Monday, 19 February 2024

Be Careful What You Wish For...

2024 has already become synonymous with some pretty weird twists and turns adding excitement to our rather action-packed lives. We are only just over half way through February and I am wondering, once more, what else the universe could have in store for us...

We started the year with two absolutely spectacular wins. Think the Big 4 banks are immovable? Think again. After three months of financial stress, woeful customer service, exposure of appalling bank practices and a vast miasma of misinformation and misdirection, we applied to the Australian Financial Complaints Authority (AFCA) to examine our case. An offer for compensation appeared faster than a speeding bullet. Would I tackle one of these juggernauts again? Yep, by going directly to the AFCA, rather than farting around with an organisation unwilling to assist a customer.

Then, there was my battle with the NDIA/S over eleven months to be reimbursed for the purchase of Alex's CPAP machine, which we tackled as improving his daily functionality, reducing his anxiety and allow him to live safely in his own home by having restful sleep. In addition, we wanted to access Alex's existing funding for this refund of $1694, not more funding. 

Eleven months of stalling, squirming, and stymieing. We were repeatedly told we needed to have three internal reviews before applying to the Administrative Appeals Tribunal (AAT). We were caught in a web of Chinese Whispers where even Alex's Local Area Coordinator (LAC) was confused and misled. That assertion about the number of internal reviews - total fiction.

Eventually, we applied to the AAT in December. We were set for our first meeting with the AAT on 15 January to discuss the process. I had been warned that the Tribunal did not move quickly and their decision could take up to a year to deliver. Surprisingly, I was comfortable with the concept of waiting.

Out of the blue came an offer from the NDIA. An offer to reimburse $1694 for Alex's CPAP machine. Golly gosh. We accepted with alacrity. Needless to say, the actual payment took as long as pulling a tooth out with a piece of string. Two days before I was due to speak to an AAT lawyer, the refund lobbed quietly into our account.

The whole episode was handled like two blokes in sweaty suits passing a money in a grubby brown paper bag under the dashboard. We were not offered a receipt. The payment was directly from the NDIA without touching Alex's funding. No paperwork, no trail. 

I would love to believe the NDIA had a change of heart. Unfortunately, our refund was all about economics. Payment for Alex's reasonable needs versus the cost of a NDIA lawyer for one day. I didn't have to be a rocket scientist to work that one out.

I have always believed that knowledge is power. I want to know the truth. I want the details so I understand and can make informed decisions. I also dislike not being taken seriously when I know otherwise. 

Thirty years ago, I was involved in a quest of a diagnosis for Alex. Hyperactivity with developmental delay didn't quite cut it. We kept seeing specialists, accruing more information, trying different treatments, supporting the skills he had. ABA therapy, which we began when Alex was four years old, was, for us, a miracle. We knew he was going to do well. We knew he had normal intelligence. And in November 1995, Alex was diagnosed with Autism. I was triumphant for about five minutes. Then I cried for eight weeks. 

Fast forward to recent times. Alex was finally diagnosed with an Acquired Brain Injury in 2022, which most likely occurred after cardiac surgery when he was seventeen months old. Thirty years of being disbelieved was sorted by a Neurosciences assessment and one MRI. Once more, I was elated. And I was livid with rage for all that lost time.

Now we come to the crux of this post. Last year, I had a mild dose of COVID. Mild because our doctor put me on anti-virals immediately. My symptoms mimicked a bad cold.  Seven days later, I tested negative and returned to the usual circus of our lives. But what was COVID's possible legacy?

In early October, I started becoming breathless. When this unpleasant issue didn't pass, I saw our GP. Apparently, I had some sort of odd lung inflammation and I was gathering fluid around my lungs. Antibiotics really didn't help. And then, I boarded the merry-go-round of tests and specialists. Chest X-ray, chest CT, ECG, Echocardiogram, exercise test, bloods and a Doppler to look for blockages. Discovery of two heart defects I'd had from birth. A couple of leaky valves that are currently non-problematic. A cardiologist with a poor bedside manner who did not impart any findings I so desperately craved.

My final port of call was to visit Scott Claxton, who is both Alex's and Michael's respiratory specialist. We first met Scott in 2014 whilst Michael was treated for double pneumonia in Joondalup Hospital. Scott is approachable, compassionate, thorough and crystal clear. However, I was still expecting to be told I was just a fat. lazy, anxious woman who needed a kick in the pants.

The appointment with Scott was last Friday. Michael was also seeing Scott for a review and general check. Scott knows Michael's lungs very well indeed. The mere mention of Michael's throat infection that was not responding to standard antibiotics sent Scott reaching for his prescription pad for stronger antibiotics.

