In June 2013, the ACT Disability Advisory Council (DAC) commissioned Women With Disabilities ACT (WWDACT) to undertake work to find what survey and data information about women with disabilities in the ACT is available in the areas of services for health and wellbeing and participation in social and economic life. The work was also to investigate how this information can enable the DAC to provide policy advice to the Minister for Disability, Children and Young People.
The first section of the report sets out the objectives of the commission in more detail and includes the underlying rationale for the study. The direction of the study is aligned with the ACT Government’s Triple Bottom Line Assessment Framework which examines the economic environmental and equity impacts of policies. In turn, the ACT Women’s Plan 2010 – 2015 contains Economic, Social and Environmental strategic outcomes.
The rationale is in three major areas. Firstly, it examines the complex nature of the intersection of disability and gender, acknowledging the diversity of vulnerable groups and various forms of inequality. Any action to address the challenges of this intersectionality must be based on sound evidence. Secondly, this section establishes the grounds on which public authorities are obligated to respond to the needs of women with disabilities. Thirdly, it stresses the role of
information in guiding policies as well justifications for the participation of public authorities in generation and dissemination of information.
The remainder of the document contains the study methodology, a review of 13 data sets that are identified as relevant to women with disabilities in the ACT, and findings resulting from the review. The main outcome of the study is to provide systematised information regarding available data sources. This information is summarised in a Table (Table 1, page 35). The study recommendations identify some of the current gaps in data collection or where analysis could be expanded in a way that would be helpful to ACT policy makers. It further identifies which body could be responsible for making the suggested data collection changes. The concluding section explains the central place of statistical evidence in guiding policies and actions, as well as outlining the joint responsibilities of all participants in the ACT community.
You can read the full report below.