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Yes, I didn't know much about PETA but I'm learning a lot of things since I improved my English. I'm not from the US and English isn't my language, but I'm improving in the language and I ended up reading about it.
Ahhh yeah sorry that makes sense. Back in the day there was lots of discourse between Black people and white vegans and how they (Peta and white vegans in general) would compare farm raised animals to slavery and or the holocaust. I remember seeing Black bloggers being harassed by white vegans.
mod laina
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I discovered that PETA is against guide dogs (comparing it to slavery/slave owners) and has harassed and blocked blind people for having guide dogs. And found out they are extremely racist, they made several anti-indigenous, anti-black, anti-Asian publications. In addition to making advertisements that cow's milk causes autism. Sad how they still have many followers and activists.
so I know they have incredible resources from the white ppl but I'm surprised you're just finding out about this. The campaign about cows milk causing autism is new to me though. That is straight up eugenics shit.
Like ok so I'm not blaming you for not knowing I want to make that clear.
I know some of my older blogs have sources from years ago that They've been doing though I'll try to find them.
mod laina
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I really appreciate the body neutrality posts that people make about how “even if you can’t love the way your body looks, appreciate the things your body does for you”. And sometimes there are examples. It’s a really great message.
I just want to take a minute to shoutout to my fellow disabled people who feel trapped in their body, or who may feel their body lets them down. Maybe sometimes you’re angry at your body or resent it for the things you can’t do. Maybe sometimes these posts remind you of these things and I just want you to know that you’re valid. Your feelings are valid.
You aren’t failing if body neutrality doesn’t work for you. I know it’s often said to be a good alternative if body positivity isn’t for you but you aren’t failing if you can’t get there.
I just want you to know that your worth doesn’t change, regardless of what your body can and can’t do. You are always worthy.
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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
youtube
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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