#bcs im neurodivergent
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i really don’t understand the hate towards Becky cause like??? Imagine this, your best friend is always emotional drained and fucking bored and doesn’t want to do jack shit with you like??
Helloooo I’m sorry but if my friend was like that I would also be fucking pissed at her and still make out with MY BOYFRIEND who happen to have beaten up ur brother 😭 like fights happen all the time it’s no biggie, plus Charlie seemed like he didn’t give a fuck.
But tori had to turn around and word vomit all the shit she hate about her "best friend"..!?!? Like what!! Both Becky and tori were fucking assholes to each other and I’m glad they’re friendship fell apart for a while.
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#osemanverse#becky allen#tagging with#character hate#bcs im neurodivergent#aaand cant rlly understand the tone of this ask#(not ur fault anon#im just bad at reading tones)
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hey btw if you're in the USA at 2:20 p.m. ET on Wednesday, Oct. 4, they're testing the emergency broadcast system. your phone is probably going to make a really loud noise, even if it's on silent. there's a backup date on the 11th if they need to postpone it.
if you're not in a safe situation and have an extra phone, you should turn that phone completely off beforehand.
additionally, if you're like me, and are easily startled; i recommend treating it like a party. have a countdown or something. be surrounded by your loved ones. take the actions you personally need to take to make yourself safe.
i have already seen mockery towards any person who feels nervous about this. for the record, it completely, completely valid to have "emergency broadcast sounds" be an anxiety trigger. do not let other people make fun of you for that. emergency sounds are legitimately engineered to make us take action; those of us with high levels of anxiety and/or neurodivergence are already pre-disposed to have a Bad Time. sometimes it is best to acknowledge that the situation will be triggering for some, and to prepare for that; rather than just saying "well that's stupid, it's just a test."
"loud scary sound time" isn't like, my favorite thing, but we can at least try to prevent some additional anxiety by preparing for it. maybe get yourself a cake? noise cancelling headphones? the new hozier album? whatever helps. love u, hope you're okay. we are gonna ride it out together.
#watching ppl go from being like ''support neurodivergent ppl~~!"#to being like ''if this is going to give u a panic attack ur fuckken stupid''#like..... gets me#yeah man. i know im going to be triggered by it . in the old fashioned term. it is GOING to give me a panic attack. it's pretty much certai#and i shouldn't have to tell u about what i have survived for you to be okay with that.#you can just trust that i ALSO don't want me to react to it. i'm not gonna be having a FUN time.#dismissing that bc you think it's stupid.... like is the whole problem.#these sounds are workshopped by entire teams of people to get you to pay attention and move quickly.#they arent meant to be fun and exciting.#OBVIOUSLY it's gonna set ppl off.#but yeah there's something so fuckken demeaning about ppl being like. well that trigger isn't valid bc u haven't undergone X#dude i have ptsd bc i was abused as a child. like plain and simple. the fact im 30 and afraid of the dark tells you how bad it was.#i shouldn't have to ask u for permission to be mentally ill.#the reason it's a fucking disorder and not a fucking choice is that I DO NOT CONTROL IT.#like how is it any different from when ppl are like ''oh public speaking isn't that scary'' like FOR YOU#for YOU this isn't scary. now if i could fucking eat my own amygdala...
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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.)
#for this disability pride month burn an ableist person's house#that's what makes you a true disability ally trust#btw with nts i mean mostly abled nts but i didnt know how to word it ;w;#and before anyone says anything im just fine with people calling themselves neurospicy#what i have a problem with is when NTs use it as a way to invalidate neurodivergent people's struggles#or to infantilise nds#or both#autism#actually autistic#neurodivergent#neurodiversity#neurodiverse stuff#autistic#neurodivergency#autistic experiences#autistic things#actually autism#ableism#ableist language cw#tw ableist language#tw ableism#neurospicy (interlude)#disabled pride month#disability pride month#wrath month#(<-just tagging that bc it's accurate since im currently pretty pissed off)
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i wish i had a purpose in life and a supportive network of friends!!!!!!!!!!!!!!!!!!!!!!!!!!!
