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#disabilties
justsomerandomgay · 2 days
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i remember being ten years old and wishing to die rather than experience the pain i was in yet still my parents and my doctors didn’t believe me. sometimes it just hits me. that wasn’t a normal experience for a ten year old, was it?
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loonarmuunar · 1 day
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Robot disabilities. Robot who charges slowly and loses power incredibly fast and is always tired. Robot with malfunctioning lenses and can’t process visual information properly. Robot that can’t process anything too large and at a fast rate or else they’ll shut down. Robot with limbs screwed on too loose/just can’t attach correctly, so if they’re not careful they fall out. Robot disabilities,,,
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cyborgqueenkelly · 2 days
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The first message was a voice mail left by police after the first of FOUR swatting attempts by #yellowjackets fans who have harassed me and put me in danger for speaking out about ableism. The second image shows me saying in code so as to not trigger anyone “So sick of waiting around to die” - because I can’t get treatment and everything keeps getting taken from me. The person responded in code “Then do it”. The others are just some recent hate messages I got, except for the last one. The last one is a direct response to my public posts about ableism, and their ego getting bruised because they tried to make an ableism issue all about them. This is silencing disabled people. No one is messaging anyone in an unsafe way. This is about PUBLIC posts. But as you see, they don’t consider ableism a real issue. They’re expressing hurt feelings from disabled people telling them they’re being ableist.
I found out 2 people who worked to gain my trust and were enthusiastically messaging me lied to people, telling them that I messaged them inappropriately. I can’t trust ANYONE.
Let it also be known that the false story keeps changing. First I was messaging minors inappropriately; then I guess that wasn’t believable enough so they changed it to inappropriate messages in general. Now it’s literally, “How dare you respond to someone’s message”. Anything to get the focus off of their ableism.
I have been terrified for 2 days that I or my dogs are gonna get shot by one of the armed men that keep showing up at my place. All of this happened because people refuse to speak up. They’ll gladly watch me die first. I had to go on Lithium as a sui**** preventative in response to this.
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dilemma-danger · 7 hours
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this‼️
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mrs-snape5984 · 9 hours
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“Oh, breathe, just breathe…”
“'Cause you can't jump the track, we're like cars on a cable. And life's like an hourglass glued to the table. No one can find the rewind button, girl. So cradle your head in your hands and breathe, just breathe…” (“Breathe (2AM)” by Anna Nalick)
Sometimes, you just have to accept, that there are things, that can’t be changed or fixed anymore…at least not right now. I guess, I’m more and more coming to terms with this insight, considering the fact, that it just doesn’t make sense to wrap my head around the reason for my disease ME/CFS.
I can’t alter my previous decisions. For the past two years, I’ve blamed myself for catching Covid on an Open Air concert of my German favourite punk rock band “Die Ärzte”…especially viewed in the context that I avoided social gatherings since late 2019 because of my medicinal immune suppression. But when I got these tickets as a gift in 2022, my brain must have shut down and I started to belittle the potential risks of catching the virus by telling myself, that I would stand in the back of the crowd, beneath the open sky. This was also the first occasion, when I didn’t wear my mask…after enduring being bullied and mocked for wearing masks everywhere and rejecting every single invitation to parties and simple get-togethers.
Well…only one week later, my life- as I knew it before - came to an abrupt halt. I don’t want to go into detail about my current situation in this post. Whoever knows me and also my prior posts, is probably already fed up with my complaints about ME/CFS and its results for my life.
So, all I can do now, is to breathe. Deliberately slowly…breathing in…and breathing out. Calming my nerves…soothing my troubled mind with my fantasies of Severus and my absolutely self-inserted OC Jules…
I’ve commissioned someone new for this project. Someone different from all those lovely artists of Snapedom, who I usually contacted for my usual coping mechanism of commissioning artworks of Sevy and Jules.
This time, I reached out to @pinklovecharm, an incredibly kind and understanding artist, who made me speechless with this drawing. I asked her to help my imagination of Severus and Jules, being on a walk in the forest, come to life.
I can’t tell you, how much I’m missing this simple activity of enjoying the autumn sunshine and some fresh air on a walk in the woods. In my fantasy, Severus would apparate us to a secluded path in the middle of the forest, wrapping his arm around my waist to support my steps. We wouldn’t talk much…but Severus would remind me of the importance of breathing…and he would exercise it with me…patiently waiting for me to eventually calm down. He’s my safe haven…my home.
