This exploratory study examines the situation of a heterogeneous group
of 46 cancer patients from one general hospital in the Stockholm area
who were diagnosed with a malignant disease in 1987. Forty-six patien
ts were interviewed to determine how they experience and cope with the
ir sickness. Although age-related issues were not directly addressed b
y the interviewer, they were frequently commented upon by the responde
nts. A questionnaire was also used to quantify various psychosocial as
pects of the individual's cancer experience. Quantitative and qualitat
ive data were used in a complementary fashion. The patients interviewe
d ranged in age from 29 to 88 years (median 61). Issues related to age
were frequently addressed spontaneously by the interviewed persons, w
hich led to further exploration of age-related aspects of care. Althou
gh few age-related differences in symptom distress were found, some di
fferences were seen in patients' perceptions of the response of the pr
ofessional health-care system. The older patients related that they ha
ve less quantitative contact with specialized formal resources, and pe
rceive less sense of engagement and concern from the professional heal
th-care sector. The qualitative analysis suggests that age may be used
by patients as an explanatory factor in a variety of situations, func
tioning as a means of ''making sense'' of sickness experiences.