The Long Hello


Book Description

This sensuous memoir strips away all preconceptions about what it means to be, or to love, a person with Alzheimer's, giving comfort to those who have walked the caregiving path and offering insight, hope, and a compass to those embarking on the journey. -- Cover, p. [4].




The Other Side of Alzheimer's


Book Description

Alzheimers and marriage is a complex combination of emotions. You change, too, when your spouse has Alzheimers. This is a poignant collection of personal experiences, moving from confusion, loneliness, and fear to understanding and peace. Knowledge of resources and connecting with others who are, or have been, faced with this consuming task help you find your way through the maze of many unanticipated challenges. Finding the support of others is critical to achieving acceptance of this life-changing event. With a sprinkling of humor, this becomes a story of the power of love, allowing you to survive it. The Other Side of Alzheimers is written with honesty, sensitivity, and love. Every experience describes the physical, mental, and emotional challenges, while alluding to humor and hope. There are few published resources that deal with feelings of a spouse faced with a partners Alzheimers disease, and none I have read as good as this one. I found it to be a beautiful love story that any reader can appreciate. Carol Long, RN-BC Board Certified Gerontological Nurse Sozo Senior Wellness, Raleigh, North Carolina Ms. Ellis has written a beautiful, insightful account of the journey through Alzheimers. It reveals how love, understanding and the acceptance of change can overcome any adversity. It applies to us all as we navigate through the ebb and flow of a significant relationship. Karen Brisendine Retired Electronics Industry Business Manager Caregiver Martha-Lee Ellis has written a touching memoir that approaches Alzheimers from a wifes perspective of a scary and unpredictable course. The Other Side of Alzheimers offers a lifeline to others going through this experience, enabling them to see that they are not alone. This story has something to benefit anyone facing this disease with their spouse. Michelle S. Brovitz, MS PA American Society of Clinical Pathologists Former Pathologists Assistant for hospitals nationwide




Alzheimer's from the Inside Out


Book Description

Receiving a diagnosis of Alzheimer's disease profoundly alters lives and creates endless uncertainty about the future. How does a person cope with such a life-changing discovery? What are the hopes and fears of someone living with this disease? How does he want to be treated? How does he feel as the disease alters his brain, his relationships, and ultimately himself? Richard Taylor provides illuminating responses to these and many other questions in this collection of provocative essays. Diagnosed with Alzheimer's disease at age 61, the former psychologist courageously shares an account of his slow transformation and deterioration and the growing division between his world and the world of others. With poignant clarity, candor, and even occasional humor, more than 80 brief essays address difficult issues faced by those with Alzheimer's disease, including the loss of independence and personhood unwanted personality shifts communication difficulties changes in relationships with loved ones and friends the declining ability to perform familiar tasks This rare, insightful exploration into the world of individuals with Alzheimer's disease is a captivating read for anyone affected personally or professionally by the devastating disease. Individuals with early-stage Alzheimer's disease will take comfort in the voice of a fellow traveler experiencing similar challenges, frustrations, and triumphs. Family and professional caregivers will be enlightened by Taylor's revealing words, gaining a better understanding of an unfathomable world and how best to care for someone living in it.




How Not to Study a Disease


Book Description

An authority on Alzheimer's disease offers a history of past failures and a roadmap that points us in a new direction in our journey to a cure. For decades, some of our best and brightest medical scientists have dedicated themselves to finding a cure for Alzheimer's disease. What happened? Where is the cure? The biggest breakthroughs occurred twenty-five years ago, with little progress since. In How Not to Study a Disease, neurobiologist Karl Herrup explains why the Alzheimer's discoveries of the 1990s didn't bear fruit and maps a direction for future research. Herrup describes the research, explains what's taking so long, and offers an approach for resetting future research. Herrup offers a unique insider's perspective, describing the red flags that science ignored in the rush to find a cure. He is unsparing in calling out the stubbornness, greed, and bad advice that has hamstrung the field, but his final message is a largely optimistic one. Herrup presents a new and sweeping vision of the field that includes a redefinition of the disease and a fresh conceptualization of aging and dementia that asks us to imagine the brain as a series of interconnected "neighborhoods." He calls for changes in virtually every aspect of the Alzheimer's disease research effort, from the drug development process, to the mechanisms of support for basic research, to the often-overlooked role of the scientific media, and more. With How Not to Study a Disease, Herrup provides a roadmap that points us in a new direction in our journey to a cure for Alzheimer's.




Kill Me First


Book Description

This is the moving true story of two women: a mother, falling into Alzheimer's disease, and her daughter, struggling to protect her from herself.




