Kimberly Zieselman | |
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Nationality | American |
Occupations |
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Known for | Intersex advocacy, executive director of interACT |
Website | xoxykz |
Kimberly Zieselman is an attorney, human rights advocate, author, and intersex woman, [1] with androgen insensitivity syndrome. [2] She currently serves as executive director of interACT (formerly Advocates for Informed Choice), [3] and is a signatory of the Yogyakarta Principles plus 10. In 2020, her memoir XOXY was published. [4]
Zieselman has described how, at age 15 and because she hadn't menstruated, she was referred to a reproductive oncologist at Massachusetts General Hospital, [5] a teaching hospital, and told that her ovaries and uterus needed to be removed to eliminate a risk of cancer. [6] [5] She had surgery at age 16, requiring a subsequent dependence on hormone replacement therapy. Neither Zieselman nor her parents were told the truth about her diagnosis, that she had androgen insensitivity syndrome, XY sex chromosomes, and internal testes. [6] [2]
Zieselman discovered her medical records at age 41, [2] including a statement that she and her parents had consented to surgery after full disclosure of a diagnosis. She described being informed she was having "a hysterectomy to remove partially developed female reproductive organs that might become cancerous in the future". [7] Discovery was disorientating, challenging her identity and that of her husband. [2] Zieselman has also described how "I felt free when I found out". [8]
Zieselman trained as a lawyer, and worked in the field of family law and assisted reproductive technology. [2]
In 2009, Zieselman discovered the peer support group AIS-DSD Support Group, and she later became a member of the board. [6] Zieselman is now executive director of interACT, an organization that promotes the rights of intersex youth, including through law and policy, development of youth leadership, and media work. [9]
The main goal of interACT is to end medically unnecessary surgeries on intersex children. Zieselman describes how intersex children just have a different type of body, and genital surgeries are not medical or social emergencies. [10] Zieselman describes how shame and secrecy, [10] and medically unnecessary surgeries on intersex infants causes devastating physical and psychological harm, [11] but they take place for sociological reasons. [10] [12] She calls for a moratorium on surgeries until children are old enough to choose for themselves, with parents given a "full spectrum of choices". [10]
Zieselman is quoted by the United Nations Human Rights Office in New York stating:
Doctors often claim there's a "silent majority" of intersex people satisfied with the way they were treated as young patients. I used to be part of that "silent majority" - but I certainly wasn't happy. Doctors draw this false conclusion because most of their young patients haven't returned as adults to complain. But their silence is just as likely to be caused by stigma and shame. [13]
Zieselman has described how the LGBT community has helped open doors, but how intersex rights are broader: "at its core this is a children's rights issue. It is also about health and reproductive rights, because these operations can lead to infertility". [10] She has described the MTV series Faking It as ground-breaking, [14] and the public disclosure by model Hanne Gaby Odiele of their intersex trait as a tipping point for the intersex movement. [15]
Zieselman is a signatory of the Yogyakarta Principles plus 10, on the application of international human rights law in relation to sexual orientation, gender identity, gender expression and sex characteristics. [16]
In 2020, her memoir XOXY was published. Chicago Review of Books described the memoir as an "impressive introduction to the powerhouse that is Kimberly M. Zieselman" that "carries the weight of what it means to be a first", showing "both the complexity and the ordinariness of intersex experiences". [4] Los Angeles Review of Books described the book as a "gripping journey she takes readers on as she slowly unravels the truth of her identity as an intersex woman", "written with the sharp, unflinching and often hilarous prose of a woman on a mission to be her authentic self". [7] In discussion with the Los Angeles Review of Books, Zieselman describes the memoir as about empowerment. [7]
The book received the Stonewall Honor Books in Non-Fiction Award in 2021. [17]
Selected publications include:
Zieselman is married to Steven. They are parents of adopted twin girls. [2]
In law, sex characteristic refers to an attribute defined for the purposes of protecting individuals from discrimination due to their sexual features. The attribute of sex characteristics was first defined in national law in Malta in 2015. The legal term has since been adopted by United Nations, European, and Asia-Pacific institutions, and in a 2017 update to the Yogyakarta Principles on the application of international human rights law in relation to sexual orientation, gender identity, gender expression and sex characteristics.
Disorders of sex development (DSDs), also known as differences in sex development or variations in sex characteristics (VSC), are congenital conditions affecting the reproductive system, in which development of chromosomal, gonadal, or anatomical sex is atypical. DSDs is a clinical term used in some medical settings for what are otherwise referred to as intersex traits. The term was first introduced in 2006 and has not been without controversy.
Hanne Gaby Odiele is a Belgian model.
