Families often talk about the range of strong emotions experienced around the time of diagnosis of disability for their child and there is research sbout the influence of the way a diagnosis is received impacting on families for years to come. In this blog, Jessica Maccallum, Social Worker from the Disability Specialist Unit, Burwood talks about the ways she works with families around the time of diagnosis, and a checklist she uses to ensure information and support is responsively and consistently provided.
Ruby Wright, Children’s Development and Disability Services Manager from Connect Child and Family Services, tells us about an innovative social skills program which is showing positive outcomes for children in schools in the Nepean and Blue Mountains region.
Knowing the most acceptable way of referring to children or adults with developmental delay or disability can be confusing. In this article we write about the importance of language and the most respectful and accepted way of referring to people with disability.