Saturday, April 15, 2017

NDIS still??

 Back in October 2015 I went to an NDIS meeting at Synapse. I blogged this in Whacksworks titled What will NDIS do for us? Have a read of that one. I don't think my questions were or will be answered.

I went to a second meeting at the City Council building soon after that, which was attended primarily by disabled people. It was supposed to give us a warm intro into NDIS but I think I already knew much about it. And I still didn't think it would work.

Over the next year I saw too many articles which said that disabled people had been broken down with their sincere effort trying to get in. On 1 July 2013 the Tasmania government signed up for a 3-year trial in 2013, and on 11 December 2015, not even 3 years, signed on to the “real” NDIS. It has causes headaches. One was the family of a 13 year old boy who has dystonic quadriplegic cerebral palsy. He wasn't eligible from July 2016, but his family has fought NDIS to get him listed. Another was the family of a 26 year old woman with autism and non-verbal. So far, after too many “plans”, they still haven't been able to get her registered.

In August 2015 in WA, the WA Today said that their own model should be supported, rather than the national scheme which “continues to face criticism”.

CEO of Nulsen, Gordon Trewern, said: “We've still got problems with the NDIS Commonwealth model. There is still a key issue around pricing. The funding is still 27 to 30 per cent below what it needs to be to run a service for five people in a group home.”

Natalie Thompson, who cares for her 16 year old son, told the Joint Standing Committee on the National Disability Insurance Scheme: “We did have funding through the old system, which worked great, and he was doing really well for a couple of years under the old system. When we went over to NDIS, that all changed. They cut our funding dramatically as well.

In December 2016, nothing had changed. One mother from Perth said: “There's ... less money handed out. Because I self-manage our funds I'm given a limit of $25 per hour to pay for support workers, which often means going for unqualified workers.” Her son is deaf, and relies on cochlear implants to access sounds. That, unfortunately, has “convinced” the Disability Insurance Commission that he's not deaf! 

On 16 April 2016 the Australian wrote a long federal article titled Monster that ate the National Disability Insurance Scheme, and said: “From today’s vantage point, the medley of early mistakes have matured into a scheme that is riddled with access issues, slow planning turnarounds and questions about future design that will have huge effects on its financial sustainability. The pace at which the NDIS must grow is about to jump astronomically: the agency says it will need to make 12,000 decisions a month for the next two years.” This is worth reading if you believe that the NDIS has problems.

In 2015 the Sydney Morning Herald wrote various articles about NDIS, including the concerns shown throughout NSW which raised “ many questions [which] remain about the future of disability services in NSW.” They wrote that: “There are about 400,000 people with a disability in NSW, with up to 240,000 having a high degree of disability, according to the Australian Bureau of Statistics. With 140,000 people expected to be eligible for the NDIS, what will happen to the other 260,000 people? Where will they get support?” 

In December 2015 the SMH wrote that disability groups had “an alarming lack of confidence in the NDIS roll out ahead of the full transition to the $22 billion scheme which will launch across the country next year.” 

Qld doesn't seem to have had articles yet, because this state isn't fully opened for NDIS until 2019. So far there are a few people who have registered: certainly not enough.

This year, in March, the ABC reported problems. It's title said National Disability Insurance Scheme rollout plagued with problems, FOI documents reveal. Much information was revealed in those documents, including the facts that NDIS “stopped processing thousands of applications from service providers, critical staff were untrained and properties were not ready when the scheme's nationwide rollout began.” Back at the first meeting which I attended (Synapse, October 2015), I had asked how the shifting of “critical staff” worked. We got ignorant replies, and we had nothing in writing to show how it would work. Recently I searched Google for organisations which would help disabled people through NDIS. Many are not listed. ABC said this year that “[b]etween 3,000 and 4,000 businesses and not-for-profit providers were blocked from entering the scheme because applications could not be transferred to a new IT system.” It is very scary to both those providers and to the disabled people who have previously used them – can they still use them?

Federal minister, Christian Porter, didn't answer questions from ABC. He sent them on to NDIA to speak to NDIA spokesperson Maryanne Diamond. There has been no real responses from her which would have answer my questions.

The NDIS website has a list of how the disabled person might be able to register as a participant. It lists the access requirements and discusses how a disabled person could get

help. It says that you have to produce proof of your disability. The scheme is not due to be fully opened in Qld until 2019, but has different dates until then – for instance, the Logan area where I live will be available from 1 July 2018.

For the NDIS, I still have a lot of questions – and I'm sure I will have problems. I had a stroke 3 years ago, I am on DSP and I have aphasia which kicks in when I am tired (constantly) or upset (too often). I'm told I can only work 8 hours a week for now. Would NDIS pay DSP? Would they rearrange my hours so they can kick me off their scheme – less money in Newstart? If the people who have already met with problems, are they worse disabled than me? If so, why were they declined?

NDIS needs to work a lot better to fix their own problems, but they also need to definitely answer the questions that any disabled person, any family supporters, any friends, any carers or anyone involved with supporting disabled people still are asking.

When will they fix that?









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