[2020] AATA 3452
General information, not legal advice.
Administrative Appeals Tribunal of Australia
2020-09-08
Original judgment source is linked above.
The Tribunal sets aside the decision under review and in substitution decides that the Applicant meets the access criteria under s 21 of the National Disability Insurance Scheme Act 2013 (Cth).
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NATIONAL DISABILITY INSURANCE SCHEME - access to scheme - disability arising from impairments resulting from autism spectrum disorder, attention deficit hyperactivity disorder, anxiety and depression - whether impairments result in "substantially reduced functional capacity" to undertake any one or more specified activities - methodology used by experts to conduct assessment of level of impairment - whether streamlined process in National Disability Insurance Agency's Operational Guidelines was considered and applied - Tribunal satisfied the Applicant met mandatory "age", "residence" and "disability" access requirements - decision set aside and substituted with decision that the Applicant met access criteria under s 21 of the National Disability Insurance Scheme Act 2013 (Cth)
National Disability Insurance Scheme (Becoming a Participant) Rules 2016
Social Security Act 1991 (Cth)
Mulligan v National Disability Insurance Agency [2015] FCA 544; (2015) 233 FCR 201
American Psychiatric Association, Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition, DSM-5
National Guideline for the Assessment and Diagnosis of Autism Spectrum Disorders in Australia
(c) either the "disability" access criteria or the "early intervention" access criteria.
(a) whether this requirement is deemed to have been met by reason of the application of the deeming provisions set out in r 5.8(a) of the National Disability Insurance Scheme (Becoming a Participant) Rules 2016 (NDIS Access Rules) applying to Mrs Ray; or
(b) the Tribunal is otherwise satisfied under s 24(1)(c) of the Act that Mrs Ray's impairment has resulted in "substantially reduced functional capacity" in any one or more of the prescribed activities referred to in this provision.
(1) A person meets the disability requirements if:
(a) the person has a disability that is attributable to one or more intellectual, cognitive, neurological, sensory or physical impairments or to one or more impairments attributable to a psychiatric condition; and
(b) the impairment or impairments are, or are likely to be, permanent; and
(c) the impairment or impairments result in substantially reduced functional capacity to undertake, or psychosocial functioning in undertaking, one or more of the following activities:
(i) communication;
(ii) social interaction;
(iii) learning
(iv) mobility;
(v) self-care;
(vi) self-management; and
(d) the impairment or impairments affect the person's capacity for social or economic participation; and
(e) the person is likely to require support under the National Disability Insurance Scheme for the person's lifetime.
(2) For the purposes of subsection (1), an impairment or impairments that vary in intensity may be permanent, and the person is likely to require support under the National Disability Insurance Scheme for the person's lifetime, despite the variation.
5.8 An impairment results in substantially reduced functional capacity of a person to undertake one or more of the relevant activities - communication, social interaction, learning, mobility, self-care, self-management (see paragraph 5.1(c)) - if its result is that:
(a) the person is unable to participate effectively or completely in the activity, or to perform tasks or actions required to undertake or participate effectively or completely in the activity, without assistive technology, equipment (other than commonly used items such as glasses) or home modifications; or
(b) the person usually requires assistance (including physical assistance, guidance, supervision or prompting) from other people to participate in the activity or to perform tasks or actions required to undertake or participate in the activity; or
(c) the person is unable to participate in the activity or to perform tasks or actions required to undertake or participate in the activity, even with assistive technology, equipment, home modifications or assistance from another person.
[Paragraph 5.8 is made for the purposes of paragraph 27(b) of the Act.]
8.3 Substantially reduced functional capacity to undertake relevant activities
The NDIA must be satisfied that an impairment results in substantially reduced functional capacity of a prospective participant to undertake one or more relevant activities (section 24(1)(c)).
The NDIA is required to consider whether any permanent impairment, or permanent impairments when considered together, result in substantially reduced functional capacity to undertake one or more of the following activities:
The NDIA does not need to be satisfied that a person's impairment is 'serious', or more serious than another person's. Rather, access to the NDIS is based on a functional, practical assessment of what a person can and cannot do (see Mulligan and NDIA [2015] FCA 44 at [56]).
