#THIS IS ABOUT BEING DISABLED AND NOT BEING ABLE TO DO THE THINGS YOU USED TO BE ABLE TO
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I think the ttpd requests thing is so cute I love that album!!! could I request i can fix him x toji fushiguro or i loved you the way that you were x satoru gojo (THE ANGST)? ilysm
i loved you the way that you were x satoru gojo
**part of my tortured poets concert event
--
“what did he do today?”
at the sound of megumi’s voice, coupled with his footsteps getting menacingly louder as he tracks down the hall, you immediately slam the tattered cardboard box shut, haphazardly leaning over it in some misguided attempt to prevent him from seeing the insides.
it partially does the job. true to your attempt, you covering the box with the weight of your body prevents him from seeing the contents. but the sight of you leaning over the counter, hands outstretched in a position so unnatural, doesn’t do the job of preventing him from asking again. or even raising the question as to why you were being so secretive in the first place.
“what’s in the box?” megumi asks.
“your birthday present.” you state.
megumi narrows his eyes at you.
“my birthday isn’t for another two months.”
“never hurts to start getting gifts early! especially since december can be busy with the holidays and all.” you murmur.
megumi narrows his eyes at you, his signal to you that he won’t necessarily drop his question, that instead he’ll be more adamant on the fact that he deserves the answer, as you retreat your hold on the box.
“did you want to eat breakfast?” you ask.
“sure. then, we can talk about what’s in there. and whatever tantrum gojo sensei threw this morning.”
you glare at him.
“it’s not a tantrum. he’s just…having a difficult time adjusting. it’s hard.” you insist.
megumi rolls his eyes.
“well, we’ve all had a difficult time. it’s not just him.” he mutters, the tone in his voice searingly angry.
there’s natural symptoms that you can expect from the ordeal – of satoru being put back together, inches from death, of megumi having his body used as a puppet – that you anticipate. the ones that you can expect are easy to handle, because you know what they are. could anticipate before hand what they would be.
shock.
numbness.
a loss of regular life.
megumi doesn’t say anything for two weeks. sometimes it takes a good effort to get satoru to shower. the two of them are no longer particularly fond of eating.
what you don’t expect is the disability. because in the aftermath of the loss, shoko can only put so much of satoru back together. and while mostly everything is intact – his limbs, his legs, his heart – the six eyes and the limitless technique don’t return. and in ways you can’t understand, it takes too harsh of a toll.
he can barely walk straight, slamming into doors or hitting the side edge of the coffee table because he insists he couldn’t sense it spatially, whatever that meant. the loss of limitless means that most of the times, standing still feels like he’s drowning, not being able to manipulate the space around him leaves him debilitated to the point where you sometimes find him cowering in a corner.
rambling over and over again about how he’s unprotected, far too exposed out in the open.
shoko can’t fix the six eyes or the limitless. and as long as you’re all concerned, they won’t ever return.
and neither will the satoru gojo that you knew and loved.
his frustrations drive him to be angry, withdrawn, and closed off every time you see him. unable to even ask for help.
and the byproduct of it all is just as shocking. because satoru gojo’s newfound flagrance for life is something that drives megumi fushiguro insane.
“satoru threw away his entire sunglasses collection this morning.” you state.
megumi frowns.
“isn’t it worth like…thousands of dollars?” he asks.
you shrug.
“he’s just insisting that he has no need for them anymore, so what’s the point of keeping them around where they’re just taking up space?”
megumi sucks in his teeth.
“i see. so why’d you go dig them out of the trash? you should have saved yourself the trouble than typing to help him when he’s intent on…on acting so pathetic.” he asks.
“i didn’t dig them out of the trash.” you retort.
megumi narrows his eyes at you.
“the box smells. you kind of do too. and i could hear you from my window this morning rustling with the bins, it woke me up.” he states.
you frown, before opening up the box, and reaching in for the set of sunglasses right at the top. they’re simple frames, silver on the sides, dark black shades, but now there’s a deep crack in the lens on the right. you’re afraid if you push it too hard, it’ll shatter into tiny pieces. but you throw away the thought, extending them out to megumi.
“do you remember these?” you ask.
megumi takes the frames, holding them up to the light, as he inspects them. he gives you a halfhearted shake.
“satoru wore these at our wedding. and every anniversary after, he’s…worn them to the dinner that we have together. makes some dumb joke about how he’s seeing me for the first time all over again.”
megumi gives a nod, before gently placing the frames back in the palm of your hand. he lets his hand linger in yours for a little too long, something that you’ve come to understand is his way of comforting you in the aftermath, as you give him a nod in response.
“he’ll be mad if you keep them. might even yell at you.” he murmurs.
“well, i’ll cross that bridge when i get there.”
--
you cross that bridge four days later. there’s only so many places to hide things in the apartment. your original thought – that hiding them in the kitchen because satoru can’t cook – doesn’t fare well when he decides to come poking for scissors.
“y/n.”
“hm?”
satoru’s suddenly materialized at your side, enough for you to abandon the pie crust you’re failing to mold, with his eyes narrowed at you.
“what are these?” he asks.
he holds up the sunglasses in the space between the two of you as you feel the embarrassed warmth run to your cheeks, and slightly take a step back.
“your sunglasses.” you murmur.
“i can see that. my question is what are they still doing here?” he seethes.
you shrug.
“i just thought you might want to keep them. i was holding on to them for you.”
satoru glares at you.
“you know, when i make the effort of walking all the way out to throw something in the dumpster, i’m fairly certain i don’t want them anymore. they were where they belonged.”
“i know, i know, i just thought…”
satoru heaves an exasperated sigh.
“thought what? that i’d need to use them again? i won’t fucking need to, because i can see just fine without them.”
you bite down on your lip. and he makes no signs of relenting.
“okay, but..”
