Books like Terry Pratchett — picked by fans

Like most people, the two diseases of aging that scare me the most are ischemic stroke and Alzheimer’s disease. I don’t want to lose my ability to think, and I want to preserve my memory. So...there is no time like the present to explore what I can do to learn how to prevent Alzheimer’s disease.

Bredesen is the first neuroscientist I’ve encountered who describes different types of Alzheimer’s and offers practical diagnostic and dietary advice. I’ve explored his recommendations, and I think they’re sound. I’ve suggested this to many of my friends for them and/or for their parents and loved ones.

Reading Patti Davis’s book is like sitting in her living room talking with her, one caregiver to another. Because she not only lived through Alzheimer’s disease and dementia with her father, Ronald Reagan, but ran a support group for a number of years, her knowledge is vast and she shares it with you. For example, chapters with titles such as, “Grief Arrives Early,” “Creative Lying,” “The Battle Over Bathing,” and “Where is the Person I Knew?” discuss important topics in relatable ways. Her story and the way she tells it also make this book a wonderful read.

A Doll for Grandma shows the love between a grandmother and granddaughter.

Kiera loves spending time with Grandma. They play dress-up, paint their nails, make molasses cookies, and picnic with Kiera’s doll. Over time, Grandma changed. She became forgetful, misplaced items, and could no longer live at home.

When Kiera visited Grandma at the memory care home, Grandma was different. She rarely smiled. She said odd things and thought Kiera was her childhood friend. Kiera found a way to connect with Grandma by giving her a doll. Grandma and Kiera played with their dolls, and they ate molasses cookies together.

This story reminds us that when a loved one loses their memory and their personality changes, there are ways to connect, share happy times, and make new memories. (An article titled "Helping Children Understand Alzheimer’s Disease" by Judy Cornish at the end of the story is helpful in explaining memory… show more.

Iveliz is angry and depressed, about a lot of things, including the death of her father. In an attempt to help Iveliz manage her anger and depression she sees a therapist and takes medication.

Iveliz knows taking her medications will help her, but what if the meds aren’t helping anymore? And what if seeing a therapist and talking about her problems isn’t what Iveliz wants to do? Why does no one want to listen to what she wants?

Iveliz struggles to say no and to advocate for herself and she pours all her thoughts and feelings into her journal, until she realizes that maybe using her voice is a better way to be heard. I loved the way Iveliz’s emotional journey and mental health are chronicled and treated with respect and care in this award-winning middle-grade novel in verse.

I was a new mother when I read this Alzheimer’s memoir and immediately felt that I’d found a friend. Elizabeth Cohen is funny, lyrical, and sometimes (understandably) frustrated as she takes on the bruising balance of managing a career while simultaneously caring for her aging father and her young daughter. The book is a testimony to the healing power of story and provided a valuable model to me as I sought to make sense of my own family experience by committing my memories to the page.

This book shows you how to meet many of the daily challenges of caring for someone with dementia. Illustrated through the heartfelt stories of others this book shows your how The Best Friends method brings dignity to the lives of those presenting dementia symptoms and those who are caring for them.

I found the explanation of Alzheimer’s disease and dementia symptoms very interesting and helpful, specifically how this type of loss and experience can make the individual feel. I appreciated learning additional and successful ways to respond and communicate to many situations that caregivers face when caring for any individual with any cause of dementia symptoms.

Dementia care is complex and different for every person, and I am always looking for new perspectives and care approaches to share with family and professional care providers that can give confidence and feelings of empowerment to anyone on their individual dementia care journey-and… show more.

This author does a beautiful job of explaining how individuals with dementia may not be able to recognize their friends and family, but still need love and attention.

The boy in the story figures out how to connect with his grandpa, even though he may not get a smile in return. It is really and truly delightful and reassuring.

This is both a children’s story and a guide to Alzheimer’s. The child, Mathew, tells the story.

He begins with all the fun things he and his grandma do when he visits, walking in the backyard, eating butterscotch candy, listening to the birds. As time passes, Grandma grows forgetful. She calls Mathew by his dad’s name. She stays indoors more and has a caregiver. Mathew’s parents and a nurse explain the changes happening to his grandma. Mathew learns how to talk to her. They look at pictures and Mathew tells the stories that she told him.

This book is an excellent source for explaining Alzheimer’s and memory loss to a child. I love how it gives examples on ways to communicate with someone who has this disease. 

Andrea Couture’s father, a well-known, recently retired surgeon, develops Alzheimer’s at the age of 67. As someone who also lost a parent at a young age, Embracing What Remains touched a deep place in my heart. I connected with how she processed her emotions through her writing. I also appreciated the way she balances her grief over his disease with the gratitude and joy she discovers in each moment. This is a beautifully written memoir! 

Difficult for me not to gush about this book by my good friend! It is amazingly rich. It builds on Kitwood, introducing the idea of ‘malignant positioning’. It deepens Kitwood’s approach to personhood using William Stern’s notion of ‘Critical Personalism’. Steve sets out how, from a social constructionist standpoint, we can give different accounts of selfhood. He shows how these remain relevant even as dementia advances. The richness, for me, comes from the verbatim accounts of people with whom Steve worked closely over an extended period of time. Theory and reality come together. We get to know real people and see into the intricacies of their lives. The importance of the new culture of dementia care – where seeing the person as a psychosocial being is imperative – becomes utterly compelling.