#cw disabilities

[e-m-p-error]

Valentino And His Disabilities

Valentino has never had great eyesight in Hell, but the longer he is dead the more his sight deteriorates. He has perfect vision in the dark and is able to read and do other things, but in any form of light, he is essentially blind. When Vox smiles at him with his big, blue teeth, he also gets what he calls Moon Eyes where he is transfixed and cannot stop staring despite not being able to see.

After the stripping of his left antenna, Valentino's hearing went from being able to hear up to 300hz to only 150hz. He is half-deaf, and though he is still capable of hearing better than any human and most other Sinners, he does not hear as well as he used to. When he watches TV he has it turned up loud, and prefers loud music. He has to really strain to hear whispers if they are not relatively close to him. He does hear a static hum when Vox is around and generating it.

Due to the stripped antenna, his sense of smell and taste were also damaged. He has to get his other good antenna in there if he wants to smell something, and he prefers foods that have a heavier scent so he can taste them properly.

[psychotic-tbh]

Stop saying…

“Psychotic/Schizophrenic” when you mean: unpredictable, unhinged, unreal, etc.

“Bipolar” when you mean: polarized, scattered, fickle, unstable, etc.

“Delusional” when you mean: unrealistic, unreasonable, close-minded, stubborn, etc.

“[insert “R” slur in relation to intellectual disabilities]” when you mean: unreasonable, unintelligent/ridiculous, childish, etc.

“OCD” when you mean: particular, neat, overbearing, etc.

“Narcissistic” when you mean selfish, abusive, manipulative, etc.

Note: I’m NOT saying that these are synonymous. This is also not an exhaustive list.

[saszor]

[ID in alt text]

gay people real 🌝

[everythingwasnormalhere]

There's so much wrong with "everyone is a little bit autistic"

Yes, allistic people might know a lot of facts about the things they like. Yes, allistic people might get a bit overwhelmed or underwhelmed sometimes. Yes, allistic people might not get an expression sometimes, mostly if it's the first time they hear it.

That doesn't make them autistic.

Those traits only make someone autistic when they become disabling. Because, big shock, autism is a disability. Yeah, even if someone is low support needs, because that doesn't mean they don't need any support at all.

Saying "everyone is a little bit autistic" is like saying "everyone struggles with this, so suck it up, you have no right to need help". Which is just pure ableist bullshit. It denies the fact that autistic people have higher support needs than NTs, no matter where in the autistic spectrum they are. We're not "neurospicy", we're disabled, and denying this fact is denying us the right to get the help we need, we deserve, to have a good life.

(yes, this rant is just because I made the awful decision of listening to "neurospicy (interlude)" by Jax. honestly I'd rather be called a slur than listen to that shit again.)

[glitchdollmemoria]

please can we stop describing bigots as delusional. please. im so fucking tired. someone being sucked into a hate group surrounded by others who believe minorities should be oppressed and encouraging them to believe in conspiracy theories that the rest of the group believes, is fundamentally different from someone having a mental illness that causes delusions.

delusions, by definition, cannot be explained by things like cultural background - such as having a belief constantly reinforced by intentional attempts to rationalize it for the sake of maintaining power over minorities. yes, someone can be both delusional and a bigot, and yes conspiracy theories can feed into delusions, but the two are not fucking synonymous.

i did not spend my teen years convinced that i was being stalked by demons just to hear so many of you people equate my disability with incel behavior and genocidal propaganda. stop reinforcing harmful connotations about mental health struggles.

[nepenthean-sleep]

you know what. i've always been hesitant to describe my anaphylactic food allergies as a disability because "it's just allergies" but if you look at the numerous ways this has affected my life as an adult (because everybody only talks about kids having anaphylactic allergies):

no restaurants or fast food

no store-bought food from small companies (less accountability/resources to prevent cross-contamination)

no candy or desserts (unless they are 100% homemade, which takes a lot of time and energy if you have other disabilities like i do)

no hand-washing dishes (every place i live in has to have a well-functioning dishwasher)

no kissing people on the mouth/lower half of the face

other people cannot kiss me/put their mouth on me

no allergens in the house (really difficult to enforce with non- immediate family members!!)

always having to cook my own meals/bake my own treats/desserts

no sharing drinks/food with other people

no food cooked in other people's houses/kitchens

always having to bring my own "lunchbox" to family events, work or school, all-day events, or any other situation in which i could THEORETICALLY need to eat or drink something other than bottled water

calling food manufacturers to verify label information on new/changed foods

and none of this is counting the avoidance behaviors i developed with obsessive-compulsive disorder around age 13 in response to the panic attacks i'd have remembering about the anaphylactic shock i experienced at age 10.

i was taught to read labels at age 5. i was taught how to use my own epi-pen at age 6. my parents and i have always been careful and responsible about my allergies. it's not "i just don't like this food", it's "if i eat this my throat will swell up and block my trachea AND i'll go into shock from low blood pressure." as inconvenient as it might be for YOU, you can learn these things too and save a life. happy disability pride month; stop being a dickhead

i don't usually talk about my allergies because it gives me a LOT of anxiety but i felt this was important to share, because most people have no idea what being an adult with allergies is like. life went from "everyone at the birthday party gets a cupcake but me and i'm sad" to to "if i want to kiss someone i like, i have to make sure she hasn't eaten anything i'm allergic to in the past few days" (which is like. hugely awkward to ask of someone holy shit) or "i have to turn down the meal from my friend's mom even though she has the best of intentions and now she thinks i'm an asshole"

[heyiappreciateyourshoelaces]

[cookinguptales]

You know... I had an experience about two months ago that I didn't talk about publicly, but I've been turning it over and over in my mind lately and I guess I'm finally able to put my unease into words.

So there's a podcast I'd been enjoying and right after I got caught up, they announced that they were planning on doing a live show. It's gonna be near me and on the day before my birthday and I thought -- hey, it's fate.

But... as many of you know, I'm disabled. For me, getting to a show like that has a lot of steps. One of those steps involved emailing the podcasters to ask about accessibility for the venue.

The response I got back was very quick and very brief. Essentially, it told me to contact the venue because they had no idea if it was accessible or not.

It was a bucket of cold water, and I had a hard time articulating at the time quite why it was so disheartening, but... I think I get it a little more now.

This is a podcast that has loudly spoken about inclusivity and diversity and all that jazz, but... I mean, it's easy to say that, isn't it? But just talking the talk without walking the walk isn't enough. That's like saying "sure, we will happily welcome you in our house -- if you can figure out how to unlock the door."

And friends, my lock-picking set is pretty good by this point. I've been scouting out locations for decades. I've had to research every goddamn classroom, field trip, and assigned bookstore that I've ever had in an academic setting. I've had to research every movie theater, theme park, and menu for every outing with friends or dates. I spend a long time painstakingly charting out accessible public transportation and potential places to sit down every time I leave the house.

Because when I was in college, my professors never made sure their lesson plans were accessible. (And I often had to argue with them to get the subpar accommodations I got.) Because my friends don't always know to get movie tickets for the accessible rows. Because my dates sometimes leave me on fucking read when I ask if we can go to a restaurant that doesn't keep its restrooms down a flight of stairs.

I had one professor who ever did research to see if I could do all the coursework she had planned, and who came up with alternate plans when she realized that I could not. Only one. It was a medical history and ethics class, and my professor sounded bewildered as she realized how difficult it is to plan your life when you're disabled.

This woman was straight-up one of the most thoughtful, philosophical, and ethical professors I've ever had, one who was incredibly devoted to diversity and inclusion -- and she'd never thought about it before, that the hospital archives she wanted us to visit were up a flight of stairs. That the medical museum full of disabled bodies she wanted us to visit only had a code-locked back entrance and an old freight elevator for their disabled guests who were still breathing.

And that's the crux of it, isn't it? It's easy to theoretically accept the existence of people who aren't like you. It's a lot harder to actively create a space in which they can exist by your side.

Because here's what I did before I contacted the podcasters. I googled the venue. I researched the neighborhood and contacted a friend who lives in the area to help me figure out if there were any accessible public transportation routes near there. (There aren't.) I planned for over an hour to figure out how close I could get before I had to shell out for an uber for the last leg of the trip.

Then I read through the venue's website. I looked through their main pages, through their FAQs to see if there was any mention of accessibility. No dice. I download their packet for clients and find out that, while the base building is accessible, the way that chairs/tables are set up for individual functions can make it inaccessible. So it's really up to who's hosting the show there.

So then and only then I contacted the podcasters. I asked if the floor plan was accessible. I asked if all the seats were accessible, or only some, and whether it was open seating or not. Would I need to show up early to get an accessible seat, or maybe make a reservation?

And... well, I got the one-sentence reply back that I described above. And that... god, it was really disheartening. I realized that they never even asked if their venues were accessible when they were booking the shows. I realized that they were unwilling to put in the work to learn the answers to questions that disabled attendees might have. I realized that they didn't care to find out if the building was accessible.

They didn't know and they didn't care. That, I think, is what took the wind out of my sails when they emailed me back. It's what made me decide that... yeah, I didn't really want to go through the trouble of finding an accessible route to the venue. I didn't want to have to pay an arm and a leg to hire a car to take me the last part of the journey. I didn't want to make myself frantic trying to figure out if I could do all that and still make the last train home.