“what part of this is so hard for you to understand? i don’t need your fucking help or for you to hold on to shit for me because you think i’ll regret it later. i won’t. i’m just fine without you trying to walk around, waiting hand and foot on me, because you think i’m defective.”
you frown, reaching forward to cup the side of his face. the mere gesture makes him flinch, enough for him to put distance between the two of you this time, and it makes your heart sink immeasurably.
“i don’t think you’re defective. you’re still the same and i…i’m just trying to be there for you in whatever way i can.”
“then why do you look at me like that?” he whispers.
“like what?”
“everytime, i walk into a wall by accident or brush against the table, you wince. you wince because i can’t find my fucking bearings with every stupid thing you’ve put in this apartment, and it drives me fucking insane because i don’t even want to look at you anymore. i understand it’s difficult, that you loved me the way that i was, but i’m just not the fucking same and i can’t do anything about it. you don’t have to make me these dumbass pies or cakes or whatever the fuck you’re trying to do everyday to celebrate my progress or whatever. i don’t care for any of it, so just give it a rest.”
you frown, dropping your hands to your side, as you dust away the last of the spare flour that’s melded into your hands. you can tell that he’s watching you, maybe a little too keenly, as you untie the apron around your neck and set it on the counter.
“you’re right, you know.” you mumble.
“what?”
“i loved you the way that you were.”
satoru frowns.
“the person i loved never raised his voice at me like that.” you whisper.
you reach forward, for the sunglasses discarded on the counter, and look down at the crack. it’s gotten noticeably bigger, probably from how satoru was shaking it around in the air a few seconds prior, before you look back up at him.
“the person i loved dragged these sunglasses out of his collection because they’re the exact ones he was wearing when i married him. he’d put them on and tell me that he was seeing me again for the first time, even though that wasn’t really true. and deep down, he probably knew that i thought it was a little cheesy, stupid even, but did it anyway because it made me laugh.”
you shake your head.
“he’d never throw these away. i’m sorry that i’m not…not as broken up that you’ve lost your six eyes or your limitless and i don’t know how to help you. i’m sorry i want to bake things and celebrate or whatever…but i almost lost you. i watched shoko sew you back together for hours, sat there for days when you didn’t wake up, and i was…just thankful that i got to see you again. in whatever state that you were. i’m sorry that it’s something that i thought warranted celebration, that the mere fact that you have the opportunity to struggle instead of be…be six feet under the ground…is something that i delight in.”
you sigh, before setting them back down on the counter, the warm tears bubbling in your eyes.
“but, please. by all means, throw them away. suppose they mean nothing to you when they’re not attached to the six eyes, anyways.”
and on that note, you turn on your heel and leave.
--
when you return home after three hours, there’s an almost pungent smell in the kitchen, so strong that it makes your nose water. you’re almost positive that in your absence the two of them made some horrible attempt at fixing themselves food, and you make a mental note to rectify their mess later.
you make your way over to the balcony doors to clear the air, except for the fact that the sliding door is already open, that satoru’s sitting criss crossed on the floor with megumi at his side, looking at the view of the city below.
you lightly wrap your knuckles against the door, the two of them turning their heads ever so slightly, as you lightly step out into the cold air. you crouch down, placing a hand on megumi’s shoulder and squeezing hard.
“mind if i talk to gojo alone?” you ask.
he gives you a polite smile, returning your gesture by placing his hand on your shoulder, and giving you a nod. the two of you switch spots, as you criss cross into the warmth megumi’s left behind, and hike your legs to your chest.
“so, i just wanted to say that…” you start.
satoru wordlessly slides two boxes in front of you. they’re dark black, a sparkling silver logo embossed into the material, tied together with a white ribbon. you shoot him a glare, before picking up the first box.
it makes you nervous, testing the waters with a joke when they were so tense when you left, but you do it anyways.
“are you trying to bribe me, satoru gojo?” you ask.
satoru gives you a smile. you note that it’s been extremely long since you’ve seen one.
“would that work, princess?”
“well, i didn’t marry you for your looks, pumpkin.” you joke, reaching forward to pinch his cheeks.
satoru fakes hurt, dramatically pressing his hand to his chest, as you pull the ribbon off the box. the sunglasses, glistening in perfect shape and sans cracks, are sitting in the box.
“oh, satoru. you didn’t have to…”
“yes, i did. they’re my wife glasses.”
you smile, reaching into the box and pulling the glasses out, and lightly pulling them around satoru’s ears. satoru shakes your hands off, only because you’ve horribly aimed for his ears, and readjusts them before leaning closer.
“oh my goodness.” he murmurs.
“what?” you whisper.
satoru lifts his hands and places them on your cheeks, the touch warm, as he rubs circles into your cheeks.
“my wife is so pretty.”
you can’t help but grin, the warmth rushing to your cheeks.
“is that right?”
“so so pretty. and kind, and patient, and too good for me to begin with.” he responds.
you shake your head.
“not true. you…”
“very true.” he insists.
satoru drops his hands, fingers fast as he sets the sunglasses back in the open box, before interlocking his fingers in with yours. he’s looking down at your skin, tracing the callouses left behind on your palms.
“you know the worst part of losing the six eyes?” he whispers.
you shake your head.
“i could feel your cursed energy all the time. and now i can’t.”
he’s never told you that before.
“really? was my cursed energy hot?”
satoru rolls his eyes at you, an unmistakable smile on his face.
“unbelievable.”
he’s quiet again, fingers outlining one of the red gashes leftover from months prior in your skin.
“it was comforting. knowing you were around, all the time. that you were moving from the kitchen, or coming up the stairs, or…or sleeping. i’d reach for it sometimes, straining to feel it when you were far away in another classroom or something, whenever someone pissed me off. something to just calm me down.”
you smile.
