Stemming the tide of normalisation: An expanded feminist analysis of the ethics and social impact of embryonic stem cell research [Book Review]
David Bourget (Western Ontario)
David Chalmers (ANU, NYU)
Rafael De Clercq
Ezio Di Nucci
Jack Alan Reynolds
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Journal of Bioethical Inquiry 3 (1-2):33-42 (2006)
Feminists have indicated the inadequacies of bioethical debates about human embryonic stem cell research, which have for the most part revolved around concerns about the moral status of the human embryo. Feminists have argued, for instance, that inquiry concerning the ethics and politics of human embryonic stem cell research should consider the relations of social power in which the research is embedded. My argument is that this feminist work on stem cells is itself inadequate, however, insofar as it has not incorporated an analysis of disability into its considerations of the ethical and political issues that surround the phenomena. Thus, I consider claims that disability theorists and anti-disability activists have made about the research. I conclude by indicating that stem cell research must be situated within a cultural matrix that operates in the service of normalisation.
|Keywords||Disabled persons Feminism Regenerative Medicine Models, Theoretical|
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References found in this work BETA
Allen E. Buchanan, Dan W. Brock, Norman Daniels & Daniel Wikler (2000). From Chance to Choice: Genetics and Justice. Cambridge University Press.
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Christopher Boorse (1977). Health as a Theoretical Concept. Philosophy of Science 44 (4):542-573.
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Shelley Tremain (2006). Reproductive Freedom, Self-Regulation, and the Government of Impairment in Utero. Hypatia 21 (1):35-53.
Citations of this work BETA
Shelley Tremain (2010). Biopower, Styles of Reasoning, and What's Still Missing From the Stem Cell Debates. Hypatia 25 (3):577 - 609.
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