Then, very matter-of-factly, Scott explained that I have Pulmonary Hypertension. High pressure in the arteries going from the heart to the lungs means the heart has to pump harder. Then Scott explained that he believed this diagnosis to be a symptom of another condition. This afternoon, I undertook a nuclear medicine appointment this afternoon to look at pressure in the arteries, the lungs and check for a pesky embolus that may be lurking, contributing to my breathlessness. Plus blood tests. We finally set off for home just before six o'clock.

I am researching conditions associated with Pulmonary Hypertension. This is not particularly positive reading. And I am dealing with the realisation that I have developed a chronic and potentially fatal health disorder. I don't think I was quite ready for this news. Hmmm...

How am I going to deal with this latest revelation? Do as I usually do. Seek knowledge. Make informed decisions. Never give up...

Welcome to 2024...

 
One of ANZ's problems was keeping their story straight!

 
My considered opinion late in 2023
 
 
  
 
An then...an offer for compensation just after I applied to the AFCA!
 
  
 
A miracle! 

 
What we wanted for Alex... 

 
A long and frustrating road...

 
Compassionate reimbursement or cynical economic decision...

 
One of my greatest hopes...

 
Nobody expects the Spanish Inquisition! 

 
Well that was a surprise...

 

 




Saturday, 17 February 2024

The Law IS An Ass...

Back during the 1600s, a couple of playwrights had their claim to fame by including the phrase "the law is such as ass" in a play called either "Revenge for Honour" or "The Parricide". George Chapman and/or Henry Clapthorne might have written/published the play in around 1654, but some historians disagree and suggest the play was produced in the 1620s by somebody else.

Anyway,"the law is an ass" was also mentioned by Mister Bumble, the unhappy workhouse proprietor and hen-pecked husband in Charles Dickens' "Oliver Twist", whilst in court. Mister Bumble was responding to a supposition that the law dictated his wife acted under his direction. His reply - "If the law supposes that," said Mr. Bumble, squeezing his hat emphatically in both hands, "the law is a ass - a idiot".

And there is the sledgehammer sized hint regarding the meaning of this phrase. The "ass" in question does not refer to an American's bum, but rather -

"This proverbial expression is of English origin and the ass being referred to here is the English colloquial name for a donkey... Donkeys have a somewhat unjustified reputation for obstinance and stupidity that has given us the adjective 'asinine'. It is the stupidly rigid application of the law that this phrase calls into question".

The last six months have only affirmed in my mind that the law is, indeed, an ass. Back in 2023, I presumed that the matter I can't discuss was settled during that awful Shuttle Conference I was required to attend. That debacle took months for me to recover my well being and mental health. Just when I thought "it was safe to go back in the water", I received a Summons from our very embarrassed local coppers that I had to attend court again.

Another pretty dreadful day. As the Listings Department obviously don't care about people's locations or travel time, we had a 9.30am Cattle Call. Not sleeping well the night before meant I was awake just after 3am, gave up on slumber at 5am and we left at 7am. We entered the Building and found our way to the waiting room outside the assigned court. The chairs could not have been more uncomfortable if they tried. There was no facility for making tea or coffee and no food was allowed to be consumed.  We probably committed an unpardonable offence for taking in our water bottles. 

And so, we waited. We watched people of all walks of life come and go. We stretched our legs within the waiting room from time to time. We could plead guilty to another mortal sin. We didn't turn off our phones. I was surprised that we were not struck down... 

11.30 am came and went. We had paid for parking until noon. Just as we were getting rather edgy, we were finally shown into the Inner Sanctum. The magistrate was quite personable. He explained that the Applicant hadn't turned up, which meant that "the Variation" would be dismissed. We were free to go.

That was that. By this point, I had been awake for nine hours. We had driven for two and a half hours and sat in a humourless, featureless waiting room for over another two hours. I was exhausted, confused and distraught. I queried how this farce could have been allowed to happen. I had no clue how the Applicant had obtained the an order for variation and who had supplied it. I left the court with Michael none the wiser, also knowing the Applicant could orchestrate this scenario again. The law, for us, was an ass.

But why are these fiascos acted out every day in court? Why is information so difficult to extract? Why is the jargon so incomprehensible? Why did the Magistrates Court strip away facets that make us human, like comfort and create such a sterile environment? We had almost no interaction with any court staff for over two hours. Don't they have a Duty of Care to those in attendance? 

