A disability history of the United States

Kim E. Nielsen

Book - 2012

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Subjects
Published
Boston : Beacon Press c2012.
Language
English
Main Author
Kim E. Nielsen (-)
Physical Description
xxiii, 216 p. ; 24 cm
Bibliography
Includes bibliographical references and index.
ISBN
9780807022023
  • Introduction
  • 1. The spirit chooses the body it will occupy: Indigenous North America, Pre-1492
  • 2. The poor, vicious, and infirm: Colonial Communities, 1492-1700
  • 3. The miserable wretches were then thrown into the sea: The Late Colonial Era, 1700-1776
  • 4. The deviant and the dependent: Creating Citizens, 1776-1865
  • 5. I am disabled, and must go at something else besides hard labor: The Institutionalization of Disability, 1865-1890
  • 6. Three generations of imbeciles are enough: The Progressive Era, 1890-1927
  • 7. We don't want tin cups: Laying the Groundwork, 1927-19 68
  • 8. I guess I'm an activist. I think it's just caring: Rights and Rights Denied, 1968-157
  • Epilogue
  • Acknowledgments
  • Notes
  • Index
Review by Choice Review

Organized chronologically, with chapters on the precolonial period through the Progressive Era and the civil rights era, this moving historical work challenges the conventional narrative of US history. Two kinds of problems vex this otherwise admirable project. First, shoehorning the thematically disparate and challenging materials into chapters organized chronologically reduces the effectiveness of the narrative and the analytic strength of the text, and misses the opportunity for alternative periodizations. The disposal of "defective" slaves at sea and cases of social elites sequestered by their families for aberrant behavior in the early 18th century are both in the same chapter, to the disservice of both. Second, a romantic view of Native American cultures produces predictable moral outrage at the effects of disease processes on the lives of the indigenous population after European contact. The framework does little to explain the contradictory trends in disability rights in each of the eras selected, such as the simultaneous emergence of eugenics and a nascent disability rights movement in the Progressive Era. Important yet underdeveloped is the way Nielsen (history and disability studies, Univ. of Toledo) presents productivism and ableism as enmeshed in the very founding documents of the US. Pathbreaking and important but flawed. Summing Up: Recommended. Most levels/libraries. J. L. Croissant University of Arizona

Copyright American Library Association, used with permission.
Review by Booklist Review

Individuals with physical, psychological, sensory, and cognitive disabilities occupy center stage in this unique perspective on American history. Nielsen, professor of history and mother of a disabled daughter, gives us a scholarly yet stirring narrative of our nation's uneasy relations part pity and empathy, part discrimination and social stigmatization with disabled people. Prior to 1492, most indigenous North Americans had no word for disability. European settlement of the continent injected disability via the diseases the colonists brought as well as the conflicts, displacement, and environmental changes they wrought. Some large cities implemented ugly laws, prohibiting maimed or deformed people from appearing in public places. For a time, disabled individuals were subject to restrictive immigration policies, institutionalization, and even forced sterilization. WWII saw a surge in the employment of disabled people. The rise of activism and empowerment culminated in the passage of the Americans with Disabilities Act in 1990. There is still much to do if all disabled persons are to achieve pride and place and live a good life in the U.S.--Miksanek, Tony Copyright 2010 Booklist

From Booklist, Copyright (c) American Library Association. Used with permission.
Review by Publisher's Weekly Review

This impressive, instructive book by Nielsen, a professor of history and women's studies at the University of Wisconsin-Green Bay (The Radical Lives of Helen Keller), seeks to define the pivotal role of people with disabilities in our nation's past and their contribution to our laws, policy, economics, popular culture, and our collective identity. Disability, with its presumed need for dependency, challenges the American ideal of independence and autonomy. Nielsen uses various concepts of disability and dependency that go to "the heart of both human and American experience." She accurately notes the difference of mind-body beliefs of the Native Americans from the Europeans who brought disease and death with them; the colonial definition of those considered insane or undesirable; and the many institutions housing the disabled. Nielsen does not sidestep the thorny issue of disabled war veterans, from the Revolutionary War through the Civil War to the present, with their surging costs and advances of laws protecting the rights of the disabled and guaranteeing accessibility in civilian life. Neilsen is at her best speaking not about the physically disabled and mentally ill, but of the legal and social barricades placed against women, minorities, and immigrants, who were classified "disabled" and blocked from full citizenship. (Oct.) (c) Copyright PWxyz, LLC. All rights reserved.

