#(This post is about physical disabilities

[midnight-soulless-system]

I think it's both sad and hilarious to see the difference between how small children react to disabled people and how teenagers/adults react to discabled people.

Small children are just curious and want to understand why and how things work, so of course when I'm walking with my cane and limping and taking walking breaks, they're going to be confused. Sometimes their questions are blunt but it's obvious they're just curious and mean well.

And then there's everyone else. They don't even want to know about why you're disabled or anything, they just want proof that you are allowed to be disabled (like that's a fucking thing). And every time they say shit like "well prove it. Prove that you're disabled" I just look at them with a confused face. Who the fuck do you think you are, demanding to see my personal medical records, move the fuck out of the disabled parking space you abled piece of shit.

[butchfalin]

the funniest meltdown ive ever had was in college when i got so overstimulated that i could Not speak, including over text. one of my friends was trying to talk me through it but i was solely using emojis because they were easier than trying to come up with words so he started using primarily emojis as well just to make things feel balanced. this was not the Most effective strategy... until. he tried to ask me "you okay?" but the way he chose to do that was by sending "👉🏼👌🏼❓" and i was so shocked by suddenly being asked if i was dtf that i was like WHAT???? WHAT DID YOU JUST SAY TO ME?????????? and thus was verbal again

[nightmaretour]

Anyway, people with brain damage I love you. People who have had strokes I love you, especially if you're told you were "too young" to have one. People who acquired your brain damage by less common means such as infection, lack of oxygen at birth or degenerative disease, I love you. People with moderate and severe brain damage, I love you. People who lost their sight or hearing or ability to speak because of their brain damage, I love you. People who have paralysis from their brain damage, I love you. People with amnesia and severe cognitive issues from their brain damage, I love you. People with rare and unusual symptoms from their brain damage, I love you.

You are not a punchline, you haven't lost your humanity, your thoughts and opinions are as valuable as anyone else's. We deserve respect.

[ID: a dark red banner with the words "This post is about physical disabilities, do not derail." in grey font. Either side of it is a lighter grey wheelchair user symbol with the user leaning forward with the arms raised and back, giving the appearance of wheeling fast. End ID.]

[schizoaffectively]

You are well within your right to be angry about the help you didn't get and should have gotten.

You are well within your right to be angry about having your needs neglected.

You are well within your right to be angry.

[p0is0n-is-th3-cur3]

Shout out to people who use adult diapers

Shout out to people who have chronic UTI

Shout out to people who have catheters

Shout out to people who have urostomys

Shout out to people who still wet the bed

Shout out to people with kidney scarring

Shout out to people who deal with kidney stones

Shout out to people with kidney cancer

Shout out to people with kidney failure

Shout out to people who I didn’t mention but still have kidney/urinary tract issues

I love you, I know it sucks, the judgement sucks, the symptoms suck. You’re not gross, it’s okay to talk about it. Your suffering isn’t taboo, never let anyone treat you like it is.

[varian-ross-horror-author]

"Disabled people should be allowed to be as independent as we can be" and "disabled people should not be pressured to be hyper-independent in order to not wind up in nursing homes against our will" are two thoughts that can, and should, exist at the same time.

[spooksforsammy]

Geniuenly like. So many people claim support disability. But then say something completely untrue

Y’all support autism? So what about when the person has intellectual disability or need help walk talk eat bath use bathroom? Does your support end when you see someone with higher needs?? Someone who actually genuinely won’t survive without support from others n that support is sometimes having other people do everything for them.

Y’all support depression? What about when the person can’t bring themself to get out of bed for days on end? What about when that person goes days weeks months without cleaning self because can’t get up even though need to?

Yall support schizo-spec disorders & psychosis? What about what the person get violent because of their delusions n hallucinations? The ones know are fake but still can’t help but believe in? The ones genuinely believe in their delusions/ hallucinations? What about the ones don’t don’t get violent to self n other because of the disorder? Those that just sit scared about the hallucinations n delusions. The ones that won’t leave their room/ house out of fear of their delusions/ hallucinations?

Y’all support those with physical disabilities? What about the housebound bedbound ones? The ones need gait trainers walkers wheelchairs? What about the ones who full time users? Or the ones that need power chairs to independently move around? What about the ones crying screaming throwing up from their pain?

What about the disabled that always have a horrible attitude because tired of the disrespect? Tired of having to explain everything about them to everyone even if personal? Tired being told get over it n just educate others?

The disabled ones tired telling people not use certain terms. Tired of being spoken over n for without being thought about or asked. Tired of hearing their communication isn’t valid for ‘xyz’

Y’all support but act very picky about who deserves support and who’s not worthy of it. It’s not support if you pickin n choosing

[satellite-runner]

being physically disabled as a young adult after being an physically active child in and physically active family, who still participates in the online spaces for physically active hobbies but cannot participate physically means… i’m a living nightmare. i talk to people who share this interest with me, and my existence is their worst nightmare. they see my crutches and hear that i cannot walk far or climb a ladder and think, thank god it isn’t me. my existence is horrible and unimaginable to able bodied people.

