However, evidence shows the cells are not actually exactly the same as the ones that grow in the uterus. Often, the disease is characterized as what happens when the uterine lining grows in other parts of the body. The author expresses particular frustration with the way people commonly describe endometriosis. Throughout, she discusses the science and history of the disease to demonstrate how the medical field has long failed women and gender nonbinary people.Īsk Me About My Uterus: A Quest to Make Doctors Believe in Women’s Pain by Abby Norman, $18, Amazon The memoir chronicles Norman’s battle with the illness, including her fight to receive appropriate medical care and have her pain taken seriously. Science writer Abby Norman shares her own experiences with endometriosis in her new book, Ask Me About My Uterus: A Quest to Make Doctors Believe in Women’s Pain. Nonetheless, little is known about the disease, and most people still don’t understand what it’s like to live with it. One in 10 women reportedly suffer from the disease, and it takes a serious toll on their well-being and quality of life. The annual event is meant to bring attention to a debilitating disease that afflicts millions around the world, most of whom are women. March marks a time to honor women’s history, but the 31-day stretch also features another national celebration that shouldn’t be overlooked: Endometriosis Awareness Month.
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