My rating: 5 of 5 stars
Bloody and brutal.
This is some non-fiction book.
I started reading this book in October 2022, after a family member had had years of trauma with her endometriosis.
Within just a few pages, I was shaking my head. In anger, disbelief, and pure, unadulterated outrage.
Tracey Lindeman pulls no punches, this is an unflinching and horrifying insight into the medical profession and the patients fighting to get treatment.
Lindeman doesn’t just share her own, horrendous story of living with endometriosis and fighting the doctors to get not only treated, but heard and respected. She tells us about so many women to show how widespread the misogyny really is.
She also tackles many of the elements of endometriosis care that, I am ashamed to say, I had not yet considered- trans, Black, disabled women are all discussed- and their treatment is harrowing to say the least.
The research Lindeman has collated in order to back up her claims is absolutely staggering. There are over 600 references of facts, books and quotes and just adds more weight to an already strong argument.
This is a heavy book- I have personal experience of endometriosis and the toll it can take on a woman, so I have only been able to read this in short bursts. Sometimes not for weeks, because of how shocking and upsetting it was to read. I started it 6 months ago, and have only just finished it. Then a few days ago, I thought, ‘why am I hiding from it? What about the women living through this? They can’t hide.’ So I ‘womaned-up’ and powered through the remaining pages.
This book should be read by every medical professional, not just specialists in gynaecology. I believe that so many people ouside of those particular patients and doctors could gain so much insight, perspective and awareness from reading this.
I cannot impress upon you how incredibly relevant and empowering this book truly is.
Bleed: Destroying Myths and Misogyny in Endometriosis Care by Tracey Lindeman
My rating: 5 of 5 stars
Bloody and brutal.
This is some non-fiction book.
I started reading this book in October 2022, after a family member had had years of trauma with her endometriosis.
Within just a few pages, I was shaking my head. In anger, disbelief, and pure, unadulterated outrage.
Tracey Lindeman pulls no punches, this is an unflinching and horrifying insight into the medical profession and the patients fighting to get treatment.
Lindeman doesn’t just share her own, horrendous story of living with endometriosis and fighting the doctors to get not only treated, but heard and respected. She tells us about so many women to show how widespread the misogyny really is.
She also tackles many of the elements of endometriosis care that, I am ashamed to say, I had not yet considered- trans, Black, disabled women are all discussed- and their treatment is harrowing to say the least.
The research Lindeman has collated in order to back up her claims is absolutely staggering. There are over 600 references of facts, books and quotes and just adds more weight to an already strong argument.
This is a heavy book- I have personal experience of endometriosis and the toll it can take on a woman, so I have only been able to read this in short bursts. Sometimes not for weeks, because of how shocking and upsetting it was to read. I started it 6 months ago, and have only just finished it. Then a few days ago, I thought, ‘why am I hiding from it? What about the women living through this? They can’t hide.’ So I ‘womaned-up’ and powered through the remaining pages.
This book should be read by every medical professional, not just specialists in gynaecology. I believe that so many people ouside of those particular patients and doctors could gain so much insight, perspective and awareness from reading this.
I cannot impress upon you how incredibly relevant and empowering this book truly is.
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