The Law is like a Secret Society. Another Department of Stealth and Total Obscurity. We arrived with no information except the Summons and left with precious little more. Surely, this is not how the Law is meant to be delivered.

The good news is that we now have an ally, who introduced himself to us, as I sat crying in yet another uncomfortable chair on the ground floor. He has made our world a little more secure and I thank him wholehearted for his approach to us. 

Stay tuned...

 
I am currently on this opinion...
 
  
 
I wouldn't be surprised... 

 
Do lawyers actually understand the law? 


 
Introducing Wank Words!
 
 




Then why is legal jargon used so often with people who have no idea of the meaning of this peculiar language?


Food for thought...

Adding the Law to this list...

 
And how is Justice obtained by the usage of the Law?

Thankfully, we know have a knight in shining armour to turn to in times of trouble.


Friday, 9 February 2024

Never, Ever Give Up!

Yesterday was one of those days I never believed would actually  happen....

2023 was consumed by three sagas that tested me intellectually and emotionally. A fight with one of the Big Four banks for compensation related to appalling and misleading practices plus, at times, a total lack of coherent information. That ordeal lasted three months. After I submitted this tale of woe to the Australian Financial Complaints Authority (AFCA), suddenly ANZ wanted to resolve this issue. Before any action by the Ombudsman could be taken, we were awarded what I consider to be a fair amount for the extreme mental and financial stress that the ANZ and its subsidiaries had caused. And I am far more knowledgeable about the jargon and the structures within ANZ that are designed to bamboozle their customers.

The other seemingly never-ending story concerned the NDIA (National Disability Insurance Agency). After Alex became a participant in the NDIS (National Disability Insurance Scheme) in October 2019, I thought this organisation would be a godsend for families like us. Supports tailored to individual needs, inclusivity and the chance to live as "ordinary" a life as possible were such noble ideals. We all grasped eagerly at these opportunities. 

Alas, the reality has been somewhat different. The NDIA has a language all of its own creation. They are masters in misleading not only their participants, but those who work within the constraints of this juggernaut. For example, our Local Area Coordinator (LAC) believed the NDIA had added Alex's diagnosis of Acquired Brain Injury to his profile, after she had uploaded all the required information. The NDIA do not believe Alex's ABI is disabling enough to warrant recognition as a second diagnosis to Autism.

Since 2019, every single NDIS Plan for Alex has been unsatisfactory.  When I complained that Alex does not understand his Plans, I was reminded by a delegate that was my role to translate the contents. When I pressed the issue, explaining I had difficulties comprehending all the separate funding terminology, I was met with silence. 

I also believe the NDIA engages in obstructive behaviour. We have experienced roadblock after roadblock when dealing with the NDIA. Funding for air-conditioning for his well-being refused, with excuses of lack of medical information and that we had missed an unknown deadline. Delays with review after review. Demands for further evidence to be scruntinised by the NDIA and then either dismissed or rejected.

in March 2023, Alex was diagnosed with Severe Obstructive Sleep Apnoea. He needed a CPAP machine immediately. Which we purchased as he would never have been able to afford one. Yes, there were significant health benefits but we concentrated on presenting his CPAP device as an instrument of well being. Alex's improved sleep quality would lower his anxiety, improve his daily functionality and allow him to participate in life without being exhausted. We were confident of reimbursement. Needless to say, the NDIA disagreed.

We have fought this decision for the last eleven months. Given the NDIA's propensity for smoke and mirrors, we kept appealing this decision, wasting time on internal reviews. I understood we needed to undertake three internal reviews within the NDIA before we could apply for an independent review by the Administrative Appeals Tribunal (AAT). This is not so. I could have applied to the AAT after the first decision by the NDIA. This information was never made clear, with contradictory advice given to Alex's LAC, his Support Coordinator and us.

The reimbursement for Alex's CPAP machine was never about additional funding. We just wanted to have permission to use some of his existing funding for this purpose. 

Some time ago, a crusty senior GP insulted us to our faces. He berated us - "people like you are why the NDIS is going broke". We swiftly cut ties with that practice. I doubt that ignorant and prejudiced doctor will ever change his views. If other medical professionals are spouting comments like this to vulnerable NDIA participants and families, God help us all. What his remarks did cause was creeping doubt and disillusionment in ourselves and in our quest for a better outcome for Alex and us.

We finally applied to the Administrative Appeals Tribunal (AAT) for an independent decision late last year. With help, we secured an advocate from People with Disabilities (PWD), who warned us that the process may take 12 - 18 months. I was prepared to trust the Tribunal and wait for its decision.

