Disability Empowerment Quotes

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We are not “differently abled”—we are disabled, robbed of empowerment and agency in a world that is not built for us. “Differently abled,” “handi-capable,” and similar euphemisms were created in the 1980s by the abled parents of disabled children, who wished to minimize their children’s marginalized status. These terms were popularized further by politicians[76] who similarly felt uncomfortable acknowledging disabled people’s actual experiences of oppression.
Devon Price (Unmasking Autism: Discovering the New Faces of Neurodiversity)
Many empaths try approaches that don’t work. And can’t work. Like constantly monitoring your energies. Or scaling down your activities – and ambitions. (As if you’ve got some kind of energetic disability and must learn to resign yourself.) Ridiculous! Empaths, you can do better. What you need is skill. The kind of skill that positions your flexible empath’s consciousness to support you better.
Rose Rosetree (Empath Empowerment in 30 Days (An Empath Empowerment® Book))
The problem with mainstream feminism, again and again, is the frivolity of the issues it is concerned with: manspreading, “girl power” and female “empowerment,” articles with headlines like CAN YOU BE A FEMINIST AND WEAR MAKEUP? As they fight these lesser battles, white women ignore the ways that their Black and brown, disabled, and trans sisters are still shackled by multiple forms of oppression.
June Eric-Udorie (Can We All Be Feminists?: New Writing from Brit Bennett, Nicole Dennis-Benn, and 15 Others on Intersectionality, Identity, and the Way Forward for Feminism)
Disabled, in the eyes of many is a dirty word because it shines a light on the differences of our world, and when we acknowledge difference, we must acknowledge privilege - and that opens a whole other can of worms.
Keah Brown (The Pretty One: On Life, Pop Culture, Disability, and Other Reasons to Fall in Love With Me)
Technoableism is a belief in the power of technology that considers the elimination of disability a good thing, something we should strive for. It’s a classic form of ableism—bias against disabled people, bias in favor of nondisabled ways of life.3 Technoableism is the use of technologies to reassert those biases, often under the guise of empowerment.
Ashley Shew (Against Technoableism: Rethinking Who Needs Improvement)
When feminist rhetoric is rooted biases like racism, ableism, transmisogyny, anti-Semitism, and Islamophobia, it automatically works against marginalized women and against any concept of solidarity. It's not enough to know that other women with different experiences exist' you must also understand that they have their own femiminist formed by that experience. Whether it's an argument that women who wear the hijab must be "saved" from it, or reproductive-justice arguments that paint having a disabled baby as the worst possible outcome, the reality is that feminism can be marginalizing
Mikki Kendall (Hood Feminism: Notes from the Women That a Movement Forgot)
Do you ever feel like you have been stopped dead in your tracks? That you have fallen and can’t get up? Or like you are stuck in a rut or wading in muck? Paralysis, inertia, and being stuck, can be disempowering and disabling. What is it going to take for you to restart your engines and get moving again?
Susan C. Young
We believed we were supposed to "cope" as best we could. As we talked, we realized the disability itself was not that big a deal for us. We had all learned to accept our physical limitations. What made life difficult was not the disability, but the lack of services and support, the lack of accessibility, the unfair and stereotypical ways in which we were treated, the pity doled out for us all our lives. Often, after a meeting, I wrote my thoughts down in a notebook. "It's not my fault that I'm disabled, yet I've been made to feel that it is," I wrote. "My polio never made me unhappy; people made me unhappy. Ever since I was a little girl, people have always made me feel I was no good because I was disabled. From Sicilian women and the nuns to the doctors who couldn't fix me, to my fellow students and prospective employers... and even my own parents." As I wrote, my tears fell and stained the pages - tears of anger, of relief and of new hope.
