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The Caregiving Years helps you answer these questions: Why me? Why now? What now? The stages describe how you'll feel as you care for a family member with a chronic illness. Through the stages, you'll find what you need so that you can be manage today and prepare for your tomorrow. You'll also follow the journey of two family caregivers through the six stages. Reader reviews: Absolutely terrific. You really have captured the stages well, very very well...This is a fabulous resource for caregivers. Your book, The Caregiving Years, helped me enormously. It would have saved me substantial stress had I had it at the beginning of these fours years of 24-hours a day caregiving to my husband! THANK YOU! It is a masterpiece and I've recommended it for other hard-pressed caregivers and those who are about to become 'and dread it'. I tell them if they are armed with the knowledge and know-how from this book, they will be enabled to handle it.
Family caregiving affects millions of Americans every day, in all walks of life. At least 17.7 million individuals in the United States are caregivers of an older adult with a health or functional limitation. The nation's family caregivers provide the lion's share of long-term care for our older adult population. They are also central to older adults' access to and receipt of health care and community-based social services. Yet the need to recognize and support caregivers is among the least appreciated challenges facing the aging U.S. population. Families Caring for an Aging America examines the prevalence and nature of family caregiving of older adults and the available evidence on the effectiveness of programs, supports, and other interventions designed to support family caregivers. This report also assesses and recommends policies to address the needs of family caregivers and to minimize the barriers that they encounter in trying to meet the needs of older adults.
This accessible and enaging work introduces current and future teachers, child care providers, and others interested in early childhood education to the importance for the early years in children's well-being and success. It summarizes their research on the value of high-quality services for young children, families, and society, showing why early education matters both today and into the future. Emphasizing the need to understand and respect young children's strengths and unique characteristics, the authors offer inspiration for working in the field, as well as addressing the realistic challenges of implementing developmentally appropriate care and education.
Revised edition of the best-selling memoir that has been read by over a million people worldwide with translations in 29 languages. After too many years of unfulfilling work, Bronnie Ware began searching for a job with heart. Despite having no formal qualifications or previous experience in the field, she found herself working in palliative care. During the time she spent tending to those who were dying, Bronnie's life was transformed. Later, she wrote an Internet blog post, outlining the most common regrets that the people she had cared for had expressed. The post gained so much momentum that it was viewed by more than three million readers worldwide in its first year. At the request of many, Bronnie subsequently wrote a book, The Top Five Regrets of the Dying, to share her story. Bronnie has had a colourful and diverse life. By applying the lessons of those nearing their death to her own life, she developed an understanding that it is possible for everyone, if we make the right choices, to die with peace of mind. In this revised edition of the best-selling memoir that has been read by over a million people worldwide, with translations in 29 languages, Bronnie expresses how significant these regrets are and how we can positively address these issues while we still have the time. The Top Five Regrets of the Dying gives hope for a better world. It is a courageous, life-changing book that will leave you feeling more compassionate and inspired to live the life you are truly here to live.
"Nurses play a vital role in improving the safety and quality of patient car -- not only in the hospital or ambulatory treatment facility, but also of community-based care and the care performed by family members. Nurses need know what proven techniques and interventions they can use to enhance patient outcomes. To address this need, the Agency for Healthcare Research and Quality (AHRQ), with additional funding from the Robert Wood Johnson Foundation, has prepared this comprehensive, 1,400-page, handbook for nurses on patient safety and quality -- Patient Safety and Quality: An Evidence-Based Handbook for Nurses. (AHRQ Publication No. 08-0043)." - online AHRQ blurb, http://www.ahrq.gov/qual/nurseshdbk/
Caring for a family member can be an exhausting, consuming experience. You get tired from coping, feeling guilty, losing hope and so much more. In this book, we'll explore 12 reasons for our weariness, which Denise calls our caregiving fatigues. In Healing Words, Denise shares her personal stories of her own caregiving fatigues. She also helps you pinpoint your caregiving fatigue and then offers you compassionate insights so you feel seen and appreciated. When you feel understood, you can begin to heal. Most important, you will receive the energy you need to keep going.Healing Words will become your go-to source when you need to heal your caregiving fatigues. With this book in hand, you have a resource that reminds you that the best of you can endure regardless of circumstances.
