
Welcome! About us…
We are a national charity by and for people with innate variations of sex characteristics. We promote health, human rights and bodily autonomy. Find out more about us and the population we work for.
Browse key InterAction and selected third-party resources. From early 2021, our key resources on this page are regularly updated and reviewed by a subcommittee of our staff and board.
We are a national charity by and for people with innate variations of sex characteristics. We promote health, human rights and bodily autonomy. Find out more about us and the population we work for.
GATE and American Jewish World Service have published a first-ever report on funding for the intersex movement, and the transgender movement. The results are shocking for intersex community controlled organisations.
The third edition of “The State of Intersex Organizing” has been released today. It identifies significant gaps in funding and resources, with an impact on the work of the intersex movement.
Intersex Human Rights Australia and Equality Australia have today welcomed the findings of a landmark report by the Australian Human Rights Commission on protecting the human rights of intersex people in medical settings.
How can you act as an ally to intersex people? This page contains introductory information and video resources.
A debate recorded at the 2020 Melbourne Medical Student Conference between paediatric surgeons John Hutson and Sonia Grover, and bioethicists Morgan Carpenter (IHRA) and Clare Delany.
We all have a right to bodily integrity, to not be subjected to invasive or irreversible medical procedures that modify sex characteristics, unless necessary to avoid serious, urgent and irreparable harm.
Body shaming is an intersex issue, perhaps even more than any other issue. This post intersperses quotations about intersex infants and children with quotations about the bodies of public figures.
The 2016 and 2021 censuses sought to capture data on people with innate variations of sex characteristics (intersex variations/differences of sex development), but they did so in ways that were harmful and that did not produce reliable, meaningful data. We have an opportunity to do better in the 2026 census.
Are clinical guidelines enough to eliminate human rights violations against people with innate variations of sex characteristics in medical settings? Reviewing the evidence, we believe they are inadequate, and their prerequisites do not exist.
Clinicians are increasingly raising their voices in opposition to forced and coercive interventions, including Physicians for Human Rights and the Board of Trustees of the American Medical Association. More action is needed – particularly in Australia.
Social Sciences journal has published a peer-reviewed perspective on the context and goals of the intersex movement in Australia, by Dr Morgan Carpenter.
All populations that suffer health inequalities are disproportionately affected by COVID-19, and people with intersex variations are no exception.
The Darlington Statement is a joint consensus statement by Australian and Aotearoa/New Zealand intersex organisations and independent advocates, agreed in March 2017. It sets out the priorities and calls to action by the intersex human rights movement in our countries.
This paper, by Morgan Carpenter to inform the Australian Institute of Health and Welfare, outlines the contradictory ways Australian data construct intersex and DSD.
The intersex population is far more diverse than commonly understood. This page presents details based on a 2015 independent Australian sociological survey.
A briefing on issues affecting people with innate variations of sex characteristics in detention settings.
A briefing on discrimination issues affecting people with innate variations of sex characteristics due to our bodies, identities, or assumptions about our identities.
A briefing paper on domestic and family violence and intersex people.
A briefing on issues affecting people with innate variations of sex characteristics in education settings.
We have struggled with symbols used to denote intersex people, so Morgan created one that is free for the world to use.
Guidance on including people born with variations of sex characteristics in forms and other forms of data collection.
Intersex Human Rights Australia and Intersex Peer Support Australia invite you to support the work of our organisations and realise the vision of the Darlington Statement.
Many intersex traits are genetic, with an identified origin. The elimination of such traits from the gene pool is an established and growing phenomenon.
An introduction to the health and well-being of people with innate variations of sex characteristics, with links to third party resources published by the Australian Human Rights Commission and clinical bodies.
These health and wellbeing resources work together to visually map established healthcare needs, highlight potential gaps in services, and evaluate against best practice indicators.
A briefing and guidance on understanding and respecting the diverse sex classifications and gender identities of people with intersex variations.
