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There is a growing movement to increase access to palliative care by declaring it a human right. Calls for such a rightin the form of articles in the healthcare literature and pleas to the United Nations and World Health Organizationrarely 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.
Public Health Ethics – Oxford University Press
Published: Apr 17, 2011
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