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A Memoir of Motherhood, Genetics, and Facing the Unknown
by Taylor Harris
Book Reviewed by:A Black mother bumps up against the limits of everything she thought she believed - about science and medicine, about motherhood, and about her faith - in search of the truth about her son.
One morning, Tophs, Taylor Harris's round-cheeked, lively twenty-two-month-old, wakes up listless, only lifting his head to gulp down water. She rushes Tophs to the doctor, ignoring the part of herself, trained by years of therapy for generalized anxiety disorder, that tries to whisper that she's overreacting. But at the hospital, her maternal instincts are confirmed: something is wrong with her boy, and Taylor's life will never be the same.
With every question the doctors answer about Tophs's increasingly troubling symptoms, more arise, and Taylor dives into the search for a diagnosis. She spends countless hours trying to navigate health and education systems that can be hostile to Black mothers and children; at night she googles, prays, and interrogates her every action.
Some days, her sweet, charismatic boy seems just fine; others, he struggles to answer simple questions. A long-awaited appointment with a geneticist ultimately reveals nothing about what's causing Tophs's drops in blood sugar, his processing delays—but it does reveal something unexpected about Taylor's own health. What if her son's challenges have saved her life?
This Boy We Made is a stirring and radiantly written examination of the bond between mother and child, full of hard-won insights about fighting for and finding meaning when nothing goes as expected.
The publisher is unable to provide an excerpt of this book.
This Boy We Made repeatedly surprised me. I'd assumed it would be exclusively about the medical mystery of Tophs' disability. But Harris elegantly weaves in a lot of other themes, too: mental illness, her own physical concerns, racism, faith, and advocating for her children's health and education. She recalls her teenage struggles with anxiety and the search for a medication regime that would help. A stay-at-home mother of three, she worries she's passed down her mental health issues to her older daughter...continued
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(Reviewed by Rebecca Foster).
Deesha Philyaw, author The Secret Lives of Church Ladies
Taylor Harris has masterfully captured the wonder and weight of the endurance race that is motherhood. Mothering in the face of illness and uncertainty as a Black woman is downright Olympian. Harris' beautiful, crisp prose drew me right into her family's journey. Their story is heart-wrenching, hopeful, and truly unforgettable. Nicole Chung, author of All You Can Ever Know: A Memoir
My rule to read everything Taylor Harris writes has never failed me. With wisdom, earnestness, and no small amount of humor, she reflects on parenthood and all of the unanswerable questions it raises, exploring what it means to love a child precious to but distinct from you; to wonder about mysteries you may never solve and a future you cannot possibly know. This Boy We Made is a courageous, exquisite memoir, one that will inspire and help readers understand how we can brave the unknown while living in hope. Porochista Khakpour, author of the acclaimed memoir Sick
Taylor Harris takes us on an unforgettable journey through the impossible tangles of America's healthcare system and lets us see firsthand all tiers of stakes that come with Black motherhood in this America. Disability, race, gender, class—every failing of our society and its frustrating promises of our security and freedom is examined here with clarity, courage, and so much love. The admiration I have for Harris extends far beyond her outstanding skills as a writer even—the blessing of her heart and mind truly transcend any ordinary reading experience! This is one of the most necessary entries in the medical/disability memoir canon yet.
In This Boy We Made, author Taylor Harris finds out that she has a BRCA2 genetic mutation that puts her at about a 50% higher than average risk of developing breast cancer, and decides to have a prophylactic double mastectomy.
A mutation in the BRCA1 or BRCA2 gene is associated with a higher risk of certain types of cancer. Dr. Mary-Claire King's work from the 1970s onwards was responsible for discovering the BRCA1 gene's connection to hereditary breast cancer. In 2014, she was given the Lasker–Koshland Special Achievement Award in Medical Science for this work. Her findings led to the development of genetic testing for breast cancer risk based on BRCA1 and BRCA2, after their locations on chromosomes 13 and 17 were identified. ...
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