HIV & the Law: updated content from ASHM

Australasian Society for HIV, Viral Hepatitis and Sexual Health Medicine, 2019

The NEW Guide to Australian HIV Laws and Policies for Healthcare Professionals includes two new sections on Mandatory Testing for HIV and My Health Record.

This resource aims to provide health care workers with information on legal and ethical responsibilities under various laws and regulations related to human immunodeficiency virus (HIV). It does not contain legal advice. Those seeking advice on individual cases should contact their health department, solicitor or their medical defence organisation as appropriate.

In the interests of brevity, laws have been summarised and re-written specifically as they relate to HIV. In many instances key legislation is more broadly targeted at a range of infectious diseases (with definitions varying by state).

All efforts have been made to ensure the content is current at time of publication.

A guide to My Health Record: for BBV & STI healthcare providers to support their patients

ASHM  (Australasian Society for HIV Viral Hepatitis and Sexual Health Medicine)

Healthcare providers can play a crucial role in helping patients make informed decisions about whether and indeed the extent, to engage with the My Health Record, particularly for those patients with BBVs and/or other potentially stigmatising conditions.

To support those conversations, ASHM has created A guide to My Health Record: for BBV & STI healthcare providers to support their patients. The guide outlines the key issues associated with My Health Record, and provides four key recommendations to clinicians around advising patients on how to engage with the system.

Though the opt-out period ends soon, clinicians still have an ongoing obligation to provide advice to patients around the benefits as well as the privacy and security control options available, to guide their decision-making around engaging with My Health Record.

With increased media attention on My Health Record in recent weeks, some specifics of the system may change. A guide to My Health Record is a living document and will be updated with any relevant changes as further details emerge.

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.