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Anarchist Meme Collective

@anarchistmemecollective

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prettyasapic

Every person need to be taught disability history

Not the “oh Einstein was probably autistic” or the sanitized Helen Keller story. but this history disabled people have made and has been made for us.

Teach them about Carrie Buck, who was sterilized against her will, sued in 1927, and lost because “Three generations of imbeciles [were] enough.”

Teach them about Judith Heumann and her associates, who in 1977, held the longest sit in a government building for the enactment of 504 protection passed three years earlier.

Teach them about all the Baby Does, newborns in 1980s who were born disabled and who doctors left to die without treatment, who’s deaths lead to the passing of The Baby Doe amendment to the child abuse law in 1984.

Teach them about the deaf students at Gallaudet University, a liberal arts school for the deaf, who in 1988, protested the appointment of yet another hearing president and successfully elected I. King Jordan as their first deaf president.

Teach them about Jim Sinclair, who at the 1993 international Autism Conference stood and said “don’t mourn for us. We are alive. We are real. And we’re here waiting for you.”

Teach about the disability activists who laid down in front of buses for accessible transit in 1978, crawled up the steps of congress in 1990 for the ADA, and fight against police brutality, poverty, restricted access to medical care, and abuse today.

Teach about us.

Oh! Oh! I got one! Meet Edward V. Roberts-

Ed Roberts was one of the founding minds behind the Independent Living movement. Roberts was born in 1939, and contracted polio at age 14, two years before the vaccine that ended the polio epidemic came out (vaccinate your kids). Polio left Roberts almost completely paralyzed, with only the use of two fingers and a few toes. At night, he had to sleep in an iron lung, and he would often rest there during the day as well. Other times of the day, he breathed by using his face and neck muscles to force air in and out of his lungs.

Despite this being the fifties, Roberts' mother insisted that her son continue schooling. Her support helped him face his fear of being stared at and ridiculed at school, going from thinking of himself as a "hopeless cripple" to seeing himself as a "star." When his high school tried to deny him his diploma because he had never completed driver's ed, Roberts and his mother fought the school and won.

This marked the beginning of his career as an activist.

Roberts had to fight the California Department of Vocational Rehabilitation for support to attend college, because his counselor thought he was too severely disabled to ever work or live independently. Roberts did go to school, however, first attending the College of San Marino. He was then accepted to UC Berkeley, but when the school learned that he was disabled, they tried to backtrack. "We've tried cripples before, and it didn't work," one dean famously said. The school tried to argue the dorms couldn't accommodate his iron lung, so Roberts was instead housed in an empty wing of the school's Cowell Hospital.

Roberts' admittance paved the way for other disabled students who were also housed in the new Cowell Dorm. The group called themselves "The Rolling Quads," and together they fought and advocated for better disability support, more ramps and accessible architecture like curb cut outs, founded the first formally recognized student-led disability services program in the country, and even managed to successfully oust a rehabilitation counselor who had threatened two of the Quads with expulsion for their protests.

After graduation from his master's, he served a number of other roles- he taught political science at a number of different colleges over the years, served on the board for the Center for Independent Living, confounded the World Institute on Disability with Judith E. Heumann and Joan Leon, and continued to advocate for better disability services and infrastructure at his alma mater of UC Berkeley.

Roberts also took part in and helped organize sit ins to force the federal government to enforce section 504 of the Rehabilitation Act of 1973, which stated that people with disabilities should not be excluded from activities, denied the right to receive benefits, or be discriminated against, from any program that uses federal financial assistance, solely because of their disability. The sit-in occupied the offices of the Carter Secretary of Health, Education and Welfare building in San Francisco and lasted 28 days. The protestors were supported by local gay rights organizations and the Black Panthers. Roberts and other activists spoke, and their arguments were so compelling that members of the department of health joined the sit in. Reagan was forced to acknowledge and implement the policies and rules that section 504 required. This national recognition helped to pave the way for the Americans with Disabilities Act in 1990.

Roberts died of cardiac arrest in 1995 at the age of 54, leaving behind a proud legacy of advocacy and activism. Not bad for a "hopeless cripple" whose rehab counselor thought he was too disabled to ever work.

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egg-squid

Here is a great online course for disability history!!

