Bioethics, Public Moral Argument, and Social Responsibility
Routledge Annals of Bioethics Series

Bioethics, Public Moral Argument, and Social Responsibility explores the role of democratically oriented argument in promoting public understanding and discussion of the benefits and burdens of biotechnological progress.

The contributors examine moral and policy controversies surrounding biomedical technologies and their place in American society, beginning with an examination of discourse and moral authority in democracy, and addressing a set of issues that include: dignity in health care; the social responsibilities of scientists, journalists, and scholars; and the language of genetics and moral responsibility.

Preface Editors’ Introduction Part 1: Public Moral Argument and Social Responsibility1. Arguing About Values: the Problem of Public Moral Argument David Zarefsky 2. Bioethical Deliberation in a Democracy Jonathan D. Moreno 3. Bioethics and the Law: Using Moot Court as a Tool to Teach Effective Argumentation Skills Christine Nero Coughlin, Tracey Banks Coan, and Barbara LentzPart 2: Moral Relationships and Responsibilities4. Dignity Can Be a Useful Concept in Bioethics Rebecca Dresser 5. Appeals to Human Nature in Biomedical Ethics: Managing Our Legacies, Loyalties, and Love of Champions Eric T. Juengst 6. In the Stars or In Our Genes: The Languages of Fate and Moral Responsibility Larry R. Churchill 7. Responsibility versus "Blame" in Health Communication: Where to Draw the Lines in Romancing the Gene Roxanne ParrottPart 3: The Media, the Public, and the Person 8. Media Misinformation and the Obesity Epidemic: The Conflict Between Scientific Fact and Industry Claims Stephen Giles and Marina Krcmar 9. How We Feel With Metaphors for Genes: Implications for Understanding Humans and Forming Genetic Policies Celeste M. Condit 10. An Investigative Bioethics Manifesto Carl Elliott 11. The Question of "The Public" Christian O. Lundberg and Ross Smith Afterword

Nancy M. P. King, JD, is Professor, Social Sciences and Health Policy and Internal Medicine, School of Medicine and Institute for Regenerative Medicine, and Co-Director of the Center for Bioethics, Health, and Society and the Master of Arts in Bioethics Program at Wake Forest University. Her scholarship addresses a range of bioethics issues, including: informed consent in health care and research; medical decisions at the beginning and end of life; the development and use of experimental technologies; preclinical and animal research; international and cross-cultural questions in human subjects research; benefit and uncertainty in human subjects research; and ethical issues in large-scale genetic research and biobanking, gene transfer research, and regenerative medicine. She is co-editor of The Social Medicine Reader (2nd ed., Duke University Press, 2005) and Beyond Regulations: Ethics in Human Subjects Research (UNC Press 1999). She has served on hospital ethics committees, IRBs, and DSMBs, and has taught research ethics in national and international settings. Professor King was a member of the Recombinant DNA Advisory Committee of NIH from 1998-2002.

Michael J. Hyde (Ph.D., Purdue University) is The University Distinguished Professor of Communication Ethics, Department of Communication, Wake Forest University and holds a joint appointment in the Program in Bioethics, Health, and Society, School of Medicine, Wake Forest University. He is the author of numerous articles and critical reviews appearing in various scholarly journals and texts and has published six books including: The Call of Conscience: Heidegger and Levinas, Rhetoric and the Euthanasia Debate (Univ. of South Carolina Press, awarded the National Communication Association’s [NCA’s] 2001 Diamond Anniversary Book Award and the Marie Hochmuth Nichols Award for Outstanding Research in Public Address), The Life-Giving Gift of Acknowle