The NDIA will not need to consider whether a prospective participant's impairment results in substantially reduced functional capacity in relation to all of the relevant activities for every access request.
It is sufficient for a prospective participant to have substantially reduced functional capacity in relation to one activity (see Mulligan and NDIA [2015] FCA 44 at 67).
Which activity the NDIA will need to consider will depend on the circumstances and the evidence presented by the prospective participant. For example, if a prospective participant has an impairment which results in substantially reduced functional capacity to undertake mobility, but otherwise has full cognitive capacity, it may not be necessary for the NDIA to consider whether the impairment results in substantially reduced functional capacity to undertake activities related to cognition.
An impairment results in substantially reduced functional capacity to perform one or more activities when:
The following information provides further guidance in relation to determining when an impairment results in substantially reduced functional capacity:
By itself, reliance on commonly used items will not result in a substantially reduced functional capacity to participate effectively or completely in an activity. Commonly used items include glasses, walking sticks, non-slip bath mats, bathroom grab rails, stair rails, age appropriate child safety locks, simple adapted kitchen utensils and dressing aids.
In considering the role played by assistive technology, home modifications and equipment, the NDIA will consider specific needs arising from the prospective participant's impairment, and whether those needs are met (or need to be met) through the use of specialist disability aids and/or equipment.
Such items would generally be specifically designed to assist in increasing the functional capacity and participation of people with disability and be formally prescribed by a medical practitioner, specialist clinician or allied health professional such as an occupational therapist, physiotherapist or speech therapist.
When considering whether a person requires assistance from others to participate or perform tasks associated with an activity, the NDIA will have regard to whether a person's need for assistance is consistent with normal expectations of a person of a similar age. For example, children under the age of 2 will not necessarily have a substantially reduced functional capacity because they need assistance to provide for self-care needs.
A person will be considered to be unable to participate effectively or completely in an activity if they cannot safely complete one or more of the tasks required to participate in an acceptable period of time. Undertaking a task more slowly or differently to others will not necessarily mean a person cannot participate effectively or completely in an activity.
When considering whether a fluctuating or episodic impairment results in substantially reduced functional capacity to undertake relevant activities, the NDIA will consider the impact on the person's ability to function in the periods between acute episodes.
3. Objects of Act
(1) The objects of this Act are to:
(a) in conjunction with other laws, give effect to Australia's obligations under the Convention on the Rights of Persons with Disabilities done at New York on 13 December 2006 ([2008] ATS 12); and
(b) provide for the National Disability Insurance Scheme in Australia; and
(c) support the independence and social and economic participation of people with disability; and
(d) provide reasonable and necessary supports, including early intervention supports, for participants in the National Disability Insurance Scheme launch; and
(e) enable people with disability to exercise choice and control in the pursuit of their goals and the planning and delivery of their supports; and
(f) facilitate the development of a nationally consistent approach to the access to, and the planning and funding of, supports for people with disability; and
(g) promote the provision of high quality and innovative supports that enable people with disability to maximise independent lifestyles and full inclusion in the community; and
(ga) protect and prevent people with disability from experiencing harm arising from poor quality or unsafe supports or services provided under the National Disability Insurance Scheme; and
(h) raise community awareness of the issues that affect the social and economic participation of people with disability, and facilitate greater community inclusion of people with disability; and
(i) in conjunction with other laws, give effect to certain obligations that Australia has as a party to:
(i) the International Covenant on Civil and Political Rights done at New York on 16 December 1966 ([1980] ATS 23); and
(ii) the International Covenant on Economic, Social and Cultural Rights done at New York on 16 December 1966 ([1976] ATS 5); and
(iii) the Convention on the Rights of the Child done at New York on 20 November 1989 ([1991] ATS 4); and
(iv) the Convention on the Elimination of All Forms of Discrimination Against Women done at New York on 18 December 1979 ([1983] ATS 9); and
(v) the International Convention on the Elimination of All Forms of Racial Discrimination done at New York on 21 December 1965 ([1975] ATS 40).
(2) These objects are to be achieved by:
(a) providing the foundation for governments to work together to develop and implement the National Disability Insurance Scheme launch; and
(b) adopting an insurance‑based approach, informed by actuarial analysis, to the provision and funding of supports for people with disability; and
(c) establishing a national regulatory framework for persons and entities who provide supports and services to people with disability, including certain supports and services provided outside the National Disability Insurance Scheme.