Our world is currently experiencing a global Caregiving Crisis. If you, like so many others, are increasingly concerned about your loved one's needs as they age, then ask yourself the following questions: How does your loved one see their life playing out? Where do they want to live as they age (in their own home vs. assisted living)? What kind of health do they aspire to be in? What kinds of activities do they want to engage in? If and when your loved one can no longer live independently, what is their preference (i.e., paid in-home help, assisted living or nursing facility)? Is their preference realistic considering their financial situation, and if not, what are the feasible alternatives? The Caregiving Journey goes far beyond the basics of wills and logistical funeral plans-basics many people have in place (especially where children are involved). Rather, you'll be guided and supported to create a well-thought-out plan for those three, five or even 10 or more years when your loved one needs your help because they can no longer live on their own. With the inspiration, practical steps, support, and tools provided inside these pages, you'll be well-equipped to guide your family members and loved ones to the end of their lives with love, ease and grace.Bringing together her 30+ years as a professional market analyst and her personal experience as a live-in caregiver for her mom, author Debbie Howard has integrated her experiences-along with the journeys of over 200 other caregivers-into this book to help you choose your best way forward. Learn more at www.theCaregivingJourney.com.
Just a few generations ago, serious illness, like hazardous weather, arrived with little warning, and people either lived through it or died. In this important, convincing, and long-overdue call for health care reform, Joanne Lynn demonstrates that our current health system, like our concepts of health and disease, developed at a time when life was mostly short, serious illnesses and disabilities were common at every age, and dying was quick. Today, most Americans live a long life, with the disabilities and discomforts of progressive chronic illness appearing only during the final chapters of their life stories. Sick to Death and Not Going to Take It Anymore! maintains that health care and community services are not set up to meet the needs of the large number of people who face a prolonged period of progressive illness and disability before death. Lynn offers what she calls an "owner's manual for the health care system," which lays out facts, concepts, strategies, and action plans for genuine reform and gives the reader new ways to interpret information creatively, imagine innovative possibilities, and take steps to implement them.
Experts estimate that as many as 98,000 people die in any given year from medical errors that occur in hospitals. That's more than die from motor vehicle accidents, breast cancer, or AIDSâ€"three causes that receive far more public attention. Indeed, more people die annually from medication errors than from workplace injuries. Add the financial cost to the human tragedy, and medical error easily rises to the top ranks of urgent, widespread public problems. To Err Is Human breaks the silence that has surrounded medical errors and their consequenceâ€"but not by pointing fingers at caring health care professionals who make honest mistakes. After all, to err is human. Instead, this book sets forth a national agendaâ€"with state and local implicationsâ€"for reducing medical errors and improving patient safety through the design of a safer health system. This volume reveals the often startling statistics of medical error and the disparity between the incidence of error and public perception of it, given many patients' expectations that the medical profession always performs perfectly. A careful examination is made of how the surrounding forces of legislation, regulation, and market activity influence the quality of care provided by health care organizations and then looks at their handling of medical mistakes. Using a detailed case study, the book reviews the current understanding of why these mistakes happen. A key theme is that legitimate liability concerns discourage reporting of errorsâ€"which begs the question, "How can we learn from our mistakes?" Balancing regulatory versus market-based initiatives and public versus private efforts, the Institute of Medicine presents wide-ranging recommendations for improving patient safety, in the areas of leadership, improved data collection and analysis, and development of effective systems at the level of direct patient care. To Err Is Human asserts that the problem is not bad people in health careâ€"it is that good people are working in bad systems that need to be made safer. Comprehensive and straightforward, this book offers a clear prescription for raising the level of patient safety in American health care. It also explains how patients themselves can influence the quality of care that they receive once they check into the hospital. This book will be vitally important to federal, state, and local health policy makers and regulators, health professional licensing officials, hospital administrators, medical educators and students, health caregivers, health journalists, patient advocatesâ€"as well as patients themselves. First in a series of publications from the Quality of Health Care in America, a project initiated by the Institute of Medicine