Kristien Hens – författare

This open access collection brings together a team of leading scholars and rising stars to consider what experimental philosophy of medicine is and can be.While experimental philosophy of science is an established field, attempts to tackle issues in philosophy of medicine from an experimental angle are still surprisingly scarce. A team of interdisciplinary scholars demonstrate how we can make progress by integrating a variety of methods from experimental philosophy, including experiments, sociological surveys, simulations, as well as history and philosophy of science, in order to yield meaningful results about the core questions in medicine. They focus on concepts central to philosophy of medicine and medical practice, such as death, pain, disease and disorder, advance directives, medical explanation, disability and informed consent. Presenting empirical findings and providing a crucial foundation for future work in this dynamic field, this collection explores new ways for philosophers to cooperate with scientists and reveals the value of these collaborations for both philosophy and medicine.The eBook editions of this book are available open access under a CC BY-NC-ND 4.0 licence on bloomsburycollections.com. Open access was funded by the European Research Council Starting Grant.

This open access collection brings together a team of leading scholars and rising stars to consider what experimental philosophy of medicine is and can be.While experimental philosophy of science is an established field, attempts to tackle issues in philosophy of medicine from an experimental angle are still surprisingly scarce. A team of interdisciplinary scholars demonstrate how we can make progress by integrating a variety of methods from experimental philosophy, including experiments, sociological surveys, simulations, as well as history and philosophy of science, in order to yield meaningful results about the core questions in medicine. They focus on concepts central to philosophy of medicine and medical practice, such as death, pain, disease and disorder, advance directives, medical explanation, disability and informed consent. Presenting empirical findings and providing a crucial foundation for future work in this dynamic field, this collection explores new ways for philosophers to cooperate with scientists and reveals the value of these collaborations for both philosophy and medicine.The eBook editions of this book are available open access under a CC BY-NC-ND 4.0 licence on bloomsburycollections.com. Open access was funded by the European Research Council Starting Grant.

This open access book is the first volume on the ethics of intra-familial reproduction, exploring cutting-edge debates and developments in reproductive science and their impact on how we conceptualize kinship.In recent decades, reproductive technologies have enabled novel uses of family members’ reproductive materials (such as gametes or wombs) or functions (such as pregnancy). Reproductive material has been collected from comatose or deceased people at the request of their spouses, and then used in reproduction. Invasive fertility preservation measures have been undertaken on children, at the request of their parents. Mothers have carried their adult offspring´s babies in their wombs in order to help them become parents. Such examples raise unprecedented ethical challenges. Whose interests ground the creation of offspring using a deceased person’s gametes? What is the relation between a mother and the grandchild that she gave birth to; between a deceased man and the children conceived with his sperm; or between the parents of a deceased woman and the baby that they created with her eggs? Contributors to The Ethics of Intra-familial Access to Reproductive Potential explore how these new forms of family connection will only grow in number and complexity as new technologies proliferate. Chapters contribute to ongoing debates on the moral status of children, the importance of genetic reproduction, and the clarification of claims to others’ reproductive capacities in the context of the family.The ebook editions of this book are available open access under a CC BY-NC-ND 4.0 licence on bloomsburycollections.com. Open access was funded by the Marcus and Amalia Wallenberg Foundation.

A wide-ranging exploration of a variety of viewpoints on nature and the environment that draws on philosophical traditions around the world.This open access collection explores the variety of ways we can relate to nature and the environment. It gives voice to perspectives often overlooked in mainstream approaches and calls for a new way of thinking about environmental challenges.For centuries European traditions have dominated how we see the world, approaching it in terms of isolation, passiveness, and survival. This collection shows the value of taking a more inclusive approach and makes a timely and much-needed contribution to environmental philosophy in the 21st century. A team of international contributors illustrate the richness of our connection with nature. They cover 19th and early 20th-century Japanese environmental philosophy centered around the figure of Tanaka Shozo; the Indian and African knowledge system; posthumanism and Oromo environmental ethics. By discussing how the relationship between humans and other forms of life is characterized in different cultures, they offer an holistic view of nature, emphasizing interconnectedness, agency and cooperation.The ebook editions of this book are available open access under a CC BY-NC-ND 4.0 licence on bloomsburycollections.com. Open access was funded by the University of Antwerp, Belgium.

Should parents aim to make their children as normal as possible to increase their chances to “fit in”? Are neurological and mental health conditions a part of children’s identity and if so, should parents aim to remove or treat these? Should they aim to instill self-control in their children? Should prospective parents take steps to insure that, of all the children they could have, they choose the ones with the best likely start in life? This volume explores all of these questions and more. Against the background of recent findings and expected advances in neuroscience and genetics, the extent and limits of parental responsibility are increasingly unclear. Awareness of the effects of parental choices on children’s wellbeing, as well as evolving norms about the moral status of children, have further increased expectations from (prospective) parents to take up and act on their changing responsibilities. The contributors discuss conceptual issues such as the meaning and sources of moral responsibility, normality, treatment, and identity. They also explore more practical issues such as how responsibility for children is practiced in Yoruba culture in Nigeria or how parents and health professionals in Belgium perceive the dilemmas generated by prenatal diagnosis.

Should parents aim to make their children as normal as possible to increase their chances to “fit in”? Are neurological and mental health conditions a part of children’s identity and if so, should parents aim to remove or treat these? Should they aim to instill self-control in their children? Should prospective parents take steps to insure that, of all the children they could have, they choose the ones with the best likely start in life?

This volume explores all of these questions and more. Against the background of recent findings and expected advances in neuroscience and genetics, the extent and limits of parental responsibility are increasingly unclear. Awareness of the effects of parental choices on children’s wellbeing, as well as evolving norms about the moral status of children, have further increased expectations from (prospective) parents to take up and act on their changing responsibilities. The contributors discuss conceptual issues such as the meaning and sources of moral responsibility, normality, treatment, and identity. They also explore more practical issues such as how responsibility for children is practiced in Yoruba culture in Nigeria or how parents and health professionals in Belgium perceive the dilemmas generated by prenatal diagnosis.

Should parents aim to make their children as normal as possible to increase their chances to “fit in”? Are neurological and mental health conditions a part of children’s identity and if so, should parents aim to remove or treat these? Should they aim to instill self-control in their children? Should prospective parents take steps to insure that, of all the children they could have, they choose the ones with the best likely start in life? This volume explores all of these questions and more. Against the background of recent findings and expected advances in neuroscience and genetics, the extent and limits of parental responsibility are increasingly unclear. Awareness of the effects of parental choices on children’s wellbeing, as well as evolving norms about the moral status of children, have further increased expectations from (prospective) parents to take up and act on their changing responsibilities. The contributors discuss conceptual issues such as the meaning and sources of moral responsibility, normality, treatment, and identity. They also explore more practical issues such as how responsibility for children is practiced in Yoruba culture in Nigeria or how parents and health professionals in Belgium perceive the dilemmas generated by prenatal diagnosis.

This book explores adult experiences of autism diagnosis. Focusing on the experiences of 21 interviewees, the structure of the book mirrors the seven stages undergone upon diagnosis, and raises important questions about modern society and the self, amidst this life-changing news. Analysing a broad range of empirical interview data including adults who had experiences of other diagnoses, and adults who seemed to function normally before their autism diagnosis, the authors use these stories to examine how autism diagnosis can be extremely important and helpful, but also generate a great deal of negativity.Illuminating a range of testimonies that have previously been kept in the shadows, this book will not only appeal to students and scholars of autism in adults, but also to practitioners as well as adults who have been diagnosed with autism.