(3) In giving effect to the objects of the Act, regard is to be had to:
(a) the progressive implementation of the National Disability Insurance Scheme; and
(b) the need to ensure the financial sustainability of the National Disability Insurance Scheme; and
(c) the broad context of disability reform provided for in:
(i) the National Disability Strategy 2010‑2020 as endorsed by COAG on 13 February 2011; and
(ii) the Carer Recognition Act 2010; and
(d) the provision of services by other agencies, Departments or organisations and the need for interaction between the provision of mainstream services and the provision of supports under the National Disability Insurance Scheme.
4 General principles guiding actions under this Act
(1) People with disability have the same right as other members of Australian society to realise their potential for physical, social, emotional and intellectual development.
(2) People with disability should be supported to participate in and contribute to social and economic life to the extent of their ability.
(3) People with disability and their families and carers should have certainty that people with disability will receive the care and support they need over their lifetime.
(4) People with disability should be supported to exercise choice, including in relation to taking reasonable risks, in the pursuit of their goals and the planning and delivery of their supports.
(5) People with disability should be supported to receive reasonable and necessary supports, including early intervention supports.
(6) People with disability have the same right as other members of Australian society to respect for their worth and dignity and to live free from abuse, neglect and exploitation.
(7) People with disability have the same right as other members of Australian society to pursue any grievance.
(8) People with disability have the same right as other members of Australian society to be able to determine their own best interests, including the right to exercise choice and control, and to engage as equal partners in decisions that will affect their lives, to the full extent of their capacity.
(9) People with disability should be supported in all their dealings and communications with the Agency and the Commission so that their capacity to exercise choice and control is maximised in a way that is appropriate to their circumstances and cultural needs.
(10) People with disability should have their privacy and dignity respected.
(11) Reasonable and necessary supports for people with disability should:
(a) support people with disability to pursue their goals and maximise their independence; and
(b) support people with disability to live independently and to be included in the community as fully participating citizens; and
(c) develop and support the capacity of people with disability to undertake activities that enable them to participate in the community and in employment.
(12) The role of families, carers and other significant persons in the lives of people with disability is to be acknowledged and respected.
(13) The role of advocacy in representing the interests of people with disability is to be acknowledged and respected, recognising that advocacy supports people with disability by:
(a) promoting their independence and social and economic participation; and
(b) promoting choice and control in the pursuit of their goals and the planning and delivery of their supports; and
(c) maximising independent lifestyles of people with disability and their full inclusion in the community.
(14) People with disability should be supported to receive supports outside the National Disability Insurance Scheme, and be assisted to coordinate these supports with the supports provided under the National Disability Insurance Scheme.
(15) Innovation, quality, continuous improvement, contemporary best practice and effectiveness in the provision of supports to people with disability are to be promoted.
(16) Positive personal and social development of people with disability, including children and young people, is to be promoted.
(17) It is the intention of the Parliament that the Ministerial Council, the Minister, the Board, the CEO, the Commissioner and any other person or body is to perform functions and exercise powers under this Act in accordance with these principles, having regard to:
(a) the progressive implementation of the National Disability Insurance Scheme; and
(b) the need to ensure the financial sustainability of the National Disability Insurance Scheme.
STREAMLINED PROCESS UNDER NDIA OPERATIONAL GUIDELINES
8.6 Streamlined process for determining the disability access requirement
The NDIA has developed a list of conditions and state or territory disability programs which are designed to streamline the access process in certain cases.
Where a prospective participant has a condition included in List A or List B, or is an existing client of a disability program included in List C (attached to this guideline), the NDIA will be satisfied that the person meets one or more of the disability requirements.
Where a prospective participant has been diagnosed with a condition/s on List A the NDIA will be satisfied that the person meets the disability requirements without further assessment. A person does not need to have a condition on List A to become a participant in the NDIS.
Where a prospective participant has been diagnosed with a condition/s on List B the NDIA will be satisfied that the person has a disability attributable to one or more impairments that is, or is likely to be, permanent without further assessment. For prospective participants diagnosed with a condition/s on List B, the NDIA will only need to assess whether the prospective participant:
A person does not need to have a condition on List B to become a participant in the NDIS.
