“You receive the diagnosis, but your whānau have the cancer”: patients’ perspectives on breast cancer treatment in Wellington, Aotearoa New Zealand

Abstract

Aim: This study aims to investigate the perceptions of Māori, Pacific, and non-Māori/Pacific breast cancer patients’ treatment experience in Wellington, Aotearoa New Zealand. It will also explore the support they received throughout their treatment journey and the information provided to them over the course of their care. method: Qualitative semi-structured focus groups were carried out including breast cancer patients who had completed treatment within the past 2 years. Participants were recruited through breast cancer clinics. Data were analysed using reflexive thematic analysis. results: Participants reported a need for more tailored information from health professionals. Many participants reported barriers accessing services and follow-up appointments. Additionally, many participants, especially Māori and Pacific participants, emphasised the importance of ongoing support from healthcare professionals and their personal networks. conclusion: The findings highlight the need for improving patient-centred communication, recognising the important role of patient support systems and providing more tailored information and resources throughout breast cancer treatment. Addressing these factors could improve different patient groups’ experiences and outcomes by fostering a more informed and supported treatment journey.