Media Release

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.

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?”

Sarah Martin, Political Reporter

Jedd (3) with behaviour therapist Stephanie Miller at the AEIOU Foundation, Huntfield Heights Centre.Source: News Corp Australia

SEVERELY autistic children are receiving less funding in trials of the National Disability Insurance Scheme than they were under previous funding arrangements.

Early intervention service provider the AEIOU Foundation, which set up in South Australia to test its viability under trials of the new national disability funding model, says it cannot operate effectively under the scheme.

AEIOU chief executive Alan Smith said it was able to provide only five days a fortnight of intensive therapy under the NDIS, compared with 10 days where the scheme was not yet in effect, in Queensland.

Programs for the 0.1 per cent of children with autism disorder require about $45,000 for each child, but the NDIS has set a benchmark payment of $16,000.

In this video Bob Buckley describes his recent experiences with National Disability Insurance Scheme (NDIS) planning. His advice tries to help others prepare for their transition to the NDIS. He suggests that people can reduce their stress over NDIS planning if they better understand the processes and likely outcomes.

Bob Buckley's son (who is 23yo with severe autism) has one of the earlier NDIS plans approved in the ACT. The process took 11 days and delivered substantially more support/resources than was previously provided. The plan is much more flexible than the previous arrangement.

By Rebecca Trigger

Families of children with autism are facing tens of thousands of dollars in costs and lost income, a Western Australian researcher has found.

The study — thought to be the first of its kind in WA — set out to measure whether a delayed diagnosis increased long-term costs for families.

But the paper, published in this month's edition of journal PLOS ONE, also established the median cost of a child being diagnosed with autism as $34,900 per annum.

Curtin professor and joint author Torbjorn Falkmer said the findings, drawn from the responses of 317 Western Australian families, had huge implications for parents.

"The majority of that cost, 90 per cent of it ... is because of the lack of the chance to have employment because parents have to stay home and take care of the children with autism, because they don't get the support they need," Dr Falkmer said.

"I think the system we have right now is showing us that parents are being forced to stay home, because they can't take a job because someone's got to take care of the kids.