The NDIA offered us complete reimbursement almost immediately after we applied for an independent decision by the AAT. The payment was finally released into our account yesterday.

Not surprisingly, the action was entirely economically based. I would have loved to say the NDIA had an epiphany of conscience, but they would have worked out the cost of a lawyer for a day before the AAT  would cost far more than reimbursing us for Alex's CPAP machine.

I have been told by the AAT that I can share the following information publicly. Families or NDIS participants can apply to the AAT if their internal review has been rejected once. Not twice, not three times. The AAT is entirely independent. Often an application to the AAT will result in a positive outcome as the cost of the service/device may be cheaper than a lawyer contesting the case in court. Good to know...

We have won cases with ANZ and the NDIA. I was tempted to give up so many times, such was the emotional turmoil caused by their deliberate and merciless excuses and delays. I had hellish days of doubt and misery. I had to pull myself out of the abyss and fight on because we believed we were in the right ...

The final hangover from 2023 can't be discussed publicity. Once again, our integrity and honesty is under fire. So, I shall don my invisible protective armour and prepare to engage the enemy once more. Michael is accompanying me and I am better prepared than last time.

Wish us luck..

 

ANZ and the NDIA should receive automatic honorary  membership!

Just saying...

 
Not the best experience...

 
Take a good look at Mister Shayne Elliott, CEO of the ANZ. Staff or customers? Should be have a bias?

 
Three months of harassment caused huge anxiety... 

 
And suddenly, an application to this saviour  fixed the issue!

 

What a good question!

 
Roadblocks and resistance tactics utilised by the NDIA...

The creation of a language that is deliberately complicated... 


 
An impossible dream?

 

Another pathway...

 

 
Actually, that's all I am permitted to say about that...

I discovered the following document when I Googled " NDIA Obstruction". Although the document is written about the experience of South Australian NDIS participants with high needs, the findings are relevant to the operation and structure of the NDIA in 2024. Note the date this document was submitted...Wordy but vital that this document is read and made public.
 

 "General issues around the implementation and performance of the NDIS Submission 97 - Attachment 1

NDIS Solutions Paper
This paper is to be read as Appendix 1 to ISSUES PAPER ON THE OBSERVED OUTCOMES OF THE
NDIS by Alister Morton undated paper - file saved 21/3/2021. It should also be understood in the
context of the cohort of people primarily with Intellectual Disability and who are accommodated
in Supported Residential Facilities or Community Supported Housing with predominantly 24 hour
supports.


KEY POINTS
1. Older persons in South Australia with congenital or life-long disability ARE the most
vulnerable citizens as they are mostly without significant Advocacy support from family or
significant others.                                                                                                                                  Solution – Independent Advocacy provided routinely for persons who require nominee or legal
guardian.

 
2. NDIS funding is not objective and equal or consistent across Participants in the program.
Solution – NDIS funding should be standardised and commensurate with diagnosis and objective
functional status of the participant.

 
3. NDIS funding is open to Political bias rather than individual Participant need.
Solution – NDIS funding should not either require strong advocacy or action based on Political
complaints or intervention – an agency separate from Government should administer the system

 
4. NDIS has discrimination inbuilt at core – Agency Managed Participants DO NOT have access
to providers of choice as Self and Plan Managed Participants do.
Solution – All Participants should have equal freedom for Providers of choice. NDIS Quality and
Safeguards and Provider Registration should be disbanded as had been ineffective and wasteful
and obstructive.

 
5. NDIS funding is determined by largely non-clinical NDIA Planners
Solution – All determinations and assessments should be carried out or informed by Qualified
Professionals with Specific Qualification in Disability or Health as situation requires
.


6. NDIS Planning Meetings are provided often without true Multi-disciplinary collaboration and
meetings are not minuted – minutes are not provided to Participants / Nominees as a true
record of Planning Meetings.
Solution – All Planning Meetings or formal determination meetings should be minuted and
accepted by all parties. Planning meetings should provide proper opportunity for Multidisciplinary
input.

 
7. NDIS Plans including Participant Profiles and Goals are quite often false or at least poor
constituting effective fraud on behalf of a Commonwealth Officer.
Solution – Plans should be developed by a person who has direct face to face knowledge of the
individual and their circumstances and should reflect minuted Planning meeting minutes
(currently none).

 
8. Many Participants in SRF’s have had effective funding reduction limiting access the same
amounts of funding for Accommodation Support, Day Options / Programs and Therapy.
Solution – Urgent review of pre-transition funding and services and comparison with current
funding and services. Key funding areas must be reported if Plans are assessed year after year and
cannot be reduced except for where a person’s disability has improved. The system needs toGeneral issues around the implementation and performance of the NDISSubmission 97 - Attachment 1
properly understand the needs of the majority of it’s population and not concentrate primarily on
the younger developmental cohort.

