the future meant it was only a matter of time before he found out that your dyslexic which again isn’t that big of a deal, but the fact that you also lied to him a few weeks ago. Not telling him is one thing, but lying when he asked why you were struggling to drive that day is a completely different act. 

Trying to put off the inevitable you tried to push the thought to the back of your mind. Somehow convincing yourself that if you didn’t think about it, then the problem would disappear he would never find out. I mean when you didn’t know how to spell a word while texting, you just spoke it into your phone. As far as grammar no one really had perfect grammar when texting including Trevor to be perfectly honest he probably didn’t even notice half the time. Plenty of people kept all their devices in dark mode for plenty of reasons, he had no reason to ask, although you did it because it helped your eyes stay focused on the words in front of you, not for the aesthetic. 

Even so, with all of these excuses as to why he wouldn’t notice you failed to remember that certain words you truly can’t pronounce the correct way no matter how hard you try. It all came crashing down tonight when you were at Trevor’s apartment cooking dinner for the both of you. Dinner was almost done at this point, when Trevor came behind you just now re-entering the kitchen after taking an expected call from his little sister. Trevor wrapped his arms around your waist, his head resting on top of your shoulder. 

“Everything okay?” you ask your curiosity getting the best of you, even though you know it’s none of your business. 

“Yeah she’s fine.” Pressing a kiss into where your jawline and neck meet. “smells good.” He compliments your cooking as he teases you one more time with a small nip with his teeth where he just kissed you, before pulling away and resting his head on your shoulder. 

Answering shyly, you let out a “thank you.”

“Anything I can help with?” asking genuinely although you're not sure if it’s to be kind or if it’s because he’s hungry but either way you’ll take it. As he slowly unwraps himself from you, getting ready to help you in any way you need. 

Without looking up from the chicken that you're grilling on the stove, trying to concentrate on the task at hand you answer him. “Yeah actually can you grab out the mellk from the fridge for the mashed potatoes.” Not even thinking twice about what you just said until you heard a chuckle coming from across the kitchen. 

“What babe?” standing in front of a now open fridge, he could have sworn you tried to say milk but botched the word so badly, it couldn’t have possibly been.

“the mellk” finally noticing what you asked for, knowing this is one of the words people can’t help but point out how you butcher it. 

“What are you trying to say?” he asked, truly confused now that he heard it twice. 

“M - il - k “ you repeat slowing down your mouth trying to force yourself to pronounce it properly but also not speak too slowly. Hoping that it's noticeable as you force your tongue to the roof of your mouth to make the “il” sound.  

A small chuckle leaves Trevor’s lips but it wasn’t a malicious way, it was as if he chuckled because he found it adorable. “Here's the milk baby.” walking back over to you and placing it on the empty counter space next to the bowl of steaming hot cooked potatoes. Taking the chicken off the hot burner you moved to the island to where the potatoes were. 

“Sorry” you mumble as he stands beside you, his hip resting on the side of the island. 

“For what?” His eyebrows frowned, his eyes focused the side of your face the only thing he could see. Focusing on the task at hand, you used the potato masher and mashed the potatoes. Opening the milk and adding a little along with some butter that you set out earlier. 

Feeling the rise of some anxiety in your stomach, hoping that you could procrastinate just a little longer on admitting that you didn’t tell him the whole truth. Deciding if now was the time or if you were gonna dig yourself in a bigger hole by wrapping yourself in a thicker web of tiny white lies. 

Finally turning your head to the side to face him and taking a deep breath. 

For good measure making one more deep breath before you barely utter the words, your nerves getting the better of you. “I lied.” 

Trevor’s face immediately changed from confusion and concern. In an instant it became shocking and almost hurt, that the girl he thought was actually going somewhere a month in, is admitting to lying to him. Not when he told her in the beginning that lying wasn’t something he tolerated after his ex lied to him for months and manipulated him. Not when he just told his little sister not even ten minutes ago on the phone that tonight he was gonna ask you to be his official girlfriend. “What are you talking about?” his voice cracking before he could even get the word out, quickly clearing his throat to cover up his own insecurities about the possible tension that could slowly be felt brewing in his kitchen. 