“i’m still around. you might not be able to feel me…that way…but i’m still right here. all the time.”
satoru winces.
“kind of embarrassing, isn’t it?” he murmurs.
“what?”
“i’m sitting over here, reeling in the fact that i’ve lost…lost what you feel like to me, when you’re the one who actually had to live that.” he whispers.
you flip his hand over in yours, mimicking his motions by tracing circles into his hand instead.
“it was no big deal.” you joke.
satoru narrows his eyes at you.
“you thought i was dead, didn’t you?” he asks.
you nod.
“i didn’t just think it, satoru. you were dead. for a whole three hours, you were…no heartbeat. skin cold. the whole ten miles of…of dead people. i was sitting there thinking about how i was twenty-five years old and already a widow.” you respond.
satoru sighs.
“i’m still around too. and…still me in the ways that matter to you. you don’t need to follow me around like you’re worried i’m going to break. hell, i’m surely not as strong as i was before, but i’ve…i will put in efforts to safeguard myself so you won’t have to…cut your losses again.”
you smile.
“that would be appreciated, you know that?”
satoru gives you a wink, before lifting your fingers to press a kiss against your knuckles.
“it’s a deal, princess.”
“also…i hope you know i regretted what i said earlier. right after i said it. i’d love you in any iteration. two eyes, six eyes, eleven.”
satoru smiles, before closing the distance to press three featherlike kisses to your cheek. he retreats to slide the second box over to you, the one you left unopened, and places it in the palm of your hands. you slide the ribbon off just the same, pulling off the lid, to find what might possibly be the most unflattering glasses you’ve ever seen.
bright green, hexagon shaped, and comically small.
“well, that’s a choice.” you mumble.
“if your memory’s failing you, these are the sunglasses you picked out for me on our third or fourth date. pretty sure you were half joking, but…but it felt right to buy them now. rebuild my collection.”
“how much were they?”
satoru pinches his lips together in a line.
“well, i’d prefer to save myself from another lecture today, if that’s okay with you. ask me again tomorrow, princess.”
--
taglist: @7haze
#seeingivywrites!#tortured poets concert#satoru#satoru x you#satoru x reader#satoru x y/n#satoru fluff#satoru angst#satoru hurt comfort#satoru gojo#satoru gojo x you#satoru gojo x reader#satoru gojo x y/n#satoru gojo fluff#satoru gojo angst#satoru gojo hurt comfort#gojo#gojo x you#gojo x reader#gojo x y/n#gojo fluff#gojo angst#gojo hurt comfort#gojo satoru#gojo satoru x you#gojo satoru x reader#gojo satoru x y/n#gojo satoru fluff#gojo satoru angst#gojo satoru hurt comfort
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hi, I'm new to arcane and I've been going a bit nuts trying to figure out what viktor's disability might be so I can write him right. I'm also disabled in my right leg but I know for sure we don't have the same thing at all.
I've seen people say his back brace is for scoliosis, and you write him as having a disability that leads to that, so it sounds like you have a pretty specific thing in mind! Could you please tell me what you're thinking of, so I can do my research? Or is there a lore bible or something with all this info that I just haven't been able to find? Any help would be super appreciated, thank you
Hi anon!! I'm also new to Arcane (literally became a fan less than two months ago) so I feel like we're in the same boat!! Theorizing about this was a very fun part of brainstorming for my current project, so I'm using this as an excuse to infodump about that part of the process. This might be long. Sorry (not sorry) in advance!
I wanted to write a Viktor character study informed by his experiences with ableism and classism in Piltover (be the change you wish to see in the world, and all that), and I was particularly inspired by this post discussing the specifics of his disability. Obviously, that's the only canonical disability (beyond the terminal illness caused by exposure to the fissures) that Viktor has, but I got to speculating.
There are a lot of conditions caused by poverty, whether from lack of sunlight (obviously rampant in Zaun) or food deserts (also probably common) or other socioeconomic issues. I did some research into what some of these conditions were and assigned some of the most likely ones, given what we know in-universe about living conditions and Viktor's appearance/progression, to Viktor in my series. These additional (non-canonical) conditions are as follows:
Rickets (caused by a Vitamin D deficiency, can result in bowed legs as referenced in the post about his leg, as well as progressive scoliosis if acquired in childhood)
The progressive scoliosis, as caused by the rickets.
Calcium deficiency (coupled with the Vitamin D deficiency, this is a big yikes; also causes slightly yellowed teeth if acquired in childhood. Kind of went on vibe for this one)
Ehlers-Danlos Syndrome (This is genetic, not environmental. I thought the leg brace being multi-functional was fun, and earlier drafts of the project had a section in which baby Viktor makes temporary friends by showing off "party tricks" common to those with hypermobility.)
I hope this answers your question! As far as I know, there's no lore bible, just one post that inspired me and some of my own rudimentary research. If anyone else has any additional info they'd like to add, please do! I love dissecting my blorbos.
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okay, the comment about moral purity had nothing to do with the media, it had to do with the suggestion that not using the word cripple to describe house means you don't understand the themes. not using the word "cripple" also doesn't mean you are abled lmao.
so addressing house's use of the word specifically; i do not think he finds it empowering. he uses the word to separate himself from the reality of his disability, a pretty common avoidance tactic in the same way i might call myself retarded for something as opposed to directly engaging with cognitive disability. house has a very, very, very high level of internalized ableism. we can't address the way he refers to himself without first addressing that. does he identify with the word 'cripple', or disidentify with the word 'disabled'? those are not really the same.
also worth noting, we aren't discussing a disabled person's self-identification, we're discussing the words used by a disabled fictional character written largely by abled people. i feel that they engage very sincerely with the subject matter, but we are not changing the words a real person is using for themself. the discussion of why he does this is beyond just internal thought process.
in general, i agree that the conversation surrounding house's disability is way off the mark. i disagree that the purpose is to make it 'palatable for abled folks to discuss'; among other things the majority of people having these conversations on here ARE disabled. house is deeply humiliated by being disabled; the words he uses to describe it are worth scrutinizing. the word was also much less shocking to hear on tv at time of airing.
truly struggling to engage w/ House MD fans who refer to House as "disabled" rather than "crippled" when that's very clearly his chosen self identification bc if you can't comprehend the importance of this self ID then tbh I'm not sure you've fully grappled with the themes of the show. and like, the memes and the yaoi are fun, but the real themes of the show are why I like it so much!!!! speaking as a cripple with a bunch of shitty shitty medical experiences. it's important to me. are you paying attention?