My dear Sadie, you can’t imagine, how much you soothed my soul with your mesmerising art and your kind-heartedness. You really achieved to put me into my OC Jules…with all her emotions and physical attributes….and you even integrated my cane into your drawing! Normally, I don’t show my reference pictures publicly, but I’m too impressed by your dedication to the details of my appearance, that I can’t stop myself from presenting them here. Thank you for everything, you wonderful person! I hope, we’ll stay in touch and that I may commission you again.
🖤Severus & Julia🖤
🖤Sevy and Jules🖤
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4rk-in-the-road · 3 months
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I think the reason a lot of leftists struggle with disability justice is that they haven't moved past the concept that discrimination isn't bad because it's objectively "wrong." yes, sexists are objectively wrong when they try to claim women are dumber than men. yes, antisemites are objectively wrong that jewish people are inherently greedy and run the state. yes, racists are wrong when they try to claim that white people are the superior race. and so on.
but then with disabled people, there are a lot of objective truths to the discrimination we face. people with IDs/LDs do fall behind and struggle with certain concepts. physically disabled people are often weaker and less capable of performing demanding tasks than able bodied people. many of us with mental illnesses are more reckless and less responsible. a lot of us are dependent on others and do not contribute much "worth".
and guess what? disabled people still deserve a place in the world. disabled people still deserve the supports they need. because they are people, and that should be enough to support them and believe they deserve a place at the table.
if your only rebuttal against discrimination is its objective inaccuracies, you are meeting bigots where they are at. you are validating the very concept that if and when people are truly incapable of being equal to the majority, that means they are worth less. this causes some leftists to then try to deny the objective realities of disabled people and/or become ableist themselves.
your rallying behind marginalized groups should start and end with the fact that people are completely worthy of life and equity, because they are fellow human beings and that should, frankly, be enough.
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sunnywalnut · 7 months
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Local PSA: invisible disability does NOT mean you can live your life like a "normal person" invisible disability meant that if a stranger looks at you in public they wouldn't know what's going on.
Like if a wheelchair user were to decide to run into a corner store to grab a candy bar because they know that their legs can last that long without, the cashier wouldn't know.
Or someone with "mild" scoliosis walking upright through their shoulder leans slightly to the left. Maybe they just have bad posture. The lady in the next isle thinks to herself.
The person with EDS or POTS or whatever sort of condition wearing compression gloves out and about. Perhaps it's a fashion statement?
Or what about the people with intestinal issues? They can look like "normal people" too.
You never know what someone is going through.
You never know what they might need to survive or if they're on the edge of a flare up or even if they are currently going through one just by one look.
I think both disabled and non disabled need to realize this. You're not "no longer disabled" because you can "live without" disability aids. They're there to help you. To make your life easier. If living without a cane is going to make it more likely you'll fall over and hurt yourself, use the cane.
If you need to sit down to do dishes or cut vegetables because you need to save your legs for taking out the trash, sit down.
If you need a shower chair because you don't know if you'll pass out, use the shower chair.
People are going to judge you regardless for multiple reasons out of your control.
I'd rather they judge you while you're being safe.
You don't need to struggle to be "normal."
You can just be you.
However that looks for you.
Use your disability aids.
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manyminded · 11 months
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shout out to “gross” disabled people.
people who can’t shower/bathe people who can’t shave people who can’t wash their clothes people who need help going to the bathroom people who have nasty habits (biting nails, picking nose, etc) people who can’t brush their teeth people who can’t go to the doctor people who can’t clean their room people who can’t make their beds people who vomit a lot people who wet the bed people who constantly have diarrhea people who’s physical deformities are seen as repulsive
and every other kind of person I missed that deserves to be here too.
you are people, first and foremost. your thoughts deserve to be heard, discussed, acknowledged, no matter what. you are not lesser. you are just another person. you should never be ignored for what you can/can’t do. you deserve care.
to abled people: check yourself. make sure you listen. and you can reblog, just don’t derail. maybe don’t add on, either.
EDIT: reblog this version instead, please.
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deulalune · 4 months
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Bisan brings up an excellent point about disabled Palestinians. Palestinian liberation is a climate, racism all problems. It is everyone’s business.