The Other Side of Alzheimer's, a Caregiver's Story


Book Description

How do you handle a crisis in your life? Alzheimer's is just one condition that requires loved ones to be caregivers. We become caregivers not by choice and once we are, we lose our choices. This is a story of a woman who faced those choices and survived. 13:978-0-615-32820-1




Just See Me


Book Description

Just See Me-Sacred Stories from the Other Side of Dementia will make you see dementia through the eyes of compassion and love and yet know this is just the beginning of a bigger conversation. Thirteen family caregivers teach us extraordinary lessons to Be a better caregiver. Feel inspired and encouraged. Support the caregivers you love. Appreciate each day as a splendid gift even in the midst of tragedy. Use the power of storytelling to see life in a different way. Believe in something we cannot hear, see or touch yet know to be true.




Neither Married Nor Single


Book Description

When Dr. David Kirkpatrick’s wife was diagnosed with Alzheimer’s disease in 2007, their lives—and their marriage—would change forever. In an honest, uplifting, and sometimes heartbreaking account of loving a partner with dementia, Dr. Kirkpatrick creates a clear guide for others in similar circumstances. He shares his perspective both as a loving and grief-stricken husband coping with a profound change in his marriage, and as a geriatric psychiatrist doing everything he can for his wife while continually learning throughout that experience. Dr. Kirkpatrick tackles the tough questions about caretaking, grief, loss, love, and sex for those whose partners have dementia. When is the right time to find or even to begin considering a care home for your loved one? How can you navigate the complexities of your changing sexual relationship with an Alzheimer’s partner? When is it appropriate for you to consider new relationships? With wisdom and compassion, Dr. Kirkpatrick reflects on these questions and more. Whether your partner has been recently diagnosed or has been living with dementia for many years, Neither Married Nor Single will help lead you to effective strategies for living and loving in an Alzheimer’s marriage, and for dealing with the changes ahead. And it will help you remember that you are not alone.




The Inheritance


Book Description

This gripping story of the doctors at the forefront of Alzheimer’s research and the courageous North Dakota family whose rare genetic code is helping to understand our most feared diseases is “excellent, accessible...A science text that reads like a mystery and treats its subjects with humanity and sympathy” (Library Journal, starred review). Every sixty-nine seconds, someone is diagnosed with Alzheimer’s disease. Of the top ten killers, it is the only disease for which there is no cure or treatment. For most people, there is nothing that they can do to fight back. But one family is doing all they can. The DeMoe family has the most devastating form of the disease that there is: early onset Alzheimer’s, an inherited genetic mutation that causes the disease in one hundred percent of cases, and has a fifty percent chance of being passed onto the next generation. Of the six DeMoe children whose father had it, five have inherited the gene; the sixth, daughter Karla, has inherited responsibility for all of them. But rather than give up in the face of such news, the DeMoes have agreed to spend their precious, abbreviated years as part of a worldwide study that could utterly change the landscape of Alzheimer’s research and offers the brightest hope for future treatments—and possibly a cure. Drawing from several years of in-depth research with this charming and upbeat family, journalist Niki Kapsambelis tells the story of Alzheimer’s through the humanizing lens of these ordinary people made extraordinary by both their terrible circumstances and their bravery. “A compelling narrative…and an educational and emotional chronicle” (Kirkus Reviews, starred review), their tale is intertwined with the dramatic narrative history of the disease, the cutting-edge research that brings us ever closer to a possible cure, and the accounts of the extraordinary doctors spearheading these groundbreaking studies. From the oil fields of North Dakota to the jungles of Colombia, this inspiring race against time redefines courage in the face of this most pervasive and mysterious disease.




Fighting for My Life


Book Description

A practical, helpful guide on how to fight back against Alzheimer’s disease—with expert medical advice and one woman’s inspiring personal journey. Jamie Tyrone was forty-nine years old when she learned by accident through genetic testing that she had a 91% chance of getting Alzheimer's disease. She was shocked, but after an initial bout with depression she decided to take action rather than concede defeat. Jamie teamed up with Dr. Marwan Sabbagh, a renowned neurologist, and together they created a resource detailing not just Jamie's experience, but expert medical advice for anyone facing the disease. This book is a practical, helpful guide for those who know they’re at greater risk of contracting Alzheimer’s disease. With cutting-edge medical guidance from Dr. Sabbagh about the true nature of Alzheimer’s, the risks involved, and daily steps you can take to protect yourself, Jamie’s story will encourage and empower you. In Fighting for My Life, readers will: Gain expert medical advice from Dr. Sabbagh on how to fight back against the disease Discover the pros, cons and possible dangers of genetic testing Witness a first-hand account of how to deal with the shadow of Alzheimer’s disease through Jamie’s story If Alzheimer’s has affected your life or the life of someone you know, this book is for you. You’ll be armed with information and ready to tackle Alzheimer’s head-on.