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You don't wish your disability was worse or more visible, you wish your disability was taken seriously. Please stop confusing the two, I guarantee you would not get the support you need JUST by being more severe or more visible. Please listen to visibly disabled people when we tell you it isn't better on our side
#m/cc#mine#I tried extremely hard to word this nicely because I KNOW people don't mean bad and often even know there are unique challenges#and believe me I know the challenges of invisible disability too!!#I have invisible disabilities!#but as someone who has also been at least visibly 'off' since they were 10 I am SO SICK of invisible disabilities being hailed as like#a unique extra oppression that us lucky visibly disabled people don't have to deal with#there are challenges to invisible disabilities that visibly disabled people DON'T have to deal with!#but you need to understand that *the reverse is also true*#there are MASSIVE benefits to being able to lie about your disability for example#or not dealing with the overt ableism that comes with your disability being obvious to everyone#*I do not have the option to pretend I'm not disabled.* that is never an option I have#I walk weirdly. I use a mobility aid now. my speech and face are 'off.' I lean to one side#for a long time I wore sunglasses 24/7 and often didn't make sense. I sometimes can't speak or won't react to others#for the most part people will always know that at the very least something is wrong with me#and more obviously I have people telling me they'll pray for me; telling me I can't do things I'm already in the process of doing;#wanting to shake my hand to tell me I'm an inspiration for not killing myself; giving me dirty looks for existing in public#and yes. I'm aware that this is very much an in-community issue. I know the average abled person doesn't know invisible disabilities exist#that's why there's so much awareness happening for it#but as a visibly disabled person I get SO TIRED of constantly hearing 'I wish my disability was visible :'('#it's just 'I wish I had your disability!' but from other disabled people
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There's a disabled angel in good omens 🥺
#listen im only in episode two and i know there's some drama going down but im focusing on this lol#i love that not only do they show the angel using a wheelchair and being ambulatory#but they also visibly show them miracling innaccessibility issues so that they Can still use the chair#instead of just getting rid of the disability#part of my is conflicted bc im like... there's disabilities in heaven? and that makes Me sad bc my disability is hell and painful as fuck#But getting rid of disability in fantasy is eugenist crap and showing that god made a disabled angel is a net good thing#while it personally makes me sad to think if there was a heaven i could still be in pain all the time#not all disabilites are bad and need to be cured we're a wide spectrum and we've been fighting for disabled rep esp in fantasy for ages#it's objectively good my personal feelings about my own disability aside#part of me thinks it's cliche to say 'you were made perfect' bc they're an angel But it's not we literally havent had this type of rep lol#anyways it made me happy to see#and im so glad it's a power chair user that's ambulatory it's important for abled ppl to see that#anyways y'all keep your drama and spoilers off my post im not far in and im only talking about this shoo#oh also!! love the fantasy hover chair they use in heaven specifically too i wish we had that it kicks ass#p
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at some point in disability you stop wanting to "get better" and this is just really hard for able bodied people to understand for some reason
#i had an interaction with a doctor which prompted this#theyre almost certainly a quack but they promised they could find a cure for my eds#to be unequivocal no such thing exists eds is genetic and changing that is beyond the current limits of medicine in almost every case#i was there for regular blood testing and when they said this to me my response was pretty unenthusiastic#something like 'thats not really what im here for'#which was clearly completely baffling to the doctor#part of that has to do with the way doctors are really solution oriented but also#i dont really want to be 'cured'#its hard to explain but this is my body now and ive gotten used to it#what matters is my day to day quality of life not a return to 'normal'#in my eyes disability isnt a bad thing its a neutral one#the idea that im okay with being permanently disabled is intolerable to able bodied society#this doctor has a ton of pther red flags id like to separately post about but ive gone on long enough#to the person who sent me the ask about intersectionality bw transgender and disabled identity#i see you it just turns out a lot of research has been needed to answer you#a reply is coming tho#anyway#disability#salt baby talks#chronic illness#ehlers danlos syndrome#postural orthostatic tachycardia syndrome#ableism
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you are not happy about the state of it!
#THIS IS ABOUT BEING DISABLED AND NOT BEING ABLE TO DO THE THINGS YOU USED TO BE ABLE TO#BC I'M MAD ABOUT IT SO I GOTTA THROW A LIL FIT#what do you MEEEEAN i can't fixate on doing art anymore bc it causes an incredible amount of pain!!!#what do you MEAN i can't WRITE consistently anymore bc i have debilitating migraines nearly every single day!!!!!!#it is NOOOOOT fair and i'm MAD about it!!#okay i'm fine now (no i'm not) here is a shitty doodle of siffrin throwing a tantrum#paper craft#i dont wanna tag everything ARGH!!!!!!!!!#isat siffrin#there that's all u get
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thinking yet again about Saiki‘s’s final choice in the series being “I’d rather live with my powers than die without them” bc that is seriously the single best ending of a disability narrative I’ve seen. Fuck.
