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With the development of new direct interfaces between the human brain and computer systems, the time has come for an in-depth ethical examination of the way these neuronal interfaces may support an interaction between the mind and cyberspace. In so doing, this book does not hesitate to blend disciplines including neurobiology, philosophy, anthropology and politics. It also invites society, as a whole, to seek a path in the use of these interfaces enabling humanity to prosper while avoiding the relevant risks. As such, the volume is the first extensive study in cyberneuroethics, a subject matter which is certain to have a significant impact in the 21st century and beyond.
In this book, a global panel of experts considers the international implications of legalised euthanasia based on experiences from Belgium.
Strategies or decisions aimed at affecting, in a manner considered to be positive, the genetic heritage of a child in the context of human reproduction are increasingly being accepted in contemporary society. As a result, unnerving similarities between earlier selection ideology so central to the discredited eugenic regimes of the 20th century and those now on offer suggest that a new era of eugenics has dawned. The time is ripe, therefore, for considering and evaluating from an ethical perspective both current and future selection practices. This inter-disciplinary volume blends research from embryology, genetics, philosophy, sociology, psychology, and history. In so doing, it constructs a ...
Calum MacKellar offers an accessible, inter-disciplinary analysis, blending science, history and Christian theology, enabling readers to develop an informed opinion about the topics encountered. To some degree, all members of society are affected by these new scientific developments in human reproduction, regardless of background, and will thus benefit from such a survey.
For Vol. 1, see (ISBN 9780215033512)
Combines original empirical data with theoretical and normative analysis of access to justice in the Court of Protection.
The atom. The Big Bang. DNA. Natural selection. All ideas that have revolutionised science - and that were dismissed out of hand when they first appeared. The surprises haven't stopped: here, Michael Brooks, bestselling author of 13 Things that Don't Make Sense, investigates the new wave of unexpected insights that are shaping the future of scientific discovery. Through eleven radical new insights, Brooks takes us to the extreme frontiers of what we understand about the world. He journeys from the observations that might rewrite our history of the universe, through the novel biology behind our will to live, and on to the physiological root of consciousness. Along the way, he examines how the...
Increasing quantities of information about our health, bodies, and biological relationships are being generated by health technologies, research, and surveillance. This escalation presents challenges to us all when it comes to deciding how to manage this information and what should be disclosed to the very people it describes. This book establishes the ethical imperative to take seriously the potential impacts on our identities of encountering bioinformation about ourselves. Emily Postan argues that identity interests in accessing personal bioinformation are currently under-protected in law and often linked to problematic bio-essentialist assumptions. Drawing on a picture of identity constructed through embodied self-narratives, and examples of people's encounters with diverse kinds of information, Postan addresses these gaps. This book provides a robust account of the source, scope, and ethical significance of our identity-related interests in accessing – and not accessing – bioinformation about ourselves, and the need for disclosure practices to respond appropriately. This title is also available as Open Access on Cambridge Core.
Explores how society's privileging of autonomy and of civil and political freedoms, fails to uphold the human rights of those with cognitive disability.
When we want to provide good care, we often take the will of care users as our starting point. However, how do we do this for vulnerable people who are highly dependent on care? This book offers a practical and theory-based method for ethical deliberation. It encourages care providers to engage in ethical empowerment, making their own ethically responsible decisions based on values, virtues and dialogue. This method is applied to important social developments that care providers are challenging today, from evolutions around networks and confidentiality, decision-making capacity and informed consent, assertive care and restriction of freedom to euthanasia. The foundation of this method is a relational care ethics, linking everyone who participates in care with the other parties involved. This relationship forms the link between the care user, the next of kin and the care providers. Good care starts from the connection between people. This book will appeal to all professionals in the care sectors, as well as teachers and students of the ethics of care.