When a hereditary cancer threat echoes her mother’s journey, one woman chooses to rewrite her story—crafting a radiant memoir about embracing life’s precious moments and finding strength in the infinite power of family love.
Tiffany Graham Charkosky was eleven years old when her mother, Julie, died. Eighteen years later, she discovers that the genetic mutation that took her mother has been passed down to Tiffany herself. But with this devastating news, Tiffany finds a certain strength in hope, resilience, and knowledge. She will fight for her family’s future.
In this intimate memoir, Tiffany shares her challenging journey forward, mapping out a plan for preventative screenings, genetic testing, and surgeries, as well as a reflective journey into the past as traumatic memories of her mother’s illness and death resurface. Memories, too, of an indomitable love that informed Tiffany’s adolescence, and her own motherhood, and would give Tiffany an optimistic understanding of just how precious even the smallest moments in life can be.
Now, thriving years beyond the age that claimed her mother, Tiffany embraces each day with fierce intention—her path illuminated by vigilant self-care, deep gratitude, and a family bond that proves the human spirit can transcend its darkest fears.
This may be the most beautiful memoir cover I've ever seen. It looks like art for the most gorgeous historical romance you can imagine, the heroine's face turned away from the reader, inviting you to turn, instead, to the compelling story rather than just gaze on her lovely face.
But that's not how I found her. The author did a compelling post on the blog of Jane Friedman, publishing industry Thought Leader, revealing how an analysis of memoir publishing inspired her to keep writing, keep pursuing her dream. https://janefriedman.com/all-others-t...
Tiffany, a fellow Ohioan, former journalist, and current Director of Arts & Culture for the Cleveland Public Library, reveals in her memoir the gobsmacking impact of learning that her mother had a genetic mutation that took her life when Tiffany was just eleven. The recommendation to the family was to be genetically tested, with possible other tests and procedures suggested if members had the same mutation.
I'm talking about the possibility of preventive mastectomies, hysterectomies, even in one case a decision to have one's colon removed. The gravest recommendations, which Tiffany and her family meet head on with fierce bravery.
Tiffany unscrolls her story in a cinematic style that reads like the best fiction. We learn who is tested, who has the lethal mutation, and what she and her family members decide to do.
I dare you to put this poignant, powerful story down once that stunning cover heroine propels you to the first page. You JUST CAN'T release it, and I found myself ignoring my darling husband, our precious calico kitten, and scarfing down meals while light-speeding it to the end. Highly, highly recommended!
Thanks to author Tiffany Graham Charkosky, Amazon Publishing, and NetGalley for the review copy. Opinions are mine.
Living Proof is a beautiful memoir that reflects on what it’s like to live with the genetic disorder Lynch Syndrome. For those unfamiliar, Lynch Syndrome means one or more of your genes are mutated, compromising your body’s ability to repair DNA. This puts you at a significantly higher risk for developing cancers such as colon, ovarian, stomach, and more. I also have Lynch Syndrome, which is why this book resonated with me on a profound, personal level.
What I Liked About Living Proof: My favorite part of Charkosky’s book is her honesty! I related to so much of her book that I found myself constantly highlighting sections and saying in my head, “Yes, that is so true.” When she found out that her mom had colon cancer, her life turned upside down. She was only 11, and she went from having her mom be a total participant in her and her sibling’s lives to watching her struggle through the stages of cancer.
What makes this memoir so compelling is how Charkosky structures it, alternating between her childhood, spent watching her mother struggle with cancer, and her adult life as a mother herself living with the same genetic disorder. This dual perspective is incredibly effective. She shares her worries, joys, and fears with such honesty that anyone who has dealt with illness, loss, or a chronic health condition will instantly relate.
Favorite Quotes About Living With a Parent Who Has Lynch Syndrome:
“I became afraid to ask my mom for anything, of doing something wrong, making her worse, of having any needs at all.”
If you have ever had someone sick in your household, you will be able to relate.
“A sick mother changes the entire biome of her family, with everyone around her adapting in their own ways to a new environment.”
I was 13 when my mom had colon cancer. It was one of my biggest life-changing events. Throughout her chemotherapy, she was sick after each treatment and then lost her hair. She truly tried to make things normal for her kids, and looking back, I am thankful and realize how strong she really was during that time.
