Carers

Sam Paior is a parent of two kids with disabilities. She is a staunch advocate for people with a disability and their families, and is a board member of IDASA (Intellectual Disability Association of SA) and founder of Parents Helping Parents.

As one of the two in five Australians who have a disability, care for someone who does, or both, the NDIS, the National Disability Insurance Scheme has been, to date the opposite of a death by a thousand cuts for me.

Assistance at last

The Scheme is kinda like a Medicare for services and equipment related to disability. A scheme where people who need a disability related service, equipment or support can get what they need. With Medicare, you might see a doctor (of your choice) and then pick up your antibiotic prescription (at a pharmacy of your choice), and when a blind person needs a white cane, or an intellectually disabled person needs someone to feed them, it should be just as simple, but it’s not.

Medicare is funded with a levy, but the Productivity Commission, who state that such a scheme for the disabled will self fund within five years, say the funds should come from general revenue.

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  • Dell and Michelle Stagg says:

    09:12am | 03/05/12

    As the mum of my adult daughter who is 47 years of age and just coincidently has profound severe and multiple disablities…(BTW ...we are not a “disabled family”—- her disability HAS NEVER DISABLED US…in fact we are quite capable and useful contributors to the world around us and in particular… Read more »

  • Robert Smissen of country SA says:

    12:06am | 02/05/12

    @acotrel, WOW, no matter what the post is about you still make it Abbott’s fault, acotrel you are legend in your own lunchtime Read more »

 

This week The Punch features two Angry Cripples, both anonymous. It’s fair to say they have somewhat opposing points of view to say the least. We recommend reading this one first.

If only it were this easy. Pic: Jeff Herbert

I am an angry cripple. No, I do not have a disability, but as the mother of a young woman with severe and multiple disabilities, I am as crippled by the cruel Australian disability support system as much as – and sometimes more than - many people with a disability themselves.

I have been the sole primary carer of my daughter since my divorce more than 20 years ago, with the result that - like hundreds of thousands of other sole primary carers - I subsist on the poverty line.

During the global financial crisis, when the government was throwing cash at families earning up to $110,000 a year and the widescreen TVs and handbags were rolling out shop doors, I looked at my life, my old and decrepit furniture, my second hand clothes and all the things about my health and life that desperately need work but which I have not been able to attend to because of lack of support services and/or my inability to pay.

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  • Les Cope says:

    06:51pm | 13/07/11

    Eye4anEye. It’s a very uninformed comment suggesting she should have therapy, and if that does not work then put her daughter into care. Neither of these two options will solve her issues or her daughters specific needs. As Sam Paior mentioned its just not possible for many parents to even… Read more »

  • Cathy says:

    07:40pm | 09/07/11

    Yes the love is the overwhelming feature of being a parent, particularly a parent to someone who needs so much more than others… All of you families who provide care and all of you people who need supports be a strong voice for transformational change. We can win but we… Read more »

 

“He…did not battle his illness bravely. Nor was he courageous in the face of death,” read the bold, opening paragraph of the obituary for the British journalist. John Diamond, a man almost as famous for his ten-year marriage to celebrity Nigella Lawson as the long and public battle with throat cancer that he lost in March 2001.

Told it the way it was

It was a fitting tribute. Diamond adamantly refused to fight his battle with cancer “bravely” and chose instead to write about his illness, in a raw and unforgiving fashion, in a weekly column for The Times newspaper in London.

Honesty was his only policy, as the quote below the fold reveals.

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  • Disgusted says:

    05:33pm | 21/06/11

    Actually acotrel, smoking INCREASES your RISK of throat/lung/whatever cancer. Non smokers get can and do get throat cancer.  Frequently. I hope people will be nicer to you when you are dying of some cancer caused by the over production of bile. Read more »

  • atthepub says:

    06:56am | 19/06/11

    When my mum was dying, she pretended all was well (we all deal with things our own way). I wasn’t able to visit her in hospital myself at the time. Just the same I decided to get to the bottom of it and find out why the doctors didn’t allow… Read more »

 

A couple of Sundays ago in Port Moresby, Stephanie Copus-Campbell – the head of AusAID’s program in PNG – invited me and a colleague to accompany her on a regular Sunday activity.

The cold statistical face of the human tragedy in PNG

Every Sunday, Stephanie goes to the local supermarket and buys $70 worth of oranges which she then takes to the AIDS ward at the Port Moresby hospital.

HIV infection rates are high in PNG and while antiretroviral drugs are available, people still come to this place to die.

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  • Not a great white hope says:

    09:05am | 31/05/11

    Great comment Cranky.  To be honest, I wonder how many of the comments posted under this article were written by AusAID communications staff.  The author had best leave these coms staff to do their job rather than taking on the role as a defacto AusAID cheerleader. Mr Marles, a much… Read more »

  • Cranky PNG watcher says:

    09:42pm | 27/05/11

    This is such a ludicrous hagiographic article. Written by the Parliamentary Secretary for Pacific Islands Affairs - a man who should be keeping AusAID accountable, not being a suckhole. Does anyone else see a problem here? Let me affirm the obvious - people in PNG are very hard done by,… Read more »

 

Given the vigorous responses to last week’s column by Sue O’Reilly, when The Angry Cripple heard that Todd Winther was writing a response to run on the ABC’s Ramp Up website, the AC asked him if we could run it too. The Punch is running his column under Todd’s own byline rather than the Angry Cripple’s byline for reasons that will become clear.

The Angry Cripple's symbol - not a universal sign.

Does it matter if the Angry Cripple is actually a cripple or not? You bet it does.

Others tell people with disabilities what their best interests are too often. For all of their good intentions, the people who look after us are the ones who do it the most. This is why The Angry Cripple’s identity is important. If he/she is a carer, then the column is doing itself no favours, and merely adding to the chorus of carers who already have their say in the mainstream media. If however, The Angry Cripple is disabled it represents an opportunity for a too often neglected voice to enter the mainstream.

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  • david bassett says:

    10:37am | 02/05/11

    i love this collum is there a way of obtaining a copy every week to my post box at home i would love to read it if u have a mag Read more »

  • Sam Mauchline says:

    08:24pm | 19/04/11

    Hi I am in my seventies and the father of Paul aged 40 who suffers from cerabral palsy an requires 24 hour care. I have also been a constant critic of the NDIS this led to NDIS QLD refusing my offer of assistance. My wife and I have been constantly… Read more »

 

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