Abstract
Traditionally, the cancer patient has been a passive recipient of various therapies—exerting very little personal direction over either the management or the outcome of his or her disease. Unlike patients with diabetes or hypertension,(1) for example, cancer patients generally adopt a passive role in their treatment, aside from the actual consent to therapy or refusal thereof. The cancer patient literally presents his or her body to the clinic or hospital, where it is examined by a variety of specialists, subjected to surgery, irradiated, and/or treated with toxic chemotherapeutic agents. Through all of this, the patient often feels like an object, while the family stands by, feeling uninformed and helpless, unable to assist the patient through the various discomforts and fears he or she faces.
The work described in this chapter was done while the author was Associate Director, Cancer Rehabilitation Program, Mayo Comprehensive Cancer Center. It was funded by Contract CN 45120 from the National Cancer Institute.
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References
Lazes, P. M. Health education project guides outpatients to active self-care. Hospitals, J.A.H.A.51:81–86, 1977.
Wang, V. L., Reiter, H., Lentz, G. A., Jr., and Whaples, G. C. An approach to consumer-patient activation in health maintenance. Public Health Reports 90: 449–454, 1975.
Janik, N. The shortest distance between treatment and survival: Reach to recovery. Proceedings of The American Cancer Society Second National Conference on Human Values & Cancer, Chicago, 1977, pp. 180–182.
1977 Cancer Facts & Figures. New York: American Cancer Society, 1976, pp. 24–25.
Yahle, M. E. An ostomy information clinic. Nurs. Clin. North Am. 11:457–467, 1975.
Kelly, O. E. Make Today Count. In: National Cancer Institute Response Book, Bethesda, National Cancer Institute, 1978, paragraph 9.12.
Monaco, M. The Candlelighters: Parents Dedicated to the Conquest of Cancer. Washington D.C.: Candlelighters, 1972.
Levin, L. S. Patient education and self-care: How do they differ? Nurs. Outlook 26:170–175, 1978.
Cox, B. G. The fine art of educating the patient. Med. Opinion 4:31–35, 1975.
Cox, B. G., Carr, D. T., and Lee, R. E. Living with Lung Cancer: A Reference Book for People with Lung Cancer and Their Families. Rochester, Minn.: Mayo Foundation, 1977.
Roth, B. G. Health information for patients: The hospital library’s role. Bull. Med. Libr. Assoc. 66:14–17, 1978.
Cox, B. G., and Wentworth, A. A. The Ileal Pouch Procedure: A New Outlook for the Person with an Ileostomy. Rochester, Minn.: Mayo Foundation, 1975.
Cox, B. G., and Wentworth, A. A. An evaluation model for the development of patient education literature. Biosciences Communications 2:333–341, 1976.
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© 1979 Plenum Publishing Corporation
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Cox, B.G. (1979). The Cancer Patient as Educator and Counselor. In: Taché, J., Selye, H., Day, S.B. (eds) Cancer, Stress, and Death. Sloan-Kettering Institute Cancer Series. Springer, Boston, MA. https://doi.org/10.1007/978-1-4684-3459-0_8
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DOI: https://doi.org/10.1007/978-1-4684-3459-0_8
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