LGBTIQ People In Australia
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LGBTIQ People In Australia
Intersex people are born with sex characteristics (such as genitals, gonads, and chromosome patterns) that "do not fit the typical definitions for male or female bodies". They are substantially more likely to identify as lesbian, gay, bisexual, or transgender (LGBT) than endosex people. According to a study done in Australia of Australian citizens with intersex conditions, participants labeled 'heterosexual' as the most popular single label (selected at 48%) with the rest being scattered among various other labels. According to another study, an estimated 8.5% to 20% experiencing gender dysphoria. Although many intersex people are heterosexual and cisgender, and not all of them identify as LGBTQ+, this overlap and "shared experiences of harm arising from dominant societal sex and gender norms" has led to intersex people often being included under the LGBT umbrella, with the acronym sometimes expanded to LGBTI. Some intersex activists and organisations have criticised this inclusio ...
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Intersex
Intersex people are those born with any of several sex characteristics, including chromosome patterns, gonads, or genitals that, according to the Office of the United Nations High Commissioner for Human Rights, "do not fit typical binary notions of male or female bodies". Sex assignment at birth usually aligns with a child's external genitalia. The number of births with ambiguous genitals is in the range of 1:4,500–1:2,000 (0.02%–0.05%). Other conditions involve the development of atypical chromosomes, gonads, or hormones. The portion of the population that is intersex has been reported differently depending on which definition of intersex is used and which conditions are included. Estimates range from 0.018% (one in 5,500 births) to 1.7%. The difference centers on whether conditions in which chromosomal sex matches a phenotypic sex which is clearly identifiable as male or female, such as late onset congenital adrenal hyperplasia (1.5 percentage points) and Kline ...
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Intersex Civil Society Organizations
Intersex civil society organizations have existed since at least the mid-1980s. They include peer support groups and advocacy organizations active on health and medical issues, human rights, legal recognition, and peer and family support. Some groups, including the earliest, were open to people with specific intersex traits, while others are open to people with many different kinds of intersex traits. History Intersex peer support and advocacy organizations have existed since at least 1985, with the establishment of the Androgen Insensitivity Syndrome Support Group Australia in 1985. The Androgen Insensitivity Syndrome Support Group (UK) established in 1988. The Intersex Society of North America (ISNA) may have been one of the first intersex civil society organizations to have been open to people regardless of diagnosis; it was active from 1993 to 2008. In May 2019, more than 50 intersex-led organizations signed a multilingual joint statement condemning the introduction of "dis ...
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Anne Tamar-Mattis
Anne Tamar-Mattis is an American attorney, human rights advocate, and founder of interACT (formerly Advocates for Informed Choice). She currently serves as interACT's Legal Director. Career Tamar-Mattis spent six years as the Director of the National Youth Talkline at Lavender Youth Recreation & Information Center, a national peer-support line for LGBTQ youth. She became the first Program Director for the San Francisco LGBT Community Center in 2001. In 2003, she took a hiatus to attend law school and graduated from the University of California, Berkeley School of Law in 2006. Tamar-Mattis founded interACT with the support of fellowships from Equal Justice Works (2006) and Echoing Green (2008). She has been an adjunct professor at the University of California, Berkeley School of Law since 2008 where she teaches Sexual Orientation & the Law. Selected bibliography Tamar-Mattis' selected publications include: * * * * * * * * * * * Awards and recognition In 2010, Ann ...
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Alice Dreger
Alice Domurat Dreger () is an American historian, bioethicist, author, and former professor of clinical medical humanities and bioethics at the Feinberg School of Medicine, Northwestern University, in Chicago, Illinois. Dreger engages in academic work and activism in support of individuals born with atypical sex characteristics (intersex or disorders of sex development) and individuals born as conjoined twins. She challenges the perception that those with physical differences are somehow "broken" and need to be "fixed". She has opposed the use of "corrective" surgery on babies whose genitalia are considered "ambiguous". She has criticized the failure to follow such patients in later life and reported longer-term medical and psychological difficulties experienced by some of the people whose sex is arbitrarily assigned. She supported J. Michael Bailey in the face of controversy over his book '' The Man Who Would Be Queen''. In a 2008 article and in her 2015 book, '' Galileo's M ...
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Congenital Adrenal Hyperplasia
Congenital adrenal hyperplasia (CAH) is a group of Genetic disorder#Autosomal recessive, autosomal recessive disorders characterized by impaired cortisol synthesis. It results from the deficiency of one of the five enzymes required for the Biosynthesis, synthesis of cortisol in the adrenal cortex. Most of these disorders involve excessive or deficient production of hormones such as glucocorticoids, mineralocorticoids, or sex steroids, and can alter development of primary sex characteristic, primary or secondary sex characteristics in some affected infants, children, or adults. It is one of the most common autosomal recessive disorders in humans. Types CAH can occur in various forms. The clinical presentation of each form is different and depends to a large extent on the underlying enzyme defect, its precursor retention, and deficient products. Classical forms appear in infancy and nonclassical forms appear in late childhood. The presentation in patients with classic CAH can be fu ...