Nadina LaSpina (Such a Pretty Girl: A Story of Struggle, Empowerment, and Disability Pride)
The problem with mainstream feminism, again and again, is the frivolity of the issues it is concerned with: manspreading, ‘girl power’ and female ‘empowerment’, articles with headlines like CAN YOU BE A FEMINIST AND WEAR MAKEUP? As they fight these lesser battles, white women ignore the ways that their Black and brown, disabled and trans sisters are still shackled by multiple forms of oppression.
June Eric-Udorie (Can We All Be Feminists?: Seventeen Writers on Intersectionality, Identity and Finding the Right Way Forward for Feminism)
Turn your obstacles to your advantage. If you can find a plus out of a negative, then it cannot weigh you down. I like to think I have a superpower called dyslexia. I am creative, intuitive, and empathetic. I am great with problem-solving, and I can think outside the box. Just the other day, I was helping my daughter with a crossword puzzle, and she said, “Dad, how do you find the answers so fast? And I said, “I have dyslexia, and it helps me see things differently. To which she replied, “Aw, I want that.” If we can see our differences or unique qualities as gifts, we can bypass the stigmas that come with them and impress upon ourselves and society we can do anything any other person can do, just differently, and sometimes better.
Lorin Morgan-Richards
We believed we were supposed to 'cope' as best we could. As we talked, we realized the disability itself was not that big a deal for us. We had all learned to accept our physical limitations. What made life difficult was not the disability, but the lack of services and support, the lack of accessibility, the unfair and stereotypical ways in which we were treated, the pity doled out for us all our lives. Often, after a meeting, I wrote my thoughts down in a notebook. 'It's not my fault that I'm disabled, yet I've been made to feel that it is,' I wrote. 'My polio never made me unhappy; people made me unhappy. Ever since I was a little girl, people have always made me feel I was no good because I was disabled. From Sicilian women and the nuns to the doctors who couldn't fix me, to my fellow students and prospective employers... and even my own parents.' As I wrote, my tears fell and stained the pages - tears of anger, of relief and of new hope.
Nadina LaSpina (Such a Pretty Girl: A Story of Struggle, Empowerment, and Disability Pride)
poverty and powerlessness are cornerstones of the dependency people with disabilities experience.
James I. Charlton (Nothing About Us Without Us: Disability Oppression and Empowerment)
Disability is not what we see or appear, it is all about not doing what one really wanted to do...
Seal the Smile
Steven shook his head frantically. What kind of accident? His eyes jerked from side to side, trying to see past his limited field of vision. Where are Mom and Dad?
D.A. Charles (Shattered (The Roll Models Saga, #1))
LANGUAGE AND THE POWER OF DESCRIPTION We must take language very seriously. The feeling I have is that language is always a reflection of attitude. With the advancement of the disability movement you see a change in language. Michael Masutha, director of socioeconomic rights, Lawyers for Human Rights, Johannesburg, South Africa Language informs attitudes and beliefs because it is a medium of translation of expression and thought.
James I. Charlton (Nothing About Us Without Us: Disability Oppression and Empowerment)
Oppression is a phenomenon of power in which relations between people and between groups are experienced in terms of domination and subordination, superiority and inferiority. At the center of this phenomenon is control. Those with power control; those without power lack control. Power presupposes political, economic, and social hierarchies, structured relations of groups of people, and a system or regime of power. This system, the existing power structure, encompasses the thousands of ways some groups and individuals impose control over others.
James I. Charlton (Nothing About Us Without Us: Disability Oppression and Empowerment)
Students with disabilities, as soon as their disability is recognized by school officials, are placed on a separate track. They are immediately labeled by authorized (credentialed) professionals (who never themselves have experienced these labels) as LD, ED, EMH, and so on. The meaning and definition of the labels differ, but they all signify inferiority on their face. Furthermore, these students are constantly told what they can (potentially/expect to) do and what they cannot do from the very date of their labeling. This happens as a natural matter of course in the classroom. All activists I interviewed who had a disability in grade school or high school told similar kinds of horror stories—detention and retention, threats and insults, physical and emotional abuse.
