Carers

Caring for carers

Tuesday, May 25, 2010
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Would you part with $8 to $10 a week to improve services for the 1.5 million Australians who are profoundly disabled?
Click in the video to listen to Alan Jones speak to Woman's Day readers who share their stories on caring.
Topics:
Carers
Australia’s carers are in desperate need of support and respite. Woman’s Day investigates their shocking stories.

Across the country, there are around 2.6 million Australians helping to care for a loved one with a disability. As our population ages, the number of carers is only set to increase.

“People with disabilities are no longer a tiny, voiceless minority,” says journalist and carer Sue O’Reilly, who helped start a national campaign, Mad As Hell (australiansmadashell.com.au), to demand better disability services.

“There are now 1.5 million people in Australia with a severe or profound disability – that’s the population of Perth. Half a million people are the primary carers of a person with a disability, and that’s the population of Tasmania.”

More than 2 million more are secondary carers, who share the sometimes unimaginable load of looking after a child or adult who cannot fend for themselves.

“Politicians need to remember that people who are severely disabled can still vote, and so can the rest of us,” Sue says.

Sue, whose son Shane suffered severe brain damage after acquiring a severe staphylococcus infection in a hospital neonatal unit soon after birth, and whose husband died of cancer three years ago, knows that tragedy can happen to any of us, at any time.

But compared to the UK, for example, Australia is almost Third World in its treatment of disabled citizens, says Sue. “Imagine how people would react if public hospitals throughout the country were so severely underfunded, they could only admit one in five people seeking treatment?

“Imagine if this one patient in five was selected by some form of random, lottery-type ballot, and if hospitals announced that because of funding shortfalls, they could only treat people who had broken a leg or an arm if it was the right leg or arm, but not the left?

“Imagine if cancer patients were refused chemotherapy or radiotherapy? All these scenarios seem ludicrous, yet this sort of rationing and crisis-driven response is exactly what’s happening in the disability sector.”

Sue says the only solution is to introduce a no-fault disability insurance scheme – which means average Aussies would be charged a levy, just like the Medicare levy, of about $10 a week to pay for a vast improvement in disability support services.

This proposal is currently being considered by the Federal Government.

Are you a carer? Do you have a story to share with us?

Send in your contact details, story (no longer than 300 words) and photos to wd@womansday.com.au.

To read the inspirational carers stories click here

User comments
Well done to Woman's Day for drawing attention to the challenges that carers face. It is an issue that is so close to so many, yet it has been largely ignored in the media. Well done for covering such an important topic and so well. Thank you.
How come Carers only get $100 per fortnight some people get more on the Dole sitting around onthere butts rorting the system than carere do we have to do a lot sometimes its a 24 hr job looking after a loved one my husband supports me because I CAN`T WORK he gets no extra support & noew we both look after his mum with Alziemers thats not easy either when he has to also work for 8 to 10 hrs then come home & look after both of us at times more goverment support would be great
The Govt and our hospital system should be ashamed of the way they have lack of care and support for any Australian who has a disability especialy when they and families have paid taxes and worked hard all their lives. Being a carer back in 2002 when my partner through cancer became a para for 8 months was the toughest challenge any one could go through, but you find inner stentgh to be their for them with a brave and cheerfull face. But in the back ground is bills to pay + extra costs because of disability, house to keep, working to pay the bills (carers pension is not something that will pay all bills) Keeping sane and healthy yourself and what ever other family commitments one has besides caring for someone who is so needy due to disability. To have a disability in a regional town in WA is even harder as distance is the killer when loved ones are 100's of km away for care or treatment. As in regional WA you get very little help or specialists and run a even bigger cost burden.
I thank Betsy Hilton everyday for donating part of their land at Quaarma to build Naardy House. Without it i would have a seven hour round trip to drop my son Peter off for respite in Sydney. The government really needs to take better care of the carers and provide funding so that more houses can be built. They need to walk a few steps in the shoes of carers to see exactly what we go through.
Mild to severe disability, the treatment is the same - indifference. It is a business where bulldust baffles brains. Rhetoric is strong - action is weak. The culture is dominated by dollars and politics.
Its hard for some to understand whats its like to be a carer,you can say you have a family member with this or that disability and although the disability maybe understood but what happens behind closed doors?What if life like for the carer? Here is an snippet of my life,Child with brain damage and other medical problems plus 3 more children ,3 hours of school a day, anal retintive,violent,short term memory,obsession with fire,food,runs away,bites,kicks,hits ect. Sleeps 5-6 hours a night wakes up constantly,locks on everything,one parent family,respite care one weekend a fortnight. Thats my life in 400 characters,am I coping No can anyone help NO.
semi- retired psychiatrist and on board of Aftercare. Also have several members of family disabled. Is there meeting in NSW I could come to?
Better to care for someone at home instead of putting them into Care where very often they are not bein cared for at all and have no voice to bring attention to their plight. Shut 'em up with dope is commonly used.
there is petition everyday to upgrade or change everything from state parks to un needed road works, the government should definatly contribute to needs of the many australianas with a disabilty, i say fight as hard as we can and let the govnerment who we want to be heard. il will send this on to everyone i know and get there feedback together we can make this happen
People with a disability should be the primary focus of any scheme for the future. By ensuring the needs of all people with a disability are met then the carers needs will also be met. It is the lack of proper resources and support for the individual with the disability that creates the burden for the families and carers.

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