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Autism Blows NDIS!

Autism Explosion leaves NDIS in Disorder

By Rick Morton & Sean Parnell, The Australian – July 28, 2015

As rates of autism diagnoses soar around the world, the tale of two Australian families struggling to pay for expensive early-intervention therapies for their children — one by themselves, the other through government — underscores the divisive cost.

In Sydney, Tina Lopez and her husband, Arron Dickens, are dipping into their savings to pay about $42,000 a year out of their pockets for their son James because a federal program stumps up  only $12,000 over two years.

 In South Australia, where The Australian revealed children with autism now made up 46 per cent of the delayed, oversubscribed National Disability Insurance Scheme trial, the Andrews family had to fight to get a $40,000 package from the scheme for son David, 4.

The agency responsible for the $22 billion NDIS is reeling as it comes to grips with the rising numbers of eligible children, engaging in an off-the-books "rationing" of packages lest it risk the scheme's financial sustain-ability further down the track.

At the heart of the issue is the fact the former federal government was misled over the numbers in South Australia but the NDIS agency is also struggling to apply a uniform interpretation of what are "reasonable and necessary" supports for children with autism spectrum disorders.

"Our initial planner, she actually said to us the funding was capped," said Eliza Andrews of the 18-month process to get a full-service early-intervention plan.

"She was not meant to use that terminology, she admitted to us, so we appealed."

Despite worldwide best practice indicating children need about 20 hours of intensive behavioural therapy a week to produce solid early-intervention outcomes, the scheme's planner initially offered only an hour of speech therapy, an hour of occupational therapy and an hour of applied behaviour analysis therapy (ABA).

Ms Andrews negotiated that the couple, a registered nurse and a fitter and turner, would pay for the first two therapies from their private health insurance if the NDIS funded the ABA therapy.

They were later granted 11 hours a week for a year. After fighting the determination, the family was awarded $40,000, covering 80 per cent of their annual costs. "Without the NDIS, we would have to have sold our Continued on  house to pay for the therapies," Ms Andrews said.

Technically there is no cap on services but an updated price guide for the scheme, effective from next month, offers a "benchmark" and says "early intervention ... provision of a mix of therapies, and a key worker for the family, are expected to fall into one of the three categories" between $6000 and $16,000.

Cheryl Dissanayake, director of the Olga Tennison Autism Research Centre at La Trobe University, said it was thought about 2 per cent of school-aged children had autism spectrum disorders but rates were rising and diagnoses varied between ages and states. "Most of the NDIS trial sites are experiencing a much bigger percentage of people seeking support for autism than they had anticipated," she said. "That is partly due to increased diagnosis but also reflects unmet need."

In a study published in the Medical Journal of Australia this year, Professor Dissanayake and colleagues examined data from a federal government support program and found three times as many children aged under five were enrolled in the Helping Children with Autism Package than anticipated.

Last week, a study in the American Journal of Medical Genetics showed the rate of autism had tripled in the US in recent years. Penn State University researchers concluded "much of the increase may be attributable merely to a reclassification of individuals with related neurological disorders rather than to an actual increase in the rate of new cases of autism".

Professor Dissanayake suggested other factors were at play, including increased awareness of autism spectrum disorders.

In Sydney, Ms Lopez fears the NDIS will be rationing even more stringently by the time it reaches full rollout, affecting families such as hers. "For James, we're hoping we won't have to pay for these therapies forever," she said. "Whether that means we see enough improvement early or whether he gets into the NDIS, what can parents do? If their children need help, they need help."

Autism Awareness Australia chief executive Nicole Rogerson said the NDIS was wriggling out of its core promise. "Ironically, it will become a poor investment because the cost benefit analysis has been done to death," she said. "If we spend good money in the early years, the savings in the long run are in the billions, and isn't that the point of an insurance scheme?"

An NDIS agency spokeswoman said the trials continued to provide lessons. "The NDIS takes an insurance-based approach to early intervention," she said. "This approach means many children ... accessing the NDIS for early-intervention services may not require ongoing assistance from the scheme."

NDIS Support must be Targeted _ The Australian Editorial

Autism Spectrum Disorders need a separate approach

Depending on the severity of their conditions, autism sufferers and their families need and receive assistance. But the role of the National Disability Insurance Scheme should not be primarily to deal with that spectrum of disorders but to support Australians with serious physical and mental disabilities. Severely disabled adults and children, especially those who need constant care and whose family carers are often unable to work outside the home, deserve priority. Based on expert diagnosis, severely disabled autism sufferers deserve to be helped under the NDIS.

Authorities need to learn a lesson from the NDIS trial in South Australia. As reported yesterday, children with autism spectrum have crowded into the trial, accounting for 46 per cent of its 10,000 participants aged under 14. The trial was expected to assist 5085 children. Nationally, such a pattern would severely limit resources for those most in need or cause an unsustainable cost blowout. It is not surprising parents of children with autism, however mild, would seek all available help. But boundaries must be set if the NDIS is to meet its purpose.

Autism spectrum is a broad term. It covers a vast range of people, from those who lead normal lives but struggle with communication and interaction to those with severe learning or behavioural difficulties who cannot function in ordinary schools and workplaces. It is complex and increasingly prevalent. The latest Australian Bureau of Statistics data, from 2012, shows 115,400 Australians diagnosed with autism, a marked increase from 64,400 in 2009.

The South Australian figures did not include children diagnosed with conditions sometimes related to autism such as attention deficit and attention deficit hyperactivity disorders. The incidences of those conditions have also soared in recent years, with sufferers often treated with Ritalin, a central nervous system stimulant that affects chemicals in the brain and nerves to reduce hyperactivity and improve impulse control. A University of Sydney study last year found Australia has one of the highest usage rates of such medication in the world. Prescriptions for Ritalin soared 300 per cent in Australia between 2002 and 2009 and by another 35 per cent across the next four years. In 2013-14, the number of Ritalin prescriptions filled under the Pharmaceutical Benefits Scheme rose by 15 per cent to 597,000.

Funding support for children diagnosed with autism and other disorders varies between states. In recent years, The Australian has highlighted trends in Queensland, for example, where parents and medical and educational professionals have complained about pressure being exerted by some teachers on parents of children who are struggling in the early years of school or finding difficulty fitting in socially. Reportedly, such parents have been urged to seek out doctors to diagnose their children with conditions such as autism spectrum disorder, for which support funding is available. In NSW, autism rates rose 280 per cent in the 10 years from 1997.

The upsurge in the diagnosis of autism and other disorders and the reasons so many children apparently need medication for their wellbeing needs to be reviewed and debated. The trend should not, however, compromise the viability of the NDIS, which has a vital role assisting the severely disabled.

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