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.

Wednesday, July 19, 2017

Meet Emily Page, author of "Fractured Memories"



By Emily Page
Writing about dementia came about fairly slowly and organically. I'm an artist, so when my dad was diagnosed with frontotemporal dementia at the age of 65, my natural inclination was to start doing paintings about our journey as a sort of self-prescribed art therapy. I used an elephant as both a symbol for and a talisman against dementia, because "an elephant never forgets." As I created paintings, I posted them on social media with an explanation of their meaning, and people really responded to them. At the insistence of a friend, I started a blog to help promote my artwork, and it became a kind of online journal. Before long, I was getting tons of great feedback from my readers when I posted about what we were experiencing as we coped with caregiving. "Me, too!" was a phrase I started hearing a lot.
After my dad passed away in early 2016, my readers kept calling for me to turn the writing and artwork into a book, which was a fairly terrifying thought. I don't consider myself a writer, so the thought of sitting down and writing a book was daunting, but I knew that what I'd been writing about on my blog had spoken to people, and I hoped that the book would do the same thing.
When my dad was diagnosed, he was really open about his diagnosis, and so I decided that honesty was paramount if my book was going to do him justice. In our home, honesty meant not just talking about the really hard stuff, but laughing at the ridiculous stuff, too. There's plenty of both. My motto was, "We laugh when we can, we cry when we must." So I talked about the silly things he did as a result of the disease, and I talked about the raw, painful stuff that we were going through in our efforts to give him the best care possible. There are moments when I don't make myself look so great, but I thought it was important for other caregivers to be able to see themselves in the writing and know that it's okay and forgivable to not be perfect. We're all just struggling to do our best for the people we love.
I'm getting some great reviews on Amazon, but even more important to me are the people who've been given the book by a friend and have taken the time to look me up and email me to say, "Thank you. You said all the things I've been thinking."
About the Author
Emily Page is a professional artist and part-time writer. Working out of Raleigh, NC, Page spends most of her time elbow deep in paint, but comes up for air periodically to share her art and thoughts on her blog. She translated her ridiculous musings about her family’s journey through her father’s dementia into a book, Fractured Memories: Because Demented People Need Love, Too, available at http://shop.emilypageart.com/.
Follow her on Twitter at @EmilyPageArt23, and read her blog at https://emilypageart.net/.


1 comment:

Unknown said...

Thank you so much!