“Remember a few weeks, when I was driving you to your apartment from the stad-” 

“What the FUCK does that have to do with lying to me? When did you lie to me Y/N” Not only has Trevor never once raised his voice at you in a not joking way, but he’s never cursed at you, and his tone made you close your eyes and flinch at the impact. Immediately, seeing you flinch he sighed his hand going to lightly crease her arm closest to him. “When did you lie?” asking at a much softer tone than moments before. 

“I’m trying to explain.” Trevor could have sworn he felt his chest hurt when he heard you struggling to speak, as if you were trying to get yourself not to cry. “Please let me explain.” 

“Okay” he softly let out, as he squeezed your arm not sure if he was trying to comfort you or himself as he felt the possibility of you slipping through his fingers. 

“A few weeks ago when I drove you home.” finally turning her body fully turning to face him. “I lied, When you asked me what happened. I told you I need the GPS because I get overwhelmed.” Pausing to make sure that Trevor was following along, he nodded along, “I lied, sort of,” your voice picking up in speed with each word you uttered out  “I mean I do get overwhelmed while driving but it’s not because of that it’s not that I” 

“Baby please take a breath you're scaring me” His other arm is going to cup your cheek, even though he was mad before as he heard you fixated on driving him home a few weeks ago. He knew it couldn’t have possibly been any of the terrible ideas that popped into his head, at least Trevor hoped not.

 “I sometimes get my left and right confused.” Looking up trying to gauge his reaction, watching as one of his eyebrows go down, as if to say ‘that’s all.’ 

“Okay. So that was the lie? Everyone gets confused sometimes and makes mistakes baby it’s okay” His famous smile slowly takes over his face. 

“That’s the thing is it isn’t sometimes, it’s kind of a lot when I’m driving when someone is giving me directions without pointing, and there are other things too. I mean they're small but they still affect me almost daily and I just.” 

Deciding to take a breath because if you don’t you will be more likely to trip up your words or stutter. “I’m dyslexic and it’s not really how they describe the movies.” 

His smile dropped a little and you swear it felt as if your heart felt as if it had just dropped a hundred flights down the Empire State building. “Dyslexic. Like you mix up letters when reading?”

“Yeah but it’s more than that.”

“Okay. But why didn’t you tell me when it happened? Why did you say it’s because you get overwhelmed.” 

“Because I do get overwhelmed when I make dumb mistakes like that. Plus, everytime I tell someone they never look at me the same. A lot of times they are shocked, and they also sometimes judge me because how does it not affect me the way the media portrays it? Why do I mispronounce words, why can’t I tell my left and right when someone gives me a direction, why I can’t read maps to save my fucking life but yet if I don’t have my GPS running I’m bound to a wrong turn, why does sometimes my mind decide I either can’t come up with a word at all or I can physically see it but I can’t say it and I can’t spell it because I’m such a bad speller.” 

“Shhh” not trying to cut you off but also trying to get you to breathe. “So you didn’t tell me cause you were scared I would look at you differently? Or judge you when something you can’t control comes out at random times of the day? That’s why you told me to point instead of just saying it because you didn’t wanna tell me in fear?” Not sure his tone is showing remorse for you thinking that at all or hurting that you ever would think of him in that way. 

“Yeah.” you embarrassingly admit.

Trevor spent the rest of the night listening to you and how your brain was different due to your own personal experience with being a dyslexic. The next morning you found him reading an article about the effects of different lighting and how dark mode was the best for dyslexics and certain fonts were better than others. It made you chuckle as you told him you knew and that’s why your phone was permanently in dark mode.  That day, he changed all the settings on his tv’s in his entire apartment for dark mode, even all of his own personal devices. Finding it adorable that he went on a tangent when he found out certain apps don’t support dark mode and how he said it was discriminating. Finding it harder and harder for yourself to hide your soft smile as you watched him continue his rant, your heart swelling at how passionate he sounded. 

“I really like you, you know.” you admitted when he finally stopped complaining about how Mirosoft finally started supporting dark mode it was still ‘white paper’ on black ink so they really missed the whole point. 

“Oh yeah.” as he grabs you, pulling you towards him on the couch, tangling your legs with his. 

“Yup” popping the p for emphasis.

“I really like you too. Actually I was gonna ask you.. Wanna make this official and let me call you mine.” The blush was obvious on your face, immediately turning a light red shade, nodding your head he pulled you into a soft kiss. 

