Diary of an Alzheimer's caregiver

Robert Hershberger, 1936-

Book - 2022

"One year shy of her fiftieth wedding anniversary, Dee Hershberger was diagnosed with Alzheimer's disease. Her husband, Bob, serving as her primary caregiver, kept a journal the following four and a half years. Diary of an Alzheimer's Caregiver provides an unflinchingly honest and heartbreaking account of what the couple went through. During the first two and a half years, Dee gradually lost short-term memory but maintained most physical and social abilities. Over the last two years she lost these abilities, most words, and long-term memory. She also became incontinent, suffered from undetected illnesses, and experienced psychotic episodes and uncontrollable, violent behavior. This is a brutally raw look at what it is like to... lose a loved one to Alzheimer's, including what the disease does to the patient and the effects it has on loved ones and caregivers. This personal view into caring for a spouse with Alzheimer's will help readers understand the physical, emotional, and financial consequences of the disease, as well as provide support, advice, and hope to anyone in the same situation"--

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Subjects
Genres
Biographies
Diaries
Published
West Lafayette, Indiana : Purdue University Press [2022]
Language
English
Main Author
Robert Hershberger, 1936- (author)
Physical Description
x, 184 pages : illustrations ; 22 cm
ISBN
9781612497341
Contents unavailable.
Review by Choice Review

In Diary, Hershberger journals his care for his wife, Dee. Charting her physical, emotional, and mental Alzheimer's journey, he reflects on Dee's experiences, considering them as her husband, life partner, and caregiver. Chronicling Dee's responses to the changes she experiences, he parallels this with his expectations of treatment and the long road from concern to diagnosis. At the end of those years, he offers thoughtful advice that will support both patient and caregiver. Years one and two are characterized by mild cognitive impairment (MCI). Early on, only the author notices Dee's lapses. At one point, she becomes frustrated with communication; a physician visit confirms her communication ability but identifies MCI. From this visit, the author and his wife become aware of their focus on retirement and recognize they have neither considered their mortality nor made plans. Year three is characterized by medication management, avoidance of urinary events, and the challenges of hygiene and dressing. Dee's decline accelerates in year four and is marked by mood changes and violent outbursts. In year five, Hershberger reflects on their separate futures. This diary is an exceptional read, remarkable for its humanity and compassion. An array of useful recommendations spans the five-year journey this couple makes together. Summing Up: Highly recommended. All readers. --Linda R. Barley, York College, CUNY

Copyright American Library Association, used with permission.
Review by Kirkus Book Review

Chronicle of a loving husband's five-year odyssey of caretaking for his wife. When his wife, Deanna, was diagnosed with Alzheimer's, Hershberger began journaling about his role as her caretaker, detailing the overwhelming, heartbreaking struggle it became. Beginning in 2010, the author noticed that Dee, a formerly energetic, attentive woman in her early 70s, was forgetting specific words and misplacing items throughout their home. A doctor attributed the incidences to a thyroid imbalance and prescribed medication. A year later, Dee's weight loss, increasing impatience, memory lapses, and distinctly diminished capacity to perform household tasks caused further alarm, though the couple continued to enjoy their usual physical and social activities. Dee's short-term memory continued to decline. Early on, her problems were viewed as minor mental malfunctions, but as the years progressed, the couple's lives became further complicated with a tentative diagnosis of early-onset Alzheimer's disease. Even seemingly simple daily tasks like showering, pouring water, or adhering to a medication regimen became a frustrating struggle in her "out of sight is out of mind" condition. As Dee's long-term memory became gradually impaired, the author sought out more personalized treatments and, as a man of faith, continued to pray for his wife's health. In the second half of the book, Hershberger depicts Dee's steady decline into deep dementia through his own increasingly arduous caregiving perspective, and the narrative becomes harrowing at times. "The last two years became an excruciating ordeal for Dee and an emotional roller coaster for me," he writes. Because the author solely focuses on his wife's decline, snippets of their life together with their children appear in a short family pictorial at the end of the book. While intensely sorrowful, the couple's journey is often poignant, grounded in true love and unshakeable devotion. It's also an insightful, knowledgeable guidebook with essential advice for concerned readers facing similar circumstances. A somber yet candid and emotionally supportive portrayal of a spouse's cognitive decline. Copyright (c) Kirkus Reviews, used with permission.

Copyright (c) Kirkus Reviews, used with permission.

This book provides an up close and personal view of Deanna (Dee) Hershberger?s four-and-a-half-year journey through Alzheimer?s disease, from its first manifestations in the fall of 2010 until her death on March 1, 2015. As Dee?s husband of more than fifty years and her primary caregiver, I first recorded changes as they occurred but later as an almost daily diary. I hope that this digest of the original entries will help readers appreciate what occurred throughout the course of the disease. Excerpted from Diary of an Alzheimer's Caregiver by Robert Hershberger All rights reserved by the original copyright owners. Excerpts are provided for display purposes only and may not be reproduced, reprinted or distributed without the written permission of the publisher.