8.6.3 Existing clients of defined state or territory disability programs on 'List C'
Defined programs are disability programs that have disability requirements equivalent to the NDIS. Where a prospective participant is an existing client of a defined Commonwealth, state or territory disability program on List C, the NDIA will be satisfied that the person meets the disability requirements without further assessment.
A person does not need to be a client of a defined program on List C to become a participant in the NDIS.
14. List A - Conditions which are likely to meet the disability requirements in section 24 of the NDIS Act.
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2. Autism diagnosed by a specialist multi-disciplinary team, paediatrician, psychiatrist or clinical psychologist experienced in the assessment of Pervasive Developmental Disorders, and assessed using the current Diagnostic and Statistical Manual of Mental Disorders (DSM-V) diagnostic criteria as having severity of Level 2 (Requiring substantial support) or Level 3 (Requiring very substantial support).
15. List B - Permanent conditions for which functional capacity are variable and further assessment of functional capacity is generally required.
1.Conditions primarily resulting in Intellectual/ learning impairment
16. List C - Defined programs
a. Victoria
Clients of the following Victorian schemes will generally be considered to satisfy the disability requirements without further evidence being required:
(a) communication, which includes "being understood in spoken, written or sign language, understanding others and expressing needs and wants by gesture, speech or context appropriate to age";[4]
(b) learning, which includes "understanding and remembering information, learning new things, practicing and using new skills";[5]
(c) self-care, which includes "activities related to personal case, hygiene, grooming and feeding oneself, including showering, bathing, dressing, eating, toileting, grooming, caring for own health care needs";[6] and
(d) self-management, which includes "the cognitive capacity to organise one's life, to plan and make decisions, and to take responsibility for oneself, including completing daily tasks, making decisions, problem solving and managing finances".[7]
(a) reject Ms Barry's diagnosis of "Autism Spectrum Disorder, Level 3 Requiring Substantial Support"; and
(b) prefer the evidence of Mr Ronald Barry, psychologist, who initially diagnosed Mrs Ray in 2006 with, what was then termed, "high functioning autism".
(a) did not undertake a comprehensive needs assessment for the purpose of expressing her opinion;
(b) did not conduct a clinical interview with Mrs Ray for the purpose of expressing her opinion; and
(c) instead, had relied upon and accepted the assertions in the report prepared by Ms Cathy Saleta, Mrs Ray's advocate from the Villamanta Disability Rights Legal Service Inc, and had also relied upon her own clinical observations.
(b) "undertook a practical functional assessment of [Mrs Ray's] capacity which focussed upon the particular activities prescribed by paragraph 24(1)(c) of the NDIS Act" using a recommended method for assessing functional capacity as detailed in the "National Guideline for the Assessment and Diagnosis of Autism Spectrum Disorders in Australia".[20]
...the Applicant:
(a) is able to mobilise independently;
(b) does not require disability specific assistance to support her to effectively manage any of her self-care tasks;
(c) does not require assistance to support her to learn new things;
(d) is able to independently self-manage and make appropriate decisions;
(e) does not require assistance to support her to effectively communicate with others, although she finds it difficult to parent her daughters with ASD.
Diagnostic Features
The essential features of autism spectrum disorder are persistent impairment in reciprocal social communication and social interaction (Criterion A), and restricted, repetitive patterns of behavior, interests, or activities (Criterion B). These symptoms are present from early childhood and limit or impair everyday functioning (Criteria C and D). The stage at which functional impairment becomes obvious will vary according to characteristics of the individual and his or her environment. Core diagnostic features are evident in the developmental period, but intervention, compensation, and current supports may mask difficulties in at least some contexts. Manifestations of the disorder also vary greatly depending on the severity of the autistic condition, developmental level, and chronological age; hence, the term spectrum. Autism spectrum disorder encompasses disorders previously referred to as early infantile autism, childhood autism, Kanner's autism, high-functioning autism, atypical autism, pervasive developmental disorder not otherwise specified, child-hood disintegrative disorder, and Asperger's disorder.
