This study explores and describes experiences of chronic liver disease
from the patient's perspective. No qualitative research studies appea
r to have examined the experiences of these patients. In-depth focused
interviews and grounded theory data collection and data analysis meth
ods were used. ii two-stage theoretical framework (becoming ill, and n
ot living) of the experience of transcending chronic liver disease is
presented. Sociological and psychological literature on common sense m
odels of health and illness are briefly reviewed. Several suggestions
for further research are made. The way in which this qualitative resea
rch study is leading to a quantitative and qualitative appraisal of th
e psychological adjustment in end-stage chronic liver disease patients
is outlined.