“…Additional approaches include cancer education programmes which support the role of Indigenous Health Workers (Le et al, 2013;Murphy et al, 2015;Smith, 2012;Whop et al, 2012;Zorbas & Elston, 2016), a key source of cancer information, health promotion and support for Indigenous patients undergoing cancer treatment (Bernardes et al, 2012). Studies from other countries have consistently attributed the well-documented poorer breast cancer survival (Dachs et al, 2008;DeSantis et al, 2014;Javid et al, 2014;Lawrenson et al, 2016;Nishri et al, 2015) in Indigenous populations to greater comorbidity burden, socioeconomic disadvantage, geographic location, cultural issues and variations in the timeliness, accessibility and quality of cancer services involving early detection, diagnosis and treatment (Javid et al, 2014;Kolahdooz et al, 2014;Lawrenson et al, 2016;Seneviratne et al, 2014;Tranberg et al, 2015). For example, Maori women are more likely to be diagnosed with advanced disease and experience delays in receiving treatment than non-Maori women in New Zealand (Lawrenson et al, 2016;Seneviratne et al, 2014) while in the United States, American Indians/Alaskan Native women are less likely to receive guideline concordant care than White women (Javid et al, 2014).…”