(c) Copyright PWxyz, LLC. All rights reserved
Review by Kirkus Book Review

American history examined sensitively and skillfully from the bottom up, grounded in the often shabby and sometimes exemplary treatment of disabled individuals. Nielsen's (History and Women's Studies/Univ. of Wisconsin, Green Bay; The Radical Lives of Helen Keller, 2004, etc.) interest in the treatment of the disabled began with research into the political activism of Helen Keller, perhaps the most famous of severely disabled Americans. The author organizes the book chronologically, beginning with the handling of disabled women and men by Native Americans. The disability spectrum within indigenous North American cultures expanded in unwelcome ways as European settlers spread disease among the Indians. Nielsen then moves on to the stories of newly arrived immigrants from Europe and Africa who were not fully functional physically or mentally. "Disability" has always been an elastic term; Nielsen explains how the definitions solidified in the legal and social sense in the 19th and 20th centuries. The definitions would deprive many individuals of full citizenship rights as institutionalization became a trend. That institutionalization fell disproportionately on the enslaved (usually but not always because of skin color), women and those individuals sometimes inaccurately characterized as lunatics or idiots. In a slightly more upbeat chapter, Nielsen explains how those marked as disabled slowly banded together to fight for their civil rights. Slowly, individuals with potential, despite being branded, began to receive educational and vocational opportunities. The final chapter marks the year 1968 as the beginning of improved understanding and enlightened policies. Individuals previously kept out of sight and mind began to enter the mainstream culture. A lively historical record that fills a gap in the literature.]] Copyright Kirkus Reviews, used with permission.

Copyright (c) Kirkus Reviews, used with permission.