 
9. Most Participants (almost all) have lost the standard yearly Respite / Holiday away from the
SRF due to insufficient funding for specialling or respite staffing
Solution – All participants should have adequate staffing SIL funding to enable individual activities
on a weekly basis and at least yearly respite from the principal place of residence if appropriate.

 
10. Participants in the Govt and NGO sector have had an effective cut in Support Coordination
funding of about 75% per person as well as Service Coordinators being more disconnected.
Solution – All participants who cannot act for themselves should have at least 12K Support
Coordination – ideally this should be undertaken by a Key person acting as a Local Area
Coordinator according to the original principal. This equates to only approx. 1 day of active
coordination per month. This was the approximate level of Program Service Coordinator funding
provided prior to transition in Govt and NGO Accommodation Services for this cohort.

 
11. Govt Accommodation Services or NGO’s who were primary advocates for many Participants
are now reduced to a position of conflict of interest in being the ‘Service Provider’
Solution – Independent Advocate to be provided.

 
12. Participants do not have easy and User-friendly access to NDIA support – the LAC system
that was meant to be incorporated into the NDIS seems to have diminished.
Solution – LAC system rediscovered and reintroduced to deliver person-centred, direct,
accountable, Case-management style coordination.

 
13. Access is difficult and impersonal for contact with NDIA Agents (Planners etc.)
Solution – Eliminate the Centrelink style Federal system and provide a Local, Accessible,
Contactable scheme.

 
14. NDIS Satisfaction rating is possibly skewed toward those who have capacity to provide
feedback. Experience and dialogue with participants would suggest that the advertised
satisfaction rate is highly inflated either by demographic, method, or reporting. An overall
satisfaction rate approaching 90% seems incredulous and inconsistent with participant
feedback.
Solution – Urgent review of data collection and reporting. Equal weighting for participants without
ability to feedback, and review with professionals how to reasonably gain true feedback about the
system where a person cannot do this themselves. Ensure a method for staff to make confidential
complaints about loss of services or treatment for participants.

 
15. NDIA Quality and Safeguards has failed to provide reasonable outcomes and has not faced
any known consequences in the wake of the Annie Smith affair.
Solution – Disband Quality and Safeguarding as stands as it has failed to provide. It has to my
knowledge not sought to measure or appreciate any loss in Quality or safety in the provision of
services. Community Visitor Scheme should be massively upgraded and States (or perhaps even
local Councils) should be funded to monitor and report on the performance of the Commonwealth
(if it is to remain a federal system).

 
16. Govt COS Program Participants have extreme limitation with services only able to be
delivered by one specific provider under agreement with SA Govt. The COS unit is somewhat
obscure with very limited ease of contact and information to Participants.General issues around the implementation and performance of the NDISSubmission 97 - Attachment 1
Solution – All Participants irrespective of funding relationship should be provided with equal
access to personal choice and freedom of provider in a truly ethical fair system.

 
17. NDIS Finance Committee has failed to appreciate market forces in relation to Therapy and
the function and efficacy of Allied Health Assistants.
Solution – Allied Health Assistant rates should be dramatically increased to reflect the real cost of
delivery of these services and to appreciate the benefit of delivering more services for less. Why
not motivate a market that looks for more cost effective options rather than providing incentive
for increased professional and more expensive input. This also helps to increase employment and
status of lowest paid workers (essentially paid commensurate with Personal Support Workers).
An Allied Health Assist may cost $55/hr to retain their services and NDIS funds at $48 if under AHP
direct supervision and $86 if under indirect supervision. Employees may make 70% billable KPI
which means there is a slimmest of margins even for an AHA level 2. An AHP (PT) may cost $75 /hr
to retain and NDIS funds at $224 / hr. Once billable potential taken into account the margin here
might be 50% ($112 / hr). Why would an employer faced with this reality look at increasing it’s
workforce / capacity with a larger number of personnel that bring little or no margin? AHA level 1
rates should be deleted as the same skill set and employee cost is most often required whether
the Physiotherapist is providing direct supervision or not and the Assistant is paid no less because
they are assisting the Therapist directly with a complex participant. AHA rates should be increased
to $120 / hr. Higher PT rates should be reviewed as this causes market forces that may alter
preference for therapist for similar work e.g. AT provision by OT rather than PT.

