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dc.contributor.authorMacDonald, Catherine D.
dc.date.accessioned2013-09-03T13:00:19Z
dc.date.available2013-09-03T13:00:19Z
dc.date.issued2013-09-03
dc.identifier.urihttp://hdl.handle.net/10222/36294
dc.description.abstractMi’kmaq women in Nova Scotia are reported to have lower rates of Papanicolaou (Pap) smear screening and have higher rates of cervical cancer compared to non-Aboriginal women. Much of the cervical cancer literature reflects mainstream values and tends to essentialize Aboriginal women as one at-risk homogenous group lacking knowledge about cervical cancer prevention. The primary purpose of this qualitative participatory study was to explore Mi’kmaq women’s and primary healthcare providers’ experiences with Pap smear screening and to consider the broader historical, economic, and socio-political contexts that shape those healthcare experiences. Mi’kmaq women’s experiences accessing Pap screening services, their encounters with healthcare providers and the health care system, and women’s past experiences with Pap smear screening were also explored. This inquiry was grounded in postcolonial feminist perspectives and Indigenous principles in a two-eyed seeing approach. Community facilitators were identified to assist with recruitment and the research process. Women participated in talking circles to learn about and shape the study. Sixteen Mi’kmaq women and five healthcare providers participated in two semi-structured interviews. Five themes were identified from the women: a) Finding Our Way, b) Our Understanding and Perceptions about Pap Smear Screening, c) The Impact of History on Our Health and Healthcare Experiences, d) Healthcare Providers’ Encounters: “Making a Difference in Our Path to Paps,” and e) “The Healthcare System is Complicating Our Going for Paps.” Two themes were identified from healthcare providers: a) Understanding the Realities of Aboriginal Women’s Lives and b) Fostering Aboriginal Women’s Access to Pap Smear Screening. This research contributes to an understanding of the continued impact of wider historical, political, and socioeconomic conditions that have resulted from colonialism, residential schools, and assimilation on Pap smear screening. It reinforces the importance of not essentializing women’s views or experiences and recognizing that some are accessing Pap smear screening regularly in spite of challenging circumstances. Mi’kmaq women have been underrepresented in the previous Pap smear screening literature. It is critical that healthcare providers understand how they can improve access to Pap smear screening and the screening process itself.en_US
dc.subjectMi'kmaq Women, Pap Smear Screening, Participatory Action Researchen_US
dc.titleExploring Mi'kmaq Women's Experiences with Pap Smear Screening in Nova Scotiaen_US
dc.date.defence2013-07-31
dc.contributor.departmentSchool of Nursingen_US
dc.contributor.degreeDoctor of Philosophyen_US
dc.contributor.external-examinerDr. Sylvia Bartonen_US
dc.contributor.graduate-coordinatorDr. Marilyn Macdonalden_US
dc.contributor.thesis-readerDr. Annette Browne, Dr. Charlotte Loppie-Reading, Dr. Marilyn Macdonalden_US
dc.contributor.thesis-supervisorDr. Audrey Steenbeek, Dr. Ruth Martin-Miseneren_US
dc.contributor.ethics-approvalReceiveden_US
dc.contributor.manuscriptsNot Applicableen_US
dc.contributor.copyright-releaseNot Applicableen_US
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