Dementia Memoir

Christine Bryden was a top civil servant and single mother of three children when she was diagnosed with dementia at the age of 46. Since then she has gone on to challenge almost every stereotype of people with dementia. This is a vivid account of the author's experiences of living with dementia, exploring the effects of memory problems, loss of independence, difficulties in communication and the exhaustion of coping with simple tasks. She describes how, with the support of her husband, Paul, she continues to lead an active life and explains how professionals and carers can help.

Dealing with Early-Onset Alzheimer’s: Love, Laughter & Tears is Sonia Discher’s heartbreaking but empowering story of caring for her husband, Steve. The story follows Steve’s diagnosis of early-onset Alzheimer’s at age 50 through treatment, care, and his passing. Sonia provides a look behind the curtain of this terrible sickness to reveal a treasure trove of tips and tricks she used to understand the disease, advocate for her husband, care for her family, and preserve her sanity throughout a confusing and sad time.

What happened to the kind, lighthearted gentleman whose strong faith had grounded him for eighty years? When I was growing up, Dad was a playful, happy man who enjoyed bringing pleasure to his loved ones. Constructing a skating rink in the barnyard, planning trailer trips to Disneyland or Montana, building a wakeboard to tow us behind his boat were gifts. Hard-working and ingenious, his whimsy disguised the changes taking place. Dads mission to protect and care for others, while seeking his childhood dream of owning a farm, triggered a slow slide into the current of dementia.

Step into a life filled with unforgettable moments and extraordinary experiences. Diamonds, Dogs, and Dementia takes you on an exciting journey through the highs and lows of Teresa Martin Pike’s life. From a birth just before the historic moon landing to heartwarming stories of family, friendships, and unexpected adventures, Teresa's story is one you won't want to miss.

Diagnosed with a disease that can't be reversed? Learn how to keep living life to the fullest. Have you received a terminal or chronic diagnosis? Can you ever find joy, peace, or fulfillment in these challenging conditions? The answer is a resounding yes. When author Jarem Sawatsky was diagnosed with Huntington's Disease, he found there were no guides for those living with incurable illness. He quit his job as a professor and devoted his life to exploring the possibilities of living with chronic conditions. Now he's bringing his findings and insights to you.

If you know anyone with dementia, have been diagnosed in the early stages of dementia, or if you are caring for a person with dementia, then you should definitely listen to this story of love, loyalty, passion, and patience. A tale of never-ending belief in the future.

In Not How It Was Supposed to Be, author Allison Crabtree takes a poignant look at her mom's obsessive and eccentric life, and the complexities of a mother-daughter relationship fraught with tension and disappointment.

Mom’s Gone Missing is not a how-to book. It’s a here’s-what-unfolded book, a story of a daughter’s experience with a father’s decade-long Alzheimer’s journey and a mother’s lightning fast dementia decline and both of their deaths.

DEMENTIA and OUR LOVE, Caregiving as spiritual practice, is the story of Gary and Heather's love that sustained them through an unusual and courageous life across continents, including tending Gary and his onset of dementia at 73 years. The story helped them remember their love and use this energy to move through the hard times. We will always remember us this way, a song by Lady Gaga, was pivotal in keeping Heathers focus.

It’s morning at Meadow Brook Nursing Home. During the last 10 months, this has been my mother’s abode. Most days, I feel it is mine, too. Life, as I have known it, is a blur. Alzheimer’s has taken mother from herself, her family, and her friends. It has demanded a grit and grace in our everyday lives beyond human comprehension. I know that I must tell her story - which ultimately is my story, too - with hope that it may bring a degree of peace to the hearts of those who have walked, or will walk, the same road.

What do you do when your reality slips away? If you're Sky Yardley and Jane Dwinell, you accept each new challenge, reshape your life, and write. When Sky was diagnosed with "probable early stage Alzheimer's" at age 66, he was determined to live as fully as possible. He researched dementia, talked about dementia, connected with other people with the disease, and wrote about it.

This book explores Alzheimer’s disease through the intertwined perspectives of a patient and her devoted caregiver, offering a deeply personal look at the emotional, physical, and mental challenges they face. From the first signs of memory loss to the final days of care, listeners are taken on a raw and honest journey through the daily struggles, heartbreaks, and small victories of providing care for a loved one with Alzheimer’s.

In 1992, Franziska Thomas had her first seizure and her whole world was turned upside down - literally. In Fits and Starts, Franziska gives a compelling personal description of living with epilepsy, an illness shrouded in secrecy and antiquated myths. Laden with self-deprecating humor, she describes her own coming of age - as an epileptic, a teacher, and ultimately, a mother.

In diesem bewegenden Buch teilt die Autorin ihre persönlichen Erinnerungen und Erlebnisse aus den letzten Jahren mit ihrer Mutter. Liliana gewährt uns tiefe Einblicke in ihr Familienleben, die ersten Anzeichen der Krankheit und die intensiven, schmerzhaften Erinnerungen, die sie für immer begleiten werden.

When my wife Cheryl saw what I was doing, she asked me to chronicle our almost 30-year journey through Alzheimer's. As I began to write and post blogs of the trip, it became apparent that I had a love of writing and an audience for our story. I soon developed a large following, and the blog almost took on a life of its own. The blog has morphed into much more than I ever dreamed. From the comments and feedback I received on many posts, it became apparent that I needed to try and turn this into a book. Many people battling this disease and being caregivers need to know they are not alone.