If they didn't care, I guess I didn't either.

If they'd apologized and said that the only venue they could get was inaccessible, I actually would have understood. I know that small shows don't always get their pick of venues. I get it. I even would have understood if they'd been like "oh dang, I actually don't know -- but I'll find out."

But to be told that they didn't know and didn't intend to find out... oof. That one stung.

Because.... this is the thing. This is the thing. I may be good at it by now, but I'm so tired of picking locks. I'm tired of doing all the legwork because no one ever thinks to help me. I'm tired of feeling like an afterthought at best, or at worst utterly unwelcome.

If you truly want to be inclusive, you need to stop telling people that you're happy to have them -- if they can manage to unlock the door. You need to fucking open it yourself and welcome them in.

What brought all this back to me now, you may be asking? Well... I guess it's just what I was thinking to myself as I was tidying up my phone.

Today I'm deleting podcasts.

[captainjimothy]

personally i do think julian bashir is trans, but not in a way that sublimates his genetic alterations into a trans allegory. i think he's disabled and trans at the same time, but i think his rebellion against his parents--the symbolic death of his old self with the name change--that's not about gender, for him, at all.

it's about the incredible violation of autonomy he experienced as a disabled person under the knife of a eugenicist society. it's about the need to reclaim some, any, of the agency that was so completely stolen from him by his parents.

it's about discovering that his entire self was deconstructed and reconstructed, without his knowledge or consent, for the express purpose of being less of a burden on his parents.

because let's not forget that the death of julian's old self was not his decision. it was his parents who killed the old self and created a new one.

let's not forget that human society in star trek is still recovering from the eugenics wars--that just because it's post-scarcity doesn't mean it's a utopia.

let's not forget the multiple episodes where bashir is forced to confront the fact that his "success story" is truthfully a gross reminder of how deeply his society (and his family) hates disabled people, not only shown in how they tried to fix him, but also in the fact that the process so rarely works as intended, yet is still done anyway--and the failures and the ones too far gone to save are locked away! with no connection to general society, and only the bare minimum provision for their physical needs, with no privacy and no autonomy!

and let's not forget that julian sees these people and is torn between the empathy he has for them, and his urge to fix them. and he goes through with this urge on Sarina, "fixing" her to conform to his idea of what she ought to be, treating her as a problem to be solved, objectifying her via "my ideal woman was trapped in this disabled body/mind and i saved her," thus continuing the cycle of violence, because even he can't conceive of a world where the disabled do not need to be fixed. where the violence done to him was wrong. fuck man

[talkingattumble]

Hi guys! Here’s some advice from a cane user on how to spot a fake cane user/disability faker!

YOU CANT

You can not spot a “fake disabled” cane user. You can not know if someone’s “really disabled”, much less by just looking at them. Here are some common misconceptions.

“Cane users always need their canes. If they walk without it or put it away when it’s inconvenient, they’re faking”: WRONG! Many cane users are what we call “ambulatory” cane users. This means they don’t always need their canes to walk. I’m an ambulatory cane user, and I experience really horrible leg pain on the daily. However, I don’t always use my cane, and when I don’t need to walk or stand a lot in a certain place I don’t use it. And when I do use it, I may lift it off the ground or carry it in places that are sandy, gravelly, or otherwise hinder my cane.

“Cane users walk abnormally without their canes, someone who walks normally without their cane is faking”: WRONG! Many ambulatory cane users can walk in a way that seems “normal”. This doesn’t mean they’re not in pain, or not “really disabled”. This just means that their condition doesn’t cause a noticeable difference in walking, and likely manifests in a different way.

“Cane users always need their cane, someone who doesn’t use their cane at home is faking”: WRONG! Cane users may not use their canes at home, because at home they may be able to do things like sit down wherever and whenever, regain more spoons, and use other mobility aids. Additionally, some ambulatory cane users only need or use their canes when they are doing something physically taxing, like going on a hike or standing in a long line.

“My cane user friend told me this person looks like they’re faking, so it must be true”: WRONG! Being a cane user doesn’t immediately make you an expert on all different conditions and experiences. Your friend does not know the random cane user walking down the street, they are going off looks and stereotypes. Disabled people are not immune to being ableist.

“They enjoy their cane too much/they’re too happy/they decorate their cane, so they can’t actually be in enough pain to need a cane” WRONG! We’re people like everyone else, and we experience positive emotions too, even if we go through a lot of pain. To me, customizing my cane is like getting a tattoo or putting streaks in my hair, it’s a way of self expression. And we deserve to be able to talk openly about our full experience, which include the parts we’re neutral or happy about.

