#physics c

[asexual-amanita]

Unpopular opinion

I don’t want a self driving wheelchair that can go up stairs. I want ramps elevators, and curb cuts.

I don’t want a solution in 20 years, I want it now. I wanna be able to go to the mall with my friends and not have to worry about stairs. I want to go the movies and actually chose where I sit. I want to go to a park without having to parkour my way through cracked pavement and curb drops.

I want accessibility and I want it today.

[crippledpunks]

i wanna say fuck you to anyone who shame disabled, chronically ill & neurodivergent people, especially homebound folks, for "spending too much time on their phone/on the internet/etc." when it's the only (Somewhat) accessible way for them to experience the world. many people don't get to get out much even if they want to because of their disabilities. shaming someone for trying to connect with the world, make friends and engage with hobbies in ways that are accessible to them is beyond cruel and unnecessary

[extreme-dyke-syndrome]

POV: you are physically disabled

[nightmaretour]

What a lot of abled people don't understand is that when you get more sick as someone who was already physically disabled/chronically ill, you don't get the sympathy, you don't get people sending you cards and coming to visit and help you with things. Everyone just kind of assumes that you can handle it, that it's not *really* anything new. Maybe people might acknowledge it for a week or two, but then to them it's just normal. You were already sick, so why would being a little more sick be disruptive to you, right?

[21stc3nturyd1gitalb0y]

it shouldn’t be taboo to admit that there are disabled people who are more or less disabled than you.

i consider myself mid support needs. i am in pain every day of my life, all the time, and am significantly impaired by that. i can’t work full time. i require significant support to get through the day. i need my service dog to function properly. i can’t live alone, at least not right now. i can’t effectively mask my autism.

but i still have privilege over other disabled people. i can walk. i don’t have to worry about wheelchair accessibility when i travel. i have no visible deformities or intellectual disabilities. i am verbal.

some people are more disabled and others are less disabled. it’s okay. it doesn’t mean that you’re not valid or that you don’t deserve help. it just means you do not have the exact same needs as someone else.

[saint-hymn]

a minor inconvenience, really

[a-sassy-bench]

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?

[satellites-halo]

If you have to use single use plastics bc of disability I love you. I love you and your existence is not bad, you deserve to live.

[disbabeled]

Do you know how many times a day I want to scream at people "THIS ISN'T FOR YOU!" ?

Just yesterday, I was ten minutes late to my tutorial class because for whatever reason, almost every single person in my lecture decided to use the elevator instead of going down one flight of stairs while me and my classmates -- the ones who didn't have that choice -- were stuck waiting for the next elevator.

I constantly have to navigate around people walking up the ramps -- or, worse, standing in the middle of them -- because they couldn't get off their phones for two seconds to use the stairs instead.

At least twice a week I end up in far more pain than usual because people who don't need them take up the accessible seats on the bus and I either have to stand there and wait for somebody to get up (Which is already hard on my body) or just wrap my arm around the pole and try to suffer through a few stops until somebody gets off (Which has already caused several dislocations). As much as people like to brag about how they'd "always give up their seat for a poor handicapped person", they're far more likely to stay right where they are and ignore you in favour of watching Instagram reels on their phone.

And I've tried asking people to move. Directly. Making eye contact and everything. They'll just look down at their phone and ignore me until the bus driver or somebody else says something. And only then can they magically notice me and get up.

Before I get a bunch of people leaping to yell about people with invisible disabilities: I know. I know there are people with invisible disabilities, I spent most of my life with only invisible disabilities. I can guarentee that not every single person in my lecture of 60 people has an invisible disability. This is not the problem.

The problem is that able bodied people see these resources and supports made specifically for physically disabled people and assume they're entitled to them. Most of them see it as something that's put in place just to comply with certain rules or laws or regulations as a 'just in case' thing. Nobody thinks that disabled people are actually out and about. We're an afterthought to them.

And I get it. I do. We all have our blind spots.

But seriously, this is getting ridiculous.

[cryptidslair]

been thinking a lot about ctubbo lately (when am I not)

[boyfailurr]

being disabled has an affect on the social life that not many people are willing to discuss . the reality is, being disabled means missing out on a lot. the queer bar you think everyone should go to isnt accessible. nobody in your towns high school was willing to talk to the only kid with down syndrome there. not all autistic people were accepted enough to be social in the first place, much less doing drugs and having sex.

there are so many experiences to miss out on

[chainedspectre]

here's to all the little sacrifices we have to make as disabled people.

here's to skipping a friend's party because you were in too much pain, or because you had no energy.

here's to dropping out of clubs because they became too much for you.

here's to all the times we've said "no it's okay, you guys go ahead, i'll hang back here."

here's to all the things we've held ourselves back from just in case they hurt us.

here's to moving seats in class away from your friends because your back was getting a draft and the cold hurts you.

here's to us. here's to letting ourselves heal. here's to being cautious, being safe.

here's to the things we can do. the things we're allowed to do. here's to enjoying those things, enjoying our lives.

here's to making the most of being us.

[extreme-dyke-syndrome]

Me when my able-bodied friends walk too fast

[boughkeeper-dainsleif]

big shoutout to disabled people who smell bad. disabled people who cannot shower regularly. disabled people who sweat a lot and it causes them to smell bad. disabled people who cannot apply deodorant due to mobility restrictions. disabled people who cannot do laundry regularly or at all, and end up wearing dirty clothes for a long time. disabled people who cannot clean their living space, and thus end up smelling bad themselves. disabled people who have any condition or disability that causes body odor. and any other disabled people who smell bad for reasons i didn't mention. i see you and i love you.

(this post is for all disabled people, including mental and physical disabilities)

[21stc3nturyd1gitalb0y]

people assume that being physically disabled makes you more empathetic to the pain of others, but that’s not always the case.

for me, it feels unfair when others are in pain and don’t feel the need to hide that fact, because i have internalized the idea that i’m not allowed to talk about my own. it annoys me that, while most are typically understanding if a non disabled person doesn’t operate at their full capacity due to sickness or injury, disabled people are expected to function normally as if that isn’t our every day. as much as i want to feel solidarity towards a suffering person, it feels impossible not to be envious when their illness or ailment is temporary, but i will never, ever get a break from mine.

for obvious reasons i would never say any of directly to someone, because my pain doesn’t make theirs any less valid or real. still, i can’t help but feel that my disability has made me bitter and unkind, because i can’t help but compare my own experiences with theirs.

this is the reality of disability- it does not create perfect people. many of us are broken and struggle to connect with others because of our conditions, and that does not mean we are evil people

[theresa-draws]

🌿healing, hurt, healing🫧

it's not that simple, it's that simple.