Ask me about my uterus : a quest to make doctors believe in women's pain
(Book)

Includes bibliographical references (pages 267-272).

"For any woman who has experienced illness, chronic pain, or endometriosis comes an inspiring memoir advocating for recognition of women's health issues. In the fall of 2010, Abby Norman's strong dancer's body dropped forty pounds and gray hairs began to sprout from her temples. She was repeatedly hospitalized in excruciating pain, but the doctors insisted it was a urinary tract infection and sent her home with antibiotics. Unable to get out of bed, much less attend class, Norman dropped out of college and embarked on what would become a years-long journey to discover what was wrong with her. It wasn't until she took matters into her own hands--securing a job in a hospital and educating herself over lunchtime reading in the medical library--that she found an accurate diagnosis of endometriosis. In Ask Me About My Uterus, Norman describes what it was like to have her pain dismissed, to be told it was all in her head, only to be taken seriously when she was accompanied by a boyfriend who confirmed that her sexual performance was, indeed, compromised. Putting her own trials into a broader historical, sociocultural, and political context, Norman shows that women's bodies have long been the battleground of a never-ending war for power, control, medical knowledge, and truth. It's time to refute the belief that being a woman is a preexisting condition"--,Provided by publisher.

"As patients, we're asked to rate our pain on a scale of one to ten. Yet as any woman who has experienced illness, chronic pain, endometriosis, or childbirth can attest, even if you report a level ten, you'll have to fight hard to have your pain taken seriously. In the fall of 2010, Abby Norman went from a healthy, ambitious college sophomore to an emaciated, wandering girl. Her strong dancer's body dropped forty pounds and gray hairs began to sprout from her temples. For weeks she was repeatedly hospitalized in excruciating pain, but the doctors insisted it was a urinary tract infection and sent her home with antibiotics. Unable to get out of bed, much less attend class, Norman dropped out of school and embarked on what would become a years-long journey to discover what was wrong with her. Along the way she would come to recognize--and repeatedly battle--medicine's systemic gender bias, pushing for treatment and a diagnosis as doctors shrugged at her unusual symptoms. It wasn't until she took matters into her own hands--securing a job in the hospital and educating herself over lunchtime reading in the medical library--that she found an accurate self-diagnosis of endometriosis, one that she had to convince an open-minded doctor to confirm. Here, Norman describes what it was like to have her pain dismissed, to be told it was all in her head, only to be taken seriously when she was accompanied by a boyfriend who confirmed that her sexual performance was, indeed, compromised. Through it all, Norman has become a patient activist, speaking out on behalf of female patients everywhere, and sharing her experiences wherever she can. Her story is a powerful and disturbing reminder of how far we have to go before healthcare can live up to its dictum to "do no harm.""--,Provided by publisher.