Small Ela Luk | |
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Born | Luk yiu-hung 1966 (age 58–59) |
Nationality | Chinese |
Education | Chinese University of Hong Kong |
Known for | Intersex activist and doctor of Chinese medicine |
Small Luk is an intersex human rights activist and the first intersex person to openly acknowledge her biological sex characteristics in Hong Kong. [1] She was born with partial androgen insensitivity syndrome (PAIS). [2] Luk lived as a male for 36 years, and now identifies and lives as a woman, [2] after changing her sex characteristics from intersex to female through gender-affirming surgery, upon doctors' advice to undergo the surgery because her type of PAIS would most likely have caused cancer. [2]
She founded the organization "Beyond Boundaries – Knowing and Concerns Intersex" [3] in 2011, which is concerned with, and strives for, the rights of intersex people.
Small Luk was the first child of her family. When Luk was born, the doctor found that she was intersex, with organs resembling testicles and a penis. Luk was deemed male and underwent more than 20 operations between the ages of 8 and 13 to construct a urethra – the duct that conducts urine from the bladder. When she was 12, the surgery failed. Luk found the surgery too unbearable and attempted suicide several times. News records state that Luk [4] was the only surviving person among the seven people who were operated on as children at Hong Kong's Kwong Wah Hospital in the 1970s to "fix" their anatomies. After surgery at the age of 13, Luk refused further genital reconstruction.
During adolescence, Luk developed breasts, suffered menstrual cramps, and saw blood in her urine. Doctors explained that her body did not respond to androgen and found undeveloped uterus and vagina in her body. Luk eventually underwent surgery to remove her male genitalia, and now lives as a woman. [4] [5]
Apart from the surgical pain, Luk also suffered from bullying. Luk was at the receiving end of discrimination from classmates and teachers. [2]
Despite the past, Luk has completed her education, earning degrees in social work and traditional Chinese medicine, as well as a master's in gender studies at Chinese University of Hong Kong. She now runs a holistic treatment clinic in Hong Kong. [6]
Small Luk founded the organization "Beyond Boundaries– Knowing and Concerns Intersex" [1] [3] in 2011, and it has been working to spread awareness about intersex people. The aims of the organization are to raise public awareness about intersex people and promote the rights of intersex people, including ending forced genital normalising surgery and conversion therapies. Luk urges the Hong Kong government to educate the public about intersex conditions, extend anti-discrimination laws to cover intersex people and stop foisting surgery on intersex children without consulting them. [7] Luk has been invited to various international and local events, [8] [9] including the United Nations meeting in Thailand, [4] [10] to speak on the issue of intersex people and their rights. [1] [11] In 2018, she participated in the forum where NGO Intersex Asia was founded. [12]
The history of intersex surgery is intertwined with the development of the specialities of pediatric surgery, pediatric urology, and pediatric endocrinology, with our increasingly refined understanding of sexual differentiation, with the development of political advocacy groups united by a human qualified analysis, and in the last decade by doubts as to efficacy, and controversy over when and even whether some procedures should be performed.
The Organisation Intersex International (OII) is a global advocacy and support group for people with intersex traits. According to Milton Diamond, it is the world's largest organization of intersex persons. A decentralised network, OII was founded in 2003 by Curtis Hinkle and Sarita Vincent Guillot. Upon Hinkle's retirement, American intersex activist Hida Viloria served as Chairperson/President elect from April 2011 through November 2017, when they resigned in order to focus on OII's American affiliate, OII-USA's transition into the independent American non-profit, the Intersex Campaign for Equality.
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.
Intersex Human Rights Australia (IHRA) is a voluntary organisation for intersex people that promotes the human rights and bodily autonomy of intersex people in Australia, and provides education and information services. Established in 2009 and incorporated as a charitable company in 2010, it was formerly known as Organisation Intersex International Australia, or OII Australia. It is recognised as a Public Benevolent Institution.
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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."
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".
Intersex rights in Australia are protections and rights afforded to intersex people through statutes, regulations, and international human rights treaties, including through the Sex Discrimination Act 1984 (Cth) which makes it unlawful to discriminate against a person based upon that person's intersex status in contexts such as work, education, provision of services, and accommodation.
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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 rights in China including the People's Republic of China, the Hong Kong Special Administrative Region, etc., are protections and rights afforded to intersex people through legislation and regulation. Obligations also arise in United Nations member states that sign international human rights treaties, such as the People's Republic of China. Intersex people in China suffer discrimination. Issues include both lack of access to health care and coercive genital surgeries.
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.
Intersex people in Taiwan currently face some gaps in legal protection of their rights to physical integrity and bodily autonomy, and in protection from discrimination on the basis of sex characteristics, with significant improvements in recent years.
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.