General assessment of whether "disability" requirements met by Mrs Ray
Manifestations of the social and communication impairments and restricted/repetitive behaviors that define autism spectrum disorder are clear in the developmental period. In later life, intervention or compensation, as well as current supports, may mask these difficulties in at least some contexts. However, symptoms remain sufficient to cause current impairment in social, occupational, or other important areas of functioning.
Section 24(1)(c) - substantially reduced functional capacity
I note that the Tribunal appears to have approached the concept of "substantially reduced functional capacity" in s 24(1)(c) as if it is exhaustively defined by r 5.8. That is not necessarily the case. As a deeming provision, r 5.8 has the effect of mandatorily including some people in the category of persons with substantially reduced functional capacity if the criteria in r 5.8(a), (b) or (c) are met. In that sense, a decision-maker must turn his or her mind to whether an applicant falls within the deeming effect of r 5.8. That is not necessarily the end of the exercise in terms of s 24(1)(c). The statutory task remains to consider whether a person's functional capacity is substantially reduced in any of the six specified areas.
Clause 24 sets out the disability requirements a person must satisfy in order to become a participant in the NDIS launch. The disability requirements are designed to assess whether a prospective participant has a current need for support under the scheme, based on one or more permanent impairments that have consequences for the person's daily living and social and economic participation on an ongoing basis. This clause also implements recommendation 3.2 of the Productivity Commission report.
Individuals receiving individually tailored, funded supports through the NDIS:
should have a disability that is, or is likely to be, permanent, and would meet one of the following conditions:
have significantly reduced functioning in self-care, communication, mobility or self-management and require significant ongoing support
be in an early intervention group, comprising individuals for whom there is good evidence that the intervention is safe, significantly improves outcomes and is cost effective
In exceptional cases, the scheme should also include people who would receive large identifiable benefits from support that would otherwise not be realised, and that are not covered by the groups above. Guidelines should be developed to inform the scope of this criterion and there should be rigorous monitoring of its effects on scheme costs.
Tribunal: In terms of the role that you play in Jenny's life, do you think you do more than you need to, to help her with everyday things?
Mr Ray: No, I don't. No. Most of it's because I have to. If I don't do it, things won't operate the way they need to operate and it's going to affect the kids, so I've got to keep a good balance. And I've had a lot of support from groups like (Indistinct) autistic services and other groups that have helped me understand and what I need to do. So, I tried to balance it all and yes, just my best, I guess.
Tribunal: Have there been opportunities where you've not assisted her in the way you normally do, just to see what will happen? Whether she can develop some skills to do more for herself?
Mr Ray: Yes. Look, Dr Barry was the one that told me to make sure she did the cooking. So, even he said, it doesn't matter if it takes her three hours, doesn't matter what happens. No matter, she even messes up, he said, she's got to do it. If she doesn't do it, then she's going - yes, she'll collapse anyway. So, we need to give her responsibilities that she can do. And that's the thing, she might be a slow cooker and it might take her three times longer than anyone else, but she's doing it. So, that's the important thing.
Tribunal: In your statement, you mentioned about needing to pretty much go over what she does in the garden and do a lot of those tasks again. Is that correct?
Mr Ray: Yes. We do have those problems. But I'm probably letting go a bit more. I've just decided I just can't handle it anymore. I'd like - it just frustrates me too much, so it's best for me to let it go and that's what I've been doing a bit more lately because it's just frustrating me too much and that's - I already have an anxiety disorder, which has been diagnosed by a doctor down at the medical centre. So, I don't really need that extra anxiety, so I'm letting more things go at the moment that really just aren't important.
Tribunal: Do you think that that anxiety, does that cause you to exercise too much control over Jenny?
Mr Ray: No. I don't. No. No. Because - yes, again, we've got to - everything's got to be balanced and like I said, I do get - I have got my own support workers that are helping me, like, within Australia. And they're telling me and I've been and talking about what I'm doing, what I'm not doing, so they're guiding me a bit at the moment. And they're the ones that sort of said let these things in the garden go because it's affecting my health.
Tribunal: Yes. And so we heard some evidence from Jenny that it was either you or Cathy that may have suggested not to involve Jenny's mother in this or to let Jenny's mother know about this case. Is that correct?
