Advocacy and Community Engagement
‘It’s not all just about the dying’. Kaumātua Māori attitudes towards physician aid-in dying: A narrative enquiry.
Malpas, P. J., Anderson, A., Jacobs, P., Jacobs, T., Luinstra, D., Paul, D., Rauwhero, J., Wade, J., & Wharemate, D. (2016).
Palliative Medicine, 31(6), 544–552.
Read it in full here
Kaupapa Māori qualitative study explored attitudes toward physician aid-in-dying among 20 kaumātua (Māori elders) in Auckland, before EoLC Act.
1. Attitudes and understandings of physician-assisted death (PAD) Kaumātua held diverse views influenced by media coverage:
2. Influence of power was attributed to wairua (spirit), karakia (prayer), medical professionals, kaumātua, and whānau. Wairua’s power was pivotal in comforting and guiding end-of-life proceedings.
3. Significance of kawa (protocol) Kawa provides security, safety, and guidance for everyone involved in dying and death, offering structured cultural protocols for these transitions.
4. Whānau relationships Whānau relationships and roles are pivotal to health, wellbeing, dying, death, and PAD.
5. Significance of wairua is essential to all aspects of death and dying.
Te Ao Māori: Māori nurses’ perspectives on assisted dying and the Te Ao Māori cultural guide to nursing practice
Manson, L. (2021). [Master’s thesis, Auckland University of Technology].
Read it in full here
Māori Nurses’ Perspectives on End-of-Life Care and Assisted Dying
This thesis offers valuable insights into Māori nurses’ perspectives about what is important in end-of-life care, which can provide cultural considerations to inform nurses’ practice
Themes found:
1. Patient Choice
2. Tapuhi Kaitiaki (Māori Nurses’ Practice)
3. Barriers to Care
4. Cultural Safety of Patients and Whānau
Key Concerns:
The research highlights the complex intersection of assisted dying with Māori cultural values, whānau involvement, and ongoing systemic barriers that compromise culturally safe end-of-life care for Māori patients and their whānau.
Concerns were raised about the limited secularised legislation, particularly the need for whakawhanaungatanga (the process of establishing relationships) and Te Ao Māori (Māori worldview) to be interwoven into the assisted dying journey for Māori. The lack of inclusivity in the drafting of the End of Life Choice Act means that the guiding principles of ethical care for Māori, such as rangatiratanga (autonomy and self-determination), manaakitanga (caring for others and showing kindness), and wairuatanga (holistic wellbeing) are missing from the legislation.
There are limited published works with Māori discussing their experiences and opinions about assisted dying services and the End of Life Choice Act. The following articles are part of this growing body of research:
Check here for future conferences or interesting events that may be happening in Aotearoa New Zealand about assisted dying.