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A Dialogue on Compassion and Supererogation in Medicine
Published online by Cambridge University Press: 29 July 2009
Extract
According to Frankena, “the moral point of view is what Alison Wilde and Heather Badcock did not have.” Most of us, however, are not such extreme examples. We are capable of the moral point of view, but we fail to take the necessary time or make the required efforts. We resist pulling ourselves from other distractions to focus on the plight of others and what we might do to ameliorate their suffering. Perhaps compassion is rooted in understanding what it is that connects us with others rather than what separates us, and rests on developing sufficient awareness, to internalize what our actions, or lack of them, mean in the lives of others.
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- Special Section: Compassion: What Does It Really Mean?
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- Copyright © Cambridge University Press 1995
References
Notes
1. For the meaning and development of the virtues in medicine, see: Pellegrino, ED, Thomasma, DC. The Virtues in Medical Practice. New York: Oxford University Press, 1993.Google Scholar
2. Loewy, EH. Suffering and the Beneficent Community. New York: SUNY Press.Google Scholar
3. Pope John Paul II. Humanize hospital work. Address to the Sixty-First General Chapter of the Hospital Order of St. John of God. L'Osservatore Romano 1983;01 24:3.Google Scholar
4. See note 1. Pellegrino, , Thomasma, . 1993.Google Scholar
5. See note 1. Pellegrino, , Thomasma, . 1993.Google Scholar
6. Flannery, A. Vatican II: The Conciliar and Post-Conciliar Documents. Collegeville, Minnesota: Liturgical Press, 1975. Decree on the Apostolate of the Laity.Google Scholar
7. De Unamuno, M. [Trans Kerrigan, A] The Tragic Sense of Life. Princeton, NJ: Bollingen Series, Vol LXXXV, 1972:224.Google Scholar
8. Pope John Paul II. Rick in mercy. The Encyclical Dives in Misericordia, 11 30, 1980. Washington, DC: U.S. Catholic Conference, 1981:45.Google Scholar
9. Bergsma, J, Thomasma, DC. Health Care: Its Psychosocial Dimensions. Pittsburgh, Pennsylvania: Duquesne University Press, 1982.Google Scholar
10. Pellegrino, ED, Thomasma, DC. Health and Healing [published first in Italian] Rome: Editions Deshoines [In press].Google Scholar
11. Pellegrino, ED, Thomasma, DC. For the Patient's Good: The Restoration of Beneficence in Health Care. New York: Oxford University Press, 1988.Google Scholar
12. Welie, J. Viktor Von Gebstattel's. Theoretical Medicine 1995; 16(2)Google Scholar
13. Von Gebstattel, V. Theoretical Medicine 1995; 16.Google Scholar
14. Jonsen, A. What does life support support? In: Winslade, W, Ed. Personal Choices and Public Commitments: Perspectives on the Humanities. Galveston, Texas: Institute for the Medical Humanities, 1988: 61–9, at pp. 66–67.Google Scholar
15. Raffin, TA, Shurkin, JN, Sinkler, W III. Intensive Care: Facing the Critical Issues. New York: W.H. Freeman & Co., 1988:185.Google Scholar
16. See note 15. Raffin, et al. 1988:175.Google Scholar
17. Rouse, F. Living wills in the long-term care setting. Journal of Long-Term Care Administration 1988;17:14–9.Google Scholar
18. Mehling, A. Living wills: preventing suffering or a deadly contract? State Government News, 1988;Dec:14–5.Google Scholar
19. Mehling, A, Neitlich, S. Right-to-die backgrounder. News from the Society for the Right to Die (now Choice in Dying) 1989;Jan:1–2.Google Scholar
20. Braithwaite, S, Thomasma, DC. New guidelines on foregoing life-sustaining treatment in incompetent patients: an anti-cruelty policy. Annals of Internal Medicine 1986;104:711–5.CrossRefGoogle ScholarPubMed
21. Illich, I. Medical Nemesis: The Expropriation of Health. New York: Pantheon, 1976:106.Google Scholar
22. See note 21. Illich, . 1976:154.Google Scholar
23. Le Carré, J. The Secret Pilgrim. New York: Alfred Knopf, 1991:12.Google Scholar
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