—---------------------------------------------

A few weeks later you were out to dinner with a few close friends and Trevor. Currently trying to tell a story about one of your new coworkers and how you didn’t like him but mid sentence you froze. Trevor had yet to see you freeze because the word you planned to say completely escaped you. Of course this wasn’t new to your friends as they saw the familiar signs, the way in which you paused, your lips pursed in a questioning way, your hand coming up and shaking knowing it was on the tip of your tongue and you just couldn’t think of it or couldn’t pronounce it. 

What your friends weren’t used to was seeing Trevor respond to it. His response to you struggling made all of them share a glance in approval of his small action. He took your shaking hand and slipped it into his own. Immediately your small flustered expression on your face turns to him. Your friends couldn’t hear what you were saying between yourselves if you were even talking at all, but they could see the care in Trevors eyes and how your frustration seemed to melt away.

“Hi” he whispers only for you to hear after a couple seconds pass. 

A smile breaks out on your face. “Hi” 

“What are you trying to say?” repeating the same sentence that he asked you weeks ago when you asked him to get the milk out the fridge. 

“I can’t think of it.” a sigh leaving your lips. 

“Describe it.” His forehead resting on yours as you look into his eyes. 

“You know, like a red flag.” 

“Like in dating? So a slang term?” 

“I think.” Pausing for a few seconds for your brian to catch up. “But I know it’s not called a red flag, but it’s like it, I think, like when someone does something and immediately you're like ew.” 

“An ick?” he softly suggests. Immediately your mouth forms into an o-shape in shock, making his mouth twitch into the slightest smile. Kissing his check quickly and whispering a quick ‘thanks’ and turning back to your friends. 

“Okay so like this new dude thinks he can come in and just boss all me and my other co-workers around. That’s not even the worst part like not only is he lowkey sexist, he literally only wears highwaters, immediate ick…” Trevor sat there half listening to your story with a huge smile on his face, hand on your thigh drawing patterns subconsciously as he sipped on his drink. He loves listening to you talk, how you get lost in telling stories and he’s happy he was able to help you instead of you pushing it to the side like you did all those months ago. 

That’s how it is from that night on, anytime you text him and he can’t understand it, or you can’t think of a word, or butcher the pronunciation; he will simply turn to you and ask “What are you trying to say?” 

[nekropsii]

thoughts on meulin as a whole :?

I think her Toxic Positivity as commentary on Tumblr Fandom Spaces is spot on, and I feel like no one acknowledges that trait partially because of the same reason that it’s there in the first place. The reason I say “partially” is because it mostly comes down to people not reading the Openbounds, but still professing themselves to be “experts” just because they saw a few pieces of Fan Art. Any remaining percentage goes to Misogyny. The Leijons are not allowed to be seen as complicated people because they are Cute Girls, and therefore are Dumb and Silly and Have No Humanity - I mean, Personality outside of this.

Every Abled person who has looked me in the eyes and told me she’s Bad Hearing Disabled Representation because she “isn’t using real sign”, or because she’s “still speaking verbally to people” owe me $500 per every word of their statement. Textually, she loves her disability, and she loves navigating it and the world around her. She loves the new learning opportunities, she loves learning sign. She’s open about this! Literally the only real reason she’s still speaking verbally to people is because the people around her won’t fucking take the time to learn sign for her. This is a struggle that a lot of real actual hearing disabled people face. It’s not unrealistic. Lip reading exists. Her disability was gained, so she already knew how to talk. I wish every Abled person a very Shut The Fuck Up, Forever. I wish them a very Begone, Concern Troll. I love Meulin. I’ll kill you.