#The thing people don’t tell u about being physically disabled#Is that you’ll see the physically abled people in your life start to view you as something tragic#And while they rarely say it when it comes down to things#They think you’re better dead than disabled. That you’d be happier put out of your misery.#Even with stories involving disabled characters (If we’re anything beyond a background diversity shot which is… rare)#It’s about “curing” or “overcoming” your disability which is I guess a nice sentiment but most of us won’t ever do that#Saiki doesn’t do either of those things#He wants to be cured and briefly thinks he is but then it’s discovered that he Cant be cured bc his powers are part of the whole of him#He doesn’t ever overcome them either#He just puts his glasses back on and decides that if it means he can live another day then he’ll continue to deal with them#And his powers are progressive#And that’s a thing weighing on him but it’s never treated like a death sentence#It’s just something he has to and will deal with#And it sucks but what else is he gonna do#It’s just. Aughhhhh. Aaaaaauuuuughhhhhhhhh……..#This post was brought to u by a man grieving his own mobility#physically disabled#physical disability#saiki k
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If you mess with somebody's mobility/life-preserving aid and all you got was yelled at by the disabled person in question, just know you got off easy. Fucking with somebody's aid can easily become a matter of life-or-death, so you have to understand why somebody would "lash out" about that.
#disability#ableism#ableism tw#reminder that fucking with somebody's aid can easily be classified under physical assault (which is what it is)#still fuming about the time my dad talked about how other people would fuck with his CPAP machine since it *has* to be plugged in an outlet#like. do you understand that not having a CPAP machine can easily either severely negatively affect somebody or kill them..#like why would the thought even cross your mind to risk somebody's life or wellbeing like that#but like. it just kind of reminds me that people can be really thoughtless about what they do and cause and effect#like at this point it's self-defense in my eyes and if you're yelled at i don't have sympathy#i will understand if you thought you were being nice but that's where my understanding ends#this is why i like when people have huge patches/stickers on their aids that are like 'DO NOT TOUCH ME' or 'I WILL BITE IF YOU TOUCH ME'#just as examples. but like. yes you shouldn't need to put that there in the first place but it is iconic#it is in-your-face and direct and it reminds everybody around you that it is up to *them* to treat *you* as an equal to abled people#it is bleak though and i hate that people have the need to put them there in the first place#if i ever needed to use more visible or 'obtrusive' aids then i'd absolutely do the same thing though
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Okay so I've never really joined the whole "small talk" argument that's been happening increasingly over the last years because I tend to just not agree with anyone I see discuss it. Like no I dont think people who use it are evil or making things hard on purpose, I also dont think it makes them lesser, ... I Also dont think that someone who refuses to use it / cant use it is automatically worse and will not make friends.
Importantly i also dont think everyone can learn it. I should know because I spent multiple years with professionals trying to teach me how to have a conversation At All and I still am actually nowhere near what would be expected at my age group. (Most recent reports usually go something like "makes slight improvements in having a two sided conversation" - because I can say nothing, or I can ramble on and then not react to your answer. The rest? Struggle time, to this day, in every aspect) No matter how many intricate guides you write, if I fail at the basic concept of a conversational structure very frequently then I will not succeed at small talk either. And additionally I also genuinely can not tell what might be too personal for this other person.
A lot of these people who get upset when people say "I cant do small talk because I'm autistic and I cant learn it, I tried and failed" and go "of course you can!", just sort of like. Ignore that a lot of the developmental delay in conversation and / or (nonverbal) language never closes up for many of us, the way a lot of us generally never reach the developmental level of our peers (in some areas). and it's not because we have not seen enough complex flow charts or not practiced enough. when so many of us literally spend so much additional time of our youth sitting in front of whiteboards and workbooks and such, being explained over and over how to talk to someone at all. I am 22 and after years of explicit teaching I still have to ask for verbal confirmation and explanation of any nonverbal cues that I think were used by my conversational partner, but do not know what they mean. Which is pretty much all of them. And I probably miss a lot of them existing at all. You can scream "just practice until you can recognize the other persons little cues on if they want to deepen or end this" until you turn blue but it will not actually make me accomplish it if the fucking people who've been spending their whole life teaching it didnt make me figure it out. On account of, you know, the developmental delay.
Sure some people can learn! That's why they try to teach us after all! Cause it has been successful! But generally stop with this shit of "everyone can learn this you're just choosing not to!"
I will never be rude to someone for engaging in small talk, I will obviously fail at their attempts to engage me in some, which usually makes them stop trying (thank god). But I will not tolerate others talking shit about it that is uncalled for (implying malice from every user, making fun of people who seem to crave it, ...).
But I also do not care to learn it anymore at this point? It's no goal of mine. I have made multiple friends, most non autistic, without ever using small talk. Including in adulthood. We simply skipped that stage. We went from "hi!" "Hi!" Immediately to "heres when it went wrong in my life (humorous but still often dark / personal). Also these are my political opinions. Sure I want to hear about the girl you dated for years in excruciating detail. Let me retell you the plot of this old indie movie you will never watch for 20 minutes and why I enjoy it. Let's go to a concert together after talking slightly in depth like this twice". Is this the way that you creep everyone out in everyone's friendship acquisition theory I've been seeing? Sure! It's been working perfectly fine, enough of the times for me, though.
Will this work in like a work environment or something? Most likely not, which is why I generally plan to keep to myself. Does this mean I still confuse every stranger who approaches me trying to small talk? Sure. that's why I'm still fucking disabled. But I have created meaningful relationships as an adult without small talk. I have genuinely tried learning in many ways and failed. And I'm done apologizing for that, either you take me with my inability to small talk or you wont.
