Alzheimer s and Dementia

Author: Kim Boyer
Publisher: University of Nevada Press
ISBN: 9780874176605
Format: PDF, ePub, Docs
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A comprehensive guide for Nevada patients and their caregivers offers advice on finding the right physician, available state resources, the legal and financial steps that patients and their families can take to protect themselves and their assets, and dealing with daily physical and emotional challenges. Original.

The Alzheimer s Advisor

Author: Vaughn E. JAMES
Publisher: AMACOM Div American Mgmt Assn
ISBN: 0814414389
Format: PDF, ePub, Mobi
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For anyone who has ever cared for a person with Alzheimer’s, coping with the emotional, financial, and day-to-day issues can be grueling. While many people are aware of the physical effects of this disease, very few know how to handle the practical issues that can make dealing with a loved one or patient with Alzheimer’s that much more difficult. In The Alzheimer's Advisor, Vaughn E. James offers an empathetic and straightforward guide to the legal and ethical dilemmas associated with this disorder. Using real-life situations, the author offers invaluable advice on such topics as: estate planning • the emotional issues of caring for a patient with Alzheimer’s • how to cope with the cost of care • living wills, power of attorney, and guardian­­ship • treatment and diagnosis • finding the right lawyer and paying for the cost of legal help • legal issues for the mobile Alzheimer’s patient From recognizing the early signs of the disease to understanding the legal implications, this is the one book that will enable caregivers, health-care practitioners, and family members to protect themselves and their loved ones.

Innovative Interventions To Reduce Dementia Caregiver Distress

Author: David W. Coon, PhD
Publisher: Springer Publishing Company
ISBN: 9780826148025
Format: PDF, Kindle
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Increasing evidence has demonstrated that caregivers of dementia victims are at risk for depression and other medical problems. In what ways can health care providers improve or maintain the well-being of dementia caregivers? This volume provides an overview of emerging themes in dementia caregiving research and presents a broad array of practical strategies for reducing caregiver distress, including interventions for specific populations such as ethnic minority caregivers, male caregivers, and caregivers with diverse sexual orientations. Innovative approaches include the value of partnering with primary care physicians to improve quality of life for both patient and caregiver and the use of technological advances to help distressed caregivers. A timely, cutting edge book written for clinicians of varying backgrounds who provide direct services to families of dementia victims. For Further Information, Please Click Here!

Learning to Speak Alzheimer s

Author: Joanne Koenig Coste
Publisher: Houghton Mifflin Harcourt
ISBN: 9780618485178
Format: PDF
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A new approach to dealing with Alzheimer's disease offers a five step method for caring for people with progressive dementia, while offering hundreds of practical tips to ease life for patients and caregivers.

What If It s Not Alzheimer s

Author: Gary Radin
Publisher: Prometheus Books
ISBN: 1616149698
Format: PDF, Kindle
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Although the public most often associates dementia with Alzheimer’s disease, the medical profession now distinguishes various types of “other” dementias. This book is the first and only comprehensive guide dealing with frontotemporal degeneration (FTD), one of the largest groups of non-Alzheimer’s dementias. The contributors are either specialists in their fields or have exceptional hands-on experience with FTD sufferers. Beginning with a focus on the medical facts, the first part defines and explores FTD as an illness distinct from Alzheimer’s disease. Also considered are clinical and medical care issues and practices, as well as such topics as finding a medical team and rehabilitation interventions. The next section on managing care examines the daily care routine including exercise, socialization, adapting the home environment, and behavioral issues. In the following section on caregiver resources, the contributors identify professional and government assistance programs along with private resources and legal options. The final section focuses on the caregiver, in particular the need for respite and the challenge of managing emotions. This new, completely revised edition follows recent worldwide collaboration in research and provides the most current medical information available, a better understanding of the different classifications of FTD, and more clarity regarding the role of genetics. The wealth of information offered in these pages will help both healthcare professionals and caregivers of someone suffering from frontotemporal degeneration.