[goblinrat69420]

If you ever get a chance to meet Matthew Lillard, do it. He’s the sweetest person to ever exist. I was waiting in line for a while and then my dad pointed out how he was walking around the line giving out high fives and saying hi. I reached my hand out and he high fived me. I started crying. My dad said “Matt look what you did!” Then, Matt came over and hugged me and said it happens. Then, when I got closer he said hi to me and I started crying again. He said “Stop crying people are going to think I did something to you!” He walked over to me and hugged me again and we walked up the line and he told me to hang in there. Then, when it was my turn he said Hi and I just kinda ran to him crying and we hugged. He asked me how old I was (I’m not gonna say my age) and when I told him my age he said that age was hard for him and it’s hard for probably everyone. He then said something about having a learning disability (I think I was crying a lot and it was loud) and he struggled and he had to find what he loved and it made him happy. I told him I have Autism and he’s my favorite person then he hugged me and said “I’m glad I’m your favorite person.” We got a picture then he said to me “You’re so nice” which made me cry more. I hugged him one more time and left. We talked for 10 minutes and it was the best 10 minutes of my life. I also couldn’t cry anymore throughout the day even after drinking 2 bottles of water! Matthew Lillard is the sweetest human being and his hugs are the best. If you ever have a chance to meet him, do it. You will never forget it.

[lastoneout]

It's also like super fucking infuriating to see people continue to argue that generative AI is the best way for disabled and/or poor people to make art because like, you know what helps make art more accessible? Giving poor and disabled people money.

Like take me for instance, I'm disabled. I get severe migraines and intense leg/back pain if I sit at my computer for too long, my hEDS makes holding pens and pencils hard, my ADHD makes it hard for me to start certain tasks and/or stop them before I potentially hurt myself, my neck also hurts if I look down too much, my dyslexia AND my ADHD both make it difficult to keep track of a story as I write and use correct spelling and grammar, plus, I need to prioritize taking care of myself and going to appointments and keeping my house clean and that takes up a lot of my free time. All of these things make creating the kind of art I want to create difficult if not occasionally impossible.

So what do you think would solve my problems better? Giving me money so that I can have a drawing tablet and desk chair that won't hurt my neck or back, another tablet + pen and a lap table and comfortable body pillows for drawing in bed, easier transportation to my doctors appointments, effective treatment for my chronic pain and migraines, the ability hire someone to help me keep my house clean, a spelling/grammar checker that isn't complete ass, and a therapist and psychatrist who can help me manage my ADHD better?

Or an AI program that takes my input and spits out a drawing or story made of stolen content glued together that, in the case of the art, I cannot meaningfully edit without starting over, which also destroys the environment in the process?

Seems pretty obvious to me. I don't need AI, I need help to manage the things that are actually stopping me from being able to write and draw.

Or take my mom. She's had severe rhumatoid arthritis since she was a small child, her hands are deformed and she relies on her wheelchair to get around. She doesn't need AI to help her paint, she needs special paint brushes she can actually hold, a table her wheelchair will fit at, and someone to help her with personal hygiene/keep her house clean/take her to doctors appointments so she actually has free time to paint.

Does that poor kid growing up in public housing with parents who are too poor to afford art classes or supplies or to send them to college really need a computer program to draw for them, or do they need support to help them take those classes, buy drawing supplies, and money so they can go to college.

Blind people can paint, deaf musicians exist, people with missing limbs find all sorts of ways to make art, people with parkinson's paint with typewriters, my mother can't hold a normal paintbrush and she makes some of the most beautiful watercolor paintings I've ever seen, Van Gogh had bipolar disorder and only sold like one painting when he was alive, I mean for real how many different artists have you heard of who's biographies start with them being born into poverty?

This is not meant to be inspiration porn, these people are just ones who were able to find ways to make art despite their struggles. They shouldn't have had to struggle at all, but god imagine how many more artisrs and writers we could have had if none of them had to overcome those struggles. It breaks my heart to think of all the wonderful art that never got to exist because no one helped the people who could have made it actually have the time, money, support, and safety they needed to make it. AI would not have saved them because making art isn't the problem, being disadvantaged is the problem. Living in a world that refuses to make room for you is the problem. Being fucking poor is the problem. Humans have always found ways to make art despite huge barriers, the solution isn't a computer that makes art for them, it's SUPPORT AND MONEY SO THEY CAN OVERCOME THOSE BARRIERS AND MAKE THEIR OWN ART.

As a last example: I love watching dancing and I would love to be able to dance, but I'm terrible at it(I got kicked off a dance team for not being able to learn the dance at all despite spending weeks on it, idk my brain wasn't made for dancing) and my disabled body makes it more pain than pleasure if not actively dangerous, anyway. Having a robot dressed to look like me dance next to me while I get to watch would not make me feel like I'm getting to dance. It would actually be extremely fucking demoralizing and frustrating. I would hate that!!