Video transcription (includes sign language part):
[Text says "People with disabilities in the Bombing"]
Bisan: Hey everyone. Have you ever thought about the people with disabilities in Gaza? I mean those people with disability in the hearing. How can they hear the bombings and just escape? Those who cannot move, those who cannot see the road in front of them, how can they escape? How can they just survive this? Okay, so during the past few days, I've been hearing more and more stories. One of them was on X (Twitter) and a girl was talking about an old woman. She was blind and she was killed during a bombing on the neighbourhood that they're living in. And another friend yesterday --he's deaf-- and he was talking about those people who were killed. Some of his neighbours were killed because they did not hear the soldiers, the Israeli soldiers, warning them. So, yeah. No one is safe in Gaza. You can just see the video of this friend, and I'll be translating his signs.
[Video cuts to a man speaking in sign language.]
Hello everyone. Hope you're doing well. I know people from the deaf community. They were displaced at to Khaleefa school in Jabalia - North of Gaza. They were three - and they were all killed! The Israeli soldiers told them to stop while they were escaping! But they didn't hear, so they shot and killed them! [Man shows his phone with a picture of the three boys in it on the right.
There's arabic text on the left that translates to
"The deaf martyrs, may God have mercy on them,
Lord of Paradise
(translated with Google
Translate) and below the text is a bia
emoii.
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a-sassy-bench · 5 months
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do able-bodied people not understand that if disabled people call out of work every time they don't feel good that we would call out of work every fucking day?
like honestly. what do you think being disabled means?
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fallenstarcat · 17 days
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sometimes i feel like people forget autism is a disability. and that’s not a bad thing! i’m all for disability acceptance, im proud of my disabilities. but i feel like we forget autism can hurt.
it hurts that i have to put more time and energy into socializing than others.
it hurts when i need to move so bad, usually cause im overwhelmed by either my surroundings or emotions, that i thrash and hurt myself.
it hurts that i cant be in places that are too loud or too bright, which on bad days can be as simple as a small, quiet noise or dim lights.
it hurts that i struggle to tell when im hungry, thirsty, tired, etc. so i can’t properly take care of myself. it doesn’t help my insomnia and i get very nauseas and get UTIs.
i 100% believe in autism acceptance. i don’t want a cure. but i also want us the acknowledge that it can hurt. it doesn’t mean my entire life will hurt, but some parts will. and i want a community where we can see both sides, see the hurt, and celebrate it anyway.
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I'm begging you, pleeeaaase if you live with a physically disabled person and they tell you what would make the living space more accessible, DO NOT SAY "just ask me for help." I don't want to have to ask for your help dumping out yesterday's coffee grounds in the french press.. I want to be able to make coffee without having to ask for help every. single. fucking. day.. Like, why don't able bodied people not understand that asking for help to do every little thing fucking SUCKS?? Also, when I'm upset because my own home isn't accessible, don't get mad at me as if it's something personal towards you.. It has absolutely nothing to do with you. I'm allowed to be mad at the lack of accessibility my disability creates... Don't make it about you.
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thoughtportal · 2 years
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painting made easier
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jodjuya · 10 months
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Image originally created by @brieflycleverspoons
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liberaljane · 10 months
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listen to disabled people 💖
Digital illustration of a large group of disabled people of different ethnicities, ages, and genders. Among the crowd are service and emotional support animals. There’s two smaller protest signs that read, ‘I shouldn’t lose benefits when I get married.’ And ‘ban subminimum wage’ the main sign reads, ‘disabled people are expert of their own lives and know what they need.’
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brandyschillace · 7 months
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I turned in the book manuscript for INTERMEDIARIES, the forgotten history of the first transgender clinic 1918-1933.
It follows the story of Dora Richter, the first transgender woman to undergo complete MTF surgery (not Lili Elbe; she was third!) It’s taken me two years of blood, sweat, and tears. A lot of tears, actually.
The Nazis raided the Institute for Sexual Science; they burned the library. They banned the books that remained. They attacked, arrested, and ultimately killed trans and homosexual people along with disabled people, minority groups like the Roma people, political opponents, and 6 million Jews. (One commenter suggested 11 million people over all, and really, that estimate may still be conservative).
The news today, 2023, reads a lot like news in 1923 with the rise of hatred against LGBTQ, attacks on reproductive rights, and increasing racism and antisemitism. The Nazis rose throughout the 1920s, coming into power 1930-1933.
The world said never again; we must now be the ones to stop a slide into hatred and violence. Before it’s too late.
Here is a preview of the book; it will be available for pre-order this winter (I hope), coming out in 2024.
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