Aim
This paper reports one aspect of a larger study, which aimed to explore the experience of ovarian cancer for women, partners and children. In this presentation the impact of relationships with health care professionals (HCPs) upon the experience of Australian women with a primary diagnosis of ovarian cancer will be described and interpreted.
Method
This research was informed by phenomenological philosophy. Data were collected via digitally recorded unstructured interviews with 15 Australian women with a primary diagnosis of ovarian cancer. Data collection ceased once themes became repetitive and saturation was reached. The analysis of the transcribed interviews was based upon van Manen’s (1990) method of data interpretation.
Findings
The women’s experience was explored around the themes of embodiment, relationality, spatiality, temporality and mortality. Results of the study indicate that relationships with HCPs can be viewed as critical foundations of the experience. Specifically, person-centered care, which reflected caring as an affect (caring about, as well as for women), provided stability and an ‘anchor of hope’ for many of these women experiencing uncertainty within a changing world.
Conclusions
This study presents evidence that relationships with HCPs form a strong foundation for the overall experience of ovarian cancer and were central to women’s experience of the disease. Results from this study have important implications for, and can be directly applied to, professional practice. An understanding of the importance women place upon their interactions with HCPs will support and encourage those HCPs already practicing in an engaged, person-centered manner. The information presented in this paper will be useful to researchers interested in optimising the provision of psychological support to women with ovarian cancer. It suggests that the impact of HCP relationships upon the experience of women with ovarian cancer is an area, which warrants further investigation in all cultures and countries.