#actually autistic#autistic adult#autistic community#actually disabled#developmentally disabled#idk what to tag this at idek if i want to actually post this because ive seen people get so mad abt this stuff#also putting this in the tags because the post is already too long . no i dont think the concept of small talk is ableist#insisting to people that they are 100% able to learn it after they told you they can not? that is.#“if you cant do it then those long posts telling people how to get better at it dont apply!!” when will yall learn that if you make -#-overarching statements a la “hey random reader. yes you too! all of you! you can learn this thing!” then you are including disabled people#and us telling you that we are in fact incapable of this is a fairly normal reaction to being semi directly addressed#and all youd have to do is say “anyone who is not unable to do this for disability reasons. you can do this” and move on#instead of going “hey of course when i address everyone i dont actually address disabled people. silly. want everything to be about you”#like last time i checked i was part of everybody and excluding me of that because of disability does not pass the vibe check
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if i hear one more pro-ai take i fear i may start exploding people with my brain
#for legal reasons im not gonna explode anyone#but i am gonna be extremely pissed off#i think the thing that pisses me off the most about pro ai people is this sense of entitlement i see from a lot of people#like “oh well this person posted their art/writing/creativity online#so therefore the ai (and by extension me) is entitled to be able to use it”#like its not the same at all as looking at another creators work and getting inspired#or when youre learning how to shape your style#its just taking other people’s work and passing it off as your own#like i get it sometimes youre not as good as you want to be or the motivation isnt there and you just want your ideas out there NOW#but you know what you do then?#you. fucking. practice.#if you don’t care enough to put in the effort to actually make your ideas rather than stealing for other creatives?#then i dont care at all about what you “create”#(obviously im not shaming people for being unable to put in effort due to any multitude of reasons—such as disability lack of time etc)#but even then that doesnt mean you have to resort to stealing from other people#because thats what ai is. theft. simple as that.#generative ai just makes me so fucking angry#fuck ai#anti ai#anti ai art#stop ai#fuck ai art#down with ai#fuck ai everything#fuck ai writing#fuck ai all my homies hate ai
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every so often i will see a post from a leftist on this website that is so egregiously ableist that i remember that like. oh yeah the userbase of leftists on this website is violently anti-disabled people and will jump at any chance to demonize any of us for any reason. i just forget that fact because i'm extremely dedicated to curating my space
i'm paraphrasing here but i saw a post that said, "every time i see an American [disabled person] mention being scared about the election because they're afraid of losing their benefits i have to laugh. anybody who wants blood-soaked money from the US government deserves to starve" which. like. goodness that's a lot to unpack. i think we should burn the whole suitcase instead !
#i inserted [disabled person] because they used a fucking slur instead and i didn't want that in my post#like i feel like there should be room for disabled people like me whose lives literally entirely depend on accessing said >#> extremely limited benefits in conversations about whether voting in this election makes you complicit in genocide#which like! i do understand. i do. it's nauseating to think about what this shit ass country is doing. it's horrific. i do not blame anyone#> for not wanting to be a part of that. *and* i am also terrified for my own life because i remember the first time trump won it suddenly >#> became IMPOSSIBLE for ANYONE to get on benefits. EVER. and so many disabled ppl i know went to renew benefits theyd had for decades >#> just to be denied. one of whom was a below-the-neck paraplegic. he died because he lost those benefits!!! because trump won#i really do understand why people dont feel right voting for harris. or why they don't vote at all. i truly do. but holy shit i am so scare#and yes! i am aware that people in palestine and gaza are suffering so much worse. and i wish i could change that#but every single person in power in the US is pro-israel and eagerly drinking the anti-palestine kool-aid. no matter who wins >#> things will not change in that part of the world. and it is infuriating. when the revolution comes this will change. but it hasnt.#the revolution will not save me as a physically disabled person. it will not save any of us. we do not matter to leftists. i am sorry but >#> this is the one thing i have learned after being in leftist spaces for over 10 years. and posts like the one i mentioned prove it#so i am very sorry. i really am. for being physically disabled. but i cannot survive another 4 years relying on my parents for everything#if trump wins i will be killing myself. this is a promise. i cannot do that again#i know it makes me a bad person to be afraid that harris will lose. but people on the left already think i'm a bad person for being disable#i want the genocide to stop. i absolutely do. i also want to survive. i am terrified that the US leftists will sacrifice disabled people#like me so they can feel good about being put in a real life trolley situation#again. im sorry. im so fucking sorry. i wish i was a better person. i wish i was able to give more. i know that if i was just a good#person i would be able to have a job and give to every palestinian gofundme on my dash. i would be able to do more than my daily clicks >#> and reaching out and calling representatives that don't care. if i was a good person i would be able to convince my parents that z*onism>#is deeply fucking racist. and that israel is wildly racist and killing palestinians for fun. if i was a good person i would be able to make#>them leftists too. im sorry. im sorry. im sorry im not good enough. im sorry that im scared. im so scared and it's not right for me to be#when so much worse is going on because of this countrys bloodlust. im sorry that im benefiting from being born here i dont want to be#im sorry for not having any other options. if i was a good person i know i would have them. im sorry. god im sorry im so fucking sorry
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i don't think i'll ever get over how people treat kids that aren't good in school as worthless no matter what. "oh it can't be that bad" my guy idk how to tell you this but the last time i went to a normal high school the principal called me into his office to brag about how he failed me in all of my classes before the semester was even finished & i should quit while i'm ahead cuz i'm too stupid ("officially" diagnosed as such by a school counselor & a psychiatrist!!) to succeed. & this is considered normal