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cwipple

“Black Panthers saved the 504 sit-in.” – Corbett O’Toole, participant in the 1977 504 protest in San Francisco

”Along with all fair and good-thinking people, The Black Panther Party gives its full support to Section 504 of the 1973 Rehabilitation Act and calls for President Carter and HEW Secretary Califano to sign guidelines for its implementation as negotiated and agreed to on January 21 of this year. The issue here is human rights – rights of meaningful employment, of education, of basic human survival – of an oppressed minority, the disabled and handicapped. Further, we deplore the treatment accorded to the occupants of the fourth floor and join with them in full solidarity.” – Black Panther Party media release on the protest, from website Disability Social History (click thru to see pictures of BPP news about the success of the protest!)
According to disability rights activist Corbett O’Toole, these advocates “showed us what being an ally could be. We would never have succeeded without them. They are a critical part of disability history and yet their story is almost never told.⁠”
They were running a soup kitchen for their black community in East Oakland and they showed up every single night and brought us dinner. The FBI [guarding the building entrance] was like, “What the hell are you doing?” They answered, “Listen, we’re the Panthers. You want to starve these people out, fine, we’ll go tell the media that that’s what you’re doing, and we’ll show up with our guns to match your guns and we’ll talk about who’s going to talk to who about the food. Otherwise, just let us feed these people and we won’t give you any trouble” – and that’s basically what they did.

Please read up on the Black Panthers' involvement in the 504 movement, they were integral to the occupation lasting as long as it did and were INCREDIBLY ACTIVE PARTICIPANTS! They are more than a footnote in that part of disability history, and I want more people to know this part of their legacy!

Read about Bradley Lomax (and his aid and fellow organizer Chuck Johnson, who I've struggled finding sources on outside of articles on Mr. Lomax :( ) here and here! Together the two were integral in bringing Black Panther Party organizing and activism to the disability rights movement!

I wish there were more information on Mr. Johnson, as his work is dear to my heart as someone who also requires caregiving. ;3; <3 Considering how little information there even was available online for Mr. Lomax just ten years ago I am hoping we get more coverage of Mr. Johnson's contributions to this important part of disability history sooner rather than later. I do not want his activism ignored!

Do not let the full richness of our history be whitewashed! The Black Panthers kept the protestors fed, they HEAVILY publicized the protests in their paper The Black Panther and agitated on the protest and protestors behalf, and paid organizers' way to Washington to pressure the HEW secretary to actually sign the damn act. In turn, the Panthers did this because the Oakland ILC did outreach to them, and helped Mr. Lomax with transportation. This is solidarity buried under focus on the white organizers. Please please please cherish it. Keep it close to your heart, read about it, celebrate it, share it!

Obviously there were more Panthers who helped but I have already lost the first draft of this and I'm starting to fade -- here's two more detailed sources to read for more, and I highly recommend you do!

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"low support needs disabled people are often not believed to have a disability at all and therefore struggle to get accommodations."

"high support needs disabled people's accommodations are often seen as 'too much' and therefore are not met."

"neurodivergent people's needs are often dismissed because nothing is physically wrong with them."

"physically disabled people people often cannot physically access buildings and people refuse to do anything about it."

"invisibly disabled people are seen as lazy by society."

"visibly disabled people are ostracized from society."

IT'S ALMOST LIKE THERE'S NO SUCH THING AS A SOCIALLY ACCEPTABLE DISABILITY

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Pixie lost a question tumblr post and not sure exactly what was ask . took Pixie so so long time to answer . Weeks of work … So here is answer with no question . so sorry !

A few things about being actually nonverbal ( Never able use mouth words at all , ever … “going nonverbal” is NOT A THING ) .

1- AAC Very slow compare to mouth words . Can take Pixie 10 or more minutes just to give answer to “ hello how are you ?“ Longer word things , like simple blog post , can take weeks to months . people are never that patient , even otherwise good people can just not wait , not without practice .

2- being nonverbal , needing AAC to Communicate all the time , make many things much harder or not possible at all , even with help .

example -

Most medical professionals Pixie have known will not accept communication with AAC device As genuine communication . And ! also will not accept communication from someone else , what is not biological parent , unless AAC user verbally ( not with AAC device ) give permission . Or . personally fills out in writing many forms giving permission . Even then . Is not work every time .

is Same for many many other things . banks and government agencies and schools and businesses and organizations of all sorts .