Having an AI spit out a painting or book would not make me feel like I got to paint or write a book. It's a fucking anamatronic doll running on stolen ideas and it will never be the same as getting to actually expirience the joy of creating art first hand. AI is not the solution. Helping people who need it is the solution. And I am CONSTANTLY pissed to think about all the time and money that goes into these fucking AI programs that would be better spent helping disabled and poor people get the help they need so they can make art themselves, all while the people running the nightmare plagiarism pollution machines pretend that their horrible inventions exist to help people like me.

[a-little-revolution]

heya, this might be too much for a single post, but i would delight in a ramble about the overlap between dwarfism and disability (whether or not you/the community as a whole generally consider it a capital-D Disability or if theres more nuance like with the autism or HOH/Deaf communities where it just Is and folks feel the the struggles with outgroup folks are like, culture clashes, or perhaps a secret third thing?)

similarly, id love for a ramble on the overlap between dwarfism and queerness, especially The Genders. i have ehlers-danlos syndrome and theres a huge number of us who are trans or nonbinary, to the point where masculinizing hrt is (anecdotally) understood to be a bit of a treatment for some symptoms. i know theres a lot of overlap between queerness and disability as a whole, but so far the couple of artists with dwarfism ive found and followed are all some flavor of trans or nonbinary, so id love to know if thats as common of a thing in your community as it is in mine

dwarfism is for sure underrepresented in discussion about both disability and queerness, and as a disabled queer person they are so intertwined in my head, and im forever curious about other folks experiences so your thoughts are appreciated!

Hello!! I love these questions!!

Firstly, yes, I do identify as being both a little person and disabled, but that isn't the case for everyone with dwarfism. Though dwarfism falls under the classification of a physical disability, not all little people find it physically debilitating. For me, my Achondroplasia dwarfism has resulted in sleep apnea, arthritis, chronic pain, hearing loss, limited mobility and dexterity. I cannot walk long distances and I use multiple moblility aids (wheelchair for long distance, rollator most of the time, and cane for short distances or around the house). My disability is dynamic, meaning that my ability changes day to day depending on pain levels, spoons (unit of measure for disabled energy), and activity.

Being that I am both a little person AND noticeably disabled, I have experienced ableism within both the abled community and the LP community, which is something I don't often talk about. I've been in situations where I feel alienated from my own community - additionally for my queerness. When you exist at the intersection of as many things as I do, you experience many flavours of ignorance and discrimination from the very people who should accept you.

That being said, I have also had the privilege of meeting other little people who are trans, queer, and nonbinary like I am. Our community is incredibly diverse, but spread along the globe. It is easy to feel a profound isolation, but the internet has provided me with a means of connection which I greatly appreciate.

Disability and queerness is something I discuss in depth in my public speaking roles, as I deeply value intersectionality in education and activism (I hope to share some of my talks as I record them in the future!).

I am forever painful aware that ableism is alive and will within the queer community - even when "all are welcome", we are still an after thought. I really urge my fellow queers to think beyond our own community to bipoc and disabled folks, otherwise you're really just dipping your toes into radicalism. Read more books by black disabled trans women of colour, and expand your thinking. (Thank you for coming to my Ted Talk lol)

I can't really speak to hate from the other direction, as all of the disabled folks I know on a personal level are also queer. Though I will say that I certainly receive queer-phobia from older (white) disabled folks - in my experience, when white folks become disabled with age and have not faced any other injustice in their life, they can be very hateful.

This has been quite a post, so I hope I've answered your questions in full! I would be happy to discuss it more if not/answer other related questions! Thank you so much!

Elliot (they/them)

[lostlegendaerie]

Veritas Ratio and Autistic Representation

Chances are you know autistic people in your life; autism itself is a fairly recently coined term, dating back to 1911, and can encompass a wide variety of symptoms and eccentricities which have existed since the dawn of humankind. (The 'fey-touched' child or changeling in European lore shares a lot of traits with autistic children.) Autism is a spectrum, encompassing and overlapping a lot with ADHD and other neurological disorders. There are probably millions of people out there, especially from older generations, who are on the spectrum and have no idea. I did not even get my diagnosis until I was 27.

