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My Father’s Daughter: A Story of Survival, Life, and Lynch Syndrome Hereditary Cancers
My Father’s Daughter: A Story of Survival, Life, and Lynch Syndrome Hereditary Cancers

My Father’s Daughter: A Story of Survival, Life, and Lynch Syndrome Hereditary Cancers

By Lindy Bruzzone

$3.99$34.99

As a child, Lindy Bruzzone knew how she would “someday” die. It would be from cancer as what occurred with almost everyone in her family up to her generation.

Bruzzone tells the story of an American family coming to America in the early 1600s, through today. Defying the odds of fate while pioneering a new country, the stories Lindy’s ancestors leave behind inspire the following generations to endure future challenges of facing hardship and survival.

Lindy shares the fear and uncertainty earlier family members experienced living with an unknown hereditary cancer syndrome during the eugenics movement in the early 1900s. Its mission was the mass sterilization of individuals considered “inferior” in an attempt to develop a “better breed” of persons.

Bruzzone takes the reader inside the notorious San Quentin prison and upon California’s mean streets where she works as a parole agent. There, she learns there are many ways to die as she flirts with danger and defies mortality.
Finally, embarking upon a genetic journey, Lindy recounts the challenges of her own battles with cancer and how she learns to save her family and herself from hereditary cancers.

Providing inspiration and serving as a working guide of how one family confronted difficult challenges in life, My Father’s Daughter serves as a guide in how to survive life’s challenges and live with the hereditary cancers of Lynch syndrome.
This revised 2017 edition of My Father’s Daughter: A Story of Survival, Life and Lynch Syndrome Hereditary Cancers, is scheduled to be released to the public in August of 2017.

About the Author:

Lindy Bruzzone is a retired peace officer, an investigator, and an author. In 2007, the diagnosis of a late staged, Lynch syndrome hereditary cancer changed her life. She and her husband Steve founded Lynch Syndrome International, a global, nonprofit organization.

For five years she served as the CEO and Executive Director. That commitment ended July 1, 2014, when she handed the reins to others to further its development. Lindy and her husband Steve reside in the Southern Nevada desert with their Australian shepherd, Gus.

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