3- Geting emergency services like ambulance or Police or Firefighter services require speaking . so , need someone else help by calling .

4- many programs for disabled people will not allow access to programs if person cannot *speak* independently . ( Pixie lucky have found some good programs , in big city really help have more programs to choose from )

Pixie also have cognitive disability and moderate to severe language difficulties . but ! even people what just not can speak And not have anything else disabling ( unlike Pixie ) Still need so much more help just because of not able speak ever .

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this honestly just came out of left fucking field i would have never expected to hear anything like this in this show. consider me Pleasantly Surprised tbh

This was the autism episode

people seem to forget that house was a multiply disabled man, so it should be a given that he’d be against eugenics and eugenicist doctors

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I’m psychotic. I mean that literally I experience psychosis.

I think many people don’t understand that while yes talking to myself is a symptom of my psychosis, it’s also one of my best coping skills.

It’s not scary when I mumble to myself in public, it’s me coping in a way that’s safe for you and me.

Reduce stigma for everyone no matter why someone acts like me but like in my case specifically I promise you prefer me when I can talk to myself.

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they said they might have to kick some people off the flight in order to fit my wheelchair on. I feel so bad but also why the fuck have they not designed airplanes better so that this doesn’t have to happen!! Why can’t they put in a transit strap system like on trains or buses or like literally just have a wheelchair storage area that is big enough for more than just foldable transport chairs

also like. What’s the point of registering my wheelchair beforehand, sending in photos, giving them all my device information. If they don’t like do anything about it beforehand or like proactively restrict the amount of seats or something. There’s just so many better options

they really need to update the air carrier access act tbh like. Please

they gotta make sure you feel bad for being disabled

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cyanomys

yes, there are that many really disabled people on the internet actually

When I was less sick I used to think, "It seems like such a large portion of people on the internet are disabled, it can't possibly be that large of a percentage of the population" and then let my ableism demons tell me it was because they were faking (the same ones that told me I was faking, until I made myself really ill.)

But now that I'm sicker and wiser I realize I was logically just wrong because

  1. The internet is disabled people's lifeline. There are more disabled people on the internet because OF COURSE. People who aren't disabled can be less chronically online because they don't have to be. This is textbook selection bias!
  2. But actually also I was almost right, because there are way more disabled people in society than you would think! They're just systematically hidden and excluded from public spaces for abled peoples' convenience! 🙃

Anyway maybe this will help you understand and/or explain to abled friends and family.

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see. the interesting thing to me is that the Bible tends to depict disability in four different ways:

  1. disability as the result of sin (e.g. Deuteronomy 5:9)
  2. disability as curable via the profession of faith (e.g. Matthew 9:20)
  3. disabled people as a method for the abled to demonstrate faith (e.g. John 9)
  4. disability as a metaphor for human defect (e.g. Matthew 23)

and none of these things are any less common when you think about disability in popular culture in the year of our lord 2024!! by the way!!

  1. disability as the result of immoral choices (think about popular conceptions of diabetes, for example)
  2. if someone is still disabled, it is because they haven't tried hard enough to seek a cure ("have you tried yoga?")
  3. if an abled person helps a disabled person, they are thought of as a saint. when disabled people have our autonomy removed, this is seen as a moral good
  4. many literary depictions of disability only use disability as a metaphor, and not as. y'know. an actual disability (this is common with depictions of blindness)

anyway. I'm a Christian and I definitely don't think Christianity is inherently ableist. but I do think there is a lot of ableism in the church. and that definitely makes a fuckton of sense when you look at our source text. but I think this is an interesting example of Cultural Christianity. even those who don't believe in sin DO believe that disability is the result of sin. or at least, they act like they believe that to be the case

this post is a mess but 👍 this is vaguely what I've been working on today

and this isn't even getting into "sins of the father" ideologies! on account of. well. misogyny. the modern world is much more likely to appeal to "sins of the mother". think about how many disabilities are blamed on immoral actions made by mothers either in pregnancy or early in the child's life. I could spend all day just talking about that in the context of autism. let alone physical disabilities. it is. There. if you have eyes to see it

you ask most people if they think disability is a holy punishment, and they'll probably say no (putting aside Hillsong and other evangelicals for now). but it becomes really fucking evident that they do, deep down, believe that once they start to talk about disability for more than two seconds

