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A Fair Trial for the NDIS

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The recent opinion pieces published in the West Australian by David Gilchrist, Gordon Trewern and other stakeholders in the disability sector are of great concern to Western Australians and their families. The views expressed are not the views of people with disability and their families themselves, who want a fair trial for the National Disability Insurance Scheme and the State based scheme, My Way. The West Australian Government and disability service sector have been vocal in decrying the Federal scheme, stating that ' My Way is the best way. ' But who should get to decide what the 'best way' is? Those who will be directly affected by the scheme, or those 'stakeholders' who have vested interests? In his latest opinion piece , Gilchrist not only fails to disclose his own vested interests , but tells West Australians that the scheme is destined for failure because the 'amounts being paid for services being paid for services by the NDIA will not...

Transcript of the Opinion Piece in today's West Australian.

The West Australian, Monday 28 September 2016 Summit throws down gauntlet on NDIS cost By David Gilchrist Last month’s National Reform Summit was one of he first realistic and open policy discussions we have seen in Australia for a long time. It included participants from industry, unions and non-profit and community groups and, essentially, laid down a challenge to politicians to implement real reform in a comprehensive rather than a piecemeal and politically-averse way. One of the key areas of focus was the National Disability Insurance Scheme, and for the first time industry and government leaders are realising the challenges of implementing this critically important policy. The summit identified that this important initiative was likely to be more expensive and more complex than seemed to be understood in policy circles and that the rollout of the scheme was at considerable risk if there was not a more realistic policy discussion – focused on demand and true cost. This ...

The Specificity of Pain

‘White people weaponize both the concepts of individuality and equality in order to deny that they constantly perpetrate patterns of abuse by denying the specificity of marginalized experiences and pain (which, in itself is a form of abuse).’ – Cassandra L. I sat in front of the man at the conciliation conference, and he looked at the file. For a long time, fixedly. Finally he spoke. ‘You said in your message that you were ‘slightly concerned about how this is going’. That really doesn’t reflect that you felt discriminated against, or that you were hurt in any way, does it? ‘Slightly’ concerned?’ I blinked. We were there to discuss a physical barrier that his organisation had installed to prevent cars from entering a site. That had also stopped me and other wheelchair users from entering the site, something they admitted that they hadn’t thought about. I could feel my face reddening and my throat closing up. The last time I’d been in this room, I’d been at another con...

'Oh, what a feeling...exploitation.'

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"Every year, small children die in their driveways when their parents accidentally reverse over them in their SUVs. Take a photograph of yourself doing a Toyota jump in your driveway to raise awareness about the perils of childhood!" "Too many toddlers and children drown every year. Last year, 30 children under fourteen drowned in pools, at beaches and at inland waterway locations. You can help raise awareness about the possibility of drowning by taking a photograph of yourself in your pool and posting it to Facebook! Don’t you think they’re good campaign strategies? Why not?" That’s right. They’re offensive. The idea of your healthy, live child posing in the same place that someone else’s dead child has been to ‘raise awareness’ is a horrible idea. Yet Epilepsy Australia has chosen to do just that, with their ‘epilepsy australia bubble bath challenge’ campaign. They’re saying that you can ‘raise awareness’ – and, of course, funds – by posting an ima...

'Learn, Respect, Celebrate' - and other trite, white, phrases.

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Image description: Children play in raw sewerage around a toilet block. There’s a running joke in the disability sector that goes something like this. Q: If the 3rd of December is International Day of People with a Disability, what happens on the other 364 days? A: Discrimination. I’m reminded each year on that day by the hypocrisy of the sector, who hold breakfast events to celebrate IDPwD despite most disabled people being unable to attend, who speak in glum terms about two percent employment rates and then do nothing to remedy it, who do things for us and to us but never with us, and consequently seldom get it right. But sometimes I see this happening in other sectors. That happened this week, and it hurt my heart. Down the centre streets of Perth, flags are proudly flying for NAIDOC week. There are celebrations in parks, in schools – even a ‘Miss NAIDOC Perth’ event for young Aboriginal women to be ‘trained’ in grooming and deportment and leadership skills. The the...

I'm Not Here For Your Entertainment

‘How would you do that?’ I asked the job candidate. She’d applied for a job in the disability sector, and I was interviewing – one of the questions related to the ‘how’ of making systemic change in the sector. ‘I would find people and get them to tell their stories,’ she said earnestly, and I made a mental note – she was the third in as many interviews who had spoken about the importance of using people’s stories to create systemic change. She’s not the only one. Bolstered by the success of Twenty Years: Twenty Stories, former Disability Discrimination Commissioner Graeme Innes has long been a proponent of the use of the stories of people with disability to transform the system. We all know it works – telling a personal story adds that extra, authentic, undeniably effective element. The BSWAT decision, the result of a concerted wage justice campaign, would not have been made if Messrs Nojin and Prior had not been prepared to tell their stories about being paid $1.85 an hour. D...

An Open Letter to Jules Anderson

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Dear Jules At three thirty today, Parliament are being asked to say yes to a national inquiry into disability violence, abuse and neglect. I heard today that you are standing shoulder to shoulder at Parliament with other disability advocates, making your voice heard. When I watched the Four Corners episode, where you talked about being raped by a disability support worker, I cried. You spoke out with such ferocity. You understood that this man was wrong to do what he did. You spoke up, and he went to jail, and now the nation waits to hear what our Government will do. I don’t know if you know how important your voice is. That you have made change for hundreds and thousands of Australians with disability – no matter what they say today. You were not just speaking up for yourself. You were speaking up for every single woman with disability who has been raped or who has suffered some other form of violence – that’s 90% of Australian women with an intellectual disability...