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The New Zealand Carers’ Strategy was launched in 2008 by then Minister for Senior Citizens, the Hon Ruth Dyson and can be found at the back of the latest Carers' Strategy Action Plan. The Strategy was developed in partnership by government agencies and the New Zealand Carers Alliance (which represents a network of over 45 not-for-profit organisations). It is supported by five-year action plans that address key priorities identified by carers and the Government.

The latest Carers’ Strategy Action Plan is focused on improving the wellbeing of the one in 10 New Zealanders who care for a loved one with a disability, health condition, illness or injury. Mahi Aroha includes a range of actions that we will help carry out with other government agencies and sector organisations over the next five years. Mahi Aroha was developed in partnership with the New Zealand Carers’ Alliance and a cross-government agency working group.

The Ministry of Health’s disability respite strategy, Transforming Respite: Disability Support Services Respite Strategy 2017-2022, will make it easier for carers of disabled people to have a break from their caring responsibilities. Transforming respite sets the future direction for improving disability respite support. The strategy responds directly to what disabled people and their families/whānau told us about their aspirations for the future.

The page, Carers in New Zealand, contains information about carers and their role, the Carers’ Strategy partnership between the government and Carers Alliance, and the care-related interest and responsibilities of the Ministry of Health.

A Guide for Carers is practical help for whānau, aiga and carers who assist family members and friends who need help with everyday living because of a health condition, disability or injury. It includes information on services and supports available for carers.

This page, COVID-19: Information for family, whānau, and āiga carers, contains information on the role of a carer during New Zealand’s response to the COVID-19 pandemic. This page makes it easy to find the support and advice for carers.

The purpose of this paper, Current state: Carers of people with health conditions or disabilities, is to provide information on New Zealand’s working-age carers, including how their caregiving roles affect them, and to describe the supports currently provided as well as the challenges with the current carer support system.

This book, Multiple Dimension of Caregiving and Disability, explore how caring for people with disabilities often becomes an all-encompassing responsibility for one or more family members. To manage the multifaceted demands, caregivers must possess strong multitasking skills, including the ability to assist with daily life tasks; provide emotional support; help with financial affairs; mediate and advocate with health care providers.

The goal of this edited volume, The Spectrum of Family Caregiving for Adults and Elders with a Chronic Illness, is to review the research on the caregiving role and the interventions developed to assist family caregivers of older adults and elders with different chronic conditions. An evidence table is included in each of these chapters so readers can judge more easily the quality of evidence supporting the intervention studies.

This book, Service User and Carer Involvement in Health and Social Care, was written by a collection of experts in the field, this text provides a critical and constructive analysis of the ways in which service users and carers engage with health and social care services. Covering topics such as the importance of terminology, wellbeing and resilience and the notion of tokenism, and enhanced by a wealth of first-hand experiences.

In this book, An extra pair of hands, Kate Mosse tells her personal story of finding herself as a carer in middle age: first, helping her mother look after her beloved father through Parkinson's, then supporting her mother in widowhood, and finally as 'an extra pair of hands' for her 90-year-old mother-in-law. This is a story about the gentle heroism of our carers, about small everyday acts of tenderness, and finding joy in times of crisis.

In The Soul of Care: The Moral Education of a Husband and a Doctor, Arthur Kleinman delivers a deeply humane and inspiring story of his life in medicine and his marriage to Joan, and he describes the practical, emotional and moral aspects of caretaking. He also writes about the problems our society faces as medical technology advances and the cost of health care soars but caring for patients no longer seems important.

Despite advances in detection and treatment, cancer remains a source of pain and distress to patients and of complex challenges to the loved ones caring for them. The trend toward shorter hospital stays in particular has increased the physical, psychological, and financial burden on caregivers, often leading to adverse effects on patients. Cancer Caregiving in the United States illuminates these complex concerns with authoritative detail.