Journal of Bioethical Inquiry

, Volume 5, Issue 4, pp 235–238 | Cite as

Bioethics, Disability, and the Good Life: Remembering Christopher Newell, 1964–2008

  • Gerard Goggin


The untimely passing of Reverend Canon Dr Christopher Newell, AM, came as a shock to many in the bioethics world. As well as an obituary, this article notes a number of important themes in his work, and provides a select bibliography. Christopher's major contribution to this field is that he was one of a handful of scholars who made disability not only an acceptable area of bioethics—indeed a vital, central, fertile area of enquiry. Crucially Christopher emphasised that where we do ethics is actually in everyday life—while we mourn his passing, his rich work and example will continue to inspire bioethical inquiry.


Christopher Newell Disability Bioethics Narrative Excluded knowledge Everyday practice 



  1. Goggin, G., and C. Newell. 2004. Uniting the nation?: Disability, stem cells, and the Australian media. Disability & Society 19(1): 47–60. doi: 10.1080/0968759032000155622.CrossRefGoogle Scholar
  2. Goggin, G., and C. Newell. 2005a. Disability in Australia: Exposing a social apartheid. Sydney: University of New South Wales Press.Google Scholar
  3. Goggin, G., and C. Newell. 2005b. Imagining disability tomorrow. Journal of Futures Studies 10(2): 69–74.Google Scholar
  4. Newell, C. 1992. Some ethical issues associated with genetic engineering for people with disabilities. Australian Disability Review 2: 73–86.Google Scholar
  5. Newell, C. 1996. Medical killing and people with disability: A critique. Australian Disability Review 2: 28–37.Google Scholar
  6. Newell, C. 1997. Powerful practices: An Australian case study of contested notions of ethical disability research. Disability & Society 12(5): 803–810. doi: 10.1080/09687599727065.CrossRefGoogle Scholar
  7. Newell, C. 1998. The ethics of narrative ethics: Some teaching reflections. Health Care Analysis 6(2): 171–174.PubMedGoogle Scholar
  8. Newell, C. 1999a. Critical reflections on disability, difference and genetic testing. In Goodbye normal gene, eds. G. O’Sullivan, E. Sharman and S. Short, 58–71. Sydney: Pluto Press.Google Scholar
  9. Newell, C. 1999b. The social nature of disability, disease and genetics. Journal of Medical Ethics 25(2): 172–175.PubMedCrossRefGoogle Scholar
  10. Newell, C., ed. 1999c. What is this thing called bioethics. Hobart: Australian Bioethics Association.Google Scholar
  11. Newell, C. 2000. Exploring notions of quality and ethics for consumers with disabilities: An Australian pilot study of general practitioners and people with disability. Interaction 13(4): 17–25.Google Scholar
  12. Newell, C., ed. 2002a. Exclusion & embrace: Conversations about spirituality and disability. Melbourne: Uniting Care Victoria.Google Scholar
  13. Newell, C. 2002b. Individual actions or social issues? Towards ethical biotech futures in a civil society. Nursing Ethics 9(5): 459. doi: 10.1191/0969733002ne534xx.PubMedCrossRefGoogle Scholar
  14. Newell, C. 2003. Disability: A voice in Australian bioethics? New Zealand Journal of Bioethics 4(2): 15–20.Google Scholar
  15. Newell, C. 2006a. Disability, bioethics, and rejected knowledge. The Journal of Medicine and Philosophy 31: 270.CrossRefGoogle Scholar
  16. Newell, C. 2006b. Rights, rhetoric and disability strategies: Reflections of a euphemistically challenged other. New Zealand Journal of Disability Studies 12: 62–80.Google Scholar
  17. Newell, C. 2007a. Narrating normalcy: Disability, medicine and ethics. Journal on Developmental Disabilities 13(2): 65–68.Google Scholar
  18. Newell, C. 2007b. ‘What’s wrong with you?’ Disability and genes as ethics. In Genes, eugenics and the future of the disabled, eds. J. Swinton and B. Brock, 44–56. London: Clark.Google Scholar
  19. Newell, C. 2008a. Better dead than disabled? When ethics and disability meet. In Ageing, disability & spirituality, ed. E. Mackinlay, 72–80. London: Jessica Kingsley Publishers.Google Scholar
  20. Newell, C. 2008b. God, brokenness and polity: Reflections from a hospital bed. Journal of Religion Disability & Health, in press.Google Scholar
  21. Newell, C., and A. Calder, eds. 2004. Voices in spirituality and disability from the land down under: From out back to out front. Birmingham: Haworth Press.Google Scholar
  22. Newell, C., and B. Offord, eds. 2008. Activating human rights in education. Canberra: Australian College of Educators.Google Scholar
  23. Newell, C., and T. Parmenter, eds. 2005. Disability in education: Context, curriculum and culture. Canberra: Australian College of Educators.Google Scholar
  24. Newman, C., and C. Newell 2007. Embracing cancer: A conversation of theology, health and ethics. Journal of Religion Disability & Health 11(1): 65–74. doi: 10.1300/J095v11n01_05.CrossRefGoogle Scholar
  25. Parsons, I., and C. Newell 1996. Managing mortality: Euthanasia on trial. Geelong: Villamanta Publishing.Google Scholar
  26. Tremain, S. 2008. Reconfiguring disability: From bioethics to biopolitics. Journal of Bioethical Inquiry 5(2–3): 101–277. doi: 10.1007/s11673-008-9105-6.CrossRefGoogle Scholar
  27. Wareing, D., and C. Newell 2005. Commonsense and the “doing” of supported care: a case study. Journal of Intellectual & Developmental Disability 30(2): 113–135. doi: 10.1080/13668250500125015.CrossRefGoogle Scholar

Copyright information

© Springer Science+Business Media B.V. 2008

Authors and Affiliations

  1. 1.Journalism and Media Research CentreUniversity of New South WalesKensingtonAustralia

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