Disability

"Constitutional protection for bodily autonomy is of vital importance to people with disabilities, because that protection has far too often been denied to them in both reproductive and non-reproductive contexts. Perhaps most notoriously, around 60,000 Americans were forcibly sterilized in state-sanctioned programs to prevent those adjudged to have psychiatric disabilities from reproducing."

"With disabled people in particular, police aren't trained to deal with us, they shoot first and ask questions later instead of taking the time to try and understand what we want to get across during interactions with them. Because everything is considered a threat first, we are more likely to die first. I absolutely don't think that the police are trained properly to handle calls when disability and mental illness are at play. If they did Alfred would still be alive."

"Pamela Anderson has more prosthetics in her body than I do; nobody calls her disabled."

"The provision of the wheelchairs would therefore address some challenges (for the disabled) such as integration into society as well as access to health and basic services and fill other gaps. We cannot talk about inclusivity if we do not empower people, at the grassroots level."

"He just wrote a really cogent, beautiful response online. Didn’t fight with anybody, didn’t call anybody anything, didn’t judge anybody. And he completely opened my eyes to a perspective I never thought of. He said, “I understand what an actor is. I, too, am an actor. But I’m an actor in a wheelchair, and I never see parts that are leading roles for a person in a wheelchair. And so the one time I see a role where there’s a person in a wheelchair, I think, wow, this could be it. This could be the moment where I have all of the tools necessary to play this part. Do I get a shot at playing it?” And he was like, “Because when you think of it on the flip side, they never call people with wheelchairs in to play able-bodied people, and they’ll get able-bodied people to play people in wheelchairs.” I never thought of it like that. My perspective, obviously, as someone who is not in a wheelchair—I just never thought of it that way. And I sat there and I was like, it’s powerful because you don’t think about representation, you don’t think about how important it is for people to see themselves onscreen in a real way. And at the same time, I don’t think Bryan Cranston did anything wrong. I don’t think everything has to be a fight. It’s just, like, a moment to be like, hey, maybe next time people in Hollywood can look at that and go, maybe you can get a relatively unknown actor to play that role and then put an A-lister opposite them and maybe this becomes their breakout. Maybe this becomes the thing that blows them up. And that’s where you realize how powerful representation is, because if you’re a person in a wheelchair, how many movies come along where the lead character is in a wheelchair? There’s virtually none. And even myself, I was like, oh man, I have to try and understand that a little bit more. It was eye-opening."

"When people project and understand that in an instant and as they grow older they face Parkinson's, Alzheimer's, MS, strokes, all the diseases of the brain and central nervous system, which will effect the entire population as we get older. People begin to realize hey I'm lucky, I'm just temporarily not disabled. So, the point is we're beginning to see equality, we're beginning to see new opportunities and that brings me to the other part we've already talked about, acceptance and the other part is denial. And what I mean by that, and everybody has to work it out for themselves, my point of view may not be your point of view, so please hold onto your belief and let me hold onto my belief. But my belief is that there is nothing we can't accomplish if we set our minds to it."

"Some people are able to accept living with a severe disability. I am not one of them, and that is why I have a keen interest in research and am deeply disturbed by unreasonable attempts to block scientific progress."

"While bilingual is understood as a valuable asset or goal for middle-class and upper-class students, for working-class and poor students it is framed as a disability that must be overcome"

"Due to the lack of federal record-keeping, we can’t even tell you precisely how many people are killed by police in the US in any given year, let alone how many of them are disabled. But we do know it’s a lot: A report from the Ruderman Family Foundation earlier this year found wildly varying estimates of the number of disabled people killed by police, from 25 percent to more than 40 percent of police shooting victims. For perspective, census data puts the overall incidence of disability at about 20 percent of the population."

"At the same time, people of color in the United States are generally more likely to be disabled, or to lack adequate care, due to factors like environmental racism, occupational segregation, and poor access to health care. This is a systemic inequality that begins long before a fatal interaction with police ever takes place."

"[Bioethics] is "a phony branch of elite philosophy whose principle purpose seems to be to justify allowing badly ill or disabled people to die.""

"Not only do physically disabled people have experiences which are not available to the able-bodied, they are in a better position to transcend cultural mythologies about the body, because they cannot do things the able-bodied feel they must do in order to be happy, ‘normal,’ and sane….If disabled people were truly heard, an explosion of knowledge of the human body and psyche would take place."

