The aim of this volume is to open up reflection on the nature of vulnerability, the responsibilities owed to the vulnerable, who bears these responsibilities, and how they are best fulfilled. In canvassing responses to these questions, the contributors engage with a range of ethical traditions and with issues in contemporary political philosophy and bioethics. Some essays in the volume explore the connections between vulnerability, autonomy, dignity, and justice. Other essays engage with a feminist ethics of care to articulate the relationship between vulnerability, dependence, and care. These theoretical approaches are complemented by detailed examination of vulnerability in specific contexts, including disability; responsibilities to children; intergenerational justice; and care of the elderly. The essays thus address fundamental questions concerning our moral duties to each other as individuals and as citizens. Contributing significantly to the development of an ethics of vulnerability, this volume opens up promising avenues for future research in feminist philosophy, moral and political philosophy, and bioethics.

This book addresses the problem of how to make democratically-legitimate public policy on issues of contentious bioethical debate. It focuses on ethical contests about research and their legitimate resolution, while addressing questions of political legitimacy. How should states make public policy on issues where there is ethical disagreement, not only about appropriate outcomes, but even what values are at stake? What constitutes justified, democratic policy in such conflicted domains? Case studies from Canada and Australia demonstrate that two countries sharing historical and institutional characteristics can reach different policy responses. This book is of interest to policymakers, bioethicists, and philosophers, and will deepen our understanding of the interactions between large-scale socio-political forces and detailed policy problems in bioethics. asdf

This book addresses the problem of how to make democratically-legitimate public policy on issues of contentious bioethical debate. It focuses on ethical contests about research and their legitimate resolution, while addressing questions of political legitimacy. How should states make public policy on issues where there is ethical disagreement, not only about appropriate outcomes, but even what values are at stake? What constitutes justified, democratic policy in such conflicted domains? Case studies from Canada and Australia demonstrate that two countries sharing historical and institutional characteristics can reach different policy responses. This book is of interest to policymakers, bioethicists, and philosophers, and will deepen our understanding of the interactions between large-scale socio-political forces and detailed policy problems in bioethics. asdf

Hegel has had a remarkable, yet largely unremarked, role in Canada's intellectual development. In the last half of the twentieth-century, as Canada was coming to define itself in the wake of World War Two, some of Canada's most thoughtful scholars turned to the work of G.W.F. Hegel for insight. Hegel and Canada is a collection of essays that analyses the real, but under-recognized, role Hegel has played in the intellectual and political development of Canada. The volume focuses on the generation of Canadian scholars who emerged after World War Two: James Doull, Emil Fackenheim, George Grant, Henry S. Harris, and Charles Taylor. These thinkers offer a uniquely Canadian view of Hegel's writings, and, correspondingly, of possible relations between situated community and rational law. Hegel provided a unique intellectual resource for thinking through the complex and opposing aspects that characterize Canada. The volume brings together key scholars from each of these five schools of Canadian Hegel studies and provides a richly nuanced account of the intellectually significant connection of Hegel and Canada.

A thought provoking examination of the interrelationship between and among feminist bioethics, human rights, and global development, Linking Visions addresses global concerns about oppression in the context of health care, medical research, and population health. Reflecting the ever-expanding diversity and comprehensiveness of feminist bioethics, contributors examine such topics as reproductive rights of women in India, HIV/AIDs policies, patenting genetic material, the language of human rights, and consequences of the OGlobal Gag RuleO. Linking Visions demonstrates the far-reaching effects of feminism on global bioethics, highlighting and celebrating the reality that feminist work is no longer relegated solely to the realm of reproductive, sexual, or maternal ethics.

The aim of this volume is to open up reflection on the nature of vulnerability, the responsibilities owed to the vulnerable, who bears these responsibilities, and how they are best fulfilled. In canvassing responses to these questions, the contributors engage with a range of ethical traditions and with issues in contemporary political philosophy and bioethics. Some essays in the volume explore the connections between vulnerability, autonomy, dignity, and justice. Other essays engage with a feminist ethics of care to articulate the relationship between vulnerability, dependence, and care. These theoretical approaches are complemented by detailed examination of vulnerability in specific contexts, including disability; responsibilities to children; intergenerational justice; and care of the elderly. The essays thus address fundamental questions concerning our moral duties to each other as individuals and as citizens. Contributing significantly to the development of an ethics of vulnerability, this volume opens up promising avenues for future research in feminist philosophy, moral and political philosophy, and bioethics.

Je nach Diagnosekriterium werden pro Jahr 200 bis 4000 Kinder mit Autismus geboren, die - mehr oder weniger - intensive Betreuung im Alltag benoetigen. Die Schulung von Eltern und Betreuern in den praktischen Alltagsroutinen zwischen Zahneputzen und Zubettgehen, insbesondere im Bereich der Kommunikation uber gemeinsames Tun, gelingt Susan Dodd in ihrem kompetenten und mit vielen praktischen Hilfsmitteln gespickten Buch auf nachgerade mitreissende Weise. Das Buch wird jedem, der im Umfeld einem autistischen Menschen begegnet, einen Schlussel liefern, um die kommunikativen Probleme integrativ und wirksam zu loesen - und anhand der Lernhilfen uberraschende Erfahrungen mit dem emotionalen Verstehen bis hin zum Lesen im Gesichtsausdruck machen.

Weather they are on the lookout or on the lam, love is what maps their migration.

An eccentric endodontist repairs a patient's freshly broken heart while performing a root canal.

A Haitian woman charms snakes into keeping her company in an urban cave as she safeguards her grandchildren's sleep.

A shy illustrator subsists through a long Vermont winter on occasional glimpses of a man in a blue pickup truck.

Susan Dodd, the acclaimed author of The Mourners' Bench explores the multifarious and otherworldly nature of love's in this shimmering collection of short stories.

In settings ranging from a desolate island in winter to a broken-down city bus at rush hour, Dodd shows us love's unlikely -- and often inconvenient -- landings 'in these ten diverse and uncommon stories.