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Maria New
Maria Iandolo New (December 11, 1928 - July 26, 2024 ) was a professor of Pediatrics, Genomics and Genetics at Icahn School of Medicine at Mount Sinai in New York City. She was an expert in congenital adrenal hyperplasia (CAH), a genetic condition affecting the adrenal gland that can affect sexual development. Medical education New received her undergraduate degree in chemistry with a minor in Latin from Cornell University in Ithaca, New York, in 1950, and her M. D. from the Perelman School of Medicine at the University of Pennsylvania in Philadelphia, in 1954. She completed an internship in medicine at Bellevue Hospital in New York, followed by a residency in pediatrics at the New York Hospital. From 1957 to 1958 she studied renal functioning under a fellowship from the National Institutes of Health (NIH). She was a research pediatrician to the Diabetic Study Group of the Comprehensive Care Teaching Program at the New York Hospital-Cornell Medical Center from 1958 to 1961, and ...
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17β-Hydroxysteroid Dehydrogenase III Deficiency
17β-Hydroxysteroid dehydrogenase III deficiency is a rare autosomal recessive disorder of sexual development condition that is a cause of Disorders of sex development, 46,XY disorder of sex development (46,XY DSD). The impaired testosterone biosynthesis by 17β-hydroxysteroid dehydrogenase III (17β-HSD III), presents as atypical genitalia in affected males. Signs and symptoms 17-β-Hydroxysteroid dehydrogenase III deficiency is a cause of Disorders of sex development, 46,XY disorder of sex development (46,XY DSD) that presents in males with variable effects on genitalia which can be complete or predominantly female with a blind vaginal pouch. Testes are often found in the inguinal canal or in a bifid scrotum. Wolffian derivatives including the epididymides, vas deferens, seminal vesicles, and ejaculatory ducts are present. The autosomal recessive deficiency arises are a result of homozygous or compound heterozygous mutations in HSD17B3 gene which encodes the 17β-hydroxystero ...
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Partial Androgen Insensitivity Syndrome
Partial androgen insensitivity syndrome (PAIS) is a condition that results in the partial inability of the Eukaryote#Animal cell, cell to respond to androgens. It is an X linked recessive condition. The partial unresponsiveness of the cell to the presence of androgenic hormones impairs the Development of the reproductive system#External genitalia, masculinization of male genitalia in the developing fetus, as well as the development of male Secondary sex characteristics, secondary sexual characteristics at puberty, but does not significantly impair female genital or sexual development. As such, the insensitivity to androgens is clinically significant only when it occurs in individuals with a Y chromosome (or more specifically, an SRY, SRY gene). Clinical features include ambiguous genitalia at birth and primary amenhorrhoea with clitoromegaly with inguinal masses. Müllerian duct, Müllerian structures are not present in the individual. PAIS is one of three types of androgen insen ...
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Heino Meyer-Bahlburg
Heino F. L. Meyer-Bahlburg (born 1940) is a German-born psychologist best known for his work on biology of sexual orientation, gender identity, intersexuality, and HIV. Education and career Meyer-Bahlburg earned his Diplom from University of Hamburg in 1966 and his Dr. rer. nat. in Psychology from University of Düsseldorf in 1970. He took a position at State University of New York, Buffalo and at Children’s Hospital in Buffalo, New York in 1970. Since 1977 he has held appointments at New York State Psychiatric Institute and Columbia University where he has been Professor of Clinical Psychology since 1990. In 1978, he took a position at New York Presbyterian Hospital and has been a Full Professional Psychologist there since 1990. Since 1987, he has been affiliated with the HIV Center for Clinical and Behavioral Studies. Meyer-Bahlburg believes homosexuality may be an issue of brain chemistry.Kotulak, Ron (November 17, 2003). Homosexuality may be issue of brain chemistry. ''Ch ...
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Organisation Intersex International Australia
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,About OII Australia
, Organisation Intersex International Australia, 24 July 2013
it was formerly known as Organisation Intersex International Australia, or OII Australia. It is recognised as a Public Benevolent Institution.


History

The institution was founded in 2009 and established as a company in 2010. Founding president Gina Wilson stepped down on 1 September 2013.
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Intersex Rights In Australia
Intersex rights in Australia are protections and rights afforded to Intersex, 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. Discrimination on the ground of intersex status. Australia was the first country to conduct a parliamentary inquiry into involuntary or coerced medical interventions on intersex people. A 2016 Family Court of Australia, Family Court case authorising a gonadectomy and consequential surgery on a young child has attracted public commentary for disclosing those medical interventions, their rationales, and a prior clitorectomy and labiaplasty. In March 2017, Australian and Intersex rights in New Zealand, New Zealand community organizations issued a joint call for legal reform, including t ...
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