The study aimed to understand the impact of chronic illness on the lives of
midlife women and explore and share the ways in which women adapt to and/o
r tolerate chronic illness in their lives. In 1998, 80 women participated i
n a study in which data were generated by corresponding with the researcher
. Guided by feminist principles of collaboration, reciprocity and disclosur
e, we created rich stories about what it is like to live with a chronic ill
ness. In this paper we will discuss the first phase of this inquiry which u
tilized correspondence between the researcher and the women. The issues pos
ed by the use of correspondence as an innovative data generation process wi
ll be analysed. Correspondence, at first glance, may appear to be a rather
impersonal communication medium. However, we are committed to this method o
f data generation and believe we have unlocked the doors to a viable qualit
ative research process. The literature to guide this process is scarce so w
e are keen to share work in progress. We will describe the preparation phas
e in setting up the study; discuss some practical issues, share some of the
researcher's experiences in generating narratives from dialogues and hear
from the women themselves what they consider to be significant about this r
esearch process.