Mr Ray: Yes, Jenny or me wouldn't, only because Jenny doesn't even understand the autism, and she was the one when she first got diagnosed with autism just wouldn't accept it. So it's - she's, yes, it's only - her father always thought she had autism basically when she was very long (sic), and he always thought she was autistic and he kept trying to say, 'Look, she's got to get it diagnosed', but she refused, and even went - I did get her diagnosed. I think she was more (indistinct) than anything else, so it's - yes, it's not a good place for us in that area I'm afraid.
Tribunal: All right. What do you see are the main reasons why Jenny wants to seek access to the NDIS? What sort of support do you consider needs to be available to her to assist her life within your family?
Mr Ray: I think a lot of - Dr Barry, I think, summed it up pretty well. He said she's going to need ongoing training on how to deal with the teenagers. Otherwise the relationships will just break down, and I think that's where we're coming to a point now where she really needs that ongoing training, especially at the moment because like I said, we're really at breaking point at the moment. So if something doesn't change, who knows. It might all break down and I'd hate to see that happen, but you know, [one of the daughters has] been crying on my shoulder several times lately, just not coping. So I know the NDIS could help us a lot in giving us the people we need to go through this period.
Tribunal: Coming back to her husband, do you think that he controls a lot of the day- to-day activities in the home, to a point that she's being excluded from the opportunity to undertake those activities?
Ms Barry: No, I wouldn't say so. I would say more to the point that over the years, he has learnt what she is capable of and not capable of, and taken up the slack of what she is not cognitively able to do.
Understanding Jenny's Sensory Profile
Jenny's high scores of much more than most people in each of the four quadrants indicate her pattern's (sic) of processing sensory information is complex. It is likely that Jenny has a narrow band for optimal levels of sensory input for her nervous system to respond for functional performance.
Her profile indicates there are occasions when her neurological threshold to sensory input is high and requires increased sensory input to initiate awareness of and response to sensory input. However, there are occasions when her neurological threshold to sensory input is low and requires reduced sensory input. Jenny's ability to function at home and in the community depends on achieving a balance of the nervous system activation so that she is alert to certain sensory input while being able to screen out distracting or overwhelming input. For example Jenny likes to sing or make other noises whilst working, but is distracted if there is externally generated noise around her and finds a child's screaming overwhelming. This causes shutdown and she then needs to re-group and withdraw in order to continue functioning.
An examination of Jenny's scores within the various sensory processing categories shows that across all the sensory domains (taste/smell, movement, visual, touch, activity level and auditory) Jenny's responses to sensory input vary between being passive and active. This indicates that Jenny has difficulty regulating her responses such that it may be difficult for Jenny to take control of the environment to achieve the level of sensory input that is optimal for her at any given time.
...I observed that she was able to communicate effectively with me, she was able to answer all of my questions appropriately. She - her articulation was clear, and it was a normal pace and a normal rhythm. There was no evidence of the echolalia that I talked about before or pronoun reversal that is - that can be evident in people with ASD. Her intonation was slightly different in that she was - just the melodical quality of her voice was slightly different but it wasn't significant and she was able to communicate with me at the beginning of the assessment that she was a little bit nervous and she was able to communicate and answer all of my questions as required...
... I observed that Ms Ray had no difficulties communicating her needs in written or verbal format...
... She had no - she was unable to describe any specific difficulties she had with using a phone if required, she just didn't have a need to her particular daily routine and, yes, she doesn't use social media because she doesn't want to. She did indicate she had difficulty understanding the evening news as well and she had difficulty communicating when there was a lot of people around...
My - the overview of my clinical impression is that Ms Ray is functioning reasonably well considering the diagnosis that she has. She appears to have received significant intervention in the past, and this has translated into a level of function that is adequate for her current life roles.
...