So it is entirely possible that the creators of Veritas Ratio from Honkai: Star Rail did not intend to write him as autistic and based him on people they knew in their own lives, who, diagnosed or not, are on the autistic spectrum. However, the point of this piece is to talk about the ways in which Veritas Ratio is good autistic representation (in my opinion as a autistic person), and how people who want to write characters like this can take a page out of Honkai's book in their own work.

1) SPECIAL INTEREST. Ratio shows a *staggering* amount of dedication to the pursuit of knowledge and his quest to cure the world of ignorance. This quest of his tends to supersede everything else in his life, with no mention of any friends, family connections or romantic partners in his character story. (Said as a Ratiorine shipper - not sinking any 'ships, here) His dedication to education started early, with reading college undergraduate education levels while still in middle school - seven or so years ahead of his peers. Autism is considered a disability, yes, but it does not exclude you from being smart, and the fixation on your chosen topic(s) can be extremely useful in motivating you to reach the top of your field. His path being The Hunt also outlines this dedication; he is seeking his target without rest or distraction.

2) SENSORY ISSUES. Ratio very explicitly can become distracted and disgusted by the feeling of dirt or sweat on his skin, something that tends to be more prevalent with specific clothing textures but absolutely can manifest in a need to feel clean. He also can apparently become very irritated and overwhelmed by lights and sounds, and wears his plaster mask as a way to deaden and deafen the amount of sensory input that he receives. This allows him to think better, and is a fantastic example of what it feels like to suffer from sensory overload. (If you find yourself getting stressed in crowds, try bringing earplugs and putting them in the next time you're in a noisy restaurant and see if doesn't help you out.)

3) STRONG SENSE OF MORALITY. Autistic people tend to suffer from a somewhat black-and-white feeling of right and wrong, and can hold themselves and other people to an extremely strict moral code. This does not mean that they are always correct in what they believe is right and wrong, but it means that they can be extremely passionate about following those rules. Ratio's beef with the Genius Society and their selectivity is indicative of his unwavering passion towards sharing knowledge with the masses, but the tactless way in which he wishes to cure ignorance bleeds into our fourth point.

4) DIFFICULTY WITH SOCIAL CUES. In one of his earlier conversations with Aventurine (where he is clearly irritated at how careless Aventurine seems to be about their entire mission), Ratio inadvertently insults Aventurine's his lack of education and parents. He apologizes afterwards, stating he did not intend to come across that way, but he maintains the same imperious tone of voice. Autistic people often, but not always, struggle with social cues and can often be considered rude when we are trying to be direct and easily understood; and we can especially struggle with understanding sarcasm or sounding sarcastic when we intend to be sincere.

With my reasons for believing Ratio to be Autistic coded firmly established, let's move onto why I think he is good representation. The two most important parts of representation, in my lived experience as an Autistic person, are RELATABILITY and EMPATHY.

Ratio exhibits some of the same mentalities and symptoms I've had, such as being misunderstood and accidentally offending people and becoming extremely stressed in large crowds due to overstimulation, so he checks off the first box. But the way that the other characters in the game respect him and do not ridicule him for his eccentricities marks the second. Whether in marketing material or in character dialogue options, Ratio's love of baths, his plaster bust, and his ceaseless drive to educate other people (whether they need it or not) are seen as charming and generally positive, and those attributes are not constantly brought up (and mocked) in his interactions and dialogue with other characters. Aventurine doesn't constantly ask Ratio if he needs to leave the Dream to take a bath, and the TB's text conversations with him allow you to engage with his special interests such as his requests for problems to solve and debates to wage against you. He is canonically seen and respected as a brilliant individual, and not reduced to a joke or viewed as comic relief (e.g. Sampo, who almost exclusively is given negative dialogue options for the player to use when interacting with him and who almost every character in the story openly despises.)

Some of you are going to disagree with me in the comments (which is fine, it's my opinion), but for the few of you who read this all the way through, thank you. I hope that this helps you view Ratio and Autistic people overall in a new light, and I am excited to see where else we go from here with him and the rest of the cast!

[cheeseanonioncrisps]

Boiling hot take, but we're never going to be able to tackle the problem of bullying, especially in schools but also in general, unless we address the fact that some people, especially some kids, are just… not that great to be around.

And that's not always their fault.