Favorite Quotes About Living With Lynch Syndrome:
“It was lonely having a mutation I’d never heard of and, it seemed, hardly anyone else had either.”
Even though statistics show that one in 300 people have it, most people don’t know that they carry this gene mutation. It is hereditary, but generations can pass before the mutation is discovered through genetic testing.
“I didn’t want the people I knew in real life to associate me with this mutation.”
I don’t speak about having Lynch Syndrome very often. I picture myself like a Teenage Mutant Ninja Turtle when I talk about my gene mutation. I’m starting to realize, though, that I should. The more people that have genetic testing done, the more people that can be saved with their new knowledge.
“I didn’t comprehend until that day that cancer isn’t just one disease, nor is cancer of a certain organ one disease. Cancer is a collection of thousands of different diseases, each operating in its own way to edge out a body’s healthy cells.”
My doctor explained that having Lynch Syndrome is like missing the “spell check” on a word document. I liked that analogy.
“These annual appointments were part of the Plan and they put me on edge, making me question every twinge.” “…the reality was that a lot of my plan was about finding cancer early, not stopping it altogether…” “…we didn’t talk about the ongoing emotional toll this information might have one us.”
If you have Lynch Syndrome, you know the amount of yearly tests to screen for cancer is exhausting. However, I feel so fortunate to have this knowledge. I feel blessed that my doctors get me in right away with something seems “off” on my skin or how I’m feeling. I agree with Charkoski when she talks about the anxiety that leads up to these tests and how it has almost turned her into a hypochondriac when almost anything seems wrong.
“…we want to remain healthy for ourselves and we need to respect the fear and anxiety our cancer risks instill in the people we love, particularly our spouses, who have chosen to love and build futures with us.”
Sometimes we can get so wrapped up in our life and health, that we forget what it also does to our family members. My husband is incredibly supportive, but I know it takes a toll on him as well. I did laugh at her experiences with her husband after each colonoscopy.
“It was living your life with the clear acceptance of what it was and not being destroyed by what it wasn’t.”
I want to remember this quote. I think it’s impactful advice for everyone. Live your life and try not to worry about what hasn’t happened yet.
Final Thoughts on Living Proof:
As you can see, I really enjoyed this memoir. It will speak to so many people. Even if you don’t know anyone with Lynch Syndrome or you haven’t had someone die that is close to you, you will still appreciate this memoir. The writing is honest and it pulls at your heartstrings. It also gives you hope!
Where To Buy Living Proof and More: Purchase Living Proof: https://amzn.to/4nWMJH8 (It’s also on Kindle Unlimited right now)
If you liked this book, I also recommend these other memoirs for your next read:
I read at nights and for the past few evenings, I've been eager to go to bed so I could return to LIVING PROOF! This is a beautiful book that makes the angst of the narrator's genetic diagnosis real for the reader. The way she writes about her mom while also mothering her sons struck me by its grace and presence. Even if you do not have chronic illness in your family, you will find this memoir heartwarming and inspiring.
Like the author, I also live with lynch syndrome. I learned I have one of the genes a few years ago and it turned my world completely upside down. I really wish this book existed then because I certainly would have felt less alone. So many of the thoughts, feelings, fears and ways I coped initially made me feel isolated, alone, and at times, ashamed, but after reading Tiffany’s memoir I realized that it wasn’t just me. Tiffany’s candor is this memoir is both refreshing and appreciated. She feels like a mentor, teacher, and friend through the pages of this book.
Thank you so much Tiffany for writing such a beautiful memoir that perfectly captures the anxiety and fear of living with lynch, the tough decisions that one will grapple with often at young ages (from fertility to screenings to surgical menopause and more), and the hope that comes with continued medical advances! While getting annual screenings, especially colonoscopies, will never be easy, having a book out there that can be shared widely to help people with and without lynch understand what it might be like is incredibly helpful. And even if you don’t have lynch or another genetic condition, you will find this memoir beautiful and relatable about the greater context of the human experience.
Definitely a 5 ⭐️ read for me! A huge thanks to Tiffany for the ARC!
I’m grateful for authors like this who know how to effectively share their deeply honest feelings about difficult medical experiences so that others who have experienced the same thing will know they are not alone.
