This narrative review examines the intersection of gambling harms and stigma among Māori, Pacific peoples, Asian communities and youth in Aotearoa New Zealand. The literature shows that stigma is shaped less by individual behaviour than by structural factors such as colonisation, socio-economic inequities, migration pressures and the concentration of pokies in low-income communities. We identify how stigma is experienced within each population and how it influences help-seeking, highlighting the central role of identity, cultural obligations and collective wellbeing.

In 2010, the passing of the Electoral (Disqualification of Sentenced Prisoners) Amendment Act removed voting rights for all prisoners, regardless of sentence length. A decade later, prisoners serving sentences of less than three years were re-enfranchised. Research and public discourse have highlighted the disproportionate effects of prisoner disenfranchisement for Māori, given persistent overrepresentation of Māori in prison. However, less attention has focused on the specific effects of disenfranchisement for wāhine Māori in prison.

Māori pharmacists are under-represented within the pharmacist community at 2.1%. This figure is substantially lower than the approximately 18% representation of Māori within the total population of Aotearoa New Zealand. The purpose of this research was to determine why Māori stay in the pharmacy profession, consider leaving or leave the profession, and what roles they move into if they leave. Those who had ever been a Māori pharmacist were invited to complete an anonymous online questionnaire. The responses of the 28 participants, representing approximately 26% (n = 23) of registered Māori pharmacists (n = 89), plus five who had left the profession, are presented here.

Whakataukī are metaphors that provide us with ethical guidelines, and tikanga and kawa are the wisdom, knowledge and history handed down from the past to future generations to help people navigate their lives and support aspirations for today and the future. Using a twin-hulled waka ama as a metaphor for the relationship between participants and researchers in Indigenous research, this article explores Māori and Indigenous ethics as having equal status to Western research ethics. In relation to research, ethics can be a complicated domain when working alongside Māori and Indigenous peoples.

Māori and Pacific researchers are working hard to transform our research system to enable Māori and Pacific postgraduate students to thrive in science, technology, engineering and mathematics (STEM). Yet barriers remain, and each new postgraduate generation inherits evolving challenges and opportunities to navigate. This paper is written for Māori and Pacific people who are about to enter the postgraduate STEM space, recognising that we need our own words to help future students to navigate this journey.

The study presented in this article is underpinned and guided by Kaupapa Māori theory and research principles (G. H. Smith, 1997; L. Smith, 2015). The purpose was to explore support systems comprising health, social, financial, education and whānau that exist for teenage Māori mothers/māmā Māori in Aotearoa New Zealand. Research participants were sourced from one Teen Parent Unit and are Māori who became mothers as teenagers. Effectiveness of support was assessed in terms of contribution to holistic wellbeing and success for māmā Māori.

Gut diseases are a major cause of morbidity and mortality in Aotearoa New Zealand, with higher rates of these conditions in Te Waipounamu. Māori experience both worse outcomes and different patterns of incidence in gut diseases than non-Māori. Overall, Māori have lower life expectancies than non-Māori and experience barriers to accessing determinants of health. We aim to illuminate how Māori understand the gut and navigate the health system when the topic is the gut and gut disease, based on interviews with Māori participants in a wider study of gut symptoms.

Climate change is the biggest threat to humanity through compounding ecological disasters. A focus on global averages tends to hide dramatic differences and mask health disparities that exist for Indigenous people. For 21 years, district health boards (DHBs) were responsible for providing or funding the provision of health services across Aotearoa. The introduction of the Pae Ora (Healthy Futures) Act 2022 disestablished DHBs and offered an opportunity to reshape health in ways that give serious consideration to climate change impacts. The need to give greater consideration to Indigenous people in climate change conversations is essential.

The aim of the study reported in this article was to explore the experiences of (1) people living with type 2 diabetes (T2D) and their whānau, and (2) kai manaaki, community health workers and dieticians who provide care to Māori and Pacific peoples living with T2D in the community. A key objective for this research was for its findings to inform workforce development strategies that will achieve equity for Māori and Pacific peoples with T2D and other long-term conditions.

For many Māori, it is the presence of their kin that transforms a dwelling into a home. However, when that dwelling needs repairs, it can compromise health and wellbeing and be a barrier to homemaking. Two Kaupapa Māori qualitative studies in Hawke’s Bay interviewed 24 whānau members living in 18 whānau-owned houses about the impact of government-funded critical house repairs. Thematic analysis highlighted that critical repairs were primarily needed as a result of financial hardship. Most participants were positive about the repair work done by Māori tradespeople.