Australian insurance companies have been using genetic test results to discriminate against individuals. This practice can lead to higher premiums or outright denial of coverage for those with certain genetic markers. This has directly affected members of the intersex community. In the Darlington Statement, we called for “We call for an end to genetic discrimination, including… Read more →
Announcement: A multi-institutional research team has been awarded $5M in federal government funding to help create a safer and better future for people with innate variations in sex characteristics (IVSC).
The Department of Health in Western Australia has invited submissions in response to a discussion paper on proposed legislation in relation to assisted reproductive technologies and surrogacy.
This statement follows press reports in the Daily Telegraph, suggesting that NSW Finance Minister Damien Tudehope will introduce a proposed amendment to a bill decriminalising abortion in the NSW Legislative Council to prohibit terminations on grounds of sex or intersex traits. IHRA has a longstanding position on the use of IVF technologies and terminations. We… Read more →
Many intersex traits are genetic, with an identified origin. The elimination of such traits from the gene pool is an established and growing phenomenon.
At present, a minority of Australian have digital health records, and such records are not used routinely. As the number of people with digital records increases, it is likely that they will increasingly be used as a way of documenting and tracking our health. The implementation of the government’s national My Health Records scheme for… Read more →
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.
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.
The sponsorship of LGBTI events by IVF businesses raises ethical issues not just about the elimination of intersex traits, but also about the nature of community and comprehension of issues relating to intersex bodily diversity.
In 2014, OII Australia made a lengthy submission to the National Health and Medical Research Council calling for the prohibition of genetic testing to select against intersex traits. This submission responds to subsequent draft guidelines.
Georgiann Davis’s first book, “Contesting Intersex, The Dubious Diagnosis” is hotly awaited, and the first chapter has just become available online, from the publisher. Here are a couple of quotes (references omitted): I show how contemporary U.S. medical experts on intersex, like much of society, tend to hold narrow, essentialist understandings of sex, gender, and… Read more →
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