#''poor teachers!!'' yeah well at least they can fucking quit & go work somewhere else#''okay but times are different than when you went to school in the 1970's'' this was 2016 my guy. shut the fuck up#''well maybe you were a violent & severely misbehaving kid!'' i wasn't. i have ADHD & severe anxiety disorder & depression#my biggest crime was being too exhausted & dopamine deprived to do my homework#my dad talks about how he was treated in school & i'm like damn dude i went through the same exact shit#how is it that a majority of teachers & principals are still abusive power-tripping pieces of shit 60 years later#why haven't things changed#well actually the answer is simple & it's because they want disabled people to disappear#& if abled students that simply disagree with the way things are done get caught in the crossfire then that is acceptable#because anyone not fit to make billionaires a billion more dollars should just die!#anyways here are my original tags from that gravity falls post i just reblogged:#I know this is supposed to be an appreciation post but like. ''for being the ''dumb one'' he's surprisingly rational.'' seriously??#as ''the dumb'' but ''surprisingly rational'' one of my family this is THEE biggest misunderstanding & it drives me up the fucking wall#just because a person struggles in one area doesn't mean they're stupid & should be an irrational dumb dumb idiot baby holy fuckkk#sorry to OP but even when people try to ''appreciate'' stuff like this they can't help but throw in insults#simply because they genuinely believe that ''even though you're stupid you SURPRISINGLY act competent sometimes'' is a compliment#I'm less mad about this & more sad that this kind of shit is still so prevalent in 2024#both Stanley & Stanford are smart & competent & rational#they just show it in different ways & exceed in different (sometimes overlapping) subjects#this is normal for human beings but the big societal scam is that if you don't do it in the way Ford does then you're stupid & a failure#& being surprised that Stan is also smart & competent in his own ways is the biggest sing that you fucking fell for it dude#btw before i get @ ed for this. i WAS that kid#i was so much that kid the school actually diagnosed me with stupid & spiteful & i was told to quit while i was ahead (they failed me befor#obviously this is very personal for me but also i don't think people realize the language they use is on purpose & it's used specifically t#& it's still happening right now & that just. makes me wanna cry honestly#like why are people still surprised that people can specialize in something despite bad grades in school#you know. the thing we all know is literally rigged to either put you in jail or in a factory to make billionaires more money.#man sorry for the rant the original spirit of the post is super correct but like fuck HS grade-centric judging of people's entire character#Stan being able to defeat Bill is just not at all surprising if you were him or knew/know someone like him#or really paid any attention at all to the show while watching it
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When it comes to hygiene tasks and self care with disability and chronic illness, its pretty much a constant case of: don't let perfect be the enemy of the good.
Basically: it's better to do something, than to do nothing at all.
TLDR: Just because you can't do something "properly" doesn't mean you shouldn't do it at all. Do it half-way. Do it shitty. Do it barely. Do it on a technicality. But do what you can. Just try, because doing something will help you.
If you don't have the energy to scrub your body with a sponge, just rub soap over your skin with your hands.
If you don't have the energy to wash your whole body with soap, just hit the places where sweat accumulates, or where you're smelliest.
If you don't have the energy to wash with soap AT ALL, just sitting in water is better than nothing. It will wash away dirt and oils.
If you can't bathe or shower at all, a warm wash cloth is your new best friend. If that's too much, then try bath wipes. They're a bit bigger than regular wet wipes, and a bit more heavy duty. They're designed to help keep bed ridden patients clean in hospitals.
If you don't have the energy to dry yourself after a bath or a shower, just put on a bathrobe and get into bed. If you don't have the energy to get dressed afterwards, just don't. It can wait until you can.
If you don't have energy to brush your teeth for two minutes, honestly, just a cursory scrub is better than not doing anything.
If you can't brush your teeth twice a day, brush in the evenings. It will help take away the build up of food from the day.
If you don't have the energy to brush AT ALL, honestly, just take a cloth and wipe the plaque off your teeth. Rinse with mouth wash after if you'd like. Something is always better than nothing.
If you can't floss twice a day. Try once. If that's too much, try a few times a week. If that's too much, try setting aside a day once a week as a goal. If you can't keep a schedule, do it when you're able to. Hell, I keep some floss next to my bed so that if I forget and don't have the energy to go get it, I can just reach over.
If you can't iron your clothes, don't bother. Wrinkles are fine. Wear jumpers over wrinkly t-shirts. No one will know, and honestly, most people won't even care. If it's really wrinkly and it's A Big Deal And It Needs To Be Ironed, here's my life hack. Step 1: take a spray bottle, and spritz the item of clothing (while you're wearing it is easiest) until it's lightly damp. Step 2: use a hair-dryer on the clothes until they're dry. It gets rid of creases like nobody's business, it's easier than lugging out the iron and ironing board, and you get to have nice toasty warm clothes afterwards.
If you can't fold your clothes, try just hanging them up. It's less commitment. It's quicker to do. Granted, you need to have the space in order to do this, but it is also good at helping you downsize, and lets you visualise exactly what you have.
If you can't put your clothes away, invest in a couple of laundry baskets, and then just keep your clean clothes in the baskets. You can then separate washed clothes into underwear, pants, and shirts baskets. You can just leave them like that. I'm giving you permission to never fold your laundry again if you can't. Just leave it unfolded. Who's going to care? Something is better than nothing. If you can, try to put those baskets into your closet so that you can keep the clutter out of sight, and give yourself a more restful environment.
If you can't separate your clothing out into different categories and wash them "properly" (whites, warm tones, cool tones, darks, delicates / switching between hot & cold washes / paying attention to laundry instructions on the label) then just don't worry about it. If you cold wash your clothes, colours won't bleed. Maybe gradually over the course of dozens of washes there'll be some changes in hue, but it's really not as high stakes as the One Red Sock In The Whites Turns Them Pink trope makes it out to be.
I've pretty much come to the point in my life where if a piece of clothing can't survive the washer and dryer, then it's just not meant to be. I colour separate my clothes, and if I have the energy/remember I'll take my bras and jumpers out of the washing machine to drip dry. But otherwise, I leave it to the universe.