“They’re one of those cringey teenagers who name themselves arson and like dsmp, so they’re probably faking” WRONG! Do I even have to explain why saying someone isn’t disabled because of their name and interests is messed up and also stupid? Or did you already know that and just wanted to make fun of a disabled teenager?

“They’re too young to be using a cane, so they must be faking” WRONG! there are lots of disabilities or injuries that can cause young people to need a mobility aid. For example, I use a cane for my fibromyalgia.

“They only use it in private places, and never in places where people recognize them, so they must be faking” WRONG! In a world where anyone can just randomly take out their phone, take a picture of a cane user, and post them online to be made fun of, it can be stressful to use a cane in public areas. Also, they may not want people to ask questions, or they may feel embarrassed about it.

“I saw them switch hands, so they must be faking” WRONG! There are different reasons a cane used might do this, but I’m going to use my experience as an example. My fibromyalgia is not consistent. Sometimes one leg hurts more then the other. But as I said, fibromyalgia is inconsistent, and sometimes my other leg will start to hurt more or need more support, which is when I switch hands. And when both my legs hurt equally, I may switch my hand if it’s getting too sore.

“They told me they feel like they’re faking when they use their cane, doesn’t that mean they don’t really need it?” WRONG! Imposter syndrome is strong in a lot of disabled people, especially when for a lot of our lives we were told by doctors that we were fine and just being dramatic. Anxiety is also comorbid with a lot of physically disabilities, which only strengthens this. To add to this, something that I’ve felt and seen other disabled people talk about it, when their disability aid lessens the pain, they start thinking “well I’m not in that much pain so I don’t really need it” even though the reason they’re not in that much pain is because of the aid. I know it seems dumb, but imposter syndrome can be that strong and affects disabled people a lot.

“They don’t have a diagnosis, so they must be faking” WRONG! First of all, diagnoses are expensive. On their own they’re often already expensive, but counting the tons of tests you have to take to confirm the diagnosis? Absolutely ludicrous. Some may also choose not to get a diagnosis, so that they don’t have to deal with the prejudice and setbacks of being diagnosed. Also, some people use a cane for injuries, and for stress or fatigue related pains.

These are only a few of the things I commonly hear from fakeclaimers, and I wanted to just put out a reminder that fakeclaiming hurts the disabled community much, much more than it does ableists. Next time you see someone with a cane switch hands, or someone with a wheelchair stand up, or someone with crutches put them down, before you immediately call them out to a friend, take a picture, or write a post: does your fakeclaim rely on stereotypes? Are your reasons things that apply to ambulatory aid users?

If so, just stop. Be mindful. Please.

[mxmorbidmidnight]

You know those teachers who would have posters in their classrooms like “weird is a superpower” and “in a world where you can be anything, be kind” then would proceed to scream at a neurodivergent child until they cried.

[e-m-p-error]

You've written about Val being disabled, but how much does Vox know about it and is he protective of Val because of it?

In Reference To This

[ Vox ]

Vox knows that Valentino was hurt the day his antenna got stripped. He knows that he was aching and hurting for months after. It took a while before it was able to move freely again, and he remembers when Val recognized that it was going to scar. All of this was the physical pain that he was very aware of. He is also very aware that touching the stripped antenna really, really hurts, it's a very sensitive scar.

As far as the extent of Valentino's hearing loss, however, Vox isn't totally sure. He knows that Valentino complains of people talking on his left side because he can't hear them as well. He is completely deaf on that side, and Vox kind of understands that much, but he doesn't know how his hearing works now.

He is not aware of Valentino's tasting issues, though he is very acutely aware of how he smells. He likes to get his antenna right up in Vox's cologne and rubs his face in it whenever he smells it. It's the main/only reason Vox knows about this from Val and not just in theory.

Vox is most aware of Valentino's poor eyesight, and he monitors how it gets worse over time. He's working on solutions for it because he can't stand the thought of seeing Val go entirely blind. It is important to him to do what he can to help Val in the meantime.

Actually, yes. Vox is incredibly protective of Val, especially in a fight. He always makes sure that he's got Valentino's left side since he can't hear on that side and his sight is very poor. Val is a good shot despite his eyesight, but Vox knows there are still weak spots that can be exploited.

That said, he's still trying to figure out how to give Val his hearing back, but he's been playing with a few ideas that he hopes will help.

[swollenbabyfat]

On loop

[hexcii]

Silly TNG doodles based off of your guys’ tags :]]

Clearer version under the cut

[ochako-daily]

for my first proper ochako-daily post have this absurd togachako art i gave up on

[kipskiptrip]

Happy Disability Pride Month! This comic was never meant to be pretty or neat, but rather meant to tell my story with internalized ableism and dealing with medical trauma. It's a very personal story, and even making it was a tough decision, but I went through too much recovery not to do so.