Very broadly speaking Ms Ray presented as a very warm and friendly person, she was very personable, and she was responsive in terms of her communication. Her social behaviours were appropriate in that she applied appropriate turn taking, she greeted me when I arrived, she smiled in reciprocation to my smile, she offered me a drink and - a cup of tea, and she responded to each of the questions that I asked. She was very cooperative and polite throughout. Now, my - a comparison to other people who I have assessed with autism and who are participants in this scheme, for example, they will communicate via echolalia, which is essentially where they repeat back what you have said to them, verbatim, because they don't understand the meaning of what you're asking them. So if you say, "What is your name?" They will say, "What is your name?" And they continue to repeat that as you go along. Or another example is someone who just continued to talk about their special interests without any regard at all to the question that you've asked or any direct questioning to go off that theme. At the more extreme end I have had clients who just simply don't acknowledge my presence at all, they just - I'm just an object that's in their way, so I might be speaking directly to them and they don't respond at all. And at the further extreme they might run away from the room and flap their arms, and sometimes they will throw objects. So - or they might repeat a sound that is like - just monosyllabic that has no - that has no meaning. To me it might have some meaning to a close carer who understands that that particular sound means that they want food. Or another example is that they will use pronouns incorrectly, so for example they might - I would refer to myself as [Occupational Therapist X] rather than I, so "[Occupational Therapist X] had a snack" rather than "I had a snack."
Jennifer does not require assistance to communicate based on my direct observations but also based on her self-report. She indicated that she was attending these groups and visiting her friends at houses - the houses of friends, sorry, and that she was communicating effectively in those domains. She specifically referred to difficulty with her daughters which I've listed under Social Interaction. So that's not a communication problem per se, it's difficulty interacting with her daughters which I've addressed separately and extensively. So the short answer is no, she doesn't. She does - she does receive assistance in making appointments but there's no reason why she couldn't do that herself if she was provided with a phone and she was motivated to do so. It's just (indistinct) for her to have one at the moment really based on her current routines.
Ms Anderson: And if she knows her husband's telephone number off by heart, why wouldn't she use the mobile phone that she had?
Occupational Therapist X: She - - -
Ms Anderson: - - - if there is not some difficulty with using the phone?
Occupational Therapist X: Sorry? She just didn't - she didn't like it. She just didn't want to. She didn't relate to the mobile phone. Again, if I was her treating therapist I would add a lot more functionality to that phone so that it actually became something that she would use. So for clients like her, I will often give them a lanyard, so something that's attaching to them, so the phone serves much more of a functional purpose than calling someone that you very rarely need to call. And so that's what I would do. As I said before, this couple of been together for 20 years, they have established routines and habits, and just because they're following those habits doesn't necessarily mean that they don't have capacity to learn new ones if they want to. There was no indication from either of them that this was a pattern that wasn't working for them. If it wasn't working for them, I would suggest changes. And to be honest, that is something that I would probably suggest, getting a low-cost phone and putting a lot more functionality on it, including some more rewarding functions onto the phone so that it was used by her more commonly than it would otherwise be.
I would say it is the - it's the low average intellectual function is most likely it. She doesn't watch the news so she doesn't have a lot of context to relate it to, so there's probably that as well. She just - so that if she jumps on ad hoc and watches it, there is no context to relate this story to one that was last week. So I think that she just doesn't watch it, and so there are two factors there.
Jenny has very neat handwriting and can write a birthday card or short note.
She is unable to express her wants and needs, feelings or opinions in written form.
She needs help filling in forms as she is unable to understand the meaning of the questions.
Jenny answers the mobile phone she shares with Tony. She seldom makes calls and is unable to use a computer or access the internet.
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Mrs. Ray has extreme difficulties in being able to understand most spoken language if it is not in a simplified format. She is unable to understand jokes, sarcasm, threats, lies, colloquialisms, nor irony. Mrs. Ray's comprehension skills are further retarded by her inability to infer meaning in communications, as she takes spoken and written language at its face value and believes exactly what she is told.
Further to this rigidity of language, Mrs. Ray has an extremely reduced capacity for working memory, rendering her almost incapable of holding more than two pieces of information in her working memory for more than 1 - 2 minutes. Added to this, she becomes fixated on her own ideas and does not listen to what others are communicating to her; becoming easily lost in the flow of the conversation.
Mrs. Ray is not able to read non-verbal body language. She will continue to approach individuals who are exhibiting body language that indicates that her advances are unwelcome, body language that indicates that the individual is a threat to Mrs. Ray; or will withdraw from interactions which indicate that she is welcomed.