The Yogyakarta Principles is a document about human rights in the areas of sexual orientation and gender identity that was published as the outcome of an international meeting of human rights groups in Yogyakarta, Indonesia, in November 2006. The principles were supplemented and expanded in 2017 to include new grounds of gender expression and sex characteristics and a number of new principles. However, the Principles have never been accepted by the United Nations (UN) and the attempt to make gender identity and sexual orientation new categories of non-discrimination has been repeatedly rejected by the General Assembly, the UN Human Rights Council and other UN bodies.
Advocates for Informed Choice, dba interACT or interACT Advocates for Intersex Youth, is a 501(c)(3) nonprofit organization advocating for the legal and human rights of children with intersex traits. The organization was founded in 2006 and formally incorporated on April 12, 2010.
Mauro Cabral Grinspan, also known as Mauro Cabral, is an Argentinian intersex and trans activist, who serves as the Senior Officer for Gender Justice and Equity at the Global Philanthropy Project. Before that, he was the Executive Director of GATE. His work - as a signatory of the Yogyakarta Principles - focuses on the reform of medical protocols and law reform. In July 2015, Cabral received the inaugural Bob Hepple Equality Award.
Morgan Carpenter is a bioethicist, intersex activist and researcher. In 2013, he created an intersex flag, and became president of Intersex Human Rights Australia. He is now executive director. Following enactment of legislative protections for people with innate variations of sex characteristics in the Australian Capital Territory, Carpenter is a member of the Variations in Sex Characteristics Restricted Medical Treatment Assessment Board.
Intersex people and themes appear in numerous books, comics and magazines. Intersex, in humans and other animals, describes variations in sex characteristics including chromosomes, gonads, sex hormones, or genitals that, according to the UN Office of the High Commissioner for Human Rights, "do not fit typical binary notions of male or female bodies". Morgan Holmes describes common representations of intersex people as monsters or ciphers for discussions about sex and gender, while Phoebe Hart contrasts a small number of examples of well-rounded characters with the creation of "objects of ridicule".
Intersex people are born with sex characteristics, such as chromosomes, gonads, or genitals, that, according to the UN Office of the High Commissioner for Human Rights, "do not fit typical binary notions of male or female bodies."
Sean Saifa Wall is an African-American researcher, and long-time advocate for intersex rights. He is a queer, transgender, and intersex man of color and former president of Interact Advocates for Intersex Youth. He approaches his work to end intersex oppression through an intersectional lens.
Intersex people are born with sex characteristics, such as chromosomes, gonads, or genitals that, according to the UN Office of the High Commissioner for Human Rights, "do not fit typical binary notions of male or female bodies". "Because their bodies are seen as different, intersex children and adults are often stigmatized and subjected to multiple human rights violations".
Pidgeon Pagonis is an American intersex activist, writer, artist, and consultant. They are an advocate for intersex human rights and against nonconsensual intersex medical interventions.
The following is a timeline of intersex history.
Intersex people in the United States have some of the same rights as other people, but with significant gaps, particularly in protection from non-consensual cosmetic medical interventions and violence, and protection from discrimination. Actions by intersex civil society organizations aim to eliminate harmful practices, promote social acceptance, and equality. In recent years, intersex activists have also secured some forms of legal recognition. Since April 11, 2022 US Passports give the sex/gender options of male, female and X by self determination.
Intersex people in the United Kingdom face significant gaps in legal protections, particularly in protection from non-consensual medical interventions, and protection from discrimination. Actions by intersex civil society organisations aim to eliminate unnecessary medical interventions and harmful practices, promote social acceptance, and equality in line with Council of Europe and United Nations demands. Intersex civil society organisations campaign for greater social acceptance, understanding of issues of bodily autonomy, and recognition of the human rights of intersex people.
Intersex people are born with sex characteristics, such as chromosomes, gonads, hormones, or genitals that, according to the UN Office of the High Commissioner for Human Rights, "do not fit the typical definitions for male or female bodies". Such variations may involve genital ambiguity, and combinations of chromosomal genotype and sexual phenotype other than XY-male and XX-female.
In Mexico there are no explicit rights reserved to intersex persons, no protections from non-consensual cosmetic medical interventions on intersex children and no legislative protection from discrimination. Intersex persons may have difficulties in obtaining necessary health care.
Intersex people in Argentina have no recognition of their rights to physical integrity and bodily autonomy, and no specific protections from discrimination on the basis of sex characteristics. Cases also exist of children being denied access to birth certificates without their parents consenting to medical interventions. The National Institute Against Discrimination, Xenophobia and Racism and civil society organizations such as Justicia Intersex have called for the prohibition of unnecessary medical interventions and access to redress.
Irene Kuzemko, also transcribed from Ukrainian and Russian as Irina Kuzemko, is a Russian-Ukrainian intersex woman and intersex human rights activist. She co-founded Intersex Russia in 2017, is a youth member of interACT, and an executive board member of OII Europe. She have started her human rights advocacy as a member of Association of the Russian Speaking Intersex.