Dementia Memoir

An estimated 50 million people in the world suffer from dementia. Diseases such as Alzheimer’s erase parts of one’s memory but are also often said to erase the self. People don’t simply die from such diseases; they are imagined, in the clichés of our era, as vanishing in plain sight, fading away, or enduring a long goodbye. In On Vanishing, Lynn Casteel Harper, a Baptist minister and nursing home chaplain, investigates the myths and metaphors surrounding dementia and aging....

After a near fatal stroke in 1995, Robert McCrum has gained an intimate understanding of his own mortality. Twenty-two years on, his friends have joined him in experiencing Prospero's 'every third thought' of death as a dominating theme of life. McCrum asks: can we make peace with what Freud calls 'the necessity of dying'? Searching for answers leads him to brain surgeons, psychologists, cancer patients and writers for advice and wisdom.

In Remembering the Music, Forgetting the Words, Kate Whouley strips away the romantic veneer of mother-daughter love to bare the toothed and tough reality of caring for a parent who is slowly losing her mind. Yet, this is not a dark or dour look at the demon of Alzheimer’s. Whouley shares the trying, the tender, and the sometimes hilarious moments in meeting the challenge also known as Mom.

While fighting an aggressive brain tumor, Deirdre must care for her mother with advanced Alzheimer’s, raise her teenage daughter, and help her husband chase a new dream - opening a barbecue restaurant. Her greatest defense is her sense of humor in this tender memoir chronicling life struggles that are often tragic - but can still be very funny. Grab a tissue and take a ride as one batty broad battles her way through the tragicomic trials of her most perilous adventure yet - brain cancer.

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.

Throughout her childhood in Detroit, Damian Rogers was never given a satisfactory account of the circumstances that led to her own birth. The "truth" behind the stories she was told by her mother - the free-spirited, beautiful, and troubled Joanna - constantly shifted, and Damian was left only with fragments: her mom's trip to California in 1969 after finishing high school, a mysterious trauma and psychotic break, then a return to Detroit, pregnant.

Happily married and running a successful business, Peter Berry's life changed when, at the age of 50, he was given a terminal diagnosis of early-onset dementia. Since that day, he has learned to live with his very own 'dementia monster'. From depression and suicide attempts through to his determination to confront his dementia, Peter has embarked on a series of challenges to show that 'life isn't over with dementia, it's just a little different'.

Leaving London to return home to rural South Wales, Robyn finds that it's her old life - same teddy bears resting on her pillow, their bodies tucked under the duvet; same view of the garages behind which she'd had her first cigarette and first kiss - but so much has changed. Her dad, the proud, charmingly intelligent self-made man who made people laugh, was in the grip of early onset Alzheimer's. His brilliant mind, which saw him building power stations and literally bringing light into the lives of others, had succumbed to darkness.

This is the story of Carolyn’s mother, her dementia, and how they navigated her journey together. Your loved one may not force feed stuffed animals vanilla pudding or burn their neighbor’s mail like Fay did, but if you’re living through the sad realities of your loved one’s slow and tortuous farewell, this book will help you find solace as you deal with it realistically and with a heart at peace.

Andrea struggles to mourn a man who is still alive as she witnesses her father decline into the depths of Alzheimer's. Denial and devastation color her life when she learns her father, Richard, a recently retired surgeon, is diagnosed with Alzheimer's at the age of 67. Her dream to grow closer to him is crushed as the reality of his disease is fully realized. Andrea, a mother of three young children, learns to balance motherhood with daughterhood as she grapples to accept her father's fate.

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.

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.

Forfatter og antropolog Ina Kjøgx Pedersen har været på feltarbejde i sin egen familie. Hendes idé var på nærmeste hold at følge sin mors demenssygdom; den sygdom, som er udråbt til at være en af vor tids største personlige og verdensøkonomiske katastrofer, som i ringe omfang lader sig behandle, og som i sundhedsvæsnet kun kan måles negativt: I form af rask tilbagegang. Men ville det også opleves sådan for hende i virkeligheden?

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.

I Will Never Forget is the powerful true story of the author Elaine’s talented mother's extraordinary journey through Dementia. Through superb stories from Elaine’s childhood, including her controversial name, tales of smokin’ dragons, and the feisty teenage years, Betty Ward’s wonderful character is revealed. Over time, as their relationship evolves and a new paradigm is formed, her mother begins to exhibit goofy behaviors, uncharacteristic verbal assaults, and bizarre thinking.

National Book Award winner Jonathan Kozol is best known for his 50 years of work among our nation's poorest and most vulnerable children. Now, in the most personal book of his career, he tells the story of his father's life and work as a nationally noted specialist in disorders of the brain and his astonishing ability, at the onset of Alzheimer's disease, to explain the causes of his sickness and then to narrate, step by step, his slow descent into dementia.

Am 4. Juni 2019 fährt der ehemalige ÖFB-Fußballnationaltrainer Didi Constantini auf der Brenner-Autobahn entgegen der Fahrtrichtung und verursacht einen Geisterfahrerunfall. Dieser offenbart ein "Demenz-Drama", in dessen Zentrum mit Didi Constantini ein ehemals gefeierter Star und Liebling der Sportwelt steht - und mit ihm seine Familie. Ein knappes Jahr später fasst sich Tochter Johanna ein Herz und beginnt die Geschichte dieser Demenz niederzuschreiben.

At the age of 53, Tony walks away from a life of journalism and into an unknown future dogged by self-doubt and financial worry. June is 48 years old then, a writer and a teacher, and over the following nine years she watches as her husband gradually changes - in interests, goals, and behavior - until Tony has a sudden fall, ending their life as they have known it.

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.

Freedom 55? The so-called “Golden Years”? What if you are slowly losing your memories and your motor skills? Or what if you are the devastated witness as your partner struggles with dementia? Lewy Body Disease is a form of dementia second only to Alzheimer’s in numbers, yet many doctors and almost no lay people have ever heard its name. This is the story of two courageous people, Julie and Ken Sobol, life partners as well as writing partners. Caught up in the frightening and fatal fog of Lewy Body Disease, they started writing this book together.