If you can't separate out your recycling, then don't. If you have a large amount of rubbish you need to get rid of but the idea of separating it out properly is stopping you from doing so, then just don't worry about it. I know it's not ideal, but if you have garbage in your room/house and you need to get rid of it, please just get rid of it. Don't let the problem get bigger and harder to deal with. Don't let "doing something properly" get in the way of keeping your living spaces clean. Please. Give yourself understanding.
If you can't wash your dishes, get paper plates. Obviously, it's not ideal, but it is better that you eat food than skipping meals. It is better that you have a clean kitchen, rather than having dishes piling up and making it harder to look after yourself.
If you can't prepare meals for yourself keep making the tasks easier and easier. If you can't do recipes, then simplify. Use pasta sauce from the jar instead of making it. Eat canned soup. Buy food you can just stick in the oven. If you eat fish fingers and microwave veggies every night, it's better than not eating anything at all. It's better than having to fork out money on take-out. If you need ready-made meals, then get them. If you're literally just eating a raw cauliflower for dinner; 1) I see you, 2) me too, sis, 3) something is better than nothing.
These are the basic things you need to do every day to function as a person. They are your activities of daily living. Brushing your teeth. Bathing or showering. Using the bathroom. Getting dressed. Eating. Drinking. Sleeping. Keeping your environment clean. You don't need to do these things perfectly, but they need to happen in order for you to have a decent quality of life.
And it breaks my heart, because I know that so many disabled people can't do these things every day. I'm not saying this to guilt or judge, I'm saying that these are basic needs; you deserve these things. These things bring dignity. If a disabled person is unable to do these things, it diminishes their quality of life. It robs them of dignity.
If you need help to do these things, Its okay to ask for help. It's okay to need help. But if you can't get that help and you have to do these things by yourself -- or you just plain want to be independent and do it without help-- then don't hold yourself to standards you can't meet.
Don't let perfect be the enemy of the good. Doing something is always better than doing nothing. Even if it's not perfect. Even if it's not done well. Do what you can.
#lord knows that im still trying to pull myself out of the muck and into independence and dignity#i had to set a rule for myself that i need to wear clean clothes every day. and that i need to wear pyjamas to bed#that one's been hard. sometimes I dont have the energy to do it and i just stay in the same clothes for two days at a time#or i go to sleep in what i was wearing. but when i do follow that rule my quality of life is drastically better#not feeling dirty or gross goes a long way to making you feel more like a person#i also made a rule that im not allowing myself to look frumpy outside anymore. that means clothes that look nice#no more trackies and pj pants and all that stuff. i basically lived in perpetual pyjamas for four years and im over it#i still dress comfortably but the important thing is that i dress. i look put together. i wear things that make me happy#(and i didnt need to buy anything to do so. i just needed to start taking better care of myself)#and i stopped letting perfect be the enemy of the good. i started doing things shitty rather than not doing it at all#and the more i keep pushing with my ADLs the better i feel#what helps is now i dont have to contend with stairs and that has made a dramatic change to what im able to accomplish#ive also finally built up enough strength in my body that im able to go to the shops by myself. so i can buy things to make easy meals#and mum doesnt mind if i just put some things in the oven or air fryer for us for dinner.#i still cant really cook. i felt bad about that for the longest time. i didnt even try bc i knew what id make would be disappointing#or it wouldnt be up to the standards of what everyone else was making. i was so sick of feeling like a let down all the time.#now i just make what i can and my mum doesnt complain bc shes in the same boat.#and yeah. having help would be nice. it would mean id be able to do more than what i can do by myself.#and its great to see how far ive come. but im not a burden. and when i have the accommodations i need i can do a lot more#i do something rather than nothing and my life has dramatically changed since then. ive just gotten better and better.#chronic illness#disability#chronic pain#spoonie#one things for certain and thats that im never going to let myself rely on anyone else ever again.#i never want to be on the other side of that ever again. I don't want to be anyone's burden. i dont want that hanging over me#i do things by myself or i dont do them at all. and god fucking willing i'll never go back to needing as much help as i used to#i really didnt realise just how much of an obstacle living with stairs was in my life. it was the biggest barrier against everything#stairs stopped me from being independent. if i couldnt traverse them i just didnt go anywhere. my world shrank so much#and not having the proper wheelchair shrinks my world even more. im stronger than i used to be but im still severely limited in where i go
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When a bad day at the end of a few bad weeks turns into being terrified you’re getting worse and terrified you’re never getting better
#vent#<?#I’m not doing too hot if you couldn’t tell#disabled#tourettes#mobility aid#when not being able to decide which leg feels worse right now turns into using both canes at once and then spiraling slightly over the#implications of that#I swear I’m normally positive about these kinds of things but the last few weeks have just been hell and the thought of becoming more disabl#disabled than I already am is terrifying to me#as much as I’m usually normal about this. I don’t want things to get worse. I don’t want to have to face the possibility of the things I lov#love being taken away from me because my body has decided it can’t or won’t handle them#I’m so tired.#edit: this is ok to rb btw
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#sometimes i think I'm finally immune to being hurt by the ableism and other bs that gets thrown around constantly#like ''at least you get to be home'' and ''wow i wish i could stay home in my pajamas and laze the days away in bed''#because once the first lockdown happened and some lucky fucks got put on remote work#they couldn't shut up online about being prisoners and all that#almost as if not being able to go out and do what they want to do is. idk. NOT fun#and then when they started getting sick they were complaining about how horrible it was to not have the energy to get out of bed some days#and then later how horrible it was to not be able to do things they used to do (working out or even just walking through their house easily)#and then how doctors weren't taking them and their symptoms seriously and how unfair that is etc etc etc#because THEY are different from disabled people who are just lazy and don't want to be productive members of society 😌 (sarcasm)#so I'll think I'm over it all and it usually doesn't bother me (except the incandescent rage it causes)#but then something like that will come from someone i never expected and it's a struggle to not. like. burst into tears 🙄
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