Adventures Of A Disabled Kid @8bit-autistic - Tumblr Blog

I don’t have time to unpack my full thoughts on the whole argument of ‘you shouldn’t be a burden to the healthcare system’ but I would like to chime in on it:

so, all athletes should immediately stop playing sports. construction workers, anyone with jobs that put them at risk, they need to find different employment. people with uteruses shouldn’t ever get pregnant, either. actually you know what? don’t enter a car or vehicle at all! and don’t even get me started on old people. what age do we think they should just give it up & throw in the towel? 50? 60? after that they become way too burdensome. it’s a problem.

sweet baby eugenicist, your anger is misplaced. they want you to blame yourself instead of their crumbling system. you should be asking, what kind of a fucking healthcare system is it if it can be burdened by the very thing it exists to provide? which is healthcare?!

starlight-shadowbanned

also it seems pretty adjacent to nazi “useless eater” rhetoric

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immunetoallbadthings

I think it's kind of pathetic that accessibility speech to text censors out most swear words as if people with disabilities were toddlers. No we are not toddlers, we are people who deserve to hear shit that isn't censored. We're tired of this ableism.

purple--starrrs

By the way it's like. Really fucked how society's thoughts on epilepsy is just "get over it." Seizures can cause permanent brain damage. Seizures can kill people. Seizures hurt like hell. Allow me to reiterate that seizures can kill people. And you're just gonna casually put flashing lights, a common trigger for seizures in your advertisement, in your animation meme, in your edit, on your billboards, without even thinking about putting a simple disclaimer? That's unbelievable. Your little anime edit could deadass cost a life and you're not gonna put a warning because it's "inconvenient" or "people like that shouldn't be on the internet" (ableist) (the problem exists outside the internet also). Or you'll give insufficient ones like putting it in the captions or only giving like one second before the flashing lights appear, meaning that the trigger's already in motion before anyone who needs the warning can read it and save themselves from literal physical danger.

We need to start commenting under other people's posts about how to properly warn for flashing lights and eyestrain. We need to be emailing and calling companies about their possibly triggering advertisements that could induce seizures. We need to stop tolerating ableism and start speaking up for the more vulnerable.

Also, stop putting epilepsy warnings. That's like saying "warning: schizophrenia" on a post including unreality or "warning: dyslexia" on a post with a typing quirk. First off, the disability mentioned isn't the only group of people that this could trigger. Second, it doesn't truly get the message across and instead makes it worse for those with the disability-- scrolling through the epilepsy tag on Tumblr should get you to view the content of other epileptic people, but no, you just get a bunch of flashing lights and eyestrain, even though you could instead tag for, oh I dunno, flashing lights and eyestrain.

Anyways this Disability Pride, and for every month that comes after, think about epileptic people and others who are triggered by flashing lights/eyestrain. Happy pride to those who experience seizures too frequently due to the unaccommodating and ableist societies we live in!

lumberjackloverboy-moved

for my fellow psychotics who struggle with thinking someone is in their house, a method I’ve found that really works are these guys:

i put them on my front door and anytime it opens they ring. that way if i think someone has broken in or i see someone who isn’t there i can think back to if the bells have rung, and if they haven’t i can assure myself it’s not real. obviously it’s not fool proof, like if you are prone to auditory hallucinations, but it has really helped me calm down in time to avoid major psychotic breaks. it’s a real lifesaver

nonpsychotics encouraged to rb

ryan-sometimes

When people justify using gen AI by talking about how it allows them to do (insert creative hobby) it sends me into a blind rage. The whole point of the creative hobby is to use your brain. Having a machine do it for you defeats the purpose. That’s like saying you’re getting into running marathons then just driving the 42km

rosslynpaladin

"well what if I was disable-"

Shut up. I am disabled. My brain barely works any more and my hands don't do what I want, and I don't have the strength for singing the way I did,

and I'd rather never paint again, never sew again, never sing again

than have a computer steal other people's work and call it mine.