  • if you're born with disability, everyone scrambles to blame the parents somehow
  • if you acquire disability, everyone scrambles to blame you for making the wrong lifestyle choices
  • if your disability is a chronic illness, everyone scrambles to tell you (explicitly or not) that it's your own fault that you haven't been cured yet

we still see disability as a punishment. it's everywhere. moral model of disability. sure is a trip

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I think people over seventy years old should have unrestricted access to prescription painkillers. Not to take home or anything (they might get sold or stolen, although frankly I think pain meds should be less regulated in general and the fact that such a market exists for that is a sign that they're over-restricted in the first place) but like, they should be able to show up at the hospital and flash their ID and be like "morphine please" and have a nurse shoot them up then and there. Yes this is about my stepfather who had every health problem and finally became a tolerable human being after he was put on constant pain management medication but also if you're over 70 you know how your own body works and what pain feels like and frankly if you throw away your life to a painkiller addiction at that age (way less rare than the media would have you think, most "abusers" of painkillers are self-medicating *to manage their pain that they're not being prescribed enough medication for*) then all the more power to you.

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*deep breath in*

*deep breath out*

Let AAC users say fuck!

Let them swear, let them say fuck and asshole and anything else they want.

Let them program their devices to say ‘fuck off’ instead of just ‘leave me alone, please’. Let them have language that’s adult or even offensive! Give them the ability to communicate the same as anyone else- let them have the option to be abrasive and even rude for when people are being assholes, let them swear casually so they can joke with their peers and say shit like ‘can you pass the damn ketchup’!!!!!!!!

Let disabled people say fuck!

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ashnistrike

In the year between college and grad school, I got a job at a deaf-hearing relay. This is a service that "translates" between people with text interfaces and speak-aloud interfaces - this was well before any business or indeed most of the population had regular access to online chat. So Deaf folks would call up on TTY phone and I would put the call through to a business or a friend or relative or whoever, and I would "voice" whatever the Deaf person typed and then type back to them whatever the speaking person said.

This job required two important skills. The first was typing really fast, and being able to transcribe quickly and accurately from natural speech. You could sometimes ask the speaker to slow down, but do that too much and you're keeping the conversation from flowing smoothly.

The second was the ability to say whatever the Deaf person typed with the correct emotion, and with zero embarrassment. Are they being an asshole to a service person? Sharing TMI about their weekend activities? Planning a heist? They get to do that the same as a caller who doesn't have you on the line! So the job interview involves getting handed a sheet full of dialogue, with swears and sexual innuendo aplenty, and you have to act everything out to the interviewer without crawling under a desk. Anyone can learn to type, but if you can't yell "fuck you" at an interviewer without muttering, they're gonna find someone else.

And if you can take that seriously as a requirement for actual live people, you can put it in your AAC app.

(for those that don’t know AAC is “alternative and augmented communication” and covers a very wide range of things that help people with limited or no verbal capacity, and often limited physical movement, to communicate).

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roxiqt
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hazel2468

Okay but actually like... Yeah.

I think a lot of abled people, people who aren't chronically ill or disabled. Have this idea that if they get sick, doctors will do EVERYTHING to make them better. After all, it's what they see on TV, isn't it? Doctors working to solve the mystery and save the patient. So of COURSE if they ever got sick, the doctors would fix it...

Which means that when someone is chronically ill and disabled and they don't get magically fixed... It must be their fault. I mean, doctors do everything they can, right? Doctors fix people, right? So if you get sick and stay sick, it must be YOUR fault, right?

I've noticed people get... REAL fucking mad when I say doctors are shit. When I say doctors being shitty and dismissing patients and not helping people is the rule, not the exception. I've encountered countless people who tell me that I'm wrong, that doctors are saints and angels who help the sick, and maybe if I wasn't so fat/disgusting/uncooperative/broken/dramatic that maybe I would be BETTER.

When really? The problem is that I can count the number of doctors I have had who listened to me and did more than look at my size and tell me that being fat is the problem on one hand, and those are ALL doctors I still see to this day. That out of the DOZENS of doctors I have seen in my lifetime, there are THREE who I still have who listen to me and care about me. Who did their damn JOB when I came in presenting with symptoms and decided to look for an actual cause instead of assuming it was because I am fat, or because I was an "attention seeker" or a "spoiled teenager" or just a "woman".