 
18. NDIS has failed to recognise the benefit of Govt and large NGO Agencies in promoting the
rights and programs for people with a disability, for developing links and providing
opportunities for tertiary education and research in disability, and for the progression of
ethic driven behaviours, education and training in the disability sector.
Solution – NDIS Price Catalogue should be reviewed with better appreciation of market forces and
Larger Organisations should be provided with a surcharge ability or receive some bulk / … funding
to appreciate that they carry larger overheads. The current model is selective for the benefit of
sole traders or smaller businesses with few overheads.19. NDIS’ fiscal focus has resulted in wholescale changes and loss of morale and ethic across the
disability sector where it was understood the objective was to provide a Person-Centred
Approach rather than a fiscal centred approach.
Solution – Unsure of a solution – a personalised funding model will inevitably force it to be about
the money and not about the person. The previous Block funding model meant that finance
wasn’t necessarily individualised or decisions of support were not based on this but on need and
clinical priority. Some people simply missed out on services as others presented with higher
priority. Now what determines service is funding not need or priority and sometimes funding is
mismatched with need and priority and requires too much bureaucracy to administer making it
untimely, inefficient and poor. Except for removing the funding based model unsure of how to
solve this tendency.

 
20. Clinical Funding was previously prioritised by therapists familiar with the participant who
would determine hours provided according to need at the time. Now Clinical prioritising is
effectively approved by an NDIS Planner without Clinical registration (AHPRA) who in many
cases has never met the Participant, and through a process that creates delay and increased
risk to the Participant.
Solution – Clinical decisions should be made by a Clinician with direct assessment of the
Participant. Funding in many cases is a Clinical decision – not an administrative one. 

21. Rather than 1 CSTDSA battle per year and Each Provider battle with Disability Services for
block funding each year the NDIS has reduced funding to thousands of individual battles
with each Participant or their nominees
Solution – Disband the NDIA as a scheme which has failed to realise the expected efficiencies of
the 2008 DIG Report. Go back to a sustainable model before all the Providers have been
irreversibly damaged. This may already be too late. The only other option is a funding model that
is decided through true independent assessment – not assessment tendered and responsible to
the NDIA. Then again, the relevance of having an NDIA is the question.

 
22. NDIS has increased the stress and understanding of many families, carers, nominees of
people with a Disability who are mostly themselves limited or tired. It creates a system
which is complicated and uses terminology and processes that is often confusing. It would
be worth looking at family separation rates in this cohort.
Solution – The system needs to be Objective, Determinable, Consistent, Stable and non-
adversarial. It must provide a reliable and ongoing source of funding without constant review for
those whose disability does not significantly change and there needs to be again a personable,
local, direct assessment process by suitable person who is also responsible for the outcomes.
Research should be conducted into the stress for families and relationship to the NDIS.

 
23. NDIS has resulted in an overall decline of Lifestyle Planning, Care, and Support for many
across the sector, especially those who lack advocacy.
Solution – Proper Local Area Coordination to deliver fully funded effective Support Coordination /
case Management. Independent Advocacy and Community Visitors to check on care.

 
24. The OPA in South Australia fails to appreciate in writing in its Annual report the overall
negative impact of the NDIS and although listing concerns provides descriptions that are
slightly misleading and not clearly representing the issues.
Solution – the OPA should not report findings of the NDIS but should make their own assessments
about the effectiveness and safety of the Scheme. The OPA should understand that the cohort of
currently between 900 – 1200 individuals they hold in cases reflects only a small portion of the
number of people who cannot advocate for themselves in South Australia. The OPA should seek to
find information about unmet advocacy need in South Australia.

 
25. The Majority of younger Participants have nominees that are dissatisfied with the processes
and inconsistencies or injustices of the system. Some have seen significant increase in
support however acknowledge that the process creates considerable increase in stress in
families where there is already considerable pressure.
Solution – The scheme needs to be adjusted so that it is more standardised and less subjectively
inconsistent. It should not be as is commonly stated whether you get a good Planner or not.

 
26. The NDIS has failed to enable the full utilisation of allocated funds resulting in $6B returned
to Treasury and not utilised where it was assessed that it was needed in the last financial
year.
Solution – All unallocated funds for the scheme should be returned to the scheme in Capital
funding type projects or business supplement projects as unallocated funds usually occurs because
there was insufficient providers or resources. There should not be an incentive to Government to
not spend the NDIS allocated funding.

 
27. Many Disability Organisations both GOVT and NGO have lost asset base / income and
suffered significant financial pressure as direct result of overall decreased funding through
NDIS compared with the previous Block funding. This has resulted in significantGeneral issues around the implementation and performance of the NDISSubmission 97 - Attachment 1
rationalisation of services and training resulting in decreased quality of services and also
increased risk to Participants.
Solution – Some form of business surcharge or block funding for large providers to enable
competing with small concerns with few overheads.

 
28. Financial pressures on larger organisations have resulted in staff pressure and turnover, and
specifically professionals leaving and operating as sole traders and managing the overheads
that larger organisations can not mange.
Solution – As for 27

 
29. NDIS focuses on the younger cohort and with the term ‘Maintenance’ not being supported
in essence. NDIS considers it’s role is to increase function rather than maintain it. Clinicians
with long term experience in the disability sector acknowledge that the majority of Therapy
in the older person’s context is about maintaining function and capability not about
“Capacity Building’. This leads to a ‘disingenuous’ attempt for Professionals to have to build
programs and reports around the construct of development rather than maintenance. NDIS
must recognise the concept of maintenance.
Solution – NDIS must recognise and support the notion of “maintenance therapy”. Every person in
society can help maintain their fitness, well-being, and function and so Participants must be
provided with reasonable and necessary supports to maintain their Capacity. Capacity Building
Supports to be renamed simply Capacity Supports – if we must retain categories!

 
30. NDIS had failed to understand the intersect with Health. It is important that significant
health and Rehabilitation supports can be provided by disability specific and experienced
providers rather than that provided through normal SA Health programs.
Solution – Additional funding should be provided for Health-related Incidents and Rehabilitation
for a person with a disability to be provided by people who are trained in Disability. It is
unreasonable to expect that a person suffering a health related issue such as an ankle fracture
cannot be supported by their principal provider / therapist who knows the person best. Again a
true Local Area Coordinator should be accessible and able to assess the persons immediate need
and respond with delegated authority to approve additional funding. NOTE – This would also solve
the current SA issue of hospital beds being held by NDIS particpants awaiting accommodation or
change of circumstance funding processes and stop the building of hospital wards to fill with
people who are not truly SA health patients but find themselves in SA Health system as a ‘service
of last resort’.
Additional points from consultations with other Providers

 
31. Experienced provider estimates that split families rate is higher (potentially double normal
statistic) in the disability sector and this raises issues for “duplication of supports”. NDIS
needs to understand that equipment may need to be provided for multiple residences for a
child participant and also modifications to vehicles may be required to more than one
vehicle as it unreasonable to expect that one guardian would have to take all transport
responsibility.
Solution – Assess causes of stress for families supporting people with a disability. NDIS to
appreciate living arrangements of the individual and that duplication of supports may be
reasonable and necessary.

 
32. Previous system was a “wrap around” system which meant that family issues were
addressed with Social work and Psych. Current system is participant / child focussed and can
ignore the needs of families / parents.General issues around the implementation and performance of the NDISSubmission 97 - Attachment 1
Solution – A true Local Area Coordinator Model like a Case Worker or Key Worker with adequate
funding to properly engage a multidisciplinary team. NDIS and States need to assess what was
provided prior to NDIS transition and compare with what is provided now and test whether it
meets the “no worse off” clause of the Act.

 
33. Interface with Health has been stated as an issue but also the interface with education and
DCP and Housing has ongoing and exacerbated issues as a result of the NDIS.
Solution – NDIA need to review issues of responsibility and barriers created by jurisdiction
arguments and eliminate these through proper agreement and management.

 
34. Old systems created Capacity Building – NDIS creates Dependence. One provider feels that
limitations in funding previously promoted maximising building capacity around the person
whereas a fiscal system flooding the market in some areas creates dependence and
increased use of therapy hours.
Solution – Unsure – NDIA have been fiscally reckless in many cases potentially in order to help
transition and acceptance of the scheme and then have to find ways to limit funding in subsequent
plans. Research of overall Plan trends for cohorts should be published
.


35. State V Federal funding responsibility conflicts. Example Housing HSA refuses to do home
mods as “it is a disability issue”. Before NDIS some mods ok but now it is a problem with
changes noted 6-12 months ago. Provider believes that HSA has obligation as does
Education DECD to provide Disability specific access / needs and it is not necessarily a NDIS
responsibility.
Solution – Age old problem when more than one person responsible – similar is happening even
within people’s Plans with lots of inefficiencies and duplication of roles with Support Coordinators,
Plan managers, Planners, LAC’s, SSC’s, Therapists, Nominees, Providers. Often lots of talk and no
action. Key solution is accountability and responsibility – a team decision and action list that is
minuted. A Key person (LAC) who holds responsibility.
NDIS should not continue to state its goal is to make Disability Funding Affordable or the Scheme
affordable. The NDIS Act should be ensure that a Reasonable and Necessary Support system is fully
Funded.

