Expressions of Interest Request Membership of the palliative care equity working group In Aotearoa New Zealand, people have differences in health that are not only avoidable but unjust. Equity recognises people live with differing levels of advantage, requiring different approaches and resources to get equitable health outcomes. Te Whatu Ora – Health NZ and co-sponsors Te Aka Whai Ora – Māori Health Authority are establishing the palliative care equity working group to ensure that the national palliative care work programme keeps equity front and centre. The palliative care equity working group is overseen by the national palliative care steering group, who have been tasked to deliver the national work programme. The palliative care equity working group will:
identify unwarranted variation, inequitable outcomes in the access to, and outcomes from, palliative care services and offer sustainable and practical solutions to mitigate these provide recommendations on achieving equitable access to, and outcomes from, paediatric and adult palliative care services for all New Zealanders and their whānau sense check proposals from the steering group and other working groups to ensure equity is addressed provide support and advice to the steering group and other working groups on equity issues.
See the draft palliative care equity working group terms of reference for further information.
WHO SHOULD APPLY? We are looking for those with experience or leadership in the areas of:
Wellbeing for Māori, Pacific, and Asian communities Whaikaha (disability) community People with experience of receiving palliative care services and their whānau LGBTQIA+ community Health service policy, planning and funding Improving access to palliative care services (patients and whānau) Analysis and research specifically in relation to equity in health services Primary, community and specialist palliative care services.
Consideration will be given to ensuring diversity of cultural perspectives, experience, and geographic spread.
ROLE REQUIREMENTS You’ll be:
passionate about ensuring palliative and end-of-life care meets the needs of people, regardless of who they are, where they live, or their whānau context involved in your community or professional organisations able to work collaboratively, promote trust, share information and be innovative available to attend meetings and progress work between meetings (minimum time commitment of 4 – 8 hours monthly) able to commit to approximately 2 years.
Skills/experience required: