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#I’m actually disabled
neurospicyyy · 6 months
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• Fidgeting and stuttering do NOT always indicate that someone is nervous.
• Avoiding eye contact does NOT always mean someone is lying.
• Having a hard time focusing does NOT always mean someone is lazy.
• Carrying around a stuffed animal or blanket does NOT make someone childish.
• Poor motor skills is NOT a direct indication of intelligence.
Not everyone fits into your box. Deal with it.
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phleb0tomist · 5 months
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tumblr users will have the most inaccessible, unreadable, low contrast, flashing carrd you can possibly imagine, with a dni full of insider acronyms with no translation and numerous link buttons labelled with cryptic captions, and then go ahead and put “ableists dni and kys!” on that carrd
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1980s-slasher-film · 1 year
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Accommodations are not special, they’re not a leg up, they’re not a benefit. They’re not putting anyone ahead in the race, nor are they taking anything away from others.
They exist to put us on a level playing ground to everyone else, and nothing more.
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doresworld · 2 months
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Being disabled means experiencing something terrifying health wise, but being uncertain if it’s hospital worthy
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eggings · 10 months
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happy disability pride month to anyone who has a disability from a condition that “usually isn’t a disability”. happy disability pride month to people with disabilities that aren’t often understood by able-bodied people. happy disability pride month to people who don’t have any official diagnosis yet. happy disability to people whose “labs look completely fine”. wishing you peace this july.
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I think a fair number of (able-bodied) people don’t understand that cripple is a slur. It’s a slur. It’s offensive. Physically disabled people can reclaim it *if they want to*, but they don’t have to. They can be offended by it if they want to as well. Both are valid.
Also, you can reclaim it FOR YOURSELF! You don’t just get to call other people cripples because you decided to reclaim it. That’s personal. Saying “oh, I can say that because I’m physically disabled” only applies if you’re referring to YOURSELF that way. You do not get to tell other people in your community what they should and shouldn’t be comfortable with.
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nerdyenby · 10 months
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Happy disability pride month everyone <3
Shoutout to my fellow people who
Didn’t realize their symptoms weren’t normal (I didn’t understand that people went through their days without feeling exhausted all the time until I was 20)
Flew under the radar because they function “well enough”
Aren’t good at communicating when they’re in pain and/or don’t know how to ask for support
Are still stuck in the endless cycle of doctor referrals
Still don’t have a name for what they experience
Hesitate to call themselves disabled, while also craving the validation of our pain that comes with that label
Feel like they don’t belong in this community. I promise you do. Your struggles are valid and you are always welcome here <3
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thatoneluckybee · 5 months
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Going to break into your house with pots and pans and yell at you until you reframe your thinking of productivity to include more than just schoolwork or a salary or chores and the like.
Did you do a thing? Was there a positive result for you or someone else?
Congratulations, you did a Productivity!!!
You aren’t ALWAYS going to be able to have the energy to do what we consider traditionally productive. You won’t always have the motivation.
Yeah, maybe you could have spent two hours studying for that test instead of 15 minutes. Maybe you could have cleaned the kitchen instead of the dishes. And? That’s still something!
Productivity is doing things!! Did you eat food and drink water? You did something that helped your body work! Doodled in class? You made art! Even just posting theories and memes on tumblr dot com is a thing! You thought out the post, figured out how to organize it (even if you don’t realize you did that) and you made it! And now other people can see and you DID something and you should be proud!!!
Be proud of yourself or I am going to show up outside your window tonight and scream positive affirmations louder than a cat who has just discovered her food bowl is empty.
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Who the FUCK decided that insurance companies get to decide what’s medically necessary????????
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One of my favourite things about being disabled is the excitement and happiness when you can do small things that others might find easy
It’s such simple joy to be able to make yourself a cup of tea for the first time (or the first time in a while!) or to just make a simple meal that you couldn’t before! Finally figuring out how to make something that doesn’t overwhelm you, etc etc
It’s a joy in the mundane that ableds need to learn from sometimes /lh
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dumbasswithapen · 3 months
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can we just listen to Disabled people when they say what accommodations they need??? Like it really isn’t that hard to just take someone’s word on what is best for their own body! Whether it’s more or less or different than what you deem they need it really isn’t your place to say!!!
Sometimes, people need more than they show! Especially if they’re used to being in pain all the time, then they won’t always display that discomfort.
Sometimes the accommodations someone needs are different than what you assume. A friend who struggles with noise sensitivity may ask for you to turn on a different type of music, instead of turning it down, and if that is what they express they need you don’t have to say “oh no I can just turn it down!” and ignore them saying that that isn’t necessary because your idea of noise sensitivity is different than their own experiences and needs.
And sometimes people need less than you try to provide! Or simply don’t want that accommodation at the time! And here’s the crazy part: this applies even if what they say to do could hurt them. Obviously this isn’t a rule for every situation*, but for some it absolutely is. If your friend wants to tag along for, say, a hike, and they have joint pain it isn’t your place to add in “oh no but they can’t do [the hike]! They’ll be in pain! We have to do something else to accommodate them!” If that person expressed a desire to go, especially if offered other options prior that wouldn’t hurt them, let them live. Let them do the thing that puts them in pain, because Disabled people don’t always want to be shoved into a little box of safety. Absolutely sometimes they do, and some might always want to, but if they don’t, then let them make their own choices for their body. Just as anyone else does. You go out and get drunk, even if it gives you a hangover. You go skating even if you’re shit at it and scratch up your knees a bunch. Just because someone is Disabled doesn’t mean that they can’t do the same thing and do that fun thing that hurts them.
I don’t know if I’m displaying my point how I want, so here’s my own example: I am allergic to the cold. Anything below 60 degrees (f) I get hives. Any water cooler than a fucking warm shower I get hives. My joints don’t do great when it’s cold out. This does not mean that when I say I want to go swimming, you can say “oh but you can’t you’ll get hives!” Or “no you can’t do that you’ll be in pain!” Because. I know that. I know that. I know my Disability better than anyone else can, and I can ask for accommodations I need. I am not a child to be wrapped in bubble wrap so I don’t get hurt. My body is my body and I can do with it what I want, and face the consequences. Likewise, just because I said I wanted to go swimming doesn’t mean that when I don’t want to go out and muck around in the snow it is anyone’s right to say “oh but you wanted to swim earlier, so obviously it isn’t that bad for you!” Or “oh it’s fine it’s not that cold! Just wear a sweater!” Because at that time I need and want different accommodations and that should be listened to and considered accordingly, as far as it can be in that situation.
Seriously. Just listen to us. We are in our own bodies. We know ourselves. It really isn’t that hard
*a situation where this point would be null is, for example, a situation where the person has been peer pressured into doing something, or one where you know the person well and know that the endurance of pain is a self-harming behavior
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derekhalesbian · 9 months
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genuinely how i feel sometimes
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gandalf-the-bean · 9 months
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when you have chronic pain you just kinda get used to that spot hurting but when a NEW spot that’s not a Hurty spot starts to hurt and it’s like not even that bad but suddenly you can’t do anything cause the Wrong Spot is Hurting
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manyminded · 10 months
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this post goes out to my disabled people who have to exercise/can’t use mobility aids or else their disability will get worse. we are not betraying our own community by helping ourselves
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fablesys · 1 year
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