James I. Charlton (Nothing About Us Without Us: Disability Oppression and Empowerment)
It is possible to identify numerous ways that students with disabilities are controlled and taught their place: (1) labeling; (2) symbols (e.g., white lab coats, “Handicapped Room” signs); (3) structure (pull-out programs, segregated classrooms, “special” schools, inaccessible areas); (4) curricula especially designed for students with disabilities (behavior modification for emotionally disturbed kids, training skills without knowledge instruction for significantly mentally retarded students and students with autistic behavior) or having significant implications for these students; (5) testing and evaluation biased toward the functional needs of the dominant culture (Stanford-Binet and Wexler tests); (6) body language and disposition of school culture (teachers almost never look into the eyes of students with disabilities and practice even greater patterns of superiority and paternalism than they do with other students); and (7) discipline (physical restraints, isolation/time-out rooms with locked doors, use of Haldol and other sedatives).11
James I. Charlton (Nothing About Us Without Us: Disability Oppression and Empowerment)
Ernesto learned how to use a cane in public. Socially, the cane transformed Ernesto's life. “Now, if I'm going onto the bus, they always let me sit, because of my disability, when they see the cane,” he said. “When I'm walking in the shopping mall, they never go against me. They always pull over to the side. When they teach you how to use a cane and how to walk through the people, everything changes—people respect you.
Jeffry Odell Korgen (Beyond Empowerment: A Pilgrimage with the Catholic Campaign for Human Development (Cchd-Catholic Campaign for Human Development))
Underachievement is not a disability but an opportunity to bridge the gap between potential and performance.
Asuni LadyZeal
Social Justice approaches that focus solely on group identity and neglect individuality and universality are doomed to fail for the simple reasons that people are individuals and share a common human nature. Identity politics is not a path to empowerment. There is no “unique voice of color” or of women or of trans, gay, disabled, or fat people. Even a relatively small random sample drawn from any of those groups will reveal widely varying individual views. This does not negate the likelihood that prejudice still exists and that the people who experience it are the most likely to be aware of it. We still need to “listen and consider,” but we need to listen to and consider a variety of experiences and views from members of oppressed groups, not just a single one that has been arbitrarily labeled “authentic” because it represents the view essentialized by Theory.
Helen Pluckrose (Cynical Theories: How Activist Scholarship Made Everything about Race, Gender, and Identity—and Why This Harms Everybody)
Paternalism lies at the center of the oppression of people with disabilities. Paternalism starts with the notion of superiority: We must and can take control of these “subjects” in spite of themselves, in spite of their individual will, or culture and tradition, or their sovereignty. The savages need to be civilized (for their own good). The cripples need to be cared for (for their own good). The pagans need to be saved (for their own good). Paternalism is often subtle in that it casts the oppressor as benign, as protector. The relation between ideology and power is expressed as natural to justify relations of oppression. In Roll, Jordan Roll, possibly the best-known exposition of paternalism, Eugene Genovese writes, The Old South, black and white, created a historically unique kind of paternalist society. . . . Southern paternalism, like every other kind of paternalism, had little to do with Ole Massa’s ostensible benevolence, kindness, and good cheer. It grew out of the necessity to discipline and morally justify a system of exploitation. . . . For the slaveholders, paternalism represented an attempt to overcome the fundamental contradiction in slavery: the impossibility of the slaves ever becoming the things they were supposed to be. Paternalism defined the involuntary labor of the slaves as a legitimate return to their masters for protection and direction. (1976:4–5)
James I. Charlton (Nothing About Us Without Us: Disability Oppression and Empowerment)
Paternalism often must transform its subjects into children or people with childlike qualities. This is the most salient aspect of paternalism as it concerns disability. Paternalism is experienced as the bystander grabs the arm of a blind person and, without asking, “helps” the person across the street. This happens for wheelchair users as well. It is the experience of the waiter asking a companion of a person with a disability, “What does she want to eat?” It is the institutionalization of people against their wishes. It is the child taught only handicrafts, or the charity pleading for money to help cute crippled kids. It is these and a thousand other examples of everyday life. It is most of all, however, the assumption that people with disabilities are intrinsically inferior and unable to take responsibility for their own lives.
