Australia
Disability employment scheme: sudden exclusion, fish-slapped by Departments and their "systems"
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%).
‘Greatest area of need for people with disability left unmet by Government’
said Matthew Wright, Chief Executive Officer of the Australian Federation of Disability Organisations (AFDO) and spokesperson for the disability peaks.
Responding to claims in The Australian newspaper by Minister for Social Services, Scott Morrison that the new peaks funding ‘supports the area of greatest need’, Matthew Wright said “The department has cut or not provided funding to the highest population groups of people with disability in Australia’.
Merry F#*king Xmas
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?”
Bleak Xmas: Disability Peaks Forced to Close Doors on People with Disability
For Immediate Release, 23 December 2014
‘Disability Peaks Forced to Close Doors on People with Disability’ said Matthew Wright, Chief Executive Officer of the Australian Federation of Disability Organisations and spokesperson for the disability peaks Ten peak organisations run by people with disability will be left with no choice but to either close their doors or reduce services, with seven organisations subject to drastic funding cuts by outgoing Minister for Social Services, Kevin Andrews.
Greensborough man with autism shackled in hospital after parents say pleas ignored
James Pascoe shackled to a bed after his parents? pleas for more appropriate care were ignored.
A MAN with severe autism has been shackled to a hospital bed after his parents say repeated pleas for more appropriate care were ignored by authorities
Understanding the challenges of disability care
Wendy and Henry Ponsen with their son Jonathan.
By Robert Virtue (with Diane McCracken)
For 32 years, Wendy and Henry Ponsen have been dealing with the challenges of caring for a child with a disability.
The Ponsen family of Newcastle are up-front about the difficulties in raising a child with a disability.
Wendy and Henry have been caring for their six-foot tall, 32 year-old son Jonathan for all his life.
There've been ups and downs and a myriad of challenges along the way.