Abbreviation | IHRA |
---|---|
Formation | 2009 |
Type | NGO |
Purpose | Intersex human rights, education and peer support |
Region served | Australia |
Co-executive directors | Tony Briffa and Morgan Carpenter |
Website | ihra.org.au |
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. [1] [2] Established in 2009 and incorporated as a charitable company in 2010, [3] it was formerly known as Organisation Intersex International Australia, or OII Australia. [4] It is recognised as a Public Benevolent Institution. [3]
The institution was founded in 2009 and established as a company in 2010. [3] Founding president Gina Wilson stepped down on 1 September 2013. [2] [5]
The current co-executive directors of IHRA are Morgan Carpenter, previously president, [6] [7] and Tony Briffa, known as the first publicly intersex mayor and previously vice-president. [8] [9] [10] [11] Tony Briffa is also the Vice-President of the Androgen Insensitivity Syndrome Support Group Australia.
Intersex Human Rights Australia campaigns in favour of personal autonomy in medical interventions affecting intersex people, including an end to cosmetic or "normalising" surgeries on intersex infants. [12] [13] [14] [15] [16] [17] In late 2012, the Senate's Community Affairs References Committee established an inquiry into the involuntary or coerced sterilisation of people with disabilities. In February 2013, intersex was added as an additional term of reference. [18] The Committee published a joint, cross-party report on 25 October 2013, making 15 recommendations. The conclusions of the inquiry supported much of the case and recommendations made by IHRA: [19] [6]
3.109 ... As OII commented, normalisation surgery is more than physical reconstruction. The surgery is intended to deconstruct an intersex physiology and, in turn, construct an identity that conforms with stereotypical male and female gender categories... 3.129 ... The proposals put forward by Organisation Intersex International have merit, and are consistent with the committee's conclusions. The committee believes that a protocol covering 'normalising' surgery should be developed, and then adhered to in all cases of intersex children. Such a guideline should be consistent with Organisational Intersex International's recommendations
In May 2019, IHRA published a multilingual joint statement signed by more than 50 intersex-led organizations condemning the introduction of "disorders of sex development" language into the International Classification of Diseases, stating that this causes "harm" and facilitates human rights violations, calling on the World Health Organization to publish clear policy to ensure that intersex medical interventions are "fully compatible with human rights norms". [20] [21] [22] [23] [24]
The institution also engages directly with clinicians and biologists. While opposing use of terminology that it describes as pathologising, such as "Disorders of Sex Development", [25] Carpenter is nevertheless named as a reviewer for a "DSD Genetics" website funded by the National Health and Medical Research Council Australia. [26]
In a submission to the UN Committee Against Torture in 2016, the organisation submitted that Australian governments recognise the dignity and rights of LGBTI people, but at the same time, "harmful practices" on intersex children continue. [27]
In March 2017, representatives of IHRA participated in an Australian and Aotearoa/New Zealand consensus "Darlington Statement" by intersex community organisations and others. [28] The statement calls for legal reform, including the criminalization of deferrable intersex medical interventions on children, an end to legal classification of sex, and improved access to peer support. [28] [29] [30] [31] [32]
In July 2013, the Commonwealth announced that it was removing sex or gender terms from item codes for Medicare procedures, [33] following input from IHRA. [34] IHRA noted that the changes do not ensure full access to the Pharmaceutical Benefits Scheme (PBS). [35]
In late 2012, the Australian Governments' proposed Human Rights and Anti-Discrimination Bill included intersex as a "gender identity". This was criticised by IHRA on the basis that intersex people needed protection, but biological differences should not come within the definition. [36] Writing in the Equal Rights Trust journal Equal Rights Review, Gina Wilson wrote, "Legislators initially did not have a clear understanding of what intersex was, but having given evidence to Senate Committees and spoken with legislators individually we are hopeful that intersex will be a protected attribute under the Bill." [1] [37] [38] [39]
On 25 June 2013, the Sex Discrimination Amendment (Sexual Orientation, Gender Identity and Intersex Status) Act passed with cross-party support, [40] and became law on 1 August 2013. This was the first time "intersex status" had been a protected attribute under Australian discrimination legislation. [41] [42]
The organisation has stated that "while sex or gender markers are still required", it supports binary, non-binary and multiple gender classifications for adults, but only binary classifications for infants and children, fearing stigmatisation and the potential impact on sex assignment processes for infants. [43] [44] [45] [46] The organisation cautiously acknowledged an Australian Capital Territory Bill to modify the Territory's birth registrations process to create a third sex category for infants and children, stating, "neither of the two national intersex organisations had been engaged in talks before the bill was presented in the Assembly." [47] [48] In 2017, the organisation reported that no children had been assigned to such a category, viewing this as a vindication of the argument that such classifications exacerbate parental fears. [49]
In March 2017, an Australian and Aotearoa/New Zealand community statement called for an end to legal classification of sex, stating that legal third classifications, like binary classifications, were based on structural violence and failed to respect diversity and a "right to self-determination". [28] [29]