Mrs. Ray's emotional regulation system is severely compromised in relation to communications. If something is perceived as upsetting to Mrs. Ray she will become inconsolable for an extended period of time; alternatively if she is excited she becomes overly and overtly demonstrative of her excitement which highlights the lack of maturity that she shows for an adult, behaving more like a young child. Mrs. Ray also does not show an awareness of the inappropriateness of this behaviour even when it has been pointed out to her on numerous occasions. Explicit directions must be provided for each situation for Mrs. Ray as she is unable to generalise instructions/rules from one setting to the next.
She did describe - I asked her who her closest friends were, and she said that they were the friends in the bible study group. She had concerns that there was difficulty - she had difficulty discussing things beyond the gardening. However, otherwise, she felt well-supported by the church and a member of the congregation.
The interactions with her daughters - and she has said to me on a number of occasions that her daughters are more intelligent and more capable than she is, and she is like a child to them. They outthink her, they outtalk her, they out-understand her.
And that, in and of itself, is debilitating for Mrs Ray, knowing that her own children have outgrown her, and trying to maintain her role as a mother and an authority figure within the [familial] hierarchy.
I am like a referee trying to stop it blowing it up before it even happens. (This is in relation to arguments and conflicts that Jenny has with her daughters where she cannot relate and mother them adequately due to her autism, so things escalate). I am always thinking - what could go wrong here so that we're not going to have problems. It hurts.
Mrs Ray tends not to have an awareness of the subtleties of emotions. She has an awareness of the more extreme ends of emotion.
In saying that, she can go from being quite - appearing to be quite (indistinct) and stable, to becoming very distressed very quickly, without any awareness of what the physiological or emotional amping up might be. Given that, it becomes very difficult to therefore read Mrs Ray getting more and more emotional, until she then has some kind of emotional response.
Tribunal: And can you describe what happened when you made that observation?
Ms Barry: We were talking about [details of the precipitating event have been omitted due to the sensitivity of the subject matter] that she had experienced. And in the beginning of that conversation, she was fairly what most people would call flat, monotone, not showing a large level of emotion, until she - up to the point where it had become disclosed to her husband. And then, she became extremely inconsolable for a good 15 minutes of trying to then explain that this was an understandable emotional reaction.
But there wasn't any catching the voice that you would expect. There wasn't any slowly tearing up and showing the distress of that as it went along. It was just - suddenly, she was just bawling her eyes out, is the best way of describing it, I guess. So there wasn't the usual - what you would expect in a disclosure of that kind from someone else.
When she becomes frustrated, you don't hear the usual - and the agitation in the movements that you usually see in people as they start becoming frustrated and irritated, to the point of leading up to an angry outburst, of her slamming her diary down on the desk, because she wasn't able to recall a specific date. It just, from here to here, very, very quickly. In saying that, it then becomes difficult for her family members to see how things might trigger her, because she does not show that slowly increasing in emotional instability.
Mrs Ray tends to be fairly flat. She can become quite excited as well, especially around her stuffed animals that she would bring to the office and have sitting, three or four them, on the table, and constantly petting them and going - and the visual and physical and verbal (indistinct) that you would quite often associate with excitability with people with autism.
She would become that way as well, and would engage in hand flapping and rocking when describing her garden, because she is so excited about the progress that she has made and the achievement she has made, whereas you wouldn't see that in a neurotypical individual in day-to-day life, talking about the grevilleas and the waratahs. And she's going like this, and getting very, very excited in her information.
... She has difficulty with vocabulary and with determining the point of written text...
Jennifer tries her hardest at all times. She encounters most difficulty in questions where she needs to interpret words...
Ms Crick: But she doesn't need you to attend for any communicative reasons, does she?
Mr Ray: Actually, she does, actually, because often she doesn't get what the doctor's talking about. She doesn't take things in very well so I often have to be there just so that he can, yes, explain things a little bit. If it's just basic things like filling in a medication, she's doing that, because that's simple, she can do that, but that's it.
I would say that her learning capacity is more consistent with the WAIS, in that she has low - low-average, and that she would take longer to learn things and she might require more repetition. So that would be my comment there. If I was asking about learning capacity, I wouldn't be relying on the Vineland, I would be relying on the WAIS. She's demonstrated capacity to learn at a basic functional level.
When I asked her about the garden, I asked her a lot - I know a little bit about gