Alzheimer Effects, a caregiver’s perspective

My mother was unable to eat dinner tonight. She has Alzheimer’s so it can be difficult to communicate and determine exactly what’s going on with her and when it started. Usually she doesn’t even know to tell anyone when she is cold and needs a shawl, but tonight she obviously had an upset stomach. She was put to bed early, with the hope she will feel better tomorrow. I went home and downloaded Margaret Ann Brown’s new Kindle e-book, Alzheimer Effects, a Caregiver’s Perspective. I don’t have a Kindle, but downloaded the Kindle app to my laptop and got the pdf e-book version. The Kindle app basically gives you a Kindle! Well, almost.

Margaret spent some time as a private caregiver for a number of clients with Alzheimer’s. While not a memoir, Alzheimer Effects is a type of lifewriting, giving short synopses of personal experiences caring for clients. Each little section on a client is followed by Margaret’s thoughts in prose-poetry form. At the very end is a list of suggestions that might help an Alzheimer patient remain in their home longer. I, myself, have tried most of them on my mother before having to take her to a nursing home to be watched around the clock.

Alzheimer’s is a very frustrating and confusing disease with varying symptoms and expressions that can change in a day. It took a class given by the Alzheimer’s Association for me to understand what in the world was going on with my mom. Even the experts cannot tell you much about the course of the disease because symptoms and stages are different with each person. Margaret felt a passion to write this short booklet to help others see what happens not just in one case, but several.

Alzheimer’s Effects is not a field guide to Alzheimer’s, rather a miniature window to understanding for those just beginning that journey. It is written in a homey style and with love. Anger, frustration and guilt can be alleviated a bit by knowledge, and Margaret provides us with a glimpse of what the future holds. Not pretty, but necessary.

Alzheimer Effects is downloadable for free until January 12.


About moonbridgebooks

Co-author of Cherry Blossoms in Twilight, a WWII Japan memoir of her mother's childhood; author of Poems That Come to Mind, for caregivers of dementia patients; Co-author/Editor of Battlefield Doc, a medic's memoir of combat duty during the Korean War; life writing enthusiast; loves history and culture (especially Japan), poetry, and cats
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3 Responses to Alzheimer Effects, a caregiver’s perspective

  1. Jan Morrill says:

    Thank you for sharing this book, Linda. My stepfather is in the early stages of Alzheimers, and it’s a frightening and sad disease. I’m going to download the book.

  2. Linda, my heart goes out to you. I was caregiver for my husband’s aunt who had it, and she fluctuated too, from day to day. The best way for me to meet her needs was to ask her how old her son was. If she said, “eight” I treated her as though she were thirty. If she said he was 38 we talked about current events. It helped her feel less stressed and confused for me to meet her where she “was”.

  3. What a good idea, Linda. I learned at an Alzheimer Society class not to correct or argue with the person but to live in their world, whatever it is at the moment. Jan, I wish the best for your family and want you to know there is plenty of support out there.

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