CARING FOR THE DYING is divided into four sections. The essays in section one clarify the role of hospice in providing care for the dying, debunk some commonly believed myths about hospice, and discuss such issues as the funding of hospice services by Medicare.
Section two focuses on palliative care, considering the complicated nature of pain, when and to what extent suffering should be alleviated, and the use of drugs in palliative intervention.
The authors in section three examine the spiritual needs of the dying and stress that caregivers must remain sensitive to the diverse traditions in which spiritual needs are rooted.
The concluding section addresses, among other things, the legal right to healthcare at the end of life, and the importance of legal measures such as the advance directive, the durable power of attorney, and litigation to modify the requirements for Medicare-funded hospice services and to remove restrictions that might impede physicians from prescribing adequate pain-management drugs.
An underlying theme of all the essays is that individuals face death and dying differently; consequently, end-of-life needs vary. Awareness of this is crucial both for the dying and for those who see to their care. The selections in this insightful volume will help readers recognize and prepare for the difficult decisions that must be faced at the end of life.
Included are offerings from experts in the fields of law, nursing, medicine, biology, and social work, as well as from representatives of Compassion in Dying, the American Hospice Foundation, the Oregon Hospice Association, and many others.
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