"There are days when I am shocked that I am still alive. Like millions of disabled, chronically ill, and older people, I spend an extraordinary amount of effort just existing. Beyond the efforts to keep our bodies from falling apart, we face existential threats from a society that actively silences, diminishes, excludes, and eliminates us."

"There are days when I am overwhelmed with grief and rage at the regressive attitudes toward public health and disabled people. In my opinion, the ableist, fascistic, and eugenic nature of proposed mask bans under consideration in New York City and Los Angeles is bleak. But what is happening now is not new or surprising; the hate is more explicit, that’s all."

"What is clear to me is that disabled people have never felt safe. Many of us view masking as a form of solidarity with workers, activists, and people of color all over the world fighting fascism and genocide. But mask bans send the message that it is a crime to be disabled. I think of people who have fought hard to stay relatively safe since early 2020, those who hang on a precipice that feels like it could fall at any moment. Some days I wonder what my breaking point will be."

"Disability is not a brave struggle or ‘courage in the face of adversity.’ Disability is an art. It’s an ingenious way to live."

"If there was a country called disabled, I would be from there. I live disabled culture, eat disabled food, make disabled love, cry disabled tears, climb disabled mountains and tell disabled stories…"

"Disability is a matter of perception. If you can do just one thing well, you’re needed by someone."

"The Americans with Disabilities Act (ADA) gives federal civil rights protections to individuals with disabilities similar to those provided to individuals on the basis of race, color, sex, national origin, age, and religion. It guarantees equal opportunity for individuals with disabilities in public accommodations, employment, transportation, State and local government services, and telecommunications."

"Q: Are people with HIV or AIDS protected by the ADA?"

"Q: What employment practices are covered by the ADA?"

"Of course, the idea that disability begets preternatural abilities is nothing new. The Greek seer Tiresias’ blindness gave him access to the spiritual sphere in Sophocles’ “Oedipus Cycle.” (As students of literature, we associate a similar capability with the blind poet Homer.) And so it goes for our modern mythologies: In “Rogue One: A Star Wars Story,” the blindness of Chirrut Îmwe, played by Donnie Yen, seems to connect him with the Force; Sofia Boutella’s character, Gazelle, likewise wears prosthetics that double as lethal blades in the spy thriller “Kingsman.” But I don’t feel like some “super-crip” — a supernaturally endowed disabled character — on nights when I can’t focus because of muscle spasms, on afternoons when I can’t spend time with friends because they’re playing disc golf, and on mornings when I remember how the nurses would catheterize me six times daily during that month I spent in the hospital, until they taught me to do it myself."

"It is probably safe to say that people like Franklin Delano Roosevelt (polio), Harriet Tubman (narcolepsy) or even the Oscar-winning actress Marlee Matlin (deafness) succeeded both despite and because of their impairments. Do I think that disability made an impact on these figures, that it offered up a unique brand of understanding and metamorphosed into a kind of Muse for them? Of course. But most people with disabilities will not be remembered by history. They are usually living challenging lives with little to show for it: Unemployment rates are disturbingly high, health care costs are often debilitating, and the emotional toll of living with an “aberration” can rend families apart. The only thing that a fidelity to positive stereotypes accomplishes, then, is to absolve society of maintaining commitments to the disabled, like making places more accessible, since it would be ridiculous to aid people who already have a leg up with added perks."

"And yet it is not a “perk” to take the elevator when your friends walk up the stairs or to park in one of the handicapped spaces or to use a capacious bathroom stall or to be wheeled to the gate when you fly. It’s not just convenient either. It’s essential. This is the challenging, needy underbelly of living with an impairment that positive stereotyping can obscure. Accommodations serve the invaluable purpose of ensuring the human dignity of people with disabilities — our ability to participate in society as completely as possible without being de facto quarantined for “defects” in a world that prizes fitness and forgets that disability is the most fluid identity category of all."

"The origin myths of many superheroes lie in life-altering accidents or bodily mutations. Fans of the genre emphasize that disability, largely unrepresented in other forms of fiction, is part of these characters’ stories. But those stories then go on to wish disability away, via bionic implants and armored suits. “ ‘Disabled’ superheroes aren’t disabled at all,” says Chris Gavaler, author of “On the Origin of Superheroes.”"

"The absence of characters living with permanent disabilities affects the way viewers and readers see themselves, argues Rachel Kolb, an Emory University graduate student who is deaf and writes widely about disability in literature. “If we don’t see ourselves within the cultural representations that surround us,” she says in an interview, “it becomes more difficult to imagine ourselves in various kinds of situations, various ways of exercising agency and justice and power and goodness. And all the other themes that tend to be a part of superhero movies.”"

