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abstract
Objective: Family physicians in Canada as reported in
several studies do not recognize the importance of family history in
relation to breast/ovarian cancer and thus Canadian women with strong
family histories continue to develop early-onset breast cancer without
the knowledge of or ability to make choices regarding increased
surveillance or preventative strategies. This study explored the
feelings of women who learned about their hereditary risk only after
their diagnosis younger than 52 years and who eventually tested positive
for a BRCA gene mutation.
Methods: Thirty-four such women were mailed an
invitation to participate in this research including a letter of
information, consent form, and discussion prompts for their written
narrative response. Rigorous mixed method analyses were performed using
Charmaz-based qualitative analyses as well as quantitative analyses.
Results: Thirteen women (38.2%) responded with
narratives for qualitative analysis from which 4 themes were
coconstructed as follows: I, types of emotions; II, emotional response;
III, coping with emotions; and IV, advice to women at similar risk.
Women felt they should have learned about their hereditary risk from
their family physician and through public education before their
diagnosis. Although not experienced at the time of diagnosis, anger,
frustration, and regret were experienced after receiving their BRCA
results. These emotions arose from our research participants’ lack of
opportunity for prior genetic counseling and testing opportunity for
genetic counseling and testing.
Conclusions: With increased public and physician
education, it is hoped that women with significant family histories of
breast/ovarian cancer will be identified before diagnosis and given
options regarding cancer surveillance and risk reduction strategies.
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