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Discover New Ways to Cope with Alzheimer's Now all those impacted by Alzheimer's disease can improve their quality of life, starting today. This helpful book dispels the myths and clearly lays out the truth about Alzheimer's and offers practical solutions for not only those who have the disease, but also their families and their caregivers. Inside, you'll uncover a new world of hope and the latest information on: ·The signs, symptoms, and proper diagnosis of Alzheimer's ·Living with Alzheimer's and providing the best possible care ·Cutting-edge research, including advances in biotechnology and genetics ·The latest conventional drugs and effective natural treatments, such as Ginkgo biloba and huperzine-A ·And much, much more!
Research-based advice for people who care for someone with dementia Nearly half of U.S. citizens over the age of 85 are suffering from some kind of dementia and require care. Loving Someone Who Has Dementia is a new kind of caregiving book. It's not about the usual techniques, but about how to manage on-going stress and grief. The book is for caregivers, family members, friends, neighbors as well as educators and professionals—anyone touched by the epidemic of dementia. Dr. Boss helps caregivers find hope in "ambiguous loss"—having a loved one both here and not here, physically present but psychologically absent. Outlines seven guidelines to stay resilient while caring for someone who has dementia Discusses the meaning of relationships with individuals who are cognitively impaired and no longer as they used to be Offers approaches to understand and cope with the emotional strain of care-giving Boss's book builds on research and clinical experience, yet the material is presented as a conversation. She shows you a way to embrace rather than resist the ambiguity in your relationship with someone who has dementia.
With humor, sensitivity and clarity, Frena draws on her over 20 years as a hands-on caregiver taking the approach to look at the inner world of people with Alzheimer's (or any kind of dementia) similar to when she was a foreign correspondent in Asia and India- looking with fresh and curious eyes to understand the people from their perspective, without judgments.She shares secrets of successful dementia care giving and reveals the deep spiritual and emotion growth possible in dementia. Even within the losses of Alzheimer's, insightful caregivers can discover their possible radiance and humor. This journey of continuing inner growth can renew the purpose and courage of the caregiver, while bringing peace and resolution to the elder.Most importantly, Frena shows how the care giving journey can bestow a whole new set of wonderful life skills on the caregiver. She demonstrates that there is nothing in meditation, prayer and spiritual practice that you can't learn as a dementia caregiver. In addition, you can have a whole lot of fun.
“A useful, step-by-step guide for anyone new to caring for those with Alzheimer’s.” —Library Journal H.O.P.E. for the Alzheimer’s Journey equips Alzheimer’s caregivers with knowledge, tools, and advice for their difficult road ahead. Author Carol B. Amos incorporates her own experience—including her family’s email correspondence illustrating how they coped during this particular challenge. Amos also introduces The Caregiving Principle™: a simple approach that provides a deeper understanding of a person with Alzheimer’s disease and a framework for the caregiver’s role. She provides examples of how The Caregiving Principle™ helped her connect with her mother. H.O.P.E. for the Alzheimer’s Journey encourages caregivers to take care for themselves and provides inspiration for a less stressful, more rewarding journey.
Here's a hope-filled book about Alzheimer's caregiving. It was written by Marie Marley, PhD - a well-known author on dementia issues - and neurologist Daniel C. Potts, MD, FAAN, both experts on caregiving. With a Foreword by Maria Shriver, this groundbreaking volume will give you hope in the midst of the darkness of Alzheimer's and other dementias. You can come to terms with your loved one's condition and free yourself to experience joyous interactions. Part I covers a variety of issues, such as the authors' belief that people with Alzheimer's can still enjoy life, how to overcome denial, five especially difficult situations, the role of grief on the journey to acceptance, and letting go of resentment through making peace with God. In Part II the authors provide 55 helpful tips for visiting people with Alzheimer's. Part III consists of numerous short stories illustrating the authors' joyous interactions with their loved ones. The stories will warm your heart and light your way along the path to achieving true joy.
"A new ethics guideline for caregivers of "deeply forgetful people" and a program on how to communicate and connect based on 30 years of community dialogues through Alzheimer's organizations across the globe"--
A definitive and compelling book on one of today's most prevalent illnesses. In 2020, an estimated 5.8 million Americans had Alzheimer’s, and more than half a million died because of the disease and its devastating complications. 16 million caregivers are responsible for paying as much as half of the $226 billion annual costs of their care. As more people live beyond their seventies and eighties, the number of patients will rise to an estimated 13.8 million by 2050. Part case studies, part meditation on the past, present and future of the disease, The Problem of Alzheimer's traces Alzheimer’s from its beginnings to its recognition as a crisis. While it is an unambiguous account of decades of missed opportunities and our health care systems’ failures to take action, it tells the story of the biomedical breakthroughs that may allow Alzheimer’s to finally be prevented and treated by medicine and also presents an argument for how we can live with dementia: the ways patients can reclaim their autonomy and redefine their sense of self, how families can support their loved ones, and the innovative reforms we can make as a society that would give caregivers and patients better quality of life. Rich in science, history, and characters, The Problem of Alzheimer's takes us inside laboratories, patients' homes, caregivers’ support groups, progressive care communities, and Jason Karlawish's own practice at the Penn Memory Center.
Caregiver Shouse celebrates spiritual and practical lessons learned on her unscripted yet rewarding journey with her mother through Alzheimer's disease.
As the largest generation in U.S. history - the population born in the two decades immediately following World War II - enters the age of risk for cognitive impairment, growing numbers of people will experience dementia (including Alzheimer's disease and related dementias). By one estimate, nearly 14 million people in the United States will be living with dementia by 2060. Like other hardships, the experience of living with dementia can bring unexpected moments of intimacy, growth, and compassion, but these diseases also affect people's capacity to work and carry out other activities and alter their relationships with loved ones, friends, and coworkers. Those who live with and care for individuals experiencing these diseases face challenges that include physical and emotional stress, difficult changes and losses in their relationships with life partners, loss of income, and interrupted connections to other activities and friends. From a societal perspective, these diseases place substantial demands on communities and on the institutions and government entities that support people living with dementia and their families, including the health care system, the providers of direct care, and others. Nevertheless, research in the social and behavioral sciences points to possibilities for preventing or slowing the development of dementia and for substantially reducing its social and economic impacts. At the request of the National Institute on Aging of the U.S. Department of Health and Human Services, Reducing the Impact of Dementia in America assesses the contributions of research in the social and behavioral sciences and identifies a research agenda for the coming decade. This report offers a blueprint for the next decade of behavioral and social science research to reduce the negative impact of dementia for America's diverse population. Reducing the Impact of Dementia in America calls for research that addresses the causes and solutions for disparities in both developing dementia and receiving adequate treatment and support. It calls for research that sets goals meaningful not just for scientists but for people living with dementia and those who support them as well. By 2030, an estimated 8.5 million Americans will have Alzheimer's disease and many more will have other forms of dementia. Through identifying priorities social and behavioral science research and recommending ways in which they can be pursued in a coordinated fashion, Reducing the Impact of Dementia in America will help produce research that improves the lives of all those affected by dementia.
If you are caring for or supporting a loved one with Alzheimer's or dementia you know that is not an easy journey. This book will give you practical advice mixed with spiritual wisdom and counsel gained from personal experience. The authors, Jim Henry and Deb Terry, have personally walked through the loss of a spouse and a parent to this disease. From their experiences they will help you through 18 Central Questions that you will undoubtably face from early onset through advanced stages. You will gain strength and comfort as you become the most effective caregiver possible while also taking care of yourself along the way.