"ACCORDING TO LAWRENCE Carter-Long, spokesman for the Disability Rights Education and Defense Fund , about 20 percent of Americans identify as disabled, while only about 2 percent of characters on television and in film have disabilities."

"Advocates are also wary of plots that go out of their way to portray disabilities as inconsequential, in a way that minimizes the genuine challenges they pose. When Netflix launched a show based on Marvel’s Daredevil character, a New York Times reviewer wrote that the central superhero “is sightless but not blind to crime.” In fact, he doesn’t seem blind to much of anything, including women or agile villains."

"Fundamentally, what Carter-Long and others want are more complex representations of people with disabilities — and not just in superhero blockbusters. “If there are few disabled characters being created or shown for disabled people to identify with, we then have fewer opportunities to be a meaningful part of what a huge number of non-disabled people simply take for granted,” Carter-Long said."

""It's got spastic in its name" the great philosopher Evan Mitchell once said"

"If there was anyone who actually fit the category of conservative, if there was such a category of people, they would have a very easy way to deal with the fact that 60% of the children under 2 [in Nicaragua] are suffering probable brain damage. Namely, by paying their debts. Simple conservative principle. But that's beyond unthinkable. Compassionate conservatives might want to go beyond that, if they existed. But they're much more interested in making political capital over the fact that a woman in a vegetative state shouldn't be allowed to die in dignity."

"Ladies and gentlemen, welcome to the next generation of science. The Agnate, an organic frame engineered directly into adulthood to match the client's age. You're looking at stage one - the development stage. Within 12 months, it'll be harvest-ready, providing a carrier of your baby, second pair of lungs, fresh skin - all genetically indistinguishable from your own and in compliance with the Eugenics Laws of 2015, all our Agnates are maintained in a persistent vegetative state. They never achieve conciousness. They never think or suffer or feel pain, joy, love, hate. It's a product, ladies and gentlemen, in every way that matters. Not Human!"

"I was learning as my friends were, and people I didn't know around the country, that we had to be our own advocates, that we needed to fight back people's view that if you had a disability, you needed to be cured, that equality was not part of the equation. And we were learning from the Civil Rights Movement and from the Women's Rights Movement. We were learning from them about their activism and their ability to come together, not only to discuss problems but to discuss solutions. And what was born is what we call today the Disability Rights Movement."

"You wanna know how you'll know if you're doing disability justice? You'll know you're doing it because people will show up late, someone will vomit, someone will have a panic attack, and nothing will happen on time because the ramp is broken on the supposedly "accessible" building. You won't meet your benchmarks on time, or ever. We won't be grateful to be included; we will want to set the agenda. And what our leadership looks like may include long sick or crazy leaves, being nuts in public, or needing to empty an ostomy bag and being on Vicodin at work. It is slow. It's people even the most social justice-minded abled folks stare at or get freaked out by. It looks like what many mainstream abled people have been taught to think of as failure."

"We are more disabled by the society that we live in than by our bodies and our diagnoses."

"That quote, "The only disability in life is a bad attitude," the reason that that's bullshit is because it's just not true, because of the social model of disability. No amount of smiling at a flight of stairs has ever made it turn into a ramp. Never."

"I want to live in a world where we don't have such low expectations of disabled people that we are congratulated for getting out of bed and remembering our own names in the morning. I want to live in a world where we value genuine achievement for disabled people."

"While disability theory has compellingly pointed to the ways in which the construction and production of (inaccessible) space renders disabled bodies abnormal or aberrant, Indigenous peoples informed by Indigenous epistemology, have consistently intimated that the disablement of space via settler colonial practices of land appropriation and destruction in pursuit of profit, concomitantly yields the disablement of Indigenous bodies and worldviews that are intricately woven together with space. These issues strike us as particularly urgent given that much of what is recognized as disability studies scholarship is produced by non-Indigenous people within settler-colonial states."

"Children born with Down Syndrome are not vegetables, nor are their lives demonstrably not worth living."

"Abort it and try again. It would be immoral to bring it into the world if you have the choice."

"Now she is like the others."

"He has Down's syndrome, a genetic defect involving varying degrees of mental retardation and, sometimes, serious physical defects. When he was born we were bombarded with advice and information, much of it mistaken. Eve 13 years ago there was more certitude than certainty in the prognoses, most of which were too pessimistic."