This study supports health, palliative and social care professionals
In New Zealand Palliative care is defined as:
"... the care of people who are dying from active, progressive diseases or other conditions that are not responsive to curative treatment. Palliative care embraces the physical, social, emotional and spiritual elements of wellbeing–tinana, whanau, hinengaro and wairua – and enhances a person’s quality of life while they are dying. Palliative care also supports the bereaved family/whanau." (Ministry of Health (2002). Palliative Care Strategy. Ministry of Health, Wellington.)
Hospice New Zealand has supported the Pae Herenga study from the start. New Zealand hospices, as well as health care, palliative care and social care professionals are also beneficiaries of the study. We hope that hospice health professionals will find this information useful to support Māori whānau who use their services. Hospice provides specialist palliative care (medical, psychological and social care for people with a life limiting illness and their whānau and families) and this is freely available in New Zealand for people who meet the criteria. Palliative care can help to improve the quality of life for kaumātua who are ill and dying and it can support kaumātua who have more than one health concern, or complex health issues.