imstephtacular's review

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dark emotional hopeful informative reflective sad medium-paced

4.0


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kateph's review

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challenging emotional hopeful informative inspiring reflective sad slow-paced

5.0


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kennyrae89's review against another edition

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dark emotional hopeful informative medium-paced

4.0

Great book to read for people dealing with chronic illness. 

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emfass's review against another edition

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challenging dark emotional hopeful informative reflective sad medium-paced

5.0

Part memoir, part journalism, 1000% vulnerable and a must-read, especially if you love someone with chronic illness. I cannot speak from an #OwnVoices perspective, but I hope it would also help a reader with chronic illness feel seen. I listened to this on audiobook, and it was made even more powerful by listening to Miller tell her story in her own voice.

Content warning: the author is descriptive throughout concerning the effects of IBD (inflammatory bowel disease), C. diff, and Crohn's disease) and does not hold back about what it does to her body. She also shares openly about many different traumas she has faced throughout her life. (I love The StoryGraph website for more detailed content warnings, if you need them!)

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readalongwithnat's review against another edition

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informative reflective medium-paced

5.0

I received a free ARC from Henry Holt Books in exchange for my honest review.

This was one of my most anticipated books of the year and it did not disappoint. My chronic illness differs from Tessa's, but I still found this book to be incredibly relatable. I also liked how it was part memoir and part educational. I want everyone in my life to read this so they can better understand living with a chronic illness.

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spaghettireads's review against another edition

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emotional informative reflective medium-paced

5.0


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lisabreads's review against another edition

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challenging dark emotional informative reflective slow-paced

4.0

 What Doesn’t Kill You by Tessa Miller is a chronic illness memoir. The author has Crohn’s Disease, like I do, but like many chronic illnesses, our symptoms and treatment paths are completely different. I did find this one leaning heavily on her experience in US healthcare and her persistent infections with C. Diff, neither of which I have personally experienced. She also goes a lot into her own personal history with abuse and the affects that had on her mental health during this experience as well, which was very personal to her.
So if you are reading this as a primer on Crohn’s, you’ll get some great information, especially if you are a US patient. But you will also get a lot of personal chapters that you would expect from a memoir.

Having Crohn’s can feel isolating as most people don’t love much “bathroom” talk so I appreciate anyone willing to share their story so I can feel a little less alone. 

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