Hepatitis C – Peer insights on barriers and motivators to Direct-Acting Antiviral (DAA) treatment uptake

ARCSHS, 2018

The knowledge and experience of people who inject drugs (PWID) within peer programs is a vital asset to strategies for the scale-up of DAA treatment among PWID (Brown and Reeders, 2016). This study is focused on translating these “real time” peer insights into resources that support policy and programs to tailor to the needs of communities of people who inject.

This tailoring is critical to achieving the goal of eliminating hepatitis C. This broadsheet is the first of a series that will be produced over the duration of the project. This series will present current peer insights from the peer workers and other members of the people who inject community on the access to and uptake of the new hepatitis C treatment.

This broadsheet provides background to the study and presents an overview of the attitudes, beliefs and experiences of PWID related to the access and scale-up of direct acting antiviral treatment among this community.

A research project by the Australian Research Centre in Sex, Health and Society in collaboration with peer-based organisations – Peer Based Harm Reduction WA, NSW Users and AIDS Association and Harm Reduction Victoria.

Responding to LGBT conversion therapy in Australia: report

GLHV@ARCSHS, La Trobe University & Human Rights Law Centre, 2018

This report highlights the nature, extent and impact of LGBT conversion therapies in Australia.

The report is designed to help government, support services and faith communities to better respond to those experiencing conflict between their gender identity or sexual orientation and their beliefs.

Connecting country: busting myths about Indigenous Australians (podcast)

Diversity Council of Australia, 2 Oct 2018

This 20-minute episode doesn’t just feature a beautiful Welcome to Country, but also attempts to connect Country by exploring the cultural and professional gaps that exist for Indigenous Australians at work and asking: where do these issues come from? Why do they persist? And what can we do to finally close the gap?

Helping answer these questions is Linda Burney – the first Aboriginal woman to serve in the House of Representatives, and the first Aboriginal person to serve in the NSW Parliament – as well as Karen Mundine, CEO at Reconciliation Australia.

Researched and hosted by: Andrew Maxwell. Produced and written by: Andrea Maltman Rivera. Executive produced by: Lisa Annese. Contributions from: Catherine Petterson and Simone Empacher Earl. Special thanks to Audiocraft. Welcome to Country by Aunty Norma Ingram.peer

Aboriginal and Torres Strait Islander listeners are warned.  The following podcast may contain voices of deceased people.

Understanding U=U for women living with HIV

ICASO, September 2018

Since its announcement, Undetectable equals Untransmittable (U=U) has
become a call to action to assert that when someone living with HIV has an
undetectable viral load they cannot transmit HIV. Additionally, the U=U message
is evolving to challenge notions of HIV infectivity, vulnerability and stigma.

The science behind the U=U message provides the evidence that we can reduce the anxiety related to the sexual transmission of the HIV virus with confidence.

To contribute to getting this message out, ICASO produced a Community Brief on U=U. This community brief explains why it is so important to understand what ‘U=U’ means for women. The brief documents the experiences and needs of individual women living with HIV from all over the world. Important questions still remain that need to be answered to make the U=U message relevant, understandable and more meaningful to women in their diversity.

  • Download the community brief in English here

Survey for Women living with HIV

napwha, femfatales, Relationships Australia South Australia, September 2018

WOMEN’S EXPERIENCE OF LIVING WITH HIV AND AGEING

This survey is the result of a collaboration between MOSAIC, NAPWHA and Femfatales. They encourage all women living with HIV, regardless of age, to be motivated to consider their health, to reflect on living with HIV, and to complete this survey so that their voices may be heard.

The feedback from this survey can be used to make positive changes in the delivery of support to women living with HIV. Please complete this survey by Friday October 26th 2018. The survey should take 10-15 minutes to complete.

LGBTIQ People Ageing Well Report released (SA)

COTA SA & South Australian Rainbow Advocacy Alliance (SARAA), July 2018

The LGBTIQ People Ageing Well Project commenced in April 2017 as a 12-month
joint project between COTA SA and the South Australian Rainbow Advocacy Alliance (SARAA). The main aim of the project was to engage with older people from South Australia’s LGBTIQ communities to find out what matters most to them as they age to better inform policy and create a groundswell for change to the policies that impact on the lives of older LGBTIQ people.

The project also celebrated the lives and contributions of older LGBTIQ people. Their
stories and lived experiences have the power to promote a greater understanding
of a unique set of issues, but also the power to create changes that will support and
enhance the lives of South Australia’s older LGBTIQ population.

This report makes a number of recommendations that can and will make a significant difference to the lives of older LGBTIQ South Australians, and must be addressed by all levels of government and the ageing and aged care sector.