#to genuinely have that would change everything and im just letting go of the dream bc the more i think#about how impossible it is the more miserable i am and btw it is impossible for me i have tried#and tried and tried and tried and i am just too neurodivergent and broke to sustain relationships or goals in life. so yeah#it's truly miserable
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everyones all “oh lots of autistic ppl are picky eaters thats totally understandable!” until youre a “”food snob”” picky eater instead of a chicken nuggies picky eater
like sorry i love sushi and toast with nutritional yeast and tiramisu when your 5 year old cousin only eats chicken wings w ketchup its almost like autistic ppl arent a monolith 😐
#(tbc im not passing judgement on the ‘chicken nuggies’ autistics french fries are literally one of my safe foods)#actually autistic#autism#autistic#neurodivergent#actually neurodivergent#actuallyautistic#autihd#neurodivergence#autistic experiences#picky eater#ppl actually have called me a food snob before#mostly bc i don’t eat ketchup ever
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leave him alone he's on his period...
#sorry for filler i guess im working on multiple things tho :333#projecting my adhd onto the dr skellytons but anything goes#guess who got overstimulated so bad teo days ago (me)#star trek#leonard mccoy#star trek tos#tos#leonard bones mccoy#bones mccoy#star trek fanart#star trek meme#adhd#neurodivergent#leonard mccoy fanart#adhd memes#hes so grouchy bc he is five seconds away from going kaboom
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; finding out you're neurodivergent is just an " oh " drawn out and progressively getting louder the more you learn about your neurotype.
#neurodiverse#neurodivergent#nd#autistic#adhd#ocd#anxiety#depression#bpd#npd#bipolar#scizophrenia#uuuh im js trying to tag as many neurodivergent things I can think of ..#dyscalculia#dyslexia#dyspraxia#neurodivergency#actually neurodivergent#specifically I am the Fucking Neurodivergent Mess™ discounted combo meal that you're guaranteed to choke on && get food poisoning from#text post#discovering#neurotype#is that the right word bc i think it is but i also dunno
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ik the common agreement in neurodivergent circles seems to be that we all function better at night but here's to the ones who are on the opposite end of the spectrum. To the early birds who wake at 7 and can't stay up past 10pm. To the ones who are left out of almost every social event bc everything seems to be happening after 8 but you're normally in bed by that point. To the ones who are made fun of bc "only little kids go to bed that early". To the ones who, even if they wanted to, can never seem to find their place among others bc of society's expectation that the real fun only begins after midnight. I see you, I feel you, and I wish you a very same
#it's especially annoying bc everyone around me seems to believe#that THEY are the weird one/minority for going to sleep at 4am#when i have literally never. not once. met someone who went to bed at 10pm like me#as part of their natural sleep cycle#& ik i can't be mad at others bc you don't really pick your sleep cycle but like.#a lot of the time it feels like they aren't even trying to involve me#bc 'if i wanted to be involved i should have just stayed awake longer'#instead of like. starting shit earlier or idk#and then im the idiot for not being able to force myself to stay awake#neurodivergent#actually neurodivergent#adhd#actually adhd#autistic#autism#actually autistic
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tell me what the video Basically, I’m Gay means to you?
daniel howell why did you send this ask to every phannie tumblr account you could find .
#that was my funny answer#the serious answer: i stopped watching dnp at that point and only started again after BIG#and. i related to. A LOTTT of what Dan was putting out there in that video#funnily enough not because im bi but because im trans. like. the not fitting. the finding other queer label bc i couldn't accept what i-#-actually was#the constant fear. hard growing up feeling different. etc etc.#anyway#i think he's been watching a bit too much contrapoints b4 making it. but i rly loved it. in a strange way it was very comforting#and very reassuring#bc i was always drawn to dnp as a neurodivergent & queer person and was felt. for lack of better word.#stupid for it. or mocked.#and in BIG i had this. self recognition thru other moment yknow#own post#ask#dan and phil#daniel howell#phan#dnp#dip and pip
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every time i drink coffee i just get more eepy and sometimes i have the best sleep after drinking a cup.
