What doesn't kill you A life with chronic illness-lessons from a body in revolt

Tessa Miller, 1988-

Book - 2021

"A riveting and candid account of a young journalist's awakening to a life of chronic illness, weaving together her personal story with reporting to shed light on how Americans live with long-term diagnoses today"--

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2nd Floor 616.344/Miller Due Dec 3, 2024
Subjects
Genres
Autobiographies
Published
New York : Henry Holt and Company 2021.
Language
English
Main Author
Tessa Miller, 1988- (author)
Edition
First edition
Physical Description
xiii, 302 pages ; 23 cm
Bibliography
Includes bibliographical references and index.
ISBN
9781250751454
  • Author's Note
  • Chapter 1. Blood
  • Chapter 2. Doctors
  • Chapter 3. The Most Important Poop of Your Life
  • Chapter 4. Our Grief
  • Chapter 5. Old Trauma, New Trauma
  • Chapter 6. Partners
  • Chapter 7. Family
  • Chapter 8. Ghosts
  • Chapter 9. Just a Little Longer
  • Chapter 10. The Brain and The Self
  • Chapter 11. Fight or Flight
  • Chapter 12. Friends
  • Chapter 13. A Pox
  • Chapter 14. Work
  • Chapter 15. Very, Very Not Normal
  • Chapter 16. Secrets
  • Chapter 17. Thirty-Eight Experiences of Joy
  • Acknowledgments
  • Appendix
  • Index
Review by Booklist Review

Chronically ill people, their loved ones, and their colleagues will find useful advice and food for thought in this conversational, revealing memoir and guide. Miller, a 32-year-old journalist, reflects on her experience with Crohn's, an inflammatory bowel disease that causes the immune system to attack the digestive system. Though she had suffered from severe stomache aches throughout her life, she felt "searing cramps" in early 2012. Then, during a visit home to rural Illinois, things got much worse. Miller became "a professional patient, and a good one." People like to say, "This too shall pass," but, she asks, "What happens when 'this' never goes away?" Her own tale is so gripping, it's almost a disappointment when she shifts from telling her story to offering advice. But her tips are excellent, from joining support groups to finding a doctor affiliated with a teaching hospital. She also shares the "secrets" of chronically ill people, such as how they want to be believed and how weary they are of unsolicited advice. This is page-turner and a quality resource.

From Booklist, Copyright (c) American Library Association. Used with permission.
Review by Library Journal Review

As more is learned about the long-term effects of COVID-19, health and science journalist Miller offers a timely description of the ramifications of a chronic illness. The story of her struggle with Crohn's disease provides the undergirding for a broader look at how every aspect of life is impacted by any disease that doesn't kill, but also doesn't go away. She begins with a graphic account of how her own life was upended and changed forever by the symptoms that eventually led to a correct diagnosis. Miller is open about her own struggles and intertwines autobiographical portions with reflections on life with chronic illnesses. She discusses interactions with the medical world; grieving over what will never be; evolving interactions with family, friends, coworkers, and bosses; and the reality of a new self-image. There is a chapter outlining specific things those who interact with people with chronic illness need to know (e.g. " 'inspirational' isn't exactly a compliment") and one in which others with chronic illness are quoted saying what now gives them joy. VERDICT A clear, no-holds-barred account that will be useful both to those coming to grips with their own chronic illness and also to the people in their lives.--Richard Maxwell, Porter Adventist Hosp. Lib., Denver

(c) Copyright Library Journals LLC, a wholly owned subsidiary of Media Source, Inc. No redistribution permitted.
Review by Kirkus Book Review

A young writer's unflinching account of her battle with Crohn's disease. Miller was a 24-year-old editor at Lifehacker when she was diagnosed with Crohn's disease, an incurable form of inflammatory bowel disease. In this blend of harrowing memoir and self-help tips, she chronicles how she achieved remission after nightmarish years of hospitalizations complicated by nasty attacks from the "extremely contagious and hard to treat" bacteria known as C. diff, which required three fecal microbiota transplants. Before she tamed her disease with medication, she endured countless physical indignities--from having to wear adult diapers to leaving a dinner party 20 times to use the bathroom--as well as "mental Olympics," which she powerfully describes as "the depression and anxiety that come along with a malfunctioning body; the defeat of visiting doctor after doctor only to hear 'it's all in your head'; the sick, sleepless nights worried about health insurance; the hope of a new treatment and the crushing loss when it doesn't work; the longing for loved ones to understand that you're the same you--except not; the grieving of a self that doesn't exist anymore; the PTSD from long hospital stays and invasive procedures; the new rules of an unrecognizable body; the inescapable loneliness." Miller intersperses vivid tales of her struggle with a hard sell for talk therapy and pages of overfamiliar advice on coping with chronic diseases: "Platitudes are annoying, but I've learned over the last decade that sometimes they're true: There is light at the end of the tunnel, time does heal, and the sun will come out tomorrow--so long as you do the work." Readers with Crohn's and other chronic conditions may find this book so valuable they won't mind the banalities, but more insightful writing on a similar topic appears in Everything Happens for a Reason, Kate Bowler's inspiring book about her colon cancer diagnosis. Frank reflections and well-worn advice on living with an incurable disease. Copyright (c) Kirkus Reviews, used with permission.

Copyright (c) Kirkus Reviews, used with permission.