The Meaning, Limitations and Possibilities of Making Palliative Care a Public Health Priority by Declaring it a Human Right
David Bourget (Western Ontario)
David Chalmers (ANU, NYU)
Rafael De Clercq
Ezio Di Nucci
Jack Alan Reynolds
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Public Health Ethics 4 (1):84-92 (2011)
There is a growing movement to increase access to palliative care by declaring it a human right. Calls for such a right—in the form of articles in the healthcare literature and pleas to the United Nations and World Health Organization—rarely define crucial concepts involved in such a declaration, in particular ‘palliative care’ and ‘human right’. This paper explores how such concepts might be more fully developed, the difficulties in using a human rights approach to promote palliative care, and the relevance of such an enterprise to public health ethics
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References found in this work BETA
James F. Childress, Ruth R. Faden, Ruth D. Gaare, Lawrence O. Gostin, Jeffrey Kahn, Richard J. Bonnie, Nancy E. Kass, Anna C. Mastroianni, Jonathan D. Moreno & Phillip Nieburg (2002). Public Health Ethics: Mapping the Terrain. Journal of Law, Medicine & Ethics 30 (2):170-178.
Bruce Jennings (2009). Public Health and Liberty: Beyond the Millian Paradigm. Public Health Ethics 2 (2):123-134.
Benjamin Mason Meier (2007). Advancing Health Rights in a Globalized World: Responding to Globalization Through a Collective Human Right to Public Health. Journal of Law, Medicine & Ethics 35 (4):545-555.
Mark G. Kuczewski (1996). Reconceiving the Family: The Process of Consent in Medical Decisionmaking. Hastings Center Report 26 (2):30-37.
Robert A. Pearlman, Kevin C. Cain, Donald L. Patrick, M. Appelbaum-Maizel, H. E. Starks, N. S. Jecker & R. F. Uhlmann (1993). Insights Pertaining to Patient Assessments of States Worse Than Death. Journal of Clinical Ethics 4 (1):33.
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