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Prenatal Testing and Disability Rights
As prenatal tests proliferate, the medical and broader communities perceive that such testing is a logical extension of good prenatal care—it helps parents have healthy babies. But prenatal tests have been criticized by the disability rights community, which contends that advances in science should be directed at improving their lives, not preventing them. Used primarily to decide to abort a fetus that would have been born with mental or physical impairments, prenatal tests arguably reinforce discrimination against and misconceptions about people with disabilities. In these essays, people on both sides of the issue engage in an honest and occasionally painful debate about prenatal testing and selective abortion. The contributors include both people who live with and people who theorize about disabilities, scholars from the social sciences and humanities, medical geneticists, genetic counselors, physicians, and lawyers. Although the essayists don't arrive at a consensus over the disability community's objections to prenatal testing and its consequences, they do offer recommendations for ameliorating some of the problems associated with the practice.
Women with Disabilities
Women with disabilities are women first, sharing the dreams and disappointments common to women in a male-dominated society. But because society persists in viewing disability as an emblem of passivity and incompetence, disabled women occupy a devalued status in the social hierarchy. This book represents the intersection of the feminist and disability rights perspectives; it analyzes the forces that push disabled women towards the margins of social life, and it considers the resources that enable these women to resist the stereotype. Drawing on law, social science, folklore, literature, psychoanalytic theory, and political activism, this book describes the experience of women with disabiliti...
The Disability Studies Reader
The second edition of "The Disability Studies Reader" builds and improves upon the classic first edition, which has sold well over 6000 copies since 1999. As a field, disability studies burst onto the scene across the social sciences and humanities in the 1990s, and the first edition of the reader gathered the best work that had been written on the subject, including essays by famous authors such as Susan Sontag and Erving Goffman. The new edition is more global in its coverage and adds material on genetic testing, the human genome, queer studies, and issues in developing countries. The size of the audience has grown since the first edition's publication, and the second edition's new material will make it even more useful for courses on the subject. Courses on the subject have mushroomed in the past ten years, and can now be found across the social sciences, humanities, and behavioral sciences.
Handbook of Disability Studies
This path-breaking international handbook of disability studies signals the emergence of a vital new area of scholarship, social policy and activism. Drawing on the insights of disability scholars around the world and the creative advice of an international editorial board, the book engages the reader in the critical issues and debates framing disability studies and places them in an historical and cultural context. Five years in the making, this one volume summarizes the ongoing discourse ranging across continents and traditional academic disciplines. To provide insight and perspective, the volume is divided into three sections: The shaping of disability studies as a field; experiencing dis...
Reproducing Persons
The essays next look at abortion from a variety of angles. One contends that killing fetuses is not murder; others emphasize the moral importance of access to abortion. Purdy considers the conflicting interests of women and men regarding abortion, and argues against requiring a husband's consent. The book concludes with a consideration of new reproductive technologies and arrangements, including the controversial issue of surrogacy, or contract pregnancy. Throughout, Purdy combines traditional utilitarianism with some of the most powerful insights of contemporary feminist ethics. Her provocative essays create guidelines for approaching new topics and inspire fresh thinking about old ones.
Disability Dialogues
"The author argues that postwar clinical professionals resisted adopting more positive, accepting, and sociopolitical perspectives on people with disabilities, as were espoused by self-advocates and family advocates, primarily owing to concerns about professional role, identity, and prestige"--
Arguing About Bioethics
Arguing About Bioethics is a fresh and exciting collection of essential readings in bioethics, offering a comprehensive introduction to and overview of the field. Influential contributions from established philosophers and bioethicists, such as Peter Singer, Thomas Nagel, Judith Jarvis Thomson and Michael Sandel, are combined with the best recent work in the subject. Organised into clear sections, readings have been chosen that engage with one another, and often take opposing views on the same question, helping students get to grips with the key areas of debate. All the core issues in bioethics are covered, alongside new controversies that are emerging in the field, including: embryo researc...
The Double-Edged Helix
This bioethics anthology exploring the questions and controversies surrounding the innovations of 21st century genetics. When the Human Genome Project completed its work in the early 2000s, it was hailed as a watershed moment in the history of medicine. But not everyone felt the same optimism about where the breakthrough might lead. The Double-Edged Helix explores the impact of recent genetic discoveries on society as a whole as well as individual populations and communities. This volume outlines potential positive and negative effects of genetic research on minorities, individuals with disabilities, and those of diverse sexual orientations. Presenting a wide array of perspectives, contributors address the medical and ethical implications of newly available technologies, from prenatal genetic screenings to the so-called “gay gene” debates. They emphasize the need to ensure that genetics research does not lead to discrimination against people on the basis of their DNA. A Choice Magazine Outstanding Academic Title
The Eugenic Mind Project
An examination of eugenic thinking past and present, from forced sterilization to prenatal screening, drawing on experience with those who survived eugenics. Part science and part social movement, eugenics emerged in the late nineteenth century as a tool for human improvement. In response to perceived threats of criminality, moral degeneration, feeble-mindedness, and "the rising tide of color," eugenic laws and social policies aimed to better the human race by regulating reproductive choice through science and technology. In this book, Rob Wilson examines eugenic thought and practice--from forced sterilization to prenatal screening--drawing on his experience working with eugenics survivors. ...
Ethical Issues for a New Millennium
Modern advances in science and medicine bring with them an array of complex ethical dilemmas. In Ethical Issues for a New Millennium editor John Howie addresses contemporary ethical problems with eight essays from top thinkers in the field. This collection offers new and comprehensive overviews of some very tough ethical issues that will remain foremost in our minds in the years ahead. Each essay is written by a recognized authority within his or her specific field, and brings to light ethical questions rooted in ongoing philosophical debates in arenas such as human rights, the welfare state, women's rights, genetic and gender equality, genetic equity, cloning, organ transplants, environmental ethics, insurrectionist ethics, and the erosion of moral sensibility. These lectures where originally presented at Southern Illinois University as part of the Wayne Leys Memorial Lectures series. This collection represents the fourth volume in the series.
