#disablity rambles

[artsybi]

heyyyyy reminder for other cane users.

don't forget that cane tips need to be replaced.

i've been using my cane for almost two years on a near daily basis and i JUST switched out the tip and

[image IDs in alt text]

the new tip versus the old tip. i'm not sure how clear it is but, YEAH, there's like. half a millimeter of tread left on the old tip, if that

the replacement was LITERALLY 2 dollars. i bought two to justify the four dollar shipping but. TWO BUCKS.

i had noticed that i was having slipping issues on linoleum recently, but i did not realize how bad the issue had gotten until the new tips came so. PLEASE check your cane treads and if they're notably worn out PLEASE get yourself a new tip they're SO cheap and the grip i get on the new one is INSANE

please don't forget to replace your cane tips!

[the-messy-artist]

Has this been done yet

[corinthian-og-begay-docrime]

God sometimes I hate being disabled.

Let me wander around Joanns without feeling like I’m gonna pass out.

Let me look at the crafting things without feeling like I just ran the mile.

FUCK.

[lightning-system]

As a medium/lower support needs autistic who works with young higher support needs autistic:

We all matter. We all have the same diagnosis. We all deserve to be treated with dignity and respect.

But we are not the same.

I can mask and might be seen as 'odd' or 'weird' in public. The students I work with are seen as 'dangerous' and 'practically little kids'.

I can go to university and work with accommodations. The students I work with likely will never live independently and a few might find jobs that support them but still pay them less than an abled worker.

I have full control of my finances. The students I work with aren't allowed to make independent financial decisions, even if capable.

If I say 'no,' I'm making a choice. The students I work with can't say 'no' without being labeled as defiant and difficult.

I can feed myself, bathe myself, and take care of myself with extreme challenges. The students I work with are unable to take care of themselves without high levels of support/one on one support.

I had an IEP in high school but was mainstreamed in classes. The students I work with take separate classes and some rarely get to interact with their abled peers.

Our experiences are fundamentally different. Higher support needs autistics will experience a specific type of ableism I never will, and can never fully understand.

Lower support needs autistics need to stop saying we understand what higher support needs autistics are going through and then present autism as only being disabling because of society/lack of acceptance because that is dangerous. We need to stop saying every autistic person is capable of everything if given the right support because that leaves out huge parts of our community who will never be able to do certain things, regardless of support.

We are worthy of existence regardless of our abilities.

Autism is a spectrum. It is not the same for every autistic person. Autism acceptance and advocacy has to come with accepting, acknowledging, and listening to our higher support needs peers.

[foldingfittedsheets]

A few years ago my dad got hit by a car. He was on his bike when a van merged into him and smashed him up pretty good. I found out because he posted it on Facebook, along with a comment that he’d just walk home.

I have a long history of haranguing my father about his health but this really took the cake. I called him to insist he get a ride home and go to urgent care. I was summarily ignored and once shock wore off he was in a lot of pain.

He had a cracked pelvis, fractured fingers, and a dozen scrapes and bruises. Over the course of his legal battle to get his medical shit covered there’s been several small battles. The first was his cane.

He refused to use it for ages. The physical therapist insisted he should but he stubbornly repeated, “I’m strong enough!” It took months for him to give in and walk with it, but he eventually thanked me as it makes his life easier.

The current fight is getting him a handicapped placard. He’s finally admitted after a year that he needs one but still hasn’t done it.

So we recently went to pick up my nephew from the airport and I was like my dads assigned disability advocate. We got to pass through security to meet my nephew at the gate but my dad tried to put his cane up on the conveyor and I grabbed it right back, loudly addressing TSA to ask if he really needed to scan that. The guy said he supposed not, the agent could check it out at the scanner.

Then as we were refilling our pockets and getting belts back on a TSA agent was chiding us for holding up the line. I snapped back, "My dad is disabled, he needs a minute." She glanced at him and reluctantly backed off while he slowly got all this belongings back on his person.

We had to take a train to my nephews gate. It was pretty full and a lady who'd gotten on before us plopped into one of the only handicapped seats. "Excuse me," I said as we got on, "Can my dad please use that?" She clocked his cane and moved without apology and my dad gratefully sat down.

At no point in any of those stages was he prepared to advocate for his own needs, he just decided suffering was the only recourse. I wish the world were softer, and I wish he didn't just accept hardship but I definitely know where I got it from.

[jemineye]

i cant stress this enough, disabled people know their own limits. i fucking promise you. we are not being lazy or jerks because we won't do something YOU want us to do or something YOU THINK will make us feel better. it wont. stop.

