#cripple shit

[extreme-dyke-syndrome]

Me when my able-bodied friends walk too fast

[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.

[nixxsmokeweed]

I made a new backpatch for my wheelchair. The first picture is the new one and the second is the old.

I made this new one with velcro which attaches much cleaner to the chair. That way, you can actually see all the patches.

I find these backpatches are much better than a traditional battle jacket for me. As Battle jackets get really heavy, which makes it harder to push myself. This way I can still participate.

If you make one I would love to see!

[justsomerandomgay]

something that isn’t talked about enough with chronic illness is knowing that going to your appointments and doing your exercises and all that will help but being in too much pain or too fatigued to go, so your just stuck in this constant cycle of knowing what you need to do to get better but not being able to do it because your sick

[permanently-sprained-ankle]

I love young cripples with stereotypically “old people” disorders! (Personally I have severe plantar fasciitis at 20)

You’re not “too young” to have this pain.

You don’t need to “wait until you’re older and then you’ll see”.

Your disability is a disability regardless of your age!!!!

[cistematicchaos]

Chronically ill people should be allowed to kill Anyone who tells them to be grateful or that they're "lucky" that their disease/disability isn't showing up on bloodwork/tests.

The idea that you're "lucky" if your disability/disease doesn't show up on tests because if it did, it would be worse is so fucking shit.

I need a wheelchair, I'm homebound, on heart medication, three different pain medications (and more!) and can barely navigate my house but according to doctors, I'm "lucky" my disease isn't progressive enough that they can figure it out. Apparently, since it doesn't show up on tests, that means whatever I have is considered "mild".

Personally, I think that idea should die in a ditch and chronically ill people without diagnoses should be allowed some kind of compensation for it existing in the first place.

[chronicallycouchbound]

Ugly Laws. Creepy coming from the word cripple. Freak shows. Fear of clowns. Bearded ladies with PCOS & intersex variations. Contortionists with EDS. Little people. “Missing links” people with Microcephaly. “Snake man” people with limb differences. Lack of welfare programs. Disability rights. All of these things are connected.

[azztiph]

Self destructive behavior pertaining to disability isn’t talking about enough

Forcing yourself to do activities that you know will hurt your body is bad!

Making yourself not use your mobility aid when you know you need it is bad!

Not taking your medicine because you want to get worse or just don’t care anymore is bad!!!!!

I think that mental illness can definitely manifest differently for disabled people. It’s not rlly talked about because this all stuff that ableds see as inspiring or us pushing through. It is just harmful behavior.

Since every single disabled person is or has been mentally ill this stuff is just seen as normal.