"Moving and illuminating….It is through stories like these that we begin to understand people living with Alzheimer's, and maybe—through empathy and compassion—we can heal what can't yet be cured."—Lisa Genova,, author, New York Times bestselling Still Alice This groundbreaking multicultural anthology shares moving personal stories about the impacts of Alzheimer’s and dementia. An estimated 5.7 million Americans are afflicted by Alzheimer’s disease, including 10 percent of those over sixty-five, and it is the sixth leading cause of death. But its effects are more pervasive: for the nearly 6 million sufferers, there are more than 16 million family caregivers and many more family members. Alzheimer’s wreaks havoc not only on brain cells; it is a disease of the spirit and heart for those who suffer from it but also for their families. This groundbreaking anthology presents forty narratives, both nonfiction and fiction, that together capture the impact and complexity of Alzheimer’s and other dementias on patients as well as their caregivers and family. Deeply personal, recounting the wrenching course of a disease that kills a loved one twice—first they forget who they are, and then the body succumbs—these stories also show how witnessing the disease and caring for someone with it can be powerfully transformative, calling forth amazing strength and grace. The contributors, who have all generously donated their work, include Edwidge Danticat, Julie Otsuka, Elizabeth Nunez, Meryl Comer, Greg O’Brien, Dr. Daniel Potts, Sallie Tisdale, and Nihal Satyadev. Reflecting the diversity and global nature of the dementia crisis, this anthology is published in collaboration with UsAgainstAlzheimer’s.

This volume seeks to bring readers to a deeper understanding of contemporary cultural and social configurations of Alzheimer’s disease by analyzing 21st-century U.S. novels in which the disease plays a key narrative role. Via analysis of selected works, Garrigós considers how the erasure of memory in a person with Alzheimer’s affects our idea of the identity of that person and their sense of belonging to a group. Starting out from three different types of memory (individual, social and cultural), the study focuses on the narrative strategies that authors use to configure how the disease is perceived and represented. This study is significant not only because of what the texts reveal about those with Alzheimer’s, but also for what they say about us - about the authors and readers who are producing and consuming these texts, about how we see this disease, and what our attitudes to it say about contemporary U.S. society.

The Book of Alzheimer's is a resource guide for congregations serving African Americans who desire to help families and individuals cope with Alzheimer's. According to the Alzheimer's Association, African Americans are two to three times more likely than whites to develop dementia. More than 5 million people in the United States have Alzheimer's and this number is expected to double by the year 2030. It is now estimated that one out of every nine persons over the age of 65 is living with Alzheimer's. The Book of Alzheimer's is a road map for providing compassionate support to persons living with Alzheimer's and their caregivers.

Addresses the psychology and treatment of diseases that affect the memory of an aging population The aging population is growing, with a significant portion of the population over the age of 65. Epidemiological research suggests that rates of age-related conditions like Alzheimer’s disease will increase. Older individuals and their families face a host of problems related to the diagnosis, treatment, and psychological management of these conditions. There is a growing demand for healthcare personnel and professionals in the human and social services who have the knowledge and skills to meet the needs of this special population. Dementia and Memory: Introduction for Professionals in Health and Human Services aims to provide an introduction to dementia and memory disorders for professionals in public health, nursing, social work, gerontology, psychology, and beyond. This book offers a scientifically rigorous approach with an approachable writing style, making it an ideal resource for all helping professions. All chapters take a multi-disciplinary approach to instruction, and all diseases are presented with applicable historical background. For each condition covered, from Alzheimer’s and Parkinson’s to depression and frailty, you’ll find a description of the condition, epidemiological data, pathophysiology, diagnostic criteria, clinical presentation, treatment strategies, and a case vignette. You’ll also learn about older adults’ daily needs, behavioral interventions, caregiver stress, and more. Gain background knowledge of age-related conditions including Alzheimer’s, Parkinson’s, Lewy Body dementia, multiple sclerosis, and more Learn about the neuroanatomy of the aging brain and how its manifestations lead to unique caregiving issues and challenges Discover pharmacological, management, and intervention techniques that will help you better care for aging adults Combat caregiver stress and compassion fatigue when dealing with difficult memory disorders and dementia Anyone who works with older adults in community, clinical, or research settings will benefit from this in-depth information on conditions of aging and dementia.

Caring for a loved one with Alzheimer’s disease can be a daunting task. Getting the most out of caregiving while taking care of a loved one is a challenge. When that loved one is a spouse, the tasks are doubly daunting, magnified over and over. Being mindful of your loved one’s habits, hobbies, lifestyle, and preferences is important. This book offers insights on how to reclaim and get more joy from the caregiving love journey. As an unpaid, loving caregiver, Eunice Sykes writes the book she wished she had at the beginning of her journey—one that shares, educates, and offers joy and hope to those beginning their journey or those still on the journey. Deeply personal, in-the-moment anecdotes drawn from her journals add to the honest, moving testimony that this book delivers.

Alzheimer’s disease can be scary and overwhelming, for both your loved one and for you. To help you fight fear with knowledge, this book provides information about the pathological features of Alzheimer’s and outlines the symptoms and prognosis at each stage of the disease. We explore diagnostic tests and treatment options and discuss how to find a doctor who will meet the needs of your loved one. We also look at special considerations for individuals with early-onset Alzheimer’s disease. Knowing what to expect will lessen your fears and prepare you for your future as a caregiver.

Research and Development is the vehicle by which organizations and economies create opportunity, innovation and secure a stream of future products and services.These outcomes are all critically important sources of sustainability in a world that is changing faster than most companies can keep up.The challenge behind them is the fundamental unpredictability of R&D; which is why effective project management is so important. Ron Basu's Managing Projects in Research and Development explains how and why project management can provide a means of helping to plan, organise and control multi-disciplinary research activities without stifling innovation. Combining research with practical examples and experience from a career that has included blue chip organizations such as GSK, GlaxoWellcome and Unilever, Ron Basu offers a rigorous guide to the fundamentals of R&D project management including project lifecycle management, risk management, cost, time quality and other success measures as well as the keys to operational excellence in this complicated world.

Alzheimer’s is scary. But you can still find ways to be you after the diagnosis. Rebecca Chopp never expected a routine annual checkup to uncover symptoms that ultimately revealed she has early-stage Alzheimer’s disease. The news was devastating. After recovering from the shock, Rebecca knew the next steps: retire from her stressful job leading the University of Denver, hold on to the core of herself for as long as possible, and find ways each day to live well so that her remaining time with her family and friends can be as rich and meaningful as possible. This honest and hope-filled book—Still Me—chronicles Rebecca’s efforts, with the help of her family, friends, and medical team, to reshape her life for a healthy and vibrant approach to living with Alzheimer’s. Based on research and experience, Rebecca provides many suggestions on how to accept the diagnosis and continue to live well.

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.