Keep our disabilities out of your mouth- we're not your PROP for arguments.

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creekfiend

thing I am proud of: when the doctor started going on a weird rant about long covid not being real I paused and listened to his nonsense for a bit and then very calmly said, in a polite and curious tone, "you don't believe in post-viral illness?" and he like. stammered a bunch and was like OH WELL I'M NOT SAYING -- I DON'T...I just think ..! and backpedaled awkwardly while I just sat there like :3c interesting :3c thank you so much for clarifying your stance on this :3c

creekfiend

an important skill for chronically ill people to develop is the ability to treat the doctor as though they are simply a person you are interviewing to find out how much they know about your condition.

nightmare-from-heaven

Holy shit op this is LITERALLY in the book 'Never Split The Difference: Negotiating as if Your Life Depends On It'. Written by a guy who did hostage negotiation and then tried doing business negotiation, and mopped the floor with industry experts.

I'm fortunate enough to have a primary care doctor who knows about hEDS, but it's occurring to me that the skills in this book could be medically life changing for chronically ill folks of all kinds. Like. Literally a matter of life and death, especially for BIPOC and/or fat and/or young people who are having their issues dismissed.

creekfiend

HMMM interesting!! will have to check this out

lastoneout

"I am not a vessel for your good intent" goes hard as a line from a disabled perspective. Abled people care so much more about being their idea of a good ally than they do actually being a good ally. They shove their good intent right down your throat and then act surprised when you tell them they're suffocating you.

lastoneout

persbaderse

before my egg cracked, i had noticed that trans people were often pro-accessibility and up-to-date on the needs of disabled people, but i hadn’t seen any inherent connection between the two (other than the obvious minority-looking-out-for-other-minority thing). but now that i’m trans and medically transitioning, and i have to constantly repeat myself while talking to doctors and nurses, and explain things about my own anatomy to medical staff who should already know this, and having every single problem i might have blamed on my “condition” so nothing i say is taken seriously, all of the sudden i have a little sneak peak into the life of someone who has to deal with this all the time. like shit bro, being disabled probably sucks ass, someone should do something about this

persbaderse

happy disability pride month, we all deserve autonomy and respect and access to medication

lupusbaby

Say it with me! Wheelchairs aren’t sad! Mobility aids aren’t sad! Mobility aids are instruments of freedom!

goth-princess-gwennie

Forgive me if this is inappropriate but

So are

colostomy bags

Diapers

insulin pumps

Oxygen systems

Braces

cuntpunkop-ed

catheters

rollators

hearing aids

compression garments

prosthetics

FREEDOM AIDS

creekfiend

its so awkward when people ask me why i dropped out and i have to be like "inadequate disability support" bc no one wants to hear this. they're always like i thought they had to provide that though isn't it the law? girl you might want to sit down i have some bad news about the litigation-based enforcement of the americans with disabilities act

then if i do say that theyre like, couldnt you sue? well theoretically maybe but not without spending more money than i have and putting myself through absolute hell. so no. no i can't.

mabelsguidetolife

it’s just this

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the-messy-artist

Has this been done yet

liebelesbe

june is over... goodbye pride month, hello disability pride month!!

liebelesbe

let's all be disabled this month... together 🤝

liebelesbe

if you're not disabled yet: no need to worry! i can help. come closer.

green-is-gay

i dont WANT pride months to be over,

on the other hand...

ourdisabilityexperences

Ppl saying that disabled ppl can't create art without ai is ableist and shows you don't think disabled ppl can do anything if they can't do it the way you can.

eptck

"why do you talk so much about disability"

i am never not in pain . you would talk about it a lot too

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brightlotusmoon

ancientson

I know this is meant to be funny but it actually makes such a good point about how ADHD and executive dysfunction can impact people in really major ways, including financially

sickzombi

"i need my medication please!" says the sicks guy.

"fuck you" says the fuck you pharmacy

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