 
Alister Morton
21/9/2021

Physiotherapist B.Ap.Sc. APAM _ Morton Health, based in Adelaide, South Australia - office@mortonhealth.com.au

"Advocacy, not adversary - Insurance, not welfare -Connection, not confusion 

NDIS reform - we need it now"




Thursday, 8 February 2024

If You Could Read My Mind...

Gordon Lightfoot was a prolific Canadian singer and songwriter. His song, "If You Could Read My Mind", was released in 1970, apparently conceived as he contemplated his divorce from his first wife, whilst sitting in his empty house in Toronto. I have always loved this song, the message, the emotion, the honesty he appeared to embrace on a failed marriage.

Except with a bit of digging on Google, I have discovered that Gordon was really rather a naughty boy, A serial philanderer, he was just a bloke ruled by his willy. Three wives and a notorious relationship with Cathy Smith, who was not a nice person. She was responsible for giving John Belushi a lethal cocktail of heroin and cocaine in 1982. Sadly, this information doesn't sound like Gordon was an entirely misunderstood party after all... *sigh*

In spite of this disappointment, the title of Gordon's song actually had relevant meaning at Station House this week. Towards the end of the last heatwave, I noted that the courtyards needed attention due to the winds that had blown leaves and other rubble into my previous pristine spaces. I was looking forward to the cool change to take hold of the broom for purposes other than transportation.

Lexi, our eight-month-old Poodle/Retriever has astonished us with her intelligence and her keen interest in gardening. I would swear that she was listening to my desire for a cleaning frenzy and decided to assist.Maybe she had even read my mind...

Recognising that the tissue box had shown homicidal tendencies on a regular basis, she dispatched that risk with gay abandon. In fact, we have had a number of tissue boxes annihilated over the last week, Lexi being the only keen observer to their evil intent. 

Lexi's next assessment was to realise the potential danger that my tomato plant possessed. In order to protect us from its lethal intentions, she decided that its elimination was the safest option. She efficiently exterminated this predatory bush, dragging the corpse and most of the potting mix into the house and onward to the dog crate. There, she ripped the final mangled remains asunder, making quite sure it posed no threat to us ever again.

She had also entered the house via her wading pool, sliding delightedly across the lino, leaving a trail of muddy paw prints in her wake. With her lack of attention to avoid leaving forensic details, a future career as a successful burglar will have to be put on the back burner. 

Upon arising on that momentous morning, Lexi was basking in her triumph, Stella was avoiding eye contact with any of us, the cat was thoroughly disinterested and the pirate parrot was giggling and chatting. In a final flourish, Lexi had piddled on the floor, knowing that I would have a handy pile of slightly chewed tissues within reach to facilitate the necessary mopping up.

Our Number 1 priority was watering, as per usual. Michael started in the front courtyard, I set the hose in the back courtyard and by the time we met in the middle, our main courtyard had been thoroughly swept and returned to some sense of normality.

 One of the fabulous attributes of being somewhat aged is that situations like this merry catastrophe do not upset me anymore. Instead, I stood there, roaring with laughter as Stella discussed beating a fast retreat with Lexi in case my mood altered. What would have been the point of becoming angry? Our puppy on stilts has entered teenagedom and we just have to endure antics of this sort until she grows out of them. Stella, our previous Destructo Dog was particularly famous for chomping her way through innumerable thongs, two leather couches and three club chairs during her teenage months. She is now a thoroughly sensible four year old, who apart from annoying the cat, has settled into a very mellow existence.

The moral of this story? Even during trying or irritating times, we have a bunch of comedic pets whose lives revolve around us, showering us with unconditional love and putting smiles on our faces every single day.


 
Gordon Lightfoot in his younger days...

 
 

 
One never knows if a psychotic teabag is going to sneak up behind us...
 

 See, "Mythbusters" agreed with Lexi's assessment...
 
 
 
Adam with the killer tissue box...

 
Our first hint that Lexi had been busy - an empty cat kibble bowl...

 
Beware of the tissues!

 
Lexi just can't help protect us enough...

 
Do you think she might be cranky?

 
Introducing the indoor garden crate!

 
There had obviously been quite a battle...

 
The heroine...

 
The bystander...

 
The scene of Lexi's brave stand...

 
 

 
That tomato bush might have put up quite a fight!