pls tell me this is not an autism/neurodivergent thing
#im convinced everything weird w me is bcs of autism#im self diagnosing here#dsm-5 who?#actually autistic#autism#austism spectrum disorder#neurodivergent#how do i use tumblr#chronically online
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adhd/autism is when you're having suicidal thoughts but there is also hamilton soundtrack permanently playing in the background of your mind
#“or” bcs im undiagnosed and have bo idea what it is#don't take this too seriously#neurodivergent#neurodiversity#autism#adhd#audhd#adhd jokes#autism jokes
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also on ao3
(cw: tics, bullying)
Eddie started shivering in seventh grade.
Even when it was hot, even when he was sweating and desperately wanted a non-rattly fan or a better air conditioner. They weren't normal shivers. He wasn't cold. But his shoulders would jerk or shake, or he would tremble for a second, and he didn't know what else it could have been. Others didn't question it for a while, because it started in October. Everyone was shivering. But by March, it hadn't stopped, and he had to explain himself when people gave him questioning looks or asked if he was okay. (Back when people cared.)
'S just a shiver, I'm fine.
He wasn't fine. It got worse over time. He got used to it, to the weird feeling that took over his body for a few seconds, got used to telling people he was cold, joking that he must be low on vitamins or iron, joking that in the future, someone is walking over his grave. But other people didn't get used to it. They thought he was weird. That was fine with him. Wayne realised something was wrong before Eddie started the tenth grade, because he wasn't just shivering anymore. His whole body was jerking sharply, suddenly, his shoulders drawing up, fists clenching. Eddie didn't question it. Wayne did.
It wasn't normal. But nothing about Eddie was normal. Wayne took him to see a doctor. The doctor make him do things, walk in a line, hold his arms out and push the doctor's hands away as hard as he could, follow a flashlight with his eyes without moving his head. It was all weird. It kind of scared Eddie. The doctor kept writing things in a notebook, and Eddie couldn't tell if he was doing well or not. But Wayne was there, watching and listening intently.
The doctor said he had tics. It sounded funny to Eddie, but then it wasn't funny, because the doctor didn't give him anything for it. He just said there wasn't anything really wrong with him. His brain just worked a little differently. (Which Eddie was already used to hearing.) That his tics could get better or go away as he got older, or they could get worse.
They got worse.
By the end of that summer, his arms were moving, flying over his head suddenly, randomly, and his head was jerking back so sharply it hurt. Wayne was worried about him getting whiplash. Eddie was worried about going to school.
That year, he became the freak.
At first, he tried to explain it to people. The movements were involuntary, he couldn't control them. Wayne contacted all his teachers, who mostly got it, but still preferred to make him sit in the hallway so he didn't distract the class. But the other students thought he was possessed, faking it for attention, and everything in between. They'd throw things at him, and complain to the teachers that he was distracting even when he wasn't moving, just to get him out of the room. They would mimic him, make fun of him, and by September, he learned that the tics get worse when he's upset. He could hear them all snickering and giggling as he shoved his hands under his legs and tucked his chin to his chest or held his shirt over his face, as he held his limbs tense so they wouldn't move, so tense he was exhausted and sore all the time, and then he'd go home and cry because he couldn't control his own body.
He'd have to sit on the sofa so when his head threw itself back, it would hit the back of the sofa instead of the wall, and Wayne would just wait, watching with that fucking sadness in his eyes that made Eddie ache even more. When it finally stopped, sometimes after a few minutes, sometimes after an hour or two, he was so exhausted he'd fall asleep right there on the sofa. He couldn't do his homework. His grades dropped even more, but he managed to keep himself afloat. He did the best he could, doing his homework early in the morning before school or in detention. (Some of his teachers thought he was faking. Mr Peterson was in charge of detention, and he was nice. Considerate. Eddie counted him as one of his few blessings.)
His tics got worse.
In December of his junior year, he started making noises. Short screams, grunts, quiet vocalizations. It scared him. He didn't want to go back to school, but he did. The laughter around him got louder, and he was sent out to the hallways more. He started skipping classes. He knew he'd be forced to leave anyway. So he'd sit in the boys' room, on top of a lidded toiler, his feet up on the stall door, and he'd leave cigarette burns on the walls.