[azztiph]

Sometimes u just need to sob and scream and cry and bitch about ur disability

I think a lot of people feel like they need to be at completely at peace with their disability

And you don’t!

Be mad be sad be pissed off!

[wheelchairtetris]

It's okay if you've pushed yourself too far. It's okay if you overdid it and are dealing with the consequences. It's okay if you did something that made your condition worse, intentionally or unintentionally. You have autonomy & do not have to only do things that make you "better".

[spookietrex]

I hate the look on able-bodied people's faces when you can't do a thing that you could do the day before. The look of disappointment, confusion, the "Oh but you could do it before. Are you SURE you can't do it?" Like yes, Brenda, I'm sure that I am in too much pain to function/move from my bed right now so going for a walk when I could move 50 feet yesterday without my cane IS too much.

[midnight-soulless-system]

Sometimes being disabled means you can't go to college, can't get a job, have to live with your parents and that's ok. For a lot of us it means not being able to go outside most days, not being able to get up or move at all. It can mean needing someone to wash us or feed us or help us with the bathroom and that is ok. It doesn't mean that we're less than or that we aren't worth anything.

And it's valid for us to be mad about it. Even if we can overcome some of these things with accomodations we're allowed to be mad that we're in this situation, and wish that we weren't disabled because I sure as hell hate this shit.

[thedisablednaturalist]

sorry you think physically disabled people setting boundaries on their posts is annoying but y'all lost your privileges long ago

There is a long history of neurodivergent people talking over physically disabled people on this site and irl. That is why we get upset when we make a post sharing our experience and suddenly 90% of the comments/discussion are neurodivergent people talking about themselves. It's not cause we don't like hearing about other people's experiences, but y'all gotta listen to us sometimes. I'd rather that you'd all just continue to ignore us than actively talk over our community.

[bixels]

What's K.O. CRISIS?

Hey all. Over the past couple months, I've gotten a lot of followers who probably don't know about my OCs and portfolio projects that I'm also working on, so I'm making a quick master-post for it!

K.O. CRISIS is a series of artwork––character designs, illustrations, sketches, and animations––inspired by late-90s/early-2000s anime and Y2K culture.

Set in an alternate-history Los Angeles in the year 2001, the story follows disabled Taiwanese-American Ashley Tang as she fights her way to the top of the bracket in the national augmented boxing championship.

As the youngest female fighter in the championship, she'll have to fight tooth-and-nail to defend her place amongst the heavy-weights. While her rare dual arm prosthetics help even the playing fields, it'll take more than brute strength to prove her worth.

But this isn't a story about an underdog triumphing against all odds. Throughout the story, Ashley will push herself to the limit for the sake of validating her existence under the grinding heel of the sports media machine, in a world that values disabled bodies more than their lives. As the championship rages on, one question seems to linger through the roar: Is Ash strong enough to win, or is she brave enough to quit?

Through the project, I'm hoping to explore representations of prosthetic-users in pop culture as "enhanced superheroes," as well as discussions of trans-humanism under medical capitalism, the fetishization of new technology, and the commodification of disabled people as entertainment.

Accompanying her journey include characters like Noora Balakrishnan, a local transfem prosthetics engineer who doubles as Ashley's ringside mechanical cutwoman.

The project is still in its early stages, especially since I sorta rebooted it earlier this year (meaning I'm no longer using past, outdated art for the project). If you enjoy it, you can find more artwork for the project under the #ko crisis tag!

[consider-your-potatoes-mashed]

Why the fuck is it so hard for able bodied people to get their heads around the fact that specifically physically disabled people are not actually accommodated most of the time?

Whether it be the inaccessibility of a building due to stairs, heavy non auto doors, ramps that are too steep, broken elevators or just non existent elevators, etc the list goes on and on. Or now public spaces that let’s say are otherwise perfectly accessible are now inaccessible to so many people because so many people refuse to wear a fucking mask when it would cause then no harm (maybe just a bit of sweat) to wear one.

The fact that abled people don’t see just how fucked up and inaccessible the world is blows my fucking mind. Just because someone “can” do something or go somewhere doesn’t mean they should have to do that or that it’s safe for them to do so. Like sure I can do stairs but holy shit by the time I’m at the top I’m in so much pain and I feel like I’m gonna pass the fuck out man.

Bottom line, the world is really fucking inaccessible and that needs to be fixed. Physically disabled people’s voices need to be listened to and not talked over by ableds who think they know what’s best for us or who think the world is perfect as it is

[extreme-dyke-syndrome]

DO YOU WANNA HELP YOUR DISABLED NEIGHBORS?

Rake up the wet leaves before we eat shit on the sidewalk! Your city or town should be doing it, but why would they??