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yknow i never noticed the sheer rareness of images having ids or alt text on this website until i started adding alt text to my art (and trying to remember to add it to any images i post in general, especially text screenshots) and that makes me kinda sad
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"As soon as possible" means a few weeks as subtitles sadly take a lot of time.
-mod Tallys
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Autistic (Coded) Characters I Actually Relate To
That easy little video I made for Autism Acceptance Month ended up being nearly forty minutes and took me quite a while.
And yeah, I will add subtitles as soon as possible, just would not have managed to finish this before the end of the month otherwise.
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As a disabled person who's loved LEVERAGE and LEVERAGE REDEMPTION since the beginning - for the characters but also the whole ethos of performing acts that help people against crap systems, it's wonderful to be reminded that it springs from reality.
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this is your daily reminder to stop being abusive and mean toward people with bladder and bowel issues.
im tired of hearing people mock those who struggle with bladder/bowl control, for people who can't tell when they need to go until it's too late or at all, for people who have uncontrollable voidings and leaking, for people who need to wear incontinence products around the clock, for people who need them influctuating amounts and need different kinds of products, for those who bedwet, for those who can't afford incontinence products so their clothes get dirty- to everyone with bowel and bladder issues.
we are human. we are still people. we are not gross, we are disabled. we are struggling with a disability. if you make cutesy posts about canes and wheelchairs, you need to include people who wear diapers, people who need plastic pants, plastic bedsheets and absorbent bed pads. you need to include people who can't tell when they need to go. people who need/use catheters. people who have colostomy bags. people with stained and dirty clothing. people who have to change their incontinence products in public.
you need to include autistic and ADHD and ND and disabled people who feel unsafe without diapers. you need to include people with spinal injuries and ehlers danlos syndrome and muscular control disorders with need incontinence products and feel safe with them. you need to include people who like their diapers and not just tragic stories where it's never discussed or doesn't negatively impact their life and livelihood.
please include all disabilities in your disability positivity posts, and please be kind and treat all disabled people with respect and humility, including those of us with symptoms you may find "gross".
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Protect yourself during earthquakes!
If possible, DROP! COVER! HOLD ON!
Using cane, DROP! COVER! HOLD ON!
Using walker, LOCK! COVER! HOLD ON!
Using wheelchair LOCK! COVER! HOLD ON!
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Your parents are not "narcissists". They're typical authoritarian assholes who treat you like their property because society allows them to.
Your ex boyfriend is not a "narcissist". He's a typical misogynistic douchebag who treats women like shit because society allows him to.
Your boss is not a "narcissist". They're a typical classist dipshit who thinks workers' entire purpose in life is to generate profit because society allows them to.
And even if they happen to be a "narcissist", that's not what gave them the power to get away with abuse.
So stop blaming mental illness and start blaming society's normalization of abuse. Stop acting like someone has to have a mental illness in order to do something cruel when ordinary people have been doing atrocious things since forever.
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the lack of compassion that a good portion of lotr fans show for frodo ("why can't he fight or do simple tasks" "why is he so weak" "why does he always need help / to be rescued") mirrors the lack of compassion of people for those who bear the burden of invisible disabilities. he's struggling against an immense weight at every step! something that actively tries to destroy him, worsening at every moment! his heroism is in just continuing to walk his path, step by step. his bravery is in just existing as himself under the debilitating weight of the ring. but because the influence of the ring is invisible, it is forgotten, and frodo is written off as a weak, cowardly, and/or useless character, much like disabled people irl. in this household we do not stand for frodo slander!!!
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the lack of compassion that a good portion of lotr fans show for frodo ("why can't he fight or do simple tasks" "why is he so weak" "why does he always need help / to be rescued") mirrors the lack of compassion of people for those who bear the burden of invisible disabilities. he's struggling against an immense weight at every step! something that actively tries to destroy him, worsening at every moment! his heroism is in just continuing to walk his path, step by step. his bravery is in just existing as himself under the debilitating weight of the ring. but because the influence of the ring is invisible, it is forgotten, and frodo is written off as a weak, cowardly, and/or useless character, much like disabled people irl. in this household we do not stand for frodo slander!!!
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when someone points out that something is ableist you actually don't have to admit to doing it
like when I talk about discrimination I do not want to hear "I've done this before. [insert story about how they were bigoted towards people like me] I will do better though" do you want an award? for doing the bare minimum of not continuing to harass and belittle disabled people?
literally no one wants to hear about your bigotry
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People have gotten way too comfortable risking serious disability just because they feel they have the right to selfish.
Do you want to kill your parents?
Do you want to disable your partner?
Do you want your friends to lie in bed wishing for death?
Wear a fucking mask.
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One of those going-over-the-fandom's-head memes about Shuro Dungeonmeshi being hopelessly infatuated with Falin and loathing Laios even though they have basically identical personalities where the direct takeaway is "lol, Shuro is dumb" and the part going over the reader's head is "people decide whether your autistic traits are charming quirks or red flags based on whether they find you fuckable".
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i think the way tiktok and tumblr (yes i am unifying these two sites together for this, for shame!) talk about autism and adhd (n honestly ocd too) as this quirky party trick has really damaged The Youths, at least in america (n they enact that damage on the rest of us, per usual)
like you guys will CONTINUE as usual to mock n harass anyone who is slightly "weird" or "offputting" bc well YOURE autistic and YOU dont do that, so it must be a them problem. well, YOU live on your own and YOU have a job and YOU have tons of friends and YOU go to uni and YOU go to the club and YOU arent weird. its not an "autism thing", this persons just weird. weird for being a picky eater, for using scripts in conversations, for avoiding crowded places n having meltdowns while in them, for living w their parents or in assisted living, for going on about their special interests, for missing social ques, for speaking "weird", for stimming, for having little or no friends, for being unemployed, for having motor issues, for being nonverbal, for not being able to handle the school/academy system, for being autistic.