Guides to inclusive practice, to help make your service, program or project intersex-friendly.
The rights and concerns of intersex people overlap and intersect with the rights and concerns of women, LGBT people, and disabled and racialised peoples.
The lived experience of intersex people, and the intersex movement, have many intersectionalities with experiences of disability and the disability movement.
IHRA’s Morgan Carpenter wrote and presented this paper at the After ‘Homosexual’ conference in Melbourne in February 2012. The focus is on intersectionalities with same-sex attracted people.
This page details some of the general differences and similarities between the experiences of transgender and gender diverse people, and people with intersex variations.
Between 29 November and 1 December 2013, the Third International Intersex Forum, supported by ILGA and ILGA-Europe, took place in Valletta, Malta. The event brought together 34 activists representing 30 intersex organisations from all continents, and produced a common declaration.
This submission to a Senate inquiry on an exposure draft marriage bill discusses the role of medical interventions in preparing intersex bodies for marriage, as well as issues accessing marriage. It analyses the implications of marriage laws in Australia before marriage equality.
If you are writing about intersex people, our bodies, identities and human rights concerns, this page outlines why we use words the way we do.
This page is for new parents of an intersex child, prospective parents planning a pregnancy or undergoing genetic or preconception screening, and also parents of older children.
How many people have innate variations of sex characteristics (IVSCs), also known as intersex variations or differences of sex development?
Intersex refers to atypical internal and/or external anatomical sexual characteristics, where features usually regarded as male or female may be mixed to some degree. This is a naturally occurring variation in humans.
The Australian Journal of Human Rights has published this peer-reviewed commentary by Morgan Carpenter on reforms to protect people with innate variations of sex characteristics from harmful medical practices in the ACT.
Guidance on including people with innate variations of sex characteristics in research studies and surveys.
In the Commonwealth Parliament tonight, senators from each of the three main parties gave extraordinary and powerful speeches. We heard clear recognition that the medical treatment of intersex people is a human rights issue, that intersex is not a disorder, and that intersex people must be heard.
This paper was updated in September 2013, with a new final “impact” section that reflects the discontinuation of “SGD” and “DSG” terminology by the National LGBTI Health Alliance and many other organisations. We recommend browsing the Videos, Audio and Personal Stories sections of this website to gain familiarity with the diversity of intersex identities, genders,…
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A briefing on issues affecting people with innate variations of sex characteristics in sport settings.
In TEDx-style, Steph Lum (then IHRA co-chair) presents experiences of some intersex women, in personal relationships and accessing appropriate healthcare, at the Women Deliver 2019 conference in Vancouver.
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This report, on the ways that intersex is used by educators, was published in June 2001. The analysis and recommendations are as valid today as they were then.
We present our Theory of Change. The diagram is intended to set out why and how we do what we do, and with what goals and outcomes. Now finalised after a period of pubic consultation, comments and feedback remain welcome.
A timeline of legal, community and other key reforms in Australian jurisdictions. This page highlights good practice and documents the history of them and other developments.
The UN Office of the High Commissioner for Human Rights has published an essential new background note on human rights violations against intersex people.
Multiple UN Treaty Body committees have issued concluding observations to Australia on the rights of children with intersex variations.
A briefing on our population, including working, Australian and international definitions.
Guidance for employers, union representatives and staff on intersex issues and inclusion in the workplace.
An important and long-awaited supplement to the Yogyakarta Principles is published today. The Principles apply international human rights law in relation to sexual orientation, gender identity, and now also gender expression and sex characteristics.
Finding out you have an intersex variation can be a surprise! It doesn’t mean you’re alone. There are heaps of us out here with different intersex variations.
In YOUth & I, intersex youth tell their own stories, how they want to and in their own way. YOUth & I is an Australian publication created and edited by Steph Lum, and supported by the ACT Capital of Equality grants program. Download a free copy.
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