James I. Charlton (Nothing About Us Without Us: Disability Oppression and Empowerment)
Another example, one that touches more people, is the nursing home industry. Numerous studies have shown that living at home, in a house or an apartment, is better psychologically, more fulfilling, and cheaper than living in nursing homes.14 Yet these institutions prosper when federal programs that foster living in the community are cut. There are also funding disincentives that the U.S. Congress, through Medicare and Medicaid, has created to ensure the profit bonanza of nursing homes. According to the activist disability journal Mouth (1995), there are 1.9 million people with disabilities living in nursing homes at an annual cost of $40,784, although it would cost only $9,692 a year to provide personal assistance services so the same people could live at home. Sixty-three percent of this cost is taxpayer funded. In 1992, 77,618 people with developmental disabilities (DD) lived in state-owned facilities at an average annual cost of $82,228, even though it would cost $27,649 for the most expensive support services to live at home. There are 150,257 people with mental illness living in tax-funded asylums at an average annual cost of $58,569. Another 19,553 disabled veterans also live in institutions, costing the Veterans Administration a whopping $75,641 per person.15 It is illogical that a government would want to pay more for less. It is illogical until one studies the amount of money spent by the nursing home lobby. Nursing homes are a growth industry that many wealthy people, including politicians, have wisely invested in. The scam is simple: get taxpayers to fund billions of dollars to these institutions which a few investors divide up. The idea that nursing homes are compassionate institutions or necessary resting places has lost much of its appeal recently, but the barrier to defunding them is built on a paternalism that eschews human dignity. As we have seen with public housing programs in the United States, the tendency is to warehouse (surplus) people in concentrated sites. This too has been the history with elderly people and people with disabilities in nursing homes. These institutions then can serve as a mechanism of social control and, at the same time, make some people wealthy.
James I. Charlton (Nothing About Us Without Us: Disability Oppression and Empowerment)
We do have better models and evidence of the superiority of these alternative models to nursing homes and other institutionalized living arrangements. People with severe disabilities who are living at home with personal assistance have demonstrated that living in an environment they control is far superior to institutionalized care. But according to the World Institute on Disability, “9.6 million people with disabilities live in the U.S. who need help with daily activities like washing, dressing and household chores. Less than 2 million receive paid assistance. Most rely on family and friends” (WID 1995). All of the 7.6 million people dependent on family or friends for personal assistance are thus vulnerable to future institutionalization.
James I. Charlton (Nothing About Us Without Us: Disability Oppression and Empowerment)
Whereas people with disabilities have always struggled to survive, many are now struggling to change their world as well. The replacement of the false consciousness of self-pity and helplessness with the raised consciousness of dignity, anger, and empowerment has meaningfully affected the way in which many people with disabilities relate personally and politically to society.
James I. Charlton (Nothing About Us Without Us: Disability Oppression and Empowerment)
In doing so, I attempt to answer, among other questions, why so many people acquiesce to oppression and why some people not only individually resist these conditions but also actively organize to change them.
James I. Charlton (Nothing About Us Without Us: Disability Oppression and Empowerment)
All governments treat disabled people badly. They all see us as a burden. All governments, whether socialist or capitalist, have separated us from the rest of society. By the end of the day, people are judged by their own activity. Until we are businessmen, politicians, community leaders, people at all levels of society, we will be marginalized and segregated.
James I. Charlton (Nothing About Us Without Us: Disability Oppression and Empowerment)
Oppression occurs when individuals are systematically subjected to political, economic, cultural, or social degradation because they belong to a social group. Oppression of people results from structures of domination and subordination and, correspondingly, ideologies of superiority and inferiority.
James I. Charlton (Nothing About Us Without Us: Disability Oppression and Empowerment)