Alzheimer's Daughter

The Story

Alzheimer’s Daughter introduces the reader to my healthy parents, Ed and Ibby, years before their diagnosis, then recounts painful details as our roles reversed and I became my parents’ parent.

Their disease started as translucent, confused thoughts and ended in a locked memory care unit after a near decade of descent into the opaque world of Alzheimer's.

I began writing Alzheimer’s Daughter one week after my mother's death––when I was stunned, realizing Dad had no memory of her or their 66-year marriage.

I write to pay tribute to the undying spirit at Ed and Ibby's core, and with the hope that the story of their parallel decline might be helpful to others.

Saturday, June 4, 2016


If you have not been a caregiver--if you’re not living with the disease, you may not understand the concept of secrets when dealing with Alzheimer’s.

If I had been an observer I would have thought, why would anyone keep a diagnosis a secret?

But, I was not an observer. Alzheimer’s invaded and took over my parents’ lives as well as my own when they were both diagnosed on the same day. I was working full time as an elementary teacher, living in the same small town in which I’d grown up, when I assumed the primary caregiving, decision-making role with my 86-year-old parents. They were small business owners, my father still drove, and they lived independently in their own home.

On the day of their diagnosis my dad struggled to his feet shouting, “How dare you use the A. word with me.” as Mom wagged her finger at the doctor scolding, “Shame on you.”

We came home from that appointment and conversation about the diagnosis stopped, unless I brought it up. They denied, saying they didn’t want anyone to know, to think they were crazy, or start gossip.

To respect the parents who had given me everything, I propped them up, protected them and their dignity, while I felt immense guilt whittling everything away piece by piece: their independence, their driving, forcing my dad to retire, moving them eventually to a locked memory unit.

I did not write, Alzheimer’s Daughter, to come clean, be honest, or tell secrets. Through the journey I sought support by reading about personal experiences. Each time I found a similar situation, I thought, If this person survived, so will I. Keep breathing. One week after my mother’s death, when I realized my father had no memory of her or their 66-year marriage, my secrets could no longer be contained, so I wrote the book I needed to read all along. Reviewers say it is written with wincing honesty about the cruel affects of the disease, but a WWII love story held together by faith and family is contained within the pages.

I see a new openness about the disease, especially in those touched by early onset, through books like Greg O’Brien’s On Pluto, B.Smith and Dad Gasby’s Before I Forget as well as Kimberly Williams Paisley’s Where the Light Gets In. When each of us tell our stories and combine our voices, we form a large pool of collaborators offering resources, support, understanding, and empathy.

Let’s not keep secrets any longer. Join us during June, Alzheimer’s and Brain Awareness Month. Speak out.

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