One who Forgets and One who is Forgotten One in eight over the age of sixty-five and one in three over the age of eighty will be diagnosed with Alzheimers Disease. In her memoir, author Joan Sutton narrates a moving account of her years as caregiver to her husband, noting that Alzheimers is a disease of the brain that is paid for with the currency of the heart. A member of the board of overseers of The Alzheimers Drug Discovery Foundation, she stresses the need to develop more effective treatment for the five million Americans currently diagnosed with this incurable disease, pointing out that for every patient there is a large circle of others also affected. Sutton offers practical advice for the care of the caregiver and the patient, and shares the pain that came as she watched pieces of her husbands self disappear. Following his death, after what Nancy Reagan described as the long goodbye, she writes candidly about coping with her new status as a widow and the aching loneliness of the heart that is the price paid for having known a great love. 100% of the authors royalties (20 to 40% of the purchase price) will benefit the Alzheimers Drug Discovery Foundation/Canada. Cover design by John R. Lewis

One who Forgets and One who is Forgotten One in eight over the age of sixty-five and one in three over the age of eighty will be diagnosed with Alzheimer's Disease. In her memoir, author Joan Sutton narrates a moving account of her years as caregiver to her husband, noting that "Alzheimer's is a disease of the brain that is paid for with the currency of the heart." A member of the board of overseers of The Alzheimer's Drug Discovery Foundation, she stresses the need to develop more effective treatment for the eight million Americans currently diagnosed with this incurable disease, pointing out that for every patient there is a large circle of others also affected. Sutton offers practical advice for the care of the caregiver and the patient, and shares the pain that came as she watched pieces of her husband's self disappear. Following his death, after what Nancy Reagan described as "the long goodbye", she writes candidly about coping with her new status as a widow and the aching loneliness of the heart that is the price paid for having known a great love. All profits from the sale of this book will benefit The Alzheimer's Drug Discovery Foundation/Canada. Cover design by John R. Lewis

A Caregiver’s Diary (Struggling With Alzheimer’s) By: William Franklin Kerns This is a love story. William and his wife, Dora, shared a beautiful marriage of fifty-four years when Alzheimer’s disease began to take a fierce grip on Dora’s health and mind. Intimate and deeply moving, William beautifully captures snippets of their daily interactions and conversations, revealing how this disease not only ravaged Dora’s mind and well-being but also challenged his relationship with his longtime love. William details his daily struggles as Dora’s sole caregiver as her disease progressed and as their marriage moved from a mutually supportive one to one that required William’s constant support and care. This diary details the harsh reality of Alzheimer’s while also capturing touching moments shared between a husband and wife. This story is an honest, often raw look at the effects of this disease, not only on the afflicted but on those who love them.

Keith Oliver was diagnosed with Alzheimer's in 2010, and has since become a leading activist for dementia care, and an international speaker. Telling his story through a diary format, this book gives an unparalleled insight into what day-to-day life with dementia is like, and how he continued to live a full life after diagnosis.

Today, there is a disease afflicting many people and arousing fear in those whose ages can start as young as forty years, and moving on through the sixties, seventy and eighty year old groups. It is known as Alzheimers Disease. This book is about sharing this experience with my sister-in-law who came down with this disease in her later years. She was eighty-four at the time and lived to be ninety four years old. I was encouraged to take notes and write about this by a doctor who told me I would be in a position to see its development every day for as long as she remained with me. He said, Take lots of notes. You will be able to observe so much more than I, because I dont spend that much time with a patient, and you will be with her day and night and observe the changes as they happen and what triggers her behavior. Good Luck! With that I started out on my ten year trip through the ups and downs, the good days and bad days of Alzheimers disease. Our days were laced with pain and humor, but I was determined to see it through, laughing a little and crying a lot, hoping the scenery would change, but finally surrendering to this fate that had come upon us. Our mantra became Lets laugh because if we dont we shall most certainly cry! I chose to care for her because I wanted her to be surrounded by love, music and laughter, in a place where we could laugh with her and cry with her and never be alone. Im glad I did.

Longlisted for the School Library Association's Information Book Award 2017 - 'Over 12' category. Brie's Granddad has always been a serious man, never without a newspaper and knowing the answer to everything. But now he keeps losing track of the conversation, and honestly, Brie doesn't really know how to speak to him. At first, Fred was annoyed that Gramps had come to live with them, it meant he had to give up his room! But then he starts to enjoy watching old films with him and spending time together... although there's the small problem of Gramps calling him Simon. Follow the stories of Brie, Fred, and other young carers as they try to understand and cope with their grandparents' dementia at all stages of the illness. Adapted from true stories, and supplemented with fun activities and discussion ideas, this book for children aged approximately 7-14 cuts to the truth of the experience of dementia and tackles stigma with a warm and open perspective.