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Journal of Medicine and Philosophy
A Forum for Bioethics and Philosophy of Medicine
Volume 31, 2006 - Issue 3
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Original Articles

Disability, Bioethics, and Rejected Knowledge

CHRISTOPHER NEWELL University of Tasmania, Hobart, Tasmania, AustraliaCorrespondence[email protected]
Pages 269-283 | Published online: 17 Aug 2006

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Alise de Bie, Andrea Daley, Lori E. Ross & Sean A. Kidd. (2021) Resisting Unmet Expectations as Service User Ethics: Implications for Social Work. Journal of Progressive Human Services 32:3, pages 177-196.
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Gerard Goggin & Katie Ellis. (2020) Disability, communication, and life itself in the COVID-19 pandemic. Health Sociology Review 29:2, pages 168-176.
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Cate Thill. (2015) Listening for policy change: how the voices of disabled people shaped Australia’s National Disability Insurance Scheme. Disability & Society 30:1, pages 15-28.
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Nicola J. Marks. (2012) Cyborg stem cells in public: deconstructing and taking responsibility for categorizations. New Genetics and Society 31:4, pages 359-384.
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Timothy Lillie. (2010) What Took So Long? The Disability Critique Recognized. The American Journal of Bioethics 10:1, pages 57-58.
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Gerard Goggin. (2009) Disability and the ethics of listening. Continuum 23:4, pages 489-502.
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Gerard Goggin & Christopher Newell. (2007) The Business of Digital Disability. The Information Society 23:3, pages 159-168.
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