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Mary, Talbot, ‘In a secular age, what does it mean to die a good death? | Aeon Essays’. [Online]. Available: https://aeon.co/essays/in-a-secular-age-what-does-it-mean-to-die-a-good-death
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D. Clark, ‘Palliative care in the global context: Understanding policies to support end-of-life care’, in A Public Health Perspective on End of Life Care, J. Cohen and L. Deliens, Eds. Oxford University Press, 2012, pp. 215–226 [Online]. Available: http://www.oxfordscholarship.com/view/10.1093/acprof:oso/9780199599400.001.0001/acprof-9780199599400-chapter-020
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Clare Humphreys, ‘“Waiting for the last summons”: The establishment of the first hospices in England 1878-1914’, Mortality, vol. 6, no. 2, 2001 [Online]. Available: https://ezproxy.lib.gla.ac.uk/login?url=https://www.tandfonline.com/doi/abs/10.1080/13576270120051875a?src=recsys
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The Economist Intelligence Unit, ‘The 2015 Quality of Death Index: Ranking palliative care across the world’. [Online]. Available: http://www.apcp.com.pt/uploads/2015-EIU-Quality-of-Death-Index-Oct-6-FINAL.pdf
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D. Vijay and M. Kulkarni, ‘Frame Changes in Social Movements: A Case Study’, Public Management Review, vol. 14, no. 6, pp. 747–770, Sep. 2012, doi: 10.1080/14719037.2011.642630.
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A. A. Abraham and V. Jithesh, ‘The Kerala Experience in Palliative Care: An Ethical Exploration from the Public Health Perspective’, Asian Bioethics Review, vol. 4, no. 1, pp. 14–28 [Online]. Available: https://ezproxy.lib.gla.ac.uk/login?url=https://muse.jhu.edu/article/469744
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F. Norwood, ‘Nothing More To Do: Euthanasia, General Practice, and End-of-Life Discourse in the Netherlands’, Medical Anthropology, vol. 26, no. 2, pp. 139–174, Apr. 2007, doi: 10.1080/01459740701283165.
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R. Pool, Negotiating a good death: euthanasia in the Netherlands. New York: Routledge, 2013 [Online]. Available: https://ebookcentral.proquest.com/lib/gla/detail.action?docID=1683677
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I. G. Finlay and R. George, ‘Legal physician-assisted suicide in Oregon and The Netherlands: evidence concerning the impact on patients in vulnerable groups--another perspective on Oregon’s data’, Journal of Medical Ethics, vol. 37, no. 3, pp. 171–174, Mar. 2011, doi: 10.1136/jme.2010.037044.
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N. Richards, ‘Assisted Suicide as a Remedy for Suffering? The End-of-Life Preferences of British "Suicide Tourists”’, Medical Anthropology, vol. 36, no. 4, pp. 348–362, May 2017, doi: 10.1080/01459740.2016.1255610.
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R. J. Chan, J. Webster, J. Phillips, and D. C. Currow, ‘The withdrawal of the Liverpool Care Pathway in the United Kingdom: what are the implications for Australia?’, The Medical Journal of Australia, vol. 200, no. 10, pp. 573–573, Jun. 2014, doi: 10.5694/mja13.10998.
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Alexi A. Wright, ‘Associations Between End-of-Life Discussions, Patient Mental Health, Medical Care Near Death, and Caregiver Bereavement Adjustment’, JAMA, vol. 300, no. 14, pp. 1665–1673, doi: 10.1001/jama.300.14.1665.
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Zur Soziologie Des Sterbens: Aktuelle Theoretische Und Empirische Beitrage. Springer vs, 2016 [Online]. Available: https://contentstore.cla.co.uk//secure/link?id=ddec9556-c840-e911-80cd-005056af4099
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A. Gawande, Wellcome Collection, and Ebooks Corporation Limited, Being mortal: aging, illness, medicine and what matters in the end. London: Profile Books, 2014 [Online]. Available: http://ebookcentral.proquest.com/lib/gla/detail.action?docID=1819882
