Bøger i International Library of Ethics, Law, and the New Medicine serien

The book analyzes attitudes to people with various disabilities based on Muslim jurists' works in the Middle Ages and the modern era. Very little has been written so far on people with disabilities in a general Islamic context, much less in reference to Islamic law.

How can we ensure that pharmaceutical research helps all communities, even those who cannot afford to pay for the products? While broadly covering global health law, the book adopts an inter-disciplinary approach that draws on public international law, philosophy, international relations, human rights law, and healthcare economics.

This book presents the findings of a study into the social shaping of reproductive genetics in Germany and Israel. A close analysis of the ways that these two societies handle the balance between the quality and sanctity of life illuminates controversies over reproductive genetics in an original and provocative way.

Elsewhere the contemporary critique of autonomy appears in a variety of alternative ethical models like narrative ethics, casuist ethics, and contextualism.

The Dutch experience has influenced the debate on euthanasia and death with dignity around the globe, especially with regard to whether physician-assisted suicide and euthanasia should be legitimized or legalized.

Islamic Bioethics presents a critical analysis of legal and political debates resulting from biomedical technologies. Perspectives from traditional Muslim law are compared with contemporary religious authorities, medical associations, as well as individuals.

This highlights not only particular bioethical themes such as social justice, choices in health care, and health policy (e.g., in post-communist countries), it also emphasizes specific approaches in ethical theory, in relation to Continental philosophies such as phenomenology and hermeneutics.

This text explores the field of medical ethics and health care decision-making through hypothetical case studies. The volume covers a variety of issues including HIV, the health care rights of minors, consent and confidentiality, assisted reproductive technology, and research ethics.

Leading scholars from a range of disciplines examine some of the most emotive topics in the study of aging: assessing quality of life, improving end-of-life care, palliative care, euthanasia, and consent to research.

Positive conceptions of 'healthy aging' are rightly displacing negative ageist perceptions of older members of our society. Nevertheless, at some stage, most elderly citizens will require some form of assistance from other members of society. When the body or mind begins to fail, a legitimate need for intervention and care will arise.

In the mid-1990s new treatment options introduced a new era of AIDS. This book is a sophisticated study of the shaping of this new era. In doing so, the book captures the new era of AIDS from multiple perspectives and through the voices of physicians as well as people with HIV.

This is the first of three volumes on Aging conceived for the International Library of Ethics, Law, and the New Medicine. Leading scholars from a range of disciplines contest some of the predominant paradigms on aging, and critically assess modern trends in social health policy.

This book addresses the ways in which the metaphor of the criminal as monster is used to scapegoat certain categories of crimes and criminals for anxieties about our own potential for deviant, and, indeed, dangerous interests.

Bringing a person into an existence that is truly awful-not worth having-can be wrong, and so can bringing a person into an existence that is worth having when we had the alternative of bringing that same person into an existence that is substantially better.

One of the first publications to synthesize reproductive ethics and post-structuralist philosophy, this monograph offers insightful discussion of key issues in reproductive ethics such as liberal eugenics, human enhancement and disability discrimination.

This book completes medical care by adding the comprehensive humanistic perspectives and philosophy of medicine. It discusses many issues of medical treatment, moral approaches or legal advice and offers a new way of thinking which it explains and illustrates.

This book analyzes definitions, concepts and recent research to offer a new model of malingering, feigning and other biases, and develops an associated diagnostic system applicable to PTSD, chronic pain and TBI. Presents ideas on practice and future research.

For instance, should a patient with Amyotrophic lateral sclerosis (ALS) who is mentally alert yet unable to move from the neck down be allowed to refuse medical treatment; Is there a difference between not inserting a respirator into a patient who is unable to breathe and not inserting a feeding tube into a patient who is unable to eat?

Throughout the book it is argued that some moral concerns about prevention - namely concerns about medicalization - cannot be adequately grasped in terms of strict and binding moral norms.

This book offers a group of essays published in memory of David Thomasma, one of the leading humanists in the field of bioethics during the twentieth century. The volume deals with the pressing issue of how to ground a universal bioethics in the context of the conflicted world of combative cultures and perspectives.

Written in a lucid style, this unique book will appeal to scholars and students in the fields of sociology, social psychology, social anthropology, social theory and philosophy, as well as anybody interested in the relationship between the self and society or the experience of living with HIV/AIDS.

For decades, health professionals have asserted the importance of public participation in interventions for health. In this innovative work, the author contrasts public and professional understandings of health and the best ways to achieve health.

Mental health issues are a growing concern in our modern Western society. However, most of what has been written so far has had its focus on mental illness or disease, the negative side of the coin, and few attempts have been made to discuss more thoroughly, from a philosophical perspective, what it is to be mentally healthy.

How can we ensure that pharmaceutical research helps all communities, even those who cannot afford to pay for the products? While broadly covering global health law, the book adopts an inter-disciplinary approach that draws on public international law, philosophy, international relations, human rights law, and healthcare economics.

Bringing a person into an existence that is truly awful-not worth having-can be wrong, and so can bringing a person into an existence that is worth having when we had the alternative of bringing that same person into an existence that is substantially better.

This book develops a novel justificatory framework for making judgments of decisional competence to consent to biomedical research. This is the first book to focus exclusively on this subject, which also has implications for the emerging field of neuroethics.

The book will help academics, healthcare professionals, legal practitioners and the educated reader to understand the challenges of creating and implementing advance directives, anticipate clinical realities, and preparing advance directives that reflect a higher degree of assurance in terms of implementation.

There are ethically relevant differences between rural health practice and rural health services delivery and urban practice and delivery that go beyond the stereotypes associated with rural life and rural health services.

The people who suffer from mental or neurological disorders in the continent form a vulnerable section of society and often face stigma, discrimination and marginalization in all societies, and this increases the likelihood that their human rights will be violated This book tackles the issue of mental health legislation in South Asia.