Healthy people who don't have these experiences with doctors will not learn this until it's too late. And then they not only have to deal with doctors telling them that there is nothing wrong with them...

They'll have to deal with people saying the exact same shit they always said to chronically ill and disabled people.

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the cultural boogeyman of the faker is such a convenient lie for ableism. Waste your time fighting about who does and does not deserve help, and maybe you wont realizes that there was never any help to begin with. The is no epidemic of malingerers taking up resources they don't need, there is a lack of resources for disabled people

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mental illness hasn’t been destigmatised but commercialised

Sooo true.

You can’t have serious conversations about your mental illness and you can’t even mention having one of the more stigmatized mental illnesses.

But you can endure a long line of ads recommending medications, self-care products, gym memberships, self-help books, online seminars, crystals, plants, sunlight lamps and other overpriced shit that’s supposed to be good for your mental health but is mainly just there to take advantage of people who are at a vulnerable place in life. Disgusting.

Marta Russel called this “handicapitlaism” and identified it as one of the traps of bourgeoisie/free market disability rights activism 

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Anonymous asked:

I noticed you have tagged posts ableist language on posts which I haven’t noticed the ableist language in. Sometimes in further reflection I can see why you have added that tag, and sometimes not. If you’ve ever got the time/inclination, could you explain some of the more nuanced ableist language usages?

sure thing! (and obviously, trigger warning for ableist language to follow)

I know many may feel I take a pretty radical stance, but i've studied enough linguistics to know how powerful the words we use can be, even when we don't intend it in that way. so I use the ableist language tag for when people are not being ableist but are using language which reinforces ableism. this can get a bit tricky as the people who are the subjects of ableist terms may often identify with or reclaim those terms, like calling someone a cripple is ableist, but many people self-identify as cripples, like the cripple punk movement.

I think they generally fall in three categories:

intelligence: stupid, idiot, moron, etc. intelligence and iq are not real, they're eugenicist myths and insulting people's intelligence only feeds these myths and serves the ruling class. build solidarity by seeing everyone as your equal. there is no moral value to having received a better or worse education than someone else. also many of these terms come directly from eugenics, such as their classifications of types or degrees of autism.

diagnoses: psycho, dumb, schizo, bipolar etc. these are real health conditions and i shouldn't have to explain why using them as insults is deeply offensive.

saneism: insane, crazy, mad, etc. the sane/insane dichotomy, if it was ever helpful, which I doubt, has been outdated for generations. there is no medical diagnosis of 'insane', there are hundreds of mental health conditions and an infinite number of combinations which we are barely beginning to understand. but none of them have or convey a moral value. using them as insults only stigmatizes those of us who have them, to the benefit of the ruling class and detriment of solidarity.

even if you are skeptical or attached to this language I'd challenge you to try not using it. you'll find it improves your vocabulary and your speaking and writing skills. not just that but it will deepen how you think about your fellow humans.

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bismuth-209

to everyone in the notes saying "i'm able-bodied but standing for more than 10 minutes, or 5, or 2 makes my body hurt"

you are not able-bodied

able bodies are able to do that

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elfwreck
It is more tiring to stand in one place for an hour as it causes a few muscle groups in your feet and legs to fire for an extended period of time. When you are walking, all the muscles in your feet and legs are used as they share in the work. This prevents any one muscle from getting excessively tired.
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mckitterick

another example of how retail is brutal

our bodies are literally engineered to walk, not to stand. our ancestors spent a huge amount of their time walking (not standing) every day and it shows in basically every aspect of our physiology. like these things:

like each time you take a step, your calf muscles help pump your blood up your leg against gravity. they cannot do that if you are standing (or sitting!) still. this is why not walking enough is associated with deep-vein thrombosis, btw - if you are able to do so, even walking for a few minutes a day is excellent for your circulatory health because it can prevent blood clots. if not, other exercises that move the calf muscles, or even simply massaging the area daily, can also have a similar preventative effect*.

*This is not medical advice. if you have DVT already or suspect you may have it, DO NOT MASSAGE YOUR LEGS. Massage could dislodge clots that have already formed and cause an embolism. Consult with your doctor.

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