More than 10,000 participants have registered for a new, free online six-week course beginning in April, which has been designed by Swinburne University to provide practical help to families with a child on the autism spectrum. Autism spectrum disorder is a lifelong condition affecting about 1 per cent of children who typically have preoccupations, aversions, obsessions and difficulties with social interaction.
6 February 2015
Note: the editorial content below.
A new Alliance representing the interests and views of all people with disability will provide advice to the Australian Government on improving social and economic participation, and breaking down barriers.
Julia May, 7/2/2015The Federal Government's cuts to the disability sector are a "catastrophic" blow and breach the United Nations convention on the rights of disabled people, advocacy groups and one of the architects of the convention says.The Department of Social Services announced yesterday it would fund an alliance of six groups representing disabled people by demographic rather than specific need.
The new arrangement threatens eight peak bodies, with 200,000 members.The former chairman of the United Nations committee representing people with disabilities has added his voice to the chorus of anger over the government's shake-up of the sector, challenging its claim it is in acting in accordance with the UN convention.Ron McCallum, who is blind, is a former dean of law at Sydney University and, until December, was chair of the United Nations Committee on the Rights of Disabled Persons in Geneva.
Autism Aspergers Advocacy Australia (known as A4), the national peak body for autism spectrum disorder (ASD), wrote an open letter to Scott Morrison MP, the new Minister for Social Security. The letter gives essential information about ASD and the impact of Government policy for people living with ASD, and asks for a meeting to discuss ways to improve outcomes.
People with autism have difficulty getting a job. The letter below describes the experience of one person and his carer on reaching a point just 2 years after leaving school.
This experience shows that the Commonwealth Government's Disability Employment Scheme (DES) is largely intractable. The Australian Bureau of Statistics describes its abysmal outcomes for people with autism/ASD (link here):
In 2012, the labour force participation rate for people with autism was 42%. This compares with 53% labour force participation rate for people with disabilities and 83% for people without disabilities.
The 41.2% of people with autism in the labour market in 2012 experienced 23% unemployment (there is improvement since 2009 when labour force participation was just 34% and unemployment was 41%).
My friend is the mother of a child who is deaf and also has autism. She has been forced on to Newstart. My friend already works five days a week but with limited hours. Luckily she works at her son’s school but must be on call to deal with any adverse behaviors that might happen. Last week, as an example, her son head-butted a glass pane door of his classroom because he could not get in. It smashed and he cut his face all over. Said my friend, “ He was damn lucky not to have cut his eyes or a major blood vessel. Bled like a stuck pig. Added 20 years and too many grey hairs to count.”
At home she also has to deal with meltdowns. ...
My friend does not get carers payment from the Government because – “ I don’t provide constant care in the home because he goes to school” ...
AND to top this off, because she has been shafted to Newstart, she is expected to apply for ten jobs per week. This single mother who can be called from work at any time to care for her child, who has the sole care of a child who is both deaf and autistic, a child that has challenging behaviour at home and school that requires her constant vigilance, who also has the sole care of another child … This mother is expected to look for ten jobs per week! Why? Because the Government thinks she is a LEANER and somehow has the capacity to not only look for ten jobs a week but also work full time. As she so eloquently put it – “How f#*ked is that?”
Federal and state Ministers are playing politics to delay reasonable and necessary early intervention services for children with disability.
The NDIA was advised from the outset that their estimates of the number of people with autism spectrum disorders (ASD) was seriously wrong (see /node/425 and the footnote on /node/695).
In South Australia, where the intake is young children, 40% NDIS participants have "autism" as their primary disability (see report here).
This appeared in the Adelaide Advertiser: