From award-winning, New York Times bestselling author and neuroscientist Lisa Genova comes a powerful new novel that does for Huntington’s Disease what her debut Still Alice did for Alzheimer’s.Joe O’Brien is a forty-four-year-old police officer from the Irish Catholic neighborhood of Charlestown, Massachusetts. A devoted husband, proud father of four children in their twenties, and respected officer, Joe begins experiencing bouts of disorganized thinking, uncharacteristic temper outbursts, and strange, involuntary movements. He initially attributes these episodes to the stress of his job, but as these symptoms worsen, he agrees to see a neurologist and is handed a diagnosis that will change his and his family’s lives forever: Huntington’s Disease.
Huntington’s is a lethal neurodegenerative disease with no treatment and no cure. Each of Joe’s four children has a 50 percent chance of inheriting their father’s disease, and a simple blood test can reveal their genetic fate. While watching her potential future in her father’s escalating symptoms, twenty-one-year-old daughter Katie struggles with the questions this test imposes on her young adult life. Does she want to know? What if she’s gene positive? Can she live with the constant anxiety of not knowing?
As Joe’s symptoms worsen and he’s eventually stripped of his badge and more, Joe struggles to maintain hope and a sense of purpose, while Katie and her siblings must find the courage to either live a life “at risk” or learn their fate.
Praised for writing that “explores the resilience of the human spirit” (The San Francisco Chronicle), Lisa Genova has once again delivered a novel as powerful and unforgettable as the human insights at its core.
Hey! Here's my review.
The O'Brien family first hear about Huntington's' Disease (HD) when Joe is diagnosed. They discover that it is a genetic disease and that each of Joe's four adult children have a 50% chance of also developing the disease. The story focusses mostly on Joe coping with HD and demonstrates how the degenerative disease actually affects him and his family. There is also a large focus on Katie, one of his children, and her journey to deciding whether she wants to have the screening test and find out her HD status.
I loved and empathised with all of the characters. I felt like I was going through this journey with them. It really made me stop and think about what I would do in this situation. I laughed with them, I cried with them and I am still thinking about them.
Lisa Genova is calling her readers to action to help find a cure for HD. You can donate to the Huntington's Disease Society of America HERE
I received this book free from NetGalley in exchange for an honest review.
★★★★★
- Where: NetGalley
- Format: ebook
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