Wise care for the dying patient is one in which the quality and fullness of life is nurtured until the end. It is care that is chosen in an informed and planned way, taking into account the progression of the disease, changes in the care environment and the medical and non-medical needs of the patient. The monograph provides information and analysis on a broad spectrum of care for the dying patient and their immediate family members in social and economic terms in the following forms::
- palliative care clinic,
- perinatal hospice,
- home hospice for children,
- home hospice for adults,
- inpatient hospice/palliative care unit.
The paper presents the system of organisation and financing of services from both public and private funds. Issues related to thanatology education and volunteering in care institutions are addressed.
The book is intended for lecturers and students of pedagogy, social work, economics, social policy, health sciences and for staff and volunteers of palliative and hospice care providers.