Not everyone was awful. Some kids were just curious about him, asked why he acted the way he did, and he did his best to calmly explain it all. I can't help it, actually. It's just my brain works different. That turned into Eddie's brain's fucked. It's broken. He's a fucking--
So he used it. Eddie the Freak. Attention-seeking, desperate for people to notice him. So he started making devil horns, yelling from tabletops, making himself The Freak so no one could use it against him.
No one, not even Wayne, saw him cry at night, because the attention he got was never the attention he wanted. Because he was tired. So fucking tired. His limbs were sore and his voice was rough, and his neck hurt, and he was sick of being laughed at. But that was all he got.
He kept counting his blessings. Mr Peterson, who never minded Eddie's noises or the way his fists would bang against the table loudly in the silent room, who scolded the other detention-goers when they tried to tease. The Hellfire guys, who got used to his tics fairly quickly, and knew when to pause whatever they were doing if Eddie couldn't hear them over a scream or was distracted by his own body. That nice girl, Chrissy Cunningham, who would slip notes from the classes he missed or skipped into his locker or backpack with sweet smiles. (If Eddie wasn't gay, he would have fallen in love with her.) The other few students that ignored him when his tics acted up, just glancing and moving on. Wayne, bless his soul, who would come to the school to confront Eddie's teachers and complain to the principal about Eddie being mistreated by the staff.
And, oddly enough, Steve Harrington.
Eddie never saw it coming. It was a particularly bad day. He was at his locker, trying to line his books up, but a tic threw his hands up, and some books fell from his locker to the floor. He watched helplessly as papers scattered across the floor, as most students stepped around them, ignoring them, as some jocks trampled over them, over Chrissy's neat handwriting, his fists clenched at his sides. When they passed, he kneeled, picking up the books, and when he looked up, Steve Harrington was kneeling too, gathering the crumpled papers and carefully straightening them out.
He gave them to Eddie with a smile, and Eddie thought he might be dying, in some weird, upside-down dimension where Steve Harrington smiles at Eddie Munson. Eddie took them hesitantly, said thank you, and then he hit him.
He was mortified, almost dropping the papers again, jumping back as his whole body flushed with heat, staring at Steve's shoulder where his hand had just landed heavily, and he burst with a Fuck, I'm so sorry, oh my god--
But Steve had just laughed. Amazingly, it was a kind laugh, with sparkling eyes, and soft cheeks, and he said It's okay.
And then he was gone. Down the hall, after his friends, and Eddie realised his hands were trembling.
Steve kept smiling at him. Even when his friends were making fun of Eddie's Satanic cult, and of the way he couldn't keep still, and of his sad, broken brain. Even when Eddie's brain made him flip Steve off across the cafeteria, Steve saw how Eddie pulled his hand down sharply, and Steve just... laughed. Eddie fell in love with his laugh. It was kind, and it made Eddie feel better, even when he wanted to cry.
Steve graduated the next year. But he didn't leave Eddie alone. Eddie couldn't stop thinking about him, and his kind laugh, and his pretty eyes, and then the sheep Eddie adopted told him all about how cool and brave Steve was, and Eddie fell harder without even seeing him.
The world went to shit. But Eddie got to see Steve again.
Steve was still kind, even though the world was ending, and even during serious discussions, plan-making, how-to-save-the-world conversations, Eddie's tics kept going. His body jerked and shivered, and his head threw back, and his fists hit his own chest and shoulders, and he had to sit down. And Eddie found out that there are more kind people than he thought. When his tics slowed, Nancy wordlessly got him an ice pack to hold to his chest, and when he flung it across the room, Robin caught it with a casual oops, and brought it back to him. No one questioned him, or stared, or laughed, even though he knew how annoying he was.
When he woke up in the hospital, he hurt so badly he couldn't move. He just cried. Steve sat by his bed and held onto his hand. He was crying too. When Eddie stopped crying, Steve carefully slid his rings, clean of blood, onto his fingers.
