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 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.
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.
Body shaming is an intersex issue, perhaps even more than any other issue. Please note that this post contains distressing images. It intersperses quotations about intersex infants and children with quotations about the bodies of public figures.
The intersex population is far more diverse than commonly understood. This page presents details based on a 2015 independent Australian sociological survey.
Intersex people have innate sex characteristics that don’t fit medical norms for female or male bodies, and that create risks and experiences of stigma, discrimination and harm. We have many different kinds of bodies and life experiences.
Intersex Human Rights Australia is a national not-for-profit company by and for people with innate variations of sex characteristics. We were formerly known as OII Australia. We promote human rights, health and bodily autonomy. Our goals are to help create a society where intersex people are not stigmatised, and where our rights are recognised. Read more →
Intersex Human Rights Australia (IHRA) can provide a range of services to individuals, organisations, institutions and community groups. Together with Intersex Peer Support Australia we deliver Yellow Tick training around Australia.
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.
There are no firm population figures for people with intersex variations, due to stigma, misconceptions, lack of accurate recording of data, arbitrary definitions, and ideological values.