Georgiann Davis – författare

Winner, 2017 Sex and Gender Distinguished Book Award, presented by the American Sociological AssociationWinner, 2016 Donald Light Award for the Applied or Public Practice of Medical Sociology, presented by the American Sociological Association A personal, compelling perspective on how medical diagnoses can profoundly hurt, or help, the lived experiences of entire communitiesWhen sociologist Georgiann Davis was a teenager, her doctors discovered that she possessed XY chromosomes, marking her as intersex. Rather than share this information with her, they withheld the diagnosis in order to "protect" the development of her gender identity; it was years before Davis would see her own medical records as an adult and learn the truth. Davis' experience is not unusual. Many intersex people feel isolated from one another and violated by medical practices that support conventional notions of the male/female sex binary which have historically led to secrecy and shame about being intersex. Yet, the rise of intersex activism and visibility in the US has called into question the practice of classifying intersex as an abnormality, rather than as a mere biological variation. This shift in thinking has the potential to transform entrenched intersex medical treatment.In Contesting Intersex, Davis draws on interviews with intersex people, their parents, and medical experts to explore the oft-questioned views on intersex in medical and activist communities, as well as the evolution of thought in regards to intersex visibility and transparency. She finds that framing intersex as an abnormality is harmful and can alter the course of one's life. In fact, controversy over this framing continues, as intersex has been renamed a 'disorder of sex development' throughout medicine. This happened, she suggests, as a means for doctors to reassert their authority over the intersex body in the face of increasing intersex activism in the 1990s and feminist critiques of intersex medical treatment. Davis argues the renaming of 'intersex' as a 'disorder of sex development' is strong evidence that the intersex diagnosis is dubious. Within the intersex community, though, disorder of sex development terminology is hotly disputed; some prefer not to use a term which pathologizes their bodies, while others prefer to think of intersex in scientific terms. Although terminology is currently a source of tension within the movement, Davis hopes intersex activists and their allies can come together to improve the lives of intersex people, their families, and future generations. However, for this to happen, the intersex diagnosis, as well as sex, gender, and sexuality, needs to be understood as socially constructed phenomena. A personal journey into medical and social activism, Contesting Intersex presents a unique perspective on how medical diagnoses can affect lives profoundly.Ask us about setting up a Skype-in with the author for your classWatch Georgiann Davis in National Geographic's Gender Revolution documentary with Katie Couric

An unforgettable journey from seventh-grade dropout to celebrated professor Her family was white, but not the right kind of white. They were five star white trash. They borrowed money and tried to buy class.In this unflinching response to JD Vance's Hillbilly Elegy, Georgiann Davis guides us through her extraordinary life, from weighing almost 300 pounds by fifth grade, to dropping out of school in the seventh and on to selling weed out of her "monkey shit green" Plymouth Neon. A tall, fat girl who only wore boy's clothing, she grew up with a turbulent family outside of Chicago: the larger-than-life mother who looked like Farah Fawcett, the father who understood cars better than children, the brother whose drug use went unchecked, and the Greek grandparents who could only love her from afar. Then there was the shocking medical secret kept from her–one that upended everything she thought she knew about herself, gender, and the human body. With unflinching candor and dark humor, Davis tells her 'stranger-than-fiction' life story in a brave voice that will have readers rooting for her. As Davis chronicles her surprising journey from middle-school dropout to professor, she reveals how whiteness colored her family's struggles. She connects her personal experiences of medical abuse, fatphobia, and fear of the intersex body with incisive critiques of whiteness, the opioid crisis, and gendered and queer oppression. Faced with unimaginable setbacks – identity theft, home eviction, medical trauma, and family betrayal – Davis relentlessly pursued education. It was this quest that transformed her life, giving her the tools to tell her own story. The result is a deeply moving memoir which complicates our understanding of upward mobility and familial love.

Winner, 2017 Sex and Gender Distinguished Book Award, presented by the American Sociological AssociationWinner, 2016 Donald Light Award for the Applied or Public Practice of Medical Sociology, presented by the American Sociological Association A personal, compelling perspective on how medical diagnoses can profoundly hurt, or help, the lived experiences of entire communitiesWhen sociologist Georgiann Davis was a teenager, her doctors discovered that she possessed XY chromosomes, marking her as intersex. Rather than share this information with her, they withheld the diagnosis in order to "protect" the development of her gender identity; it was years before Davis would see her own medical records as an adult and learn the truth. Davis' experience is not unusual. Many intersex people feel isolated from one another and violated by medical practices that support conventional notions of the male/female sex binary which have historically led to secrecy and shame about being intersex. Yet, the rise of intersex activism and visibility in the US has called into question the practice of classifying intersex as an abnormality, rather than as a mere biological variation. This shift in thinking has the potential to transform entrenched intersex medical treatment.In Contesting Intersex, Davis draws on interviews with intersex people, their parents, and medical experts to explore the oft-questioned views on intersex in medical and activist communities, as well as the evolution of thought in regards to intersex visibility and transparency. She finds that framing intersex as an abnormality is harmful and can alter the course of one's life. In fact, controversy over this framing continues, as intersex has been renamed a 'disorder of sex development' throughout medicine. This happened, she suggests, as a means for doctors to reassert their authority over the intersex body in the face of increasing intersex activism in the 1990s and feminist critiques of intersex medical treatment. Davis argues the renaming of 'intersex' as a 'disorder of sex development' is strong evidence that the intersex diagnosis is dubious. Within the intersex community, though, disorder of sex development terminology is hotly disputed; some prefer not to use a term which pathologizes their bodies, while others prefer to think of intersex in scientific terms. Although terminology is currently a source of tension within the movement, Davis hopes intersex activists and their allies can come together to improve the lives of intersex people, their families, and future generations. However, for this to happen, the intersex diagnosis, as well as sex, gender, and sexuality, needs to be understood as socially constructed phenomena. A personal journey into medical and social activism, Contesting Intersex presents a unique perspective on how medical diagnoses can affect lives profoundly.Ask us about setting up a Skype-in with the author for your classWatch Georgiann Davis in National Geographic's Gender Revolution documentary with Katie Couric