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Two families, half a continent apart, faced with a loved one struggling against the onset of Alzheimer’s Disease. Two men, who each wind up being the primary care-provider for a beloved mother-in-law. These were roles they never expected to fill. Nothing they had done previously had prepared them for this. We often hear that life is a journey, and it's the journey that matters – the path and the experiences – more than anything else. The family confronted with a loved one struggling against dementia often faces new, unexpected twists and turns in their journey. This book offers some perspective on that journey, as we were going through it. It’s part memoir, part journal, and all based on the things we were writing at the time. In seeing what we experienced, and the decisions we each made, over the arc of care-giving and then recovery, perhaps you will be better able to understand your own path, choose your own road.
- Sales Rank: #4124229 in Books
- Published on: 2011-07-15
- Original language: English
- Number of items: 1
- Dimensions: 9.00" h x .95" w x 6.00" l,
- Binding: Paperback
- 420 pages
Most helpful customer reviews
25 of 26 people found the following review helpful.
Highly recommended for anyone dealing with dementia
By Pam Crabtree
Her Final Year is a powerfully written book that is a must read for anyone dealing with a relative who has dementia. Alzheimer's and other types of dementia gradually rob a person of his/her independence and personality. While many of the available on-line sources deal with the clinical progression of dementia including loss of mobility, incontinence, loss of speech, there is very little information about the cognitive changes that accompany this disease. Dementia patients suffer hallucinations, talk to dead relatives, and perceive the world in very different ways. This book addresses these issues.
The authors also deal with the toll--both emotional and physical--that caregiving takes on the caregivers. It takes a long time to die from dementia, and the process is marked by a series of declines and plateaus. I am entering the final stage of this process with my own mom who is 92, and I found this book to be very useful and moving. I read it in a single sitting. Highly recommended.
18 of 19 people found the following review helpful.
The Best Caregiving Account That I Have Read
By Steve Austin
I've been the sole caregiver for my wife who has been in that awful journey through Alzheimer's for at least the last twelve years. The word "caregiver" means a great deal to me. I do it 24 hours a day all of the time, except for a few hours off each week. So often when I read books about the experiences of Alzheimer's "caregivers" I end up angry the way the word is used by those that use the word but don't often really do the difficult hands on work that caregiving is. Usually they do it by phone and hire the actual caregivers.
"Her Final Year" is not that way. I kept shaking my head in agreement as I read the book, knowing that the two authors and their wives had walked in my shoes and understood my feelings and frustrations. I especially liked the last section on recovery and renewal after their mothers in law had passed away, as I will shortly be in that phase myself.
This is an open and honest book about the realities of caring for someone with Alzheimer's or dementia. Expecially for those just embarking on this experience, the book is a great reality check for what probably lies ahead.
12 of 13 people found the following review helpful.
Good resource also for those not directly involved with dementia related care giving
By James Kasper
As Pam Crabtree has noted in her review, this book should be a great addition to those dealing directly with someone with dementia.
I think this book can also be of value to those who are not directly dealing with a family member with dementia. I read some of the e-mails in real time (I'm a friend of one of the families). I do not have any family currently dealing with dementia, but in the years since this book began to be assembled I now have several friends with family members afflicted with some form of dementia, as well as family and friends that need help and attention on a daily basis. Reading through the book I was surprised to find how many of the experiences there touched directly on some of my developing tangential contacts with care giving. Dealing with hospice, getting patients to the doctor, dealing with bureaucracy and the like are not unique to dementia, even if those stresses and others can be so much worse in the long term care that dementia generally requires. The book has also opened a window on to some of the stresses and experiences of those friends I have, that, due to their dealing directly with a person suffering dementia, do not have as much current social contact outside their family as earlier.
Although not "literature" the book is well written/presented and read with an intensity that became physically palpable for me.
I highly recommend this for anyone with aging friends and relatives as well as those dealing more directly with the immediate issues of care giving. Even if you are blessed enough never to have to go through what the authors did I think you will find reading the book worthwhile for the insights into what so many others are going through.
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