Tiffany Graham Charkosky’s Living Proof is a luminous testament to what it means to carry both loss and legacy in your DNA. The story opens with the devastating truth that the same genetic mutation that took her mother also lives in her. And yet, instead of being paralyzed by fear, Charkosky faces her future with strength, intentionality, and love. Her personal response to terrifying circumstances informs her gorgeous narrative voice.
Her writing is deeply honest and beautifully balanced. She weaves together losing her mother during her childhood with the more medically focused reality of her adulthood: genetic testing, difficult medical decisions, and the heavy knowledge that this kind of illness brings.
One of the most compelling parts of this memoir is Charkosky’s dual timeline structure — alternating between her memories of her mother and her own journey as a mother. We witness her grief that she somehow turns into a courageous, hopeful story infused with the light of love. What stands out most, though, is this very love. Charkosky takes the plot points of genetics and illness and turns them into a love story about family, connection, and choosing to live fully in spite of uncertainty. Through exams, difficult experiences, and moments of grief, Charkosky’s gratitude and fierce intention shine through.
Everything about this very specific memoir feels universal, not just medical. Anyone will relate to her experience.
In short, Living Proof is a beautifully written, deeply human memoir. It’s a book that keeps resonating long after we close its pages — the narrative is a reminder that while we can’t control our inherited risks, we can choose how we face them. Charkosky believes in kindness and love. Highly recommend.
I absolutely loved this book. It’s a gorgeous, powerful piece of work, and I am so thankful that Tiffany wrote it. Her story moved me deeply — both for its raw honesty and for the way she turns unimaginable pain into something luminous and full of hope.
Tiffany’s writing is intimate and brave, weaving together memory, science, and emotion with such grace. Through her story, she gives voice to what it means to live with knowledge of genetic inheritance, to confront fear head-on, and to still choose love, gratitude, and joy. I found myself completely immersed in her world — grieving with her, celebrating with her, and ultimately feeling inspired by her resilience and intention.
Living Proof isn’t just a memoir; it’s an act of generosity. Tiffany has offered us a roadmap for how to live fully, even when the future feels uncertain. I’m so grateful for this book and will be recommending it to everyone I know.
The premise of Living Proof is heart wrenching: daughter inherits the same genetic mutation that led to her own mother's early death.
But Living Proof isn't just a story about grief, motherhood, and illness. This book is compelling because the author, Tiffany Graham Charkosky, is both earnest AND witty. She's unflinchingly honest, admitting to the emotions we all share but may not care to admit to.
Reading this book felt like listening to the secret, sincere thoughts of a mother desperately longing to remain healthy for her children. You know how people often tell the cleaned up story in small talk, but if you were to peruse their Google searches, you would learn about the real stuff? This book gives you the real stuff. It's such a smart, important memoir, and you should order a copy today.
This memoir is about the narrator's experience with genetic testing and counseling after learning the illness that killed her mother far too young is a genetic condition that the narrator may also have inherited. What I especially appreciated about the book is how it shows how this experience ripples outward--inevitably affecting her siblings, spouse, children, etc. Such careful attention is paid to internal weather and family dynamics, articulating complicated situations with the nuance they deserve. This is the kind of book that can only be written by living an honest life and doing a lot of soul-searching. I imagine this book was far from easy to write, which makes it all the more rewarding to read.
Structure/pace: The book is written in short vignettes and I found it compulsively readable. I read it in 24 hours.
Living Proof is a beautiful, deep dive into the lasting impact of early mother loss on girlhood, womanhood, and motherhood set against the shadow of genetics. Tiffany Graham Charkosky’s gripping and poignant prose resonated deeply with me after losing my own mother at eight. Though this memoir is about the genetic legacy the author carries, it is also about how profoundly early mother loss impacts a woman, and the echo of grief that comes with aging and becoming a motherless mother. With grace and honesty, the author examines what it’s like to build a family against a backdrop of the seemingly faulty genetics lingering within our own bodies. I highly recommend this memoir to everyone, but especially those who have experienced mother loss or motherless motherhood.
