Bøger i Golden Age Books serien

New treatments and advances in therapy for the ravages of Parkinson's disease are constantly being researched and perfected for patients, yet those afflicted still must endure tremors, poor balance, speech problems, and lessened psychological well-being. Patients and families need the most up-to-date information available to improve quality of care and life.This new, second edition of Caring for the Parkinson Patient covers a variety of topics, providing information and helpful suggestions for patients, families, and caregivers to aid them as they grapple with this chronic, debilitating neurological disorder. Sixteen accessible and information-packed essays by noted contributors address diagnosis and treatment, new research, communication, physical/ occupational therapy, nursing care, problems faced by the caregiver, emotional changes, "neurorehab," prevention of falls, sleep problems, surgery, community supports, the family, sexuality, and safe home environments.With a wealth of information, practical advice, and encouragement, Caring for the Parkinson Patient is an indispensable resource guide for all those touched by Parkinson's disease.

This thoughtful collection based on a highly successful conference held in Calgary, Alberta, combines the views of professional gerontologists, educators, health-care specialists, and policy makers to confront the issues affecting health care for older adults in both Canada and the United States. The contributors seek not only to inform but to inspire innovative reponses from the private as well as the public sector. Experts in government, aging, medicine, public administration, social service, counseling, and consulting focus their attention on vital areas of concern to elders who are in need of assistance, to the providers of these services, and to a public who seeks assurance that its resources are cost-effectively allocated to meet present and future demand. Included are essays on the current status of health-care policy in the United States and Canada, daily money management, caring for the noncompliant elder, long-term care as an emerging women's issue, lobbying government agencies and political leaders, the role of gerontology in resolving the crisis of long-term care, and "geroethics."

Advances in technology have raised new ethical questions in medicine, concern for pollution has encouraged the growth of "environmental ethics", and the problems of corporate America have sparked more questions about "business ethics". With the population of older persons increasing every year and their social problems becoming ever more acute, it's now time for "geroethics", which assesses the impact of societal values on elders and how the aged may respond to these values. The issues are urgent and compelling: the changing face of elder America, dependence on others for care, the corporate response to agism, the healthcare crisis, how to take charge of one's life and bring meaning to it, living longer verses living better, coping with disabilities, the psychological aspects of aging, and so many others. Ethics embraces concepts of rights and privileges, duties and obligations, choices and their outcomes. In Geroethics: A New Vision of Growing Old in America author Gerald A. Larue shows how social values impact on elders in the United States and how older persons, and those who advocate on their behalf, may respond to the attitudes and actions of others. Dreams and goals, rights and responsibilities, self-respect and personal dignity shouldn't fade with the passing of youth. This latest addition to the Golden Age series offers the elderly and those who care for them a vibrant new look at the challenges of aging: the role elders can and do play in shaping and changing society's views of its oldest members, regaining control of important life choices, and the struggle to live a meaningful and independent existence free of anxiety, fear, and uncertainty. Included are chapters onstereotypes, identifying the elderly, human rights, agism, the ethics of survival, elder power, elder abuse, fear of aging, caring for elders, health care, dementia, loneliness, death and dying, and much more.

Family caregivers must often juggle their duties as parents, spouses, and employees while tending to the daily needs of a loved one who is elderly, chronically ill, or dying. As the rising cost of care forces many more people to respond to the needs of a family member, increasing numbers of primary care providers will become susceptible to anxiety, frustration, guilt, confusion, anger, emotional and physical fatigue, resentment, worry and depression, and other sources of pressure. Soon stress becomes an everyday occurrence that at times seems insurmountable. If those who care for the ill and the infirm are to remain effective, they must confront the reality of stress and their obligation, both to themselves and their loved ones, to take the time to find ways of relieving these pressures. In Taking Time for Me, Katherine L. Karr's insightful observations and suggestions - enhanced by compelling personal accounts of real care providers who are struggling with their own needs while tending to the needs of others - demonstrate that caregivers can overcome their personal conflicts and develop innovative ways of renewing their strength without jeopardizing the well-being of those who depend on them. From exercise regimens and support groups to recognizing the humor in everyday situations, this book can revitalize caregivers for the challenges ahead.