[sickly-sapphic]

this disability pride month you can help disabled people by continuing to mask up, using appropriate masks (KN95 or N95) and appropriate masking technique (wash your hands before and after putting it on, don't touch the front, make sure there's no gaping) 🫧

[starcountr]

Once again bringing up the fact that albinism is always tied to varying degrees of visual impairment. Disability is inherent in our condition and glossing over this (due to ignorance or not) is an act of ableism and fetishisation. Before you create an original character or any sort of fiction you ought to not stick to lazy research. Albinism affects real people, not just animals and social stigma because of our looks is only half of the story. Please do not contribute to a superficial understanding of an already rare and not researched enough condition, happy 10 years of international albinism awareness day.

[ween-kitchens]

happy disability pride month and FUCK all the subtitles that go [speaks foreign language] instead of just saying what was said

[sojourner-between-worlds]

Even if you, personally, don't hate Discord's new UI, I am begging ya'll to still send them the following feedback:

"The changes made to Dark Mode are an accessibility issue due to the lack of a low contrast option for those who need it."

The previous dark gray was never ideal, tbh, but it was still worlds better than what we have now. As someone who can feasibly get by with the new dark mode but vastly prefers low contrast, and as someone who knows people who do need low contrast -- please tell them about this problem.

[friendlycursedspaceotter]

Pro tip for my disabled and chronically ill friends in college: if you have to put a work order in and it is related any bit at all to your disability, write, very clearly in the "describe what needs to get done" section, "This issue is a health hazard," followed by a description of how the issue relates to your disability/chronic illness.

They are required to put it as a high-priority issue and fix it ASAP. Required BY LAW. Yes, I said it. They are legally required to fix these things, both under OSHA regulations and the ADA.

Play the disability card. I'm begging you. DISABLED IS NOT A BAD WORD. But don't abuse it. This is a fine line here.

Example: I'm heat and noise sensitive. My HVAC unit started breaking down and rattling loudly. That would be an example of a health hazard. A broken light could be a health hazard to someone with vision issues. I can only speak for myself here. But y'all have the right to speak up and advocate to yourself.

Neurodivergent people, this applies to you too. You're one of us (one of us! one of us! one of us!). Don't let the exclusionists gatekeep this information from you.

[miraculouslumination]

"But AI makes art more accessible to disabled people!" your AI schlop is clogging the search results and making it actively MUCH MORE DIFFICULT for ANY artist to find a real reference for their project

[em-the-nem]

Reasons to take a train for distance travel:

• affordable

• pretty views out the window

• no dealing with TSA

• you can bring your own snacks and drinks

• accessibility for disabled folks

• no baggage claim to break or lose your stuff

• you might meet a lesbian on there

[chronicpaingirlie]

it’s interesting to me how nondisabled people seem to have such a hard time grasping the idea that my illnesses are forever. for me it took some time for it to sink in, yeah, but other people seem to just like. refuse to even acknowledge the possibility (or reality) of disability and chronic illness.

like what’s your problem lol. why can’t you even try to imagine a world in which i am disabled forever and still a person living my life. why do you equate disabled with bad & unhappy & impossible to go on living with. why can’t you believe me when i say this is forever and im still a person and i still want to live

[thepisserrrrrr]

as an ND able-bodied person, i just wanna say that cpunks are NOT doing anything wrong by not allowing us in their community. its completely okay and im actually very very happy that physically disabled people finally have their own space where they dont have to deal with ableism toward them all the time

able-bodied NDs have it made in this sense. we have TWO communities! we have neuropunk and madpunk, and you can go on any social media platform and easily find hundreds of other NDs on there along with little communities and shit. but physically disabled people dont have it that easy. when they DO find one that isnt just about ND people, it's still full of ableism. i've seen it myself and it makes me sick

so physically disabled people decided to make their OWN community. just for them. no one else. then THATS when able-bodied NDs start getting pissy and call them ableist when they were basically doing the exact same shit before.

you can handle not being allowed in one community. theres two more you can be part of just fine

if youre an able-bodied ND who sees yourself in any of this, maybe you should stop and look at yourself. make some improvements

to the cpunk community, dont let people like this tear you down. stand your ground, push these people out. you deserve your OWN safe space and no one will take that from you

[simpystarrr]

//Helluva Boss spoilers

I LOVE the disabled representation here with the little deaf imp and how Fizz respected and supported them!!!

I don't know if the sign language is accurate but the scene is cute nonetheless