From the Introduction When I crossed the stage to receive my PhD in history in 1996, I had no plans to become a historian of disability. I love history: the captivating stories and the satisfying intellectual bite of a vigorous analysis. At the time, if asked, and if I'd been honest, I'd have considered the topic of disability too "soft"--all that pity and empathy--too boring, and too far removed from the real "hard" stories of history. Was I wrong! I've learned that disability pushes us to examine ourselves and the difficult questions about the American past. Which peoples and which bodies have been considered fit and appropriate for public life and active citizenship? How have people with disabilities forged their own lives, their own communities, and shaped the United States? How has disability affected law, policy, economics, play, national identity, and daily life? The answers to these questions reveal a tremendous amount about us as a nation. A Disability History of the United States places the experiences of people with disabilities at the center of the American story. In many ways, this is a familiar telling. In other ways, how- ever, it is a radical repositioning of US history. As such, it casts new light on familiar stories (such as slavery and immigration), while also telling new stories (such as the ties between nativism and oralism in the late nineteenth century). It also makes clear that there has been no singular disability experience. Although people with disabilities share social stigmatization, and some- times are brought together by common experiences and common goals, their lives and interests have varied widely according to race, class, sexuality, gender, age, ideology, region, and type of disability--physical, cognitive, sensory, and/or psychological. While telling the history of people with disabilities, A Disability History of the United States will also tell the history of the concept of disability. These are two very different tasks. Throughout US history, disability has been used symbolically and metaphorically in venues as diverse as popular culture (freak shows, for example) and language ("That's so lame"; "What a retard"; "special"). When"disability" is considered to be synonymous with "deficiency" and "dependency," it contrasts sharply with American ideals of independence and autonomy. Thus, disability has served as an effective weapon in contests over power and ideology. For example, at varying times, African Americans, immigrants, gays and lesbians, poor people, and women have been defined categorically as defective citizens incapable of full civic participation. The story of US history is often told as a story of independence, rugged individualism, autonomy, and self-made men (and occasionally women) who, through hard work and determination, move from rags to riches. Just as the colonists sought and gained independence from Great Britain in order to create a successful and powerful country, so must individual citizens seek and gain independence in order to create successful and powerful selves. The idealized notion holds that we are a nation of Horatio Algers, perpetual train engines chugging our way ( I think I can, I think I can ) up to the city on the hill, insisting that we can do it ourselves. And, of course, the US democracy is founded on the premise that citizens are capable. It is the responsibility and privilege of citizens to vote, contribute economically, and have a say in their government. As citizens, as good citizens, we are to "stand on our own two feet" and "speak up for ourselves" (ableist phrases, if ever there were). In this version of the national story, independence is good and dependency is bad. Dependency means inequality, weakness, and reliance on others. When disability is equated with dependency, disability is stigmatized. Citizens with disabilities are labeled inferior citizens. When disability is understood as dependency, disability is posited in direct contrast to American ideals of independence and autonomy. In real life, however, just as in a real democracy, all of us are dependent on others. All of us contribute to and benefit from the care of others--as taxpayers, as recipients of public education, as the children of parents, as those who use public roads or transportation, as beneficiaries of publicly funded medical research, as those who do not participate in wage work during varying life stages, and on and on. We are an interdependent people. As historian Linda Kerber wrote, critiquing the gendered nature of the American ideal of individualism, "The myth of the lone individual is a trope, a rhetorical device. In real life no one is self-made; few are truly alone." Dependency is not bad--indeed, it is at the heart of both the human and the American experience. It is what makes a community and a democracy. The use of disability as an analytic tool matters in our national story because it forces consideration of the strengths, weaknesses, and contradictions of American ideals. Taking note of race, class, and gender, scholars have examined the historical expansion of democracy. It is time to do the same for disability. Additionally, a richer understanding of US history demands that we use disability to better understand the interdependent nature of democratic communities. Disability is not the story of someone else. It is our story, the story of someone we love, the story of who we are or may become, and it is undoubtedly the story of our nation. It is, quite simply, the American story in all of its complexities. The story of US history is one of many efforts to define, contest, and enshrine a specific national body as best for the nation--a national body both individual and collective. But . . . what is disability? Who are people with disabilities? And conversely, what does it mean to be nondisabled? When the US Supreme Court struggled to define obscenity in 1964, Justice Potter Stewart threw up his hands in frustration and wrote, "I know it when I see it."2 It's temptingly easy to do the same about disability. We generally assume that disability is a clearly defined category, unchanging and concrete. Closer inspection, however, reveals that disability is often elusive and changing. Not only do people with disabilities have a history, but the concept of disability has a history as well. The dominant method of defining disability assumes disability to be a medical "problem" with a clear "cause" that must be "treated" in an effort to find a "cure." This framework considers disability to stem from bodily-based defects and tends to define disabled people almost exclusively by those diagnostic defects (and supposedly nondisabled people by their lack of such defects). It erroneously presumes disability to be ahistorical--that is, to have always had the same, unaltering definition. Such a narrow conception erases the widely diverse and rich lives of so many people with disabilities--for whom disability likely matters, but who also define themselves according to and whose lives are shaped by race, sexuality, gender, class, political ideology, athleticism, their favorite hobby, whether or not they like yappy dogs, and the like. Disability can include disease or illness, but it often does not, and nondisabled people can be ill. Illness some- times leads to disability (but it often does not), and when it does the illness can go away but the disability remain. Illness, disease, and disability are not synonymous. Defining disability is difficult--and that's part of my argument. Although the definition theoretically has been based on bodies, the categorization of bodies as disabled has been shaped by factors such as gender, race, sexuality, education, levels of industrialization or standardization, access to adaptive equipment or privacy, and class. With age and medical care, as well as the vagaries of life, or simply daily context, one can move in and out of the category of "people with disabilities." One can be temporarily disabled due to accident or illness. Disabilities can be easily "read" by others (signified by the presence of a wheelchair or the sounds of a speech impediment), or more difficult to discern (such as some psychological disabilities or neurological disabilities). Disability can be contextual, and its meanings have changed over time. A simplistic example: a fellow historian and I once spent a delightful few days in Montreal at an academic conference. Those around me read my body as nondisabled. The white cane of my friend led others to read her as blind and disabled. Waiters and cab drivers always looked to me to take the lead. However, and to their dismay, I don't speak French. Luckily, my colleague is fluent in French. In that context, my linguistic deficiencies became far more of an impediment, far more disabling, than her blindness. Disability is not just a bodily category, but instead and also a social category shaped by changing social factors--just as is able-bodiedness. This is not to argue that we should all hold hands and cheerfully insist that we're all disabled in some way or another. That ignores the lived reality that disability can bring physical discomfort or difficulty. It also ignores the historical reality that being defined as disabled has made access to power and resources limited or difficult; and that hierarchies of power contribute to definitions of disability. For example, in the nineteenth century, medical experts argued that menstruation and reproduction so impaired women's bodies (those of middle and upper-class white women, at least) that their exclusion from higher education and employment was absolutely necessary, for themselves and for the greater good of society. And in the early twentieth century, if public transportation was not accessible, and employers refused to hire a man with only one leg, then exclusionary ideas and re- sources--not the condition of being one-legged--generated social segregation and unemployment. These are real consequences. Excerpted from A Disability History of the United States by Kim E. Nielsen All rights reserved by the original copyright owners. Excerpts are provided for display purposes only and may not be reproduced, reprinted or distributed without the written permission of the publisher.