Event Hosted by CoPQTI and InterAction

Health and social issues for people living with innate variations of sex characteristics (IVSC), often referred to as intersex variations or differences of sex development, are frequently collapsed into discussions of sex and gender. This is a particular problem with LGBTIQ+ research that aims to be inclusive but may in fact render IVSC experience invisible. The result is that IVSCs remain misunderstood, medicalised, and marginalised within dominant research, social, and clinical frameworks. Hosted by CoPQTI and InterAction, this public lecture and panel discussion aims to critically examine how IVSC is understood, governed, and lived across different contexts. It will also provide advice on how to practice meaningful IVSC inclusivity.

This is a hybrid event and will be available both in person and online. Participants are encouraged to engage in discussion and contribute questions in advance.

Panelists:

Associate Professor Morgan Carpenter

Associate Professor Morgan Carpenter is an internationally recognised expert on human rights and ethics in relation to the treatment of people with innate variations of sex characteristics (also known as intersex variations or differences of sex development). He is an Associate Professor at Sydney Health Ethics in the University of Sydney’s School of Public Health, and leads the Interconnect Health Medical Research Future Fund Research Project on the health and wellbeing of people with innate variations of sex characteristics. He is the Executive Director of InterAction for Health and Human Rights, a national charity that engages in policy work, and provides psychosocial support, peer support and training services to promote the health and human rights of people with innate variations of sex characteristics. He is also a member of the Australian Capital Territory’s new Restricted Medical Treatment Assessment Board, and the NSW government’s LGBTIQ+ Advisory Council. Morgan has been contracted to the UN Office of the High Commissioner for Human Rights, the ACT government and the Australian Institute of Health and Welfare, and collaborates with the World Health Organization. He is or has been a reference or advisory group member for the Australian Department of Health and Aged Care, Australian Bureau of Statistics and New South Wales Health.

Bonnie Hart

Bonnie Hart is the founding Service Manager of the intersex psychosocial support service InterLink, the Deputy Executive Director of InterAction for Health & Human Rights, a Research Fellow (Intersex Psychosocial Models of Care) and PhD candidate with the University of Southern Queensland, and a Chief Investigator and Lived Experience Lead with the Interconnect Health Research Project. Bonnie uses her lived experience as an intersex woman to work with community members as an intersex peer worker and systemic advocate. She provides content expertise as a researcher, educator, consultant and mental health program designer. Bonnie was an organising signatory of the 2017 Darlington Statement of intersex community consensus and founder of the YellowTick intersex education and inclusion initiative.

Associate Professor Bridget Haire

Bridget Haire is a senior research fellow at the Kirby Institute, and an associate of the Australian Human Rights Institute. She lectures in public health and medical ethics. Prior to academia, Bridget worked in HIV and sexual and reproductive health for more than 20 years as a journalist, editor, policy analyst and advocate. She is a former consultant for the Australia-China Human Rights Technical Co-operation Program on sexual and reproductive health rights for the Australian Human Rights Commission. From 2015-18 Bridget was President of Australian Federation of AIDS Organisations (AFAO) and a member of the Ministerial Advisory Committee on Blood Borne Viruses and Sexually Transmissible Infections. She also served on the Data Safety Monitoring Board for the South African HIV prevention study CAPRISA 008 as a medical ethicist, and is the medical ethicist on the NSW HIV Assessment Panel for People who Put Others at Risk of HIV. Her research interests are ethical issues in infectious disease control with an emphasis on underserved or marginalised populations, gender, and sexual and reproductive health.

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