Like, as an autistic adult, when I look back on the ways I was treated as a kid, on the one hand I think "fuck that was shitty to live through", but on the other hand, I kinda get it?

I was loud and regularly called out in class or interrupted people when they were talking.

I had a narrow range of interests that I was very interested in, and wasn't great at recognising when the person I was discussing them with wanted to talk about something else.

I couldn't judge my tone of voice and so things I said often came across as insulting when I didn't mean them to.

I was highly opinionated and argumentative.

I would sometimes lash out at people physically (when provoked).

I growled and hissed at people like a cat when I wanted them to go away, because I didn't know how to communicate that in human terms.

I used to hit and bite myself when I felt frustrated, and a couple of times threatened to hurt myself during stressful social interactions.

I had a loose grasp of personal hygiene.

Was any of this a justifiable excuse for bullying me? No. I was a kid, struggling with a brain that was structured very differently to everyone else's. I didn't even know what I was doing wrong a lot of the time. I had a disability.

But was this a justifiable excuse for not wanting to hang out with me? Fuck yeah.

Like, I would have liked it better if I'd been able to have close friends in primary school (without the teachers having to literally set up a structured group of people who were willing to befriend me, complete with weekly meetings where we discussed our social issues with an adult mediator present)? Yeah. That would have been great.

But I was also weird and unpredictable and gross and inconsiderate, and I wouldn't have wanted to hang out with me either. The other kids didn't owe me their friendship. (Even though, again, none of those things were my fault.) But that doesn't mean I deserved mistreatment.

Basically, I think there would be less bullying if we had more preschool books and Very Special Episodes about how to handle interacting with people who are essentially harmless, but who you don't really want to be friends with all the same.

Get rid of the dichotomy in kids media where everyone is either deliberately and purposefully being unpleasant because they can, OR Just Like You with no annoying or unpleasant traits whatsoever.

Sometimes people just are Annoying. It sucks. But part of living in a society is learning to walk away from those people and leave them be, rather than treating their existence as a personal attack.

[five-thousand-loaves-of-bread]

uh hi. got some few followers because that LSN post. some points of housekeeping:

this blog rare contained little space where actually safe when wider autism & disability community very hostile to people like me. n whenever people follow me because of posts not about severe disability / level 2&3 HrSN nonverbal autism, some new people don’t know what going on & sometimes do stuff that make this space feel unsafe. you’re more than welcome to stay as long as you follow housekeeping & have general respect

1. not written by me but read this

& do search in blog for intellectual disability too

2. use stuff like autism levels & nonverbal & impairment & deficit language & severe autism & severe disability & visible autism here to describe self & have friends who also use them. while not use for self, also have friend who been called low functioning & also call themself that. you not have to like all that for yourself but don’t police what we call self don’t tell me “um actually this is ableist… but of course you call yourself whatever!” uh. we know. basically if you uncomfortable to even see these language my blog not for you.

eventually will have actual post about this instead of respond to someone rude who blocked me after this n so blocked back… but for now this will do (probably used to have one but too tired find right now)

3. 99% time post about above topic. n blog center people with those experiences & decenter LSN level 1 mild whatever language use. reflect on your experience n who you are n your privileges n your advantages bc we all have some yea even me

4. because do experience stuff post about they not just words… no empathy, can’t mask, have very bad theory of mind, often don’t understand other people exist not to mention have different thoughts feelings knowledge experience than me. am bitter a lot, mad a lot, angry a lot. think in extremes, n immediate write what think, immediate post what write. can be angry aggressive without realize n even if do realize, can’t really do anything about it. basically have level 2/3 autism have big communication struggle have big cognitive struggle & act like it

5. don’t tell me you relate to what am saying unless am know you. keep have problem of people think they experience same thing am talking about but actually turn out very different whole other world n am wish can be like them. sorry to people am not familiar with who genuinely understand n relate but please understand need this

6. am just one random nonverbal person with level 2/3 autism & higher support needs & severe disability online. human. so make mistakes. n have bad takes like anyone. don’t treat me as write universal truth never wrong

7. oh something important. no “going nonverbal” “nonverbal episode” “sometimes nonverbal” etc

should update all this on pinned

tone sound annoyed pissed off because kind of am… but not because of this so not at any of you all not personal