This one goes here, right?
Yeah.
On the second day, his brain didn't care that he hurt. As Steve was telling him about what was going on with the others (Max was staying with the Sinclairs, Dustin's leg was almost healed), Eddie's hand smacked him across the face sharply, the sting of his rings bringing tears to his eyes before he even processed what happened. Steve wordlessly crawled onto the bed, carefully pulled Eddie against himself, and set a pillow over Eddie's lap for when his fists started hitting his legs. He'd just murmured those words, the first words he'd said to Eddie years ago.
It's okay. It's okay.
And he waited until Eddie's body fell lax against him before he carefully found Eddie's hand, laced their fingers, and pressed a kiss to his forehead.
Eddie was released from the hospital a few weeks later. He stayed in the Wheelers' basement for a few days until Steve's parents left town, for good this time, and then he moved into the Harrington house.
He likes it there. Steve is still kind. Always. He lets Eddie lay his head in his lap when his body hurts or won't stop moving, and he drags his fingers through his hair or holds a joint to his lips for him, and he smiles. (Eddie would go through the end of the world all over again for that smile.) When Eddie's head hits the wall while they're in the waiting room of the hospital for a checkup, Steve just shifts to face him and holds a hand up to the back of his head so his hand hits the wall instead, saying quietly that Eddie isn't allowed to beat his record number of concussions. He drives Eddie to Wayne's even though Eddie doesn't tic when he drives except for a few facial or vocal ones.
When Eddie whistles one night, Steve just smiles at him and says Was that a tic or are you hitting on me? and Eddie freezes, his face burning. Which would you prefer, pretty boy?
Steve kisses him.
And then Steve starts holding his hand even when he isn't having tics, even when they're with the Party. Eddie moves into Steve's room. (They always slept better when they accidentally fell asleep on the sofa together anyway.) Steve holds him when his tics are bad, and Eddie holds him during his migraines, pressing kisses as softly as he can to his forehead and his temples. Steve takes his hand when it moves to hit Eddie's face or chest. Eddie stands steady and holds Steve's hand to himself when he gets dizzy. Steve keeps ready-made ice packs in the freezer to hold to Eddie's chest and legs when they bruise from his fists. Eddie keeps his handwriting as neat as possible when he writes notes in case Steve forgets anything. When they wake up at night, breathless and sweaty and crying, the other is there, arms open, lips waiting.
One night Eddie says very softly, You know, they used to say my brain was broken.
Steve just says, Mine too.
#welcome to projection central#hand wrote this during a lecture today bc i was bored and realised a lot of ppl write/hc eddie as autistic and w adhd#but usually those are the only kinda neurodivergencies i see in fan content#(pretend thats a word)#but then i thought eddie having tics would make sense for his character and i have Experience to write from so#(disclaimer i was not bullied in school nor was i removed from classes (unless i left on my accord bc i wanted to hide in the bathroom))#(some kids teased me or mimicked me or told me to 'do it again' but i dealt w them)#(and the one kid that was really a dick ended up being rly nice by the time we graduated he's cool)#(and i got lucky w my teachers i think they were all very sweet and considerate)#(but i thought this story would make sense and go along with eddies story in the canon)#anyway give eddie tics#anotther hc that his tics calm down/stop when he's playing guitar and playing d&d#mine arent as bad as they were in high school but back then (and on bad days now) they usually calm down#when im focused on something or doing something i enjoy (ie drawing or painting or st)#steddie#steddie oneshot#eddie munson#eddie munson oneshot#steve harrington#steve harrington one shot#stranger things#stranger things one shot
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i would talk about harry potter on here but no one agrees with my headcanons i fear
#rose rambling#mostly bc i hc like 90% of the main cast as poc - neurodivergent - etc#mixed/arabic harry potter.... black hermione.... dyslexic ron.... autistic luna lovegood + neville longbottom.... the list goes on...#they're also all queer in some way#i enjoy harry potter not in the canon way but in the fanon way#GOD does anyone want to hear my character analysis'#i could write an entire essay on why draco (a literal child!!) shouldve been redeemed instead of snape (incel nice guy)#like draco is actually such a nuanced character#hes not an innocent sweetheart hottie whos done no wrong (tiktok characterization) but he's not like. fucking. idk. satan#i think he deserved redemption is what im saying#more than snape anyway#im more of a marauders person too#SIRIUS BLACK I LOVE YOU SIRIUS BLACK#i love them all#hp is precious to me in a “ive been obsessed with it since my formative yesrs and it is a comfort pieve of media” way#also this has to be said#fuck dumbledore
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Tw for weight loss mention
The whole exercise will cure your disability thing is a fucking joke. Yes exercise is beneficial for your health, but only if you aren't already on shaky foundations. You need to be on a treatment plan that WORKS before going into the maintenance phase. You wouldn't do regular maintenance on a broken item, you'd work on getting it up and running first. And maybe it would even need specialized maintenance afterwards if it's especially fragile.