Living Proof: How Love Defied Genetic Legacy is an honest and heartfelt memoir that explores what it means to live under the shadow of inherited illness while still choosing joy and connection. Tiffany Graham Charkosky writes with striking vulnerability about losing her mother young, discovering her own genetic risk, and navigating motherhood with both fear and determination.
The book shines brightest in its emotional clarity—Charkosky’s reflections on love, legacy, and resilience feel authentic and deeply relatable. At times the pacing slows with medical details, but her insight and warmth keep the story grounded.
What stands out most is Charkosky's refusal to let tragedy define her. Instead, she reclaims her story, showing how understanding our past can help us build a more loving future.
Thank you to Netgalley and Brilliance Audio for the free copy in exchange for an honest review.
I would like to thank Netgalley and the publisher for providing me with an audio ARC.
This book is well written and the author really delves into her own life in this book. I really enjoyed reading what she shared about her life and her reflections. This book really delves into the uncertainty of health and those scary feelings surrounding health. I myself am having to go thorough some genetic testing and all the uncertainty that goes with it. This book is very touching and is also a bit comforting at the same time.
This amazing book takes a heartfelt, unflinching look at family, life, and how much we cannot control about our bodies. Charkosky writes with brutal honesty about her mother's death and all the emotions that come with the uncertainty of medical issues surrounding the rest of the family. She is a warrior who immerses the reader into her triumphs and heartbreaks. A truly must-read book for anyone who has experienced loss, love, or wants to learn more about rare medical conditions.
In this powerful and insightful memoir by Tiffany Graham Charkosky, readers are given a behind-the-scenes look at genetic testing and the aftermath of the results that includes heart-wrenching decisions that involve not just an individual, but an entire family. Beautifully written, vulnerable, brutally honest, and filled with hope, Living Proof is a page-turner that you won’t want to end. I highly recommend this memoir!
This book broke my heart and stitched it back together again. Beautifully told, with so many gorgeous passages. I was rooting for Tiffany and feeling her pain. Along the way, I learned about genetic mutations, and the strength that can come from testing. This book made me think about health and love and the complications in life that so many of us endure. It reconfirmed for me that knowledge can kick up difficult decisions but can ultimately provide power. I highly recommend.
An exquisitely written memoir that allows the reader to follow the author’s experiences of love, grief, fear and conviction from childhood to present day. Cleverly paced, her insights into the implications of undergoing genetic testing and the nature of genetic counseling are relevant to the general population as medical advances continue. Beautifully told and felt.
This book was so incredible!! It was super difficult to put down and kept me up late because I had to finish it. What a gift to others who may be going through similar struggles. The author writes beautifully and is very relatable. Highly recommend!!
This book is an amazing glance into the life of someone facing the challenges of genetic testing and living with loss. “Living Proof” will absolutely be a profound comfort, reassuring, inspirational and perspective giving to anyone who reads it, Lynch Syndrome or not, as it was for me. Tiffany’s writing is perfection. Her impeccable details made reading her words such a pleasure. I was captivated by the way Tiffany’s illustration of emotion penetrated my heart. It surely will help everyone who reads it to feel seen and loved. She is beyond brave for sharing her story in effort to help others in her same space in life and she has done it so eloquently.
A stunning memoir. The book is full of small, vivid details that are unique (I especially loved all of the Cleveland references), but it also captures the universal and deeply relatable swing between grief and gratitude in response to the randomness of life. The book also does a great job of capturing this wild moment we’re in with genetic testing, when we’re gaining more and more access to previously hidden information about our bodies, and with it comes both the good (prevention!) and the hard (decisions! anxiety!). Plus, the structure made it such a page-turner! I truly had a hard time putting it down. Ok, go read it!
Like the author, I have a genetic mutation that took my mom and left my sister and I with hard choices that didn't feel like choices at all, plus an anxious doom cloud that often hovers over my life. Reading this slim but evocative memoir made me feel less alone. It's not just a book for mutants, though; it's for anyone who has struggled with loss and with the challenges of living in a body they can't entirely control, which is to say, everyone.
A powerful memoir about the author's struggle with Lynch syndrome, a rare genetic defect that can lead to cancer. Deftly written, it has the pace of a compelling mystery. You can read my extended review on my Substack: https://open.substack.com/pub/keighah...