What is it like living with the diagnosis of cancer

作者: S. SAEGROV , A.-G. HALDING

DOI: 10.1111/J.1365-2354.2004.00442.X

关键词:

摘要: This article discusses in-depth interviews of 12 persons, who had been diagnosed for cancer from 6 months to 3 years earlier, concerning what it is like live with the diagnosis cancer. The persons interviewed were aged 43-70 years, and 11 received successful radical treatment; one patient was treated symptoms, but an uncertain future development. investigation shows that period waiting first suspicion until confirmation disease a great stress, following commencement treatment also very difficult one. there no follow-up individual patients their need talk about new life-situation brought by disease. Receiving remembered as being dramatic experience informants. informants satisfied medical they received, feel should have some kind programme available care psycho-social needs. In rehabilitation phase, left own resources; during this period, felt physically mentally drained, did not knowledge tackle life-situation. threat cells discovered always patients. Attending check-ups described stress.

参考文章(11)
Rosser R, The history of health related quality of life in 10 1/2 paragraphs. Journal of the Royal Society of Medicine. ,vol. 86, pp. 315- 318 ,(1993)
Tomoko Takayama, Yoshihiko Yamazaki, Noriyuki Katsumata, Relationship between outpatients' perceptions of physicians' communication styles and patients' anxiety levels in a Japanese oncology setting. Social Science & Medicine. ,vol. 53, pp. 1335- 1350 ,(2001) , 10.1016/S0277-9536(00)00413-5
JUDITH FITZGERALD MILLER, MARJORIE J. POWERS, Development of an instrument to measure hope. Nursing Research. ,vol. 37, pp. 6- 10 ,(1988) , 10.1097/00006199-198801000-00002
Sarah Ford, Lesley Fallowfield, Shôn Lewis, Doctor-patient interactions in oncology. Social Science & Medicine. ,vol. 42, pp. 1511- 1519 ,(1996) , 10.1016/0277-9536(95)00265-0
Anne P. O??Connor, Cheryl A. Wicker, Barbara B. Germino, Understanding the cancer patient's search for meaning. Cancer Nursing. ,vol. 13, pp. 167- 175 ,(1990) , 10.1097/00002820-199006000-00006
Cynthia M. Mathieson, Henderikus J. Stam, Renegotiating identity: cancer narratives. Sociology of Health and Illness. ,vol. 17, pp. 283- 306 ,(1995) , 10.1111/1467-9566.EP10933316
Rob Sanson-Fisher, Afaf Girgis, Allison Boyes, Billie Bonevski, Louise Burton, Peter Cook, , The unmet supportive care needs of patients with cancer Cancer. ,vol. 88, pp. 226- 237 ,(2000) , 10.1002/(SICI)1097-0142(20000101)88:1<226::AID-CNCR30>3.0.CO;2-P
Marieke A.E. van der Waal, Anton F. Casparie, Christiaan J. Lako, Quality of care: a comparison of preferences between medical specialists and patients with chronic diseases Social Science & Medicine. ,vol. 42, pp. 643- 649 ,(1996) , 10.1016/0277-9536(95)00200-6
Symone B. Detmar, Martin J. Muller, Liowina D. V. Wever, Jan H. Schornagel, Neil K. Aaronson, Patient-Physician Communication During Outpatient Palliative Treatment Visits: An Observational Study JAMA. ,vol. 285, pp. 1351- 1357 ,(2001) , 10.1001/JAMA.285.10.1351