I have fibromyalgia and acute degenerative disc disease. My immune system attacks my nerves and discs in my spine are slowly calcifying and causing the bones to constrict and damage my nerves (i think thats how it works). I have days where it feels like my body is on fire from nerve pain and days where it feels like my spine is about to rip from my back. And days where I have both (like today!). I get numbness in my hands and feet. I have horrible migraines. I can no longer walk unaided more than maybe 5 minutes without severe pain. I have something wrong with my knees and hips but the doctors don't know what yet.
You'd think I live an obviously seditary lifestyle correct?
Hell no.
I walk aided on average 6 miles a day over difficult terrain OUTSIDE of regular activity almost everyday. My legs are muscular and strong. I get my heart rate up and a good sweat, like all the gym rats swear on. I am often doing physical labor such as weeding, digging, sample collecting, pruning trees etc.
I'm not saying this to make other disabled people feel bad or prove that they can do anything if they just tried harder. This is an extremely painful lifestyle I've chosen that takes a lot of lifestyle management AND BOUNDARIES to keep up with the work. I also have an extremely forgiving boss who is also physically disabled and knows what I'm going through (deciding between your passion and your health and having to do so each and every day) No one should ever be expected to do what I do. I'm not even sure if I should be doing this myself.
This is to prove that exercise? Has not cured me. My muscles are strong but still hurt as if they're broken and I have to take more breaks than my coworker. I am constantly getting out of breath and I flare up regularly if I'm not careful. I am in excellent physical condition outside of my disabilities. I go to different doctors several times a month to get checked out.
I previously went through a diet program and lost a lot of weight (basically starving myself and got off my depression meds which cause weight gain but are also the only ones that work) and guess what? That didn't do shit either!!! I still felt horrible!!! I've since gained back the weight anyway after switching to focusing on adding more nutrient dense foods than taking stuff away from my diet (also muscle weighs more than fat, and fat helps cushion my aching joints and spine).
The muscle doesn't do shit for my disabilities outside of maybe some stability. Exercising everyday doesn't make the pain go away. Without my medications and aids and nutrition plans and steroid injections and spinal adjustments and physical therapy (that takes my fibro and spine into account) and alternative work methods I WOULD NOT BE ABLE TO DO WHAT I DO. Exercise alone is like trying to make a car run with no oil. Yes it'll go but it'll get more and more damaged till it can't and will need its entire engine replaced!
And yet I see new doctors and they look at me and the first thing out of their mouths is do I exercise? I should try doing a little every day :) and then i fucking blow their minds when I tell them about my job. No longer can they use that fucking cop out on me. I've been through this rodeo. Ive tried their suggestions. If you are in pain and nothing is helping? Exercise ain't going to do SHIT. You need to get to a point where you can move without severe pain first (if that's even possible). Then and only then should you consider implementing regular exercise if you can. Also weight loss talk is a red flag and a cop out. They made me lose 50+ lbs before they would look into the reasons behind my pain. Weight loss did nothing for me and exacerbated my pain.
