This post is part of a virtual book tour organized by Goddess Fish Promotions. Corinne Brown will be awarding a $10 Amazon/BN gift card to a randomly drawn winner. Click on the tour banner to see the other stops on the tour.
Blurb:
"The results of your predictive testing are here, and they show that you did inherit the gene for Huntington's disease."
Those words, delivered by the neurologist to 57-year-old Mae Brown, forever changed her life and the lives of her family. Me, Mom & the Monster is a soul-stirring memoir that follows the path of this farming wife, businesswoman, mother and grandmother who lived a life with a monster of a disease. Interwoven with Mae's story is that of her third child, Corinne, whose life is intrinsically connected to her mother's diagnosis. Told from alternating voices of Corinne and her mother, this is a candid account of the harrowing effects of living with a fatal, genetic disease. Me, Mom & the Monster captures the authenticity and vulnerability of a mother and daughter who find themselves entwined in a long dance with a neurodegenerative disease.
Purchase ME, MOM AND THE MONSTER on Amazon
Read an Excerpt
MOM
I remember hearing stories of distant aunts and uncles who were afflicted with the Devil’s Dance—a colloquialism used in some circles to refer to those who were afflicted with HD. They were said to have the Devil’s Dance because of the chorea—a movement disorder causing involuntary spasmodic movements—that looked like an awkward, uncontrolled dance. Chorea is a primary symptom of HD. The Devil’s Dance was whispered about because of the shame, stigma and fear of this disease no one knew much about.
Times were different back then. There was no genetic testing or genetic counselling. Families just waited to see if symptoms would appear in them or in loved ones. Not much was known about the genetics of this disease or what the probabilities were of being affected if a parent had the disease. All I knew was what I heard about family members being sheltered and, in some instances, locked up so they wouldn’t harm themselves. They were deemed to have the Devil’s Dance, and not everyone behaved the same way. There was shame among afflicted families. There was also incredible fear.
This was in the early to mid-1900s in a remote community in northeast Newfoundland, where not many people talked about HD. Partly because there wasn’t much known about it, and no one in these small towns knew what to do anyway, especially if the afflicted person had rage tendencies and dramatic outbursts. My aunt Edna, who, along with my aunt Marg, helped in raising me after my own mother died, often became quite violent and would hit her husband, and hit him hard. She was sent away periodically for shock therapy because that was the preferred “treatment” of a disease that no one knew much about. I had an uncle who took his own life after he started exhibiting symptoms.
I suppose they call it the Devil’s Dance because those who are afflicted can’t keep still, legs going, feet going, torso bending. And the devil part? Well, that probably doesn’t need much explanation or observation. Only the devil could conjure such a tragic infliction. Some days I do feel like I’m in hell, to be honest. Fitting, I suppose. Not like I have a choice to dance with anyone else except with this devil of a disease.
About the Author:
Corinne was 10-years old when she told her teacher that when she grew up, she was going to be an author. A few decades may have passed since then, but the author dream was realized with the publication of her debut novel, Me, Mom & the Monster in the summer of 2026.
Corinne, a native Newfoundlander, grew up surrounded by books, newspapers and magazines. Her environment must have had some impact since she graduated from Memorial University of Newfoundland with a Bachelor of Arts and then went on to pursue a Journalism diploma at Mount Royal University in Calgary, Alberta.
Although her initial intention was to write fiction, Corinne says the story of Me, Mom & the Monster needed to be told first. She says sharing the intimate story of being part of a Huntington’s disease family opened the space for other ideas.
When she isn’t creating characters, and envisioning scenes and scenarios, she finds comfort in being outside. She lives in Surrey, British Columbia, Canada where she is continuously adding to her To Be Read stack and where she is currently writing her second book.
Connect with Corinne Brown
Giveaway:
$10 Amazon/BN GC
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