THEYRE clearly just weird, THEYRE wrong for exhibiting signs and symptoms of autism. their autism is WRONG and WEIRD and OFFPUTTING. YOURE autistic and YOU dont do that, so its clearly "not about autism".
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Replacing physical buttons and controls with touchscreens also means removing accessibility features. Physical buttons can be textured or have Braille and can be located by touch and don't need to be pressed with a bare finger. Touchscreens usually require precise taps and hand-eye coordination for the same task.
Many point-of-sale machines now are essentially just a smartphone with a card reader attached and the interface. The control layout can change at a moment's notice and there are no physical boundaries between buttons. With a keypad-style machine, the buttons are always in the same place and can be located by touch, especially since the middle button has a raised ridge on it.
Buttons can also be located by touch without activating them, which enables a "locate then press" style of interaction which is not possible on touchscreens, where even light touches will register as presses and the buttons must be located visually rather than by touch.
When elevator or door controls are replaced by touch screens, will existing accessibility features be preserved, or will some people no longer be able to use those controls?
Who is allowed to control the physical world, and who is making that decision?
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Is only Alt Text enough?
[PT: Is only Alt Text enough? End PT.]
If you post something and include an image description in the alt text, that's great! But it would be even better if you included a description in the body of the post as well. Alt text doesn't always work, especially on a platform as broken as Tumblr is. An image must also load fully before the [ALT] button shows up, so people with Internet issues won't be able to see it for a long time. It also requires pressing on the small [ALT] button, which may be difficult for people with motor issues. The point I'm trying to make here is that the ability to access and read alt text is conditional, not a given. Putting the image description in the text of the post helps it be accessible to everyone.
"Okay, well can I at least put it under a readmore?"
[PT: "Okay, well can I at least put it under a readmore?" End PT]
No! If your blog or the original post is deleted, that readmore is gone forever! It also presents an extra step, another thing to push. This can be difficult for a number of reasons! I have also heard that readmores are difficult for some screenreaders, but I can't remember for sure.
"Can I at least make it pretty?"
[PT: "Can I at least make it pretty?"]
No! If you write the image description in small text, italics, bold, colored text, or other fonts that makes the description harder to read! That defeats the purpose! It can also be hard for screenreaders to read certain kinds of text, especially unicode or other fonts.
TLDR: Please include your image descriptions in the body of the post as plain text. It's the best way to make sure your post is actually accessible to everyone!
[PT: TLDR. end PT.]
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Please stop using disabilities you don't have as comparisons.
I saw a video trying to explain that autistic people don't make eye contact because it can be painful for them (good, this is true) and telling them to "just do it anyway" is ridiculous, saying "you wouldn't tell a wheelchair user to "just walk, its better for you" so don't tell autistic people to just make eye contact".
But people do. They do all the time. It's well documented that doctors will withhold their ok for patients to get a wheelchair (which is needed unless you're paying out of pocket, because insurance and most public disability services like the NDIS need proof from a doctor). I've known people who can hardly walk and are having to fight because the doctor still insists it better for them to walk, even if it's painful and sevearly limiting their quality of life.
Then in the comments, someone pointed out that people do say that to wheelchair users (good, this is true) but then continued on by saying "unless you just don't have legs" which is just as bad as the origonal.
I had to fight to get my first wheelchair as a double leg amputee, and every wheelchair since then I've had to justify not wanting the "better option" (prosthetics) to the government so they'll approve me for the funding. Doctors and even strangers too, all want to know why I'm not walking, why I'm not using prosthetics all the time. When I go on trips with my family I'm told to "just walk" so they don't have to pack my wheelchair. at my own graduation from university I was chastised by the organisers for not bringing my prosthetics (because wearing them was exceptionally painful back then and i hadnt worn them in nearly 3 months. I had asked before if this would be ok. they knew) because the venue was accessible but not the part of the venue the graduates were in. On the topic of university they also put my class in the only non-wheelchair accessible room and held meetings i was expected to take part in, in the non-accessible lunch room. When I complained, I was told to just use my legs for a few minutes so I could get into my classes. Being an amputee with no legs didn't shield me from these experiences either, it often made it worse.
I have all 3 of the disabilities mentioned (autistic, wheelchair user, amputee). If you don't have the disability you're using for a comparison, don't use it. Please
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Listen. Sit down around the fireplace with me for a moment.
Artists. Gif makers. People who like memes. Anyone who posts images.
Y'all have got to start writing your own image descriptions. You have to. You really really have to start doing it yourself.
Us, the blogs dedicated to accessibility, cannot keep doing it for you. Well, we can, but we shouldn't have to. We shouldn't have to dedicate our time and energy to make posts that are not ours accessible and you shouldn't expect strangers to do you favors, especially when the work is so thankless. For every post I describe, a hundred more are posted without one.
The original post should be accessible. Adding an image description through a reblog is a metaphorical bandaid when what's needed are metaphorical stitches. Someone's ability to access the internet should not be dependent on the goodwill of others and goodwill that can just be ignored at that. People can simply choose to not reblog an accessible version of a post, whether intentionally or out of ignorance.
We don't expect volunteers to construct temporary ramps for buildings, we expect the building to have its own ramp, built to code.
The next time you see or post art, or a meme, or a screenshot from Twitter, ask yourself- does someone with a visual impairment not deserve to know what this image is about? Why should you get to laugh at the joke and not them?
Just.....just do it. Just write image descriptions. There's loads of resources out there to help you and even more references from the people who care.
Just. Do it.
Start doing then.
Start telling other people to do them.
Start reblogging them.
Accessibility is a necessity and it is not optional.
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