Fixing Sex

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Fixing Sex: Intersex, Medical Authority, and Lived Experience
Fixing Sex, Karkazis (cover).jpg
Author Katrina Karkazis
Country United States
Language English
Genre Medicine and health sciences
Publisher Duke University Press
Publication date
November 14, 2009
Media type Print (Paperback and Hardback) and E-book
Pages 384
ISBN 978-0822343189

Fixing Sex: Intersex, Medical Authority, and Lived Experience by Stanford anthropologist and bioethicist Katrina Karkazis was published in 2008. Described as "thoughtful", "meticulous", and an "authoritative treatise on intersex",[1] the book examines the perspectives of intersex people, their families, and clinicians to offer compassionate look at the treatment of people born with atypical sex characteristics.

Synopsis[edit]

In a scholarly work, Karkazis draws heavily on interviews with intersex adults, parents, and physicians to explore how intersex is understood and treated. In part 1, she reviews the history of treatment for intersex traits, highlighting the work of John Money and the introduction of the, then new, terms "gender", "gender role" and "gender identity". She explores the events following publication of Milton Diamond's study of the David Reimer or "John/Joan" case, and the ways in which public opinion impacted on medical treatment. In part 2, Karkazis presents an analysis of current medical approaches to intersex, and the risks involved, in the wake of a 2006 "consensus statement on the management of intersex disorders".[2] She also reviews the methods utilised to assign a sex of rearing to intersex infants, such as genitals and penis size, chromosomes, fertility, "sexing of the brain", and parental wishes; these impact upon determination whether or not to proceed with early genital surgery.[3] Part 3 interviews parents of children with complete androgen insensitivity syndrome and congenital adrenal hyperplasia, and adults with intersex experiences. Part 3 also looks at activism by intersex organizations.

Reception[edit]

The book has been well received by both clinicians and intersex groups. Gary Berkovitz, writing in the New England Journal of Medicine states that Karkazis's analysis is fair, compelling, and eloquent; "Current consensus guidelines recommend early separation of the vagina and urethra for female subjects with abnormalities in the formation of the sex organs... Karkazis presents a compelling argument for the deferment of subsequent surgery until the patient is able to decide."[2] Elizabeth Reis, reviewing the book in American Journal of Bioethics, states that the book identifies risk of incontinence, fistulas, scarring and lack of physical sensation arising from surgical intervention, and the psychological harm caused by the knowledge that "one's genitals are 'wrong,' requiring constant medical scrutiny and 'fixing'. It "masterfully examines the concerns and fears of all those with a stake in the intersex debate: physicians, parents, intersex adults, and activists. . . . Karkazis’s honest, multi-pronged approach poses critical questions."[4] Mijeon in American Journal of Human Genetics writes that the "conclusion is quite fitting", "the history of thinking about the body ... can be highly politicized and controversial".[3] Kenneth Copeland MD, former president of the Lawson Wilkins Pediatric Endocrine Society describes the book as "Masterfully balancing all aspects of one of the most polarizing, contentious topics in medicine... the most recent authoritative treatise on intersex."[1]

Gayle Rubin describes the book as "meticulous, sensitive, and brilliantly executed".[1] Arlene Baratz MD, (Accord Alliance) describes the book as "a velvet-gloved punch to the gut", "astonishing, a tale told straight from the mouths of affected adults, parents, and physicians in tender and lyrical prose."[5] Intersex community organization Organisation Intersex International Australia regards the book as "approachable," "compelling and recommended reading".[6]

The book was referenced by Involuntary or coerced sterilisation of intersex people in Australia, a 2013 report of a committee of the Senate of Australia in 2013.[7]

Awards and recognition[edit]

The book was nominated for the Margaret Mead Award, 2010, and a finalist for the Lambda Literary Award, 2009.[1]

References[edit]

  1. ^ a b c d Katrina Karkazis, PhD, MPH, Stanford University School of Medicine Center for Biomedical Ethics, 2013
  2. ^ a b Fixing Sex: Intersex, Medical Authority, and Lived Experience, New England Journal of Medicine, April 16, 2009. DOI: 10.1056/NEJMbkrev0805101.
  3. ^ a b Fixing Sex: Intersex, Medical Authority, and Lived Experience, Claude Migeon in American Journal of Human Genetics, June 12, 2009; 84(6): 718-727. DOI: 10.1016/j.ajhg.2009.04.022.
  4. ^ Review of Katrina Karkazis, Fixing Sex: Intersex, Medical Authority, and Lived Experience, Elizabeth Reis in American Journal of Bioethics, Volume 9, issue 6, 2009. DOI:10.1080/15265160902790617
  5. ^ Fixing Sex, Kalahari.com
  6. ^ Katrina Karkazis, “Fixing Sex” (recommended reading), Organisation Intersex International Australia, 26 January 2010
  7. ^ Involuntary or coerced sterilisation of intersex people in Australia, Community Affairs Committee, Senate of Australia, October 2013.

External links[edit]