Intersex topics |
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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. [1] [2]
The declaration affirmed the existence of intersex people, and demanded an end to "discrimination against intersex people and to ensure the right of bodily integrity, physical autonomy and self-determination". For the first time, participants made a statement on birth registrations, in addition to other human rights issues: [3] [4] [5]
- To put an end to mutilating and 'normalising' practices such as genital surgeries, psychological and other medical treatments through legislative and other means. Intersex people must be empowered to make their own decisions affecting own bodily integrity, physical autonomy and self-determination.
- To put an end to preimplantation genetic diagnosis, pre-natal screening and treatment, and selective abortion of intersex foetuses.
- To put an end to infanticide and killings of intersex people.
- To put an end to non-consensual sterilisation of intersex people.
- To depathologise variations in sex characteristics in medical guidelines, protocols and classifications, such as the World Health Organization's International Classification of Diseases.
- To register intersex children as females or males, with the awareness that, like all people, they may grow up to identify with a different sex or gender.
- To ensure that sex or gender classifications are amendable through a simple administrative procedure at the request of the individuals concerned. All adults and capable minors should be able to choose between female (F), male (M), non-binary or multiple options. In the future, as with race or religion, sex or gender should not be a category on birth certificates or identification documents for anybody.
- To raise awareness around intersex issues and the rights of intersex people in society at large.
- To create and facilitate supportive, safe and celebratory environments for intersex people, their families and surroundings.
- To ensure that intersex people have the right to full information and access to their own medical records and history.
- To ensure that all professionals and healthcare providers that have a specific role to play in intersex people's wellbeing are adequately trained to provide quality services.
- To provide adequate acknowledgement of the suffering and injustice caused to intersex people in the past, and provide adequate redress, reparation, access to justice and the right to truth.
- To build intersex anti-discrimination legislation in addition to other grounds, and to ensure protection against intersectional discrimination.
- To ensure the provision of all human rights and citizenship rights to intersex people, including the right to marry and form a family.
- To ensure that intersex people are able to participate in competitive sport, at all levels, in accordance with their legal sex. Intersex athletes who have been humiliated or stripped of their titles should receive reparation and reinstatement.
- Recognition that medicalization and stigmatisation of intersex people result in significant trauma and mental health concerns.
- In view of ensuring the bodily integrity and well-being of intersex people, autonomous non-pathologising psycho-social and peer support be available to intersex people throughout their life (as self-required), as well as to parents and/or care providers.
The forum called on:
- International, regional and national human rights institutions to take on board, and provide visibility to intersex issues in their work.
- National governments to address the concerns raised by the Intersex Forum and draw adequate solutions in direct collaboration with intersex representatives and organisations.
- Media agencies and sources to ensure intersex people's right to privacy, dignity, accurate and ethical representation.
- Funders to engage with intersex organisations and support them in the struggle for visibility, increase their capacity, the building of knowledge and the affirmation of their human rights.
- Human rights organisations to contribute to build bridges with intersex organisations and build a basis for mutual support. This should be done in a spirit of collaboration and no-one should instrumentalise intersex issues as a means for other ends.
The Forum was organized by ILGA Europe's Silvan Agius and Ruth Baldacchino, and three intersex activists selected from an open call application process managed by ILGA Europe: Mauro Cabral, of Argentina, Mani Bruce Mitchell, of New Zealand, and Hida Viloria of Intersex Campaign for Equality. [6] Attending participants included Sean Saifa Wall and Pidgeon Pagonis for AIC (now interACT), [7] Morgan Carpenter and Tony Briffa from Organisation Intersex International Australia, [8] Intersex Austria [9] Holly Greenberry from Intersex UK, [10] [11] Miriam van der Have and Inge Intven of Nederlandse Netwerk Intersekse/DSD (NNID), [12] and representatives of Zwischengeschlecht, [13] and IVIM/OII Deutschland [14]
The declaration has been cited by numerous human rights institutions around the world, [15] including intersex human rights papers published by the Council of Europe's Commissioner for Human Rights, [16] and the Asia Pacific Forum of National Human Rights Institutions, [17] and by organizations allying themselves with the intersex human rights movement. [18]
In 2015, Malta adopted world-first legislation to protect intersex infants and children from non-consensual medical interventions. [19] [20] [21] [22]
In March 2017, the Malta declaration was acknowledged by a consensus "Darlington Statement", published by Australian and New Zealand intersex community organizations and others. [23] 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. [23] [24] [25] [26] [27]
The International Lesbian, Gay, Bisexual, Trans and Intersex Association (ILGA) is a LGBTQ+ rights organization.
ILGA-Europe is the European region of the International Lesbian, Gay, Bisexual, Trans and Intersex Association. It is an advocacy group promoting the interests of lesbian, gay, bisexual, trans and intersex (LGBTI) people, at the European level. Its membership comprises more than 500 organisations from throughout Europe and Central Asia. The association enjoys consultative status at the United Nations Economic and Social Council and participatory status at the Council of Europe.
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.
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.
The Intersex Campaign for Equality (IC4E) is a non-governmental organization that advocates for the human rights of intersex people. It was formerly the US affiliate of Organisation Intersex International.
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.
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.
OII Europe is the umbrella organisation of European human rights-based intersex organisations. It is a non-governmental organization (NGO) which is working for the protection and full implementation of intersex people's human rights in Europe.
Intersex Trust of Aotearoa New Zealand is a nonprofit organization based in New Zealand that serves as the national advocacy and peer support organization for intersex people. Operating under the name Intersex Aotearoa, and previously known as Intersex Awareness New Zealand, it is recognized as the peak body representing intersex persons, those with variations of sex characteristics, or Ira Tangata. The organization was founded in 1996 by Mani Mitchell, a prominent intersex activist and advocate.
Dan Christian Ghattas is an intersex activist, university lecturer and author who co-founded OII Europe in 2012 and is now executive director. In 2013, he authored Human Rights between the Sexes, a first comparative international analysis of the human rights situation of intersex people.
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 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".
Miriam van der Have is an intersex human rights activist and woman with androgen insensitivity syndrome. She is a co-founder and co-chair of OII Europe e.V in 2015, co-founder and managing director of NNID Foundation in the Netherlands and member of the ILGA board where she is Intersex Secretariat until spring 2019. Van der Have is also a documentary film maker and journalist.
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, 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 inclusion as distracting from intersex-specific issues such as involuntary medical interventions.
The following is a timeline of intersex history.
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.
Intersex rights in Malta since 2015 are among the most progressive in the world. Intersex children in Malta have world-first protections from non-consensual cosmetic medical interventions, following the passing into law of the Gender Identity, Gender Expression and Sex Characteristics Act in 2015. All Maltese intersex persons have protection from discrimination. Individuals who seek it can access simple administrative methods of changing sex assignment, with binary and non-binary forms of identification available.
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.