Get Free Ebook What If It's Not Alzheimer's?: A Caregiver's Guide to Dementia (Updated & Revised)
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What If It's Not Alzheimer's?: A Caregiver's Guide to Dementia (Updated & Revised)
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About the Author
Lisa Radin (Blackwood, NJ) and her son, Gary Radin (Philadelphia, PA), provided complete in-home care for husband and father Neil Radin over a four-year period. In 1998, they established the Neil L. Radin Caregivers Relief Foundation. They are both support-group facilitators and have been involved in planning and coordinating FTD caregiver conferences, most recently in June 2007.
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Product details
Paperback: 360 pages
Publisher: Prometheus Books; Revised edition (March 27, 2008)
Language: English
ISBN-10: 1591025842
ISBN-13: 978-1591025849
Product Dimensions:
6 x 0.7 x 9 inches
Shipping Weight: 1 pounds (View shipping rates and policies)
Average Customer Review:
4.6 out of 5 stars
44 customer reviews
Amazon Best Sellers Rank:
#703,255 in Books (See Top 100 in Books)
My sister has been diagnosed with Fronto-Temporal Dementia, which is rare, fatal, and relatively quick, and I could not find information on the internet that was complete and reliable enough for my needs. I felt that one site said one thing, another site said something else, and every site only told part of the story. In this book I found everything I needed to know. I had not had the benefit of going to any of the medical appointments with my sister, so I really needed a book explaining the medical information in a way I could understand but still deeply enough that it would be useful. This great book talks about everything from possible causes, prognosis, stages of disease, what is happening in the brain, how I can help, history of the disease, when to do what, to....literally everything I wanted to know, and more. It doesn't pull any punches.If you are needing more information on dementia, this is your go-to book.
Good book for those of us who have the diagnosis of Frontal Temporal Dementia of a spouse. Has a lot of information that you can not always find right away. Very glad I bought the book. Could touch more on the financial aspect especially since FTD hits younger people and the high financial situation is hard for the surviving spouse, family.
When my brother was diagnosed with FTD 18 months ago I was all over the internet trying to get answers. I'd grab a bit here and little more there but never the entire field of view. This book helped me and the professional care givers understand thebeast within that we must learn to deal with. With so few cases each year, I even recommended this book to my brothers familydoctor who was treating him for depression. I was able to come to understand his weird behavior patterns over the last seven years and now have a better understanding of how to prepare for his end time. Thinking I was to blame for his problems because of sibling rivalry caused me many years of angst. For those of you burdened with a family member or friend with FTD, this is, unfortunately, a must read. I am now better prepared to get on with my life and help my brother with his limited life.
10 stars:My best friend from grade school, now 70, was dx with FTD, a little over a year ago. This author could have been writing her story. Her family is devistated and she is so helpless. This was the brightest, prettiest, best figure, most popular and (dam it), the sweetest and kindest of all of us, her life has been amazing. She spoke 5 languages and now, can't find a word in any, although, most of the time it is obvious that she knows what she wants to say. These authors were so "right on" with this terrible dementia, that I took this book for her family during my most recent visit. We all tend to think Alzheimer's, but it is worse, and was getting worse when misdiagnoised and treated for Alzheimer's, just like the author said.I hope you and your family will never need this book, but if you do, thank goodness they wrote it.DHR, Tucson, AZ
Complements existing resources to provide additional insights on a variety of dementias. Helps caregivers to compare the symptoms they experience to those commonly documented for Alzheimer's patients so medical and support staff can be alerted to the need for additional diagnostic tests and treatments. Was helpful to me in determining that my parent may not have true Alzheimer's dementia.
My 43 year old son has FTD. Until now I had never heard of the this type of dementia. Thw book was very helpful with how to apply for Socical Security and Medicade. Without this information it would have been difficult to wade through all the paperwork. I learned why he was acting the way he was and to be able to accept the man he is now and let go of the brillant man he was before this happened to him. I have read the book several times and gain more information each time. Wish his doctors would read it.
This book was recommend to me by a local Alzheimer's organization. I have found it very useful in understanding my mother's dementia. She was re-diagnosed with Frontal Temporal Dementia and there were things that I read in the book that gave me a couple of Ah Ha moments.It's pretty straight forward and blunt. I would definitely recommend it to anyone who has a loved one with dementia.
I have been doing a lot of searching to obtain info about F TD.. Most searches take you to info about A D. While this is helpful, much is not relevant to F T D.This book relates first to F T D then expands where similarities are also involved with A D and A L S.
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