Comparative Empirical Bioethics: Dilemmas of Genetic Testing and Euthanasia in Israel and Germany

Nonfiction, Health & Well Being, Medical, Reference, Ethics, Religion & Spirituality, Philosophy, Ethics & Moral Philosophy
Cover of the book Comparative Empirical Bioethics: Dilemmas of Genetic Testing and Euthanasia in Israel and Germany by Aviad E. Raz, Silke Schicktanz, Springer International Publishing
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Author: Aviad E. Raz, Silke Schicktanz ISBN: 9783319327334
Publisher: Springer International Publishing Publication: April 29, 2016
Imprint: Springer Language: English
Author: Aviad E. Raz, Silke Schicktanz
ISBN: 9783319327334
Publisher: Springer International Publishing
Publication: April 29, 2016
Imprint: Springer
Language: English

This book is a comprehensive, empirically-grounded exploration of the relationship between bioethics, culture, and the perspective of being affected. It provides a new outlook on how complex “bioethical” issues become questions of everyday life.  The authors focus on two contexts, genetic testing and end-of-life care, to locate and demonstrate emerging themes of responsibility, such as self-responsibility, responsibility for kin, and the responsibility of society. Within these themes, the duty to know versus the right not to know one's genetic fate (in the context of genetic testing), or the sanctity of life versus self-determination (in the context of end of life care) are identified as culturally embedded dilemmas that are very much relevant for lay persons. Furthermore, cultural factors such as religion, history, utopian and dystopian views of biomedical technologies, outlooks on the body and on health/illness, and citizenship are examined. Health issues are increasingly becoming a question of assessing risk and responsibility: How can we better prepare ourselves for the future? We all make such assessments in a way that combines personal inclinations, professional recommendations, and cultural framings. There is still much to be learned about the interplay between these three dimensions. 

   

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This book is a comprehensive, empirically-grounded exploration of the relationship between bioethics, culture, and the perspective of being affected. It provides a new outlook on how complex “bioethical” issues become questions of everyday life.  The authors focus on two contexts, genetic testing and end-of-life care, to locate and demonstrate emerging themes of responsibility, such as self-responsibility, responsibility for kin, and the responsibility of society. Within these themes, the duty to know versus the right not to know one's genetic fate (in the context of genetic testing), or the sanctity of life versus self-determination (in the context of end of life care) are identified as culturally embedded dilemmas that are very much relevant for lay persons. Furthermore, cultural factors such as religion, history, utopian and dystopian views of biomedical technologies, outlooks on the body and on health/illness, and citizenship are examined. Health issues are increasingly becoming a question of assessing risk and responsibility: How can we better prepare ourselves for the future? We all make such assessments in a way that combines personal inclinations, professional recommendations, and cultural framings. There is still much to be learned about the interplay between these three dimensions. 

   

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