Citing cases where marriages have been annulled, [50] [51] and where marriage prospects are stated as a rationale for early medical interventions, [52] IHRA campaigned for marriage rights regardless of sex characteristics. [28] The institution expressed concern at the marriage implications of constructions of intersex as a third sex. [52] In 2017 the Marriage Amendment (Definition and Religious Freedoms) Bill 2017 [53] specifically refers to '2 people' rather than 'same-sex' with respect to the definition of marriage. [54]
Intersex Human Rights Australia is represented at numerous international events, including the "first United Nations Human Rights Council side event on intersex issues" in March 2014, alongside Mauro Cabral and representatives of Intersex UK and Zwischengeschlecht. [55]
The Intersex flag was created in July 2013 by Morgan Carpenter of Intersex Human Rights Australia (then known as Organisation Intersex International Australia) to be a flag "that is not derivative, but is yet firmly grounded in meaning". The circle is described as "unbroken and unornamented, symbolising wholeness and completeness, and our potentialities. We are still fighting for bodily autonomy and genital integrity, and this symbolises the right to be who and how we want to be." [56]
The organisation was nominated for a 2013 Community Organisation "Honour" Award [57] [58] for its work on anti-discrimination legislation. Founding former president Gina Wilson was a finalist for the Australian Human Rights Commission Community Individual Award in 2013, following her retirement, for her work on discrimination protections. [59] [60] [61]
Intersex Human Rights Australia is a national affiliate of Organisation Intersex International, a member of the National LGBTI Health Alliance and the International Lesbian, Gay, Bisexual, Trans and Intersex Association.
Lesbian, gay, bisexual, transgender and queer (LGBTQ) rights in Australia rank among the highest in the world; having significantly advanced over the latter half of the 20th century and early 21st century. Opinion polls and the Australian Marriage Law Postal Survey indicate widespread popular support for same-sex marriage within the nation. Australia in 2018, in fact was the last of the Five Eyes set of countries - that consisted of namely Canada (2005), New Zealand (2013), United Kingdom (2014) and the United States (2015) to legalize same-sex marriage. A 2013 Pew Research poll found that 79% of Australians agreed that homosexuality should be accepted by society, making it the fifth-most supportive country surveyed in the world. With its long history of LGBTQ activism and annual Gay and Lesbian Mardi Gras festival, Sydney has been named one of the most gay-friendly cities in the world.
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.
Intersex Awareness Day is an internationally observed awareness day each October 26, designed to highlight human rights issues faced by intersex people.
Tony Briffa is a Maltese-Australian politician who is notable for being the world's first known intersex and non-binary mayor and public officeholder.
LGBTIQ+ Health Australia is a peak health organisation for LGBT and intersex organisations in Australia. A not-for-profit company, it was established in August 2007.
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.
The International Intersex Forum is an annual event organised, then later supported, by the ILGA and ILGA-Europe that and organisations from multiple regions of the world, and it is believed to be the first and only such intersex event.
Gina Wilson is an Australian intersex human rights activist. She was the founding president of Intersex Human Rights Australia.
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 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 Peer Support Australia (IPSA), also known as the Androgen Insensitivity Syndrome Support Group Australia, is possibly the oldest known intersex organization, established in 1985. It provides peer and family support, information and advocacy. The group is run by volunteers, for people with intersex variations such as androgen insensitivity syndrome. It changed name from the Androgen Insensitivity Syndrome Support Group Australia (AISSGA) to Intersex Peer Support Australia in 2019.
Intersex people are born with sex characteristics, such as chromosomes, gonads, or genitals that, according to the United Nations 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".
Bonnie Hart is an Australian artist, film maker, and intersex human rights activist, born with androgen insensitivity syndrome and president of Intersex Peer Support Australia. Hart performs nationally and internationally, and speaks on intersex issues nationally and internationally. In 2016, Australia's Gay News Network included her in their "25 LGBTI people to watch in 2017".
Intersex people are born with sex characteristics 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 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, 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 inclusion as distracting from intersex-specific issues such as involuntary medical interventions.
Intersex rights in New Zealand are protections and rights afforded to intersex people. Protection from discrimination is implied by the Human Rights Act and the Bill of Rights Act, but remains untested. The New Zealand Human Rights Commission states that there has seemingly been a "lack of political will to address issues involved in current practices of genital normalisation on intersex children".
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.
The Malta declaration is the statement of the Third International Intersex Forum, which took place in Valletta, Malta, in 2013. The event was supported by the ILGA and ILGA-Europe and brought together 34 people representing 30 organisations from multiple regions of the world.
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.