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.