I am living proof that all that shit is a lie and a cop out. That is the point of this post. I cannot believe people with serious medical conditions are being forced to put their bodies through extreme duress just to be believed. You are not disabled because of laziness or because you sit a lot. Plenty of people live seditary lifestyles and do not live in constant excruciating pain (they may develop disabilities later in life due to this however, and should be doing preventative exercises to maintain their health)
Please, share my story with doctors. Use me as an example. I am proof that "exercise first treat later" does not work. I should not have had to wait years to have my pain validated. I'd rather hundreds of fakers get (what? A blood test? An MRI?) than one chronically ill person get told to try yoga and go away by a doctor.
#wrenfea.exe#doctors and nurses dont fucking clown on this post#anything you say needs to be backed up by sources with apa citation thrown in for good measure#this is my personal experience dont tell me im exaggerating or just havent tried hard enough#i will kick you with my horse legs and then go lie down for 4 hours#bedbound people i am sending you so much love and will probably be joining you in a few years#chronic disability#chronic pain#spoonie#fibromyalgia#disability#chronic illness#from the field#physically disabled#this also applies to neurodivergent and mentally ill people but pls don't derail#this is mainly about physical disabilities#you are welcome to make your own post and reference mine if you want @ me and ill reblog it#sometimes im like oh i cant be disabled bc i do all this stuff im a faker inflatrating the community#and then i have days like today where i cannot leave my bed#i am so pissed off that people with long covid and ME have to go through that fucking exercise rehabilitation program#that actively makes their mitochondria worse#you wouldnt start using a vase without fixing the cracks first#the water will spill out and the flower will die#degenerative disc disease
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i do think that despite being the squad's designated nerds, kon and bart struggle to watch lotr together because kon physically CANNOT stop infodumping through any of the movies (and of course they have to watch the extended editions only), but bart's like. you want me to sit in one place and watch one screen for 12 fucking hours. and on top of that you WON'T SHUT UP the ENTIRE TIME? i already can't focus on movies and you TALK THROUGH THE WHOLE THING? im going to fucking bite you--
#rimi talks#i like to hand bart my personal flavor of adhd as in ''it is physically painful to watch a movie--#--without mental preparation. stimulants. and something to fidget with''#in some cases someone talking through a thing can make it easier for me to watch it but in others im like broooo shut up 😭#bc sometimes i just can't get into a story or focus on it if someone keeps interrupting and i have to split my attention!!!#and i think handing that to bart. well it fits. movies make you sit in one place for a longass time and im not even a speedster#meanwhile kon gets neurodivergence brand ''this is one of my hyperfixations/special interests and if i don't tell you everything i know--#--about it ever at every single opportunity i WILL explode and die on the spot''. which. is also me during lotr marathons#not only will my friends know about the shaving cream used for the caradhras scenes.#they will know about the significance of celebrimbor and narvi's friendship when we see the gates of moria#and i WILL be talking balrog lore even after gandalf is already down the pit and we're in lothlórien#(obligatory break to quote ''a balrog of morgoth.'' ''what did you say?'' @ celeborn tho)#kon#bart
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Although it’s important that those of us in the aromantic community correct the assumption that ALL of us fit into the “cold emotionless aro” stereotype, it is just as important that we remember some aros do fit that stereotype, and that that’s okay. Some aros, especially neurodivergent aros, not only don’t love but also lack empathy, lack interest in close emotional bonds, don’t feel sadness/grief/anger/fear when they’re supposed to, have trouble expressing and/or feeling intense emotions, etc.
It’s very easy to fall into the trap of trying to justify our collective humanity and right to exist by attempting to distance ourselves from these individuals. However, in doing so, we not only harm many individual members of our community but also stifle the aro community as a whole. We are a community that relies heavily on dismantling the notion that certain feelings — namely romantic feelings — are a prerequisite for humanity. We cannot afford to undermine that goal by throwing “cold” and “scary” aros under the bus to make ourselves look more palatable. And even if we could afford to do so, it would not be worth it to gain societal approval of our identity at the expense of the actual people in our community.
#aro#aromantic#neurodivergent#this includes aros with personality disorders btw#i’m not sure how coherent this is bc im#very tired. but tbh idc. i think im just gonna throw it in my queue and hope for the best
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