Ethical issues arise for genetic counselors when a
client fails to disclose a genetic diagnosis of hereditary disease
to family: they must consider the rights of the individual client
to privacy and confidentiality as well as the rights of the
family to know their genetic risk. Although considerable work
has addressed issues of non-disclosure from the client’s
perspective, there is a lack of qualitative research into how
genetic counselors address this issue in practice. In this study,
a qualitative approach was taken to investigate whether
genetic counselors in Australia use a relational approach to
encourage the disclosure of genetic information from hereditary
breast and ovarian cancer (HBOC) clients among family
members; and if so, how they use it. Semi-structured qualitative
interviews were conducted with 16 genetic counselors
from selected states across Australia. Data collection and
analysis were guided by a basic iterative approach incorporating
a hybrid methodology to thematic analysis. The findings
provide indicative evidence of genetic counselors employing a
relational approach in three escalating stages––covert, overt
and authoritative––to encourage the disclosure of genetic
information. The findings lend credence to the notion that
genetic counselors envision a form of relational autonomy
for their clients in the context of sharing genetic information,
and they depart from individualistic conceptions of care/
solely client-centered counseling when addressing the needs
of other family members to know their genetic status.