BORDER mums are taking the disability service system to task in a heartfelt plea to Canberra.

Wodonga disability activist and mum to a son with autism, Jen Tait, and Gateway Health’s Community Inclusion and Population Health manager and mum to a son with a disability, Toni Reeves, have put their concerns on the public record.

Ms Tait wrote a moving letter to the member for Indi, Cathy McGowan, seeking a fair go for people living with disabilities on the Border. 

A couple of years ago, school was not going so well for Jack. He was close to failing several subjects, even at risk of dropping out. He was bright, the teachers were relaxed and friendly, but that was the problem – they were too relaxed.

Now in year 9 and doing well, Jack, 15, says he has a very particular learning style, getting teachers who match that has turned everything around.

Note: there is commentary on this article at the end.

Angela Shanahan

It seems odd in this belt-tightening age that the National Disability Insurance Scheme, one area of almost certain future overblown expenditure, seems to be isolated from scrutiny.

A report into autism diagnosis in Australia has found discrepancies in how children are assessed for the condition and calls for a national standard to ensure early intervention.

The study was produced through the Cooperative Research Centre for Living with Autism.

The senior author of the report, Professor Andrew Whitehouse from Perth's Telethon Kids Institute, said the study highlighted serious problems.

Children who do not meet the ­criteria for autism are being diagnosed with the condition, as desperate parents take their kids to private practitioners in a bid to gain a label, according to frank ­admissions from health professionals.

A report from the Australian National Audit Office (ANAO) said that in February 2014 the Department of Social Security (formerly FaHCSIA) funded $50,000 worth of research to establish "the extent of [ASD] over-diagnosis nationally".

A Deputy Secretary of DSS wrote back that

this wording is not intended to presuppose the findings of the Autism CRC report.

The following is the current editorial in the Newsletter issued monthly by ATAC  [Action for Tasmanian Autistic Children].  ATAC  was established to provide free advocacy for all those who have difficulty with government and other bureaucratic bodies when they want to gain services for members of their families who are on the spectrum.  Another key function of ATAC  is to fight for the  recognition of Autism as a brain disorder based in neurol

Members

Board of the National Disability Insurance Agency (NDIA)

Dear Board Member,