Cancer screening is a high priority within the Métis community in Alberta. Despite comparable cancer incidence rates to non-Métis Albertans, Métis people face barriers to accessing cancer screening programs. This study used community-based research approaches informed by Métis ways of knowing to engage 31 individuals across Alberta about their experiences with accessing cancer screening services. Data collection was completed through two in-person Métis gatherings and six telephone interviews. Gatherings included talking circles and cultural activities, with discussions lasting approximately three hours. Topics discussed included experiences with accessing screening services, the quality of care received during appointments, and the supports needed to improve access to screening programs. Discussions were audio-recorded, transcribed, de-identified, and thematically analyzed using NVivo Software. Four prominent themes emerged from this study: (1) the impact of patient-provider communications on cancer experiences, (2) a broken healthcare system and access to care, (3) a need for support and safety, and (4) health promotion behaviours. An overarching theme of discrimination as a social determinant of health emerged throughout the findings. Tangible barriers, including geographical, transportation, and financial, were also identified by study participants. This study provides an increased understanding of Métis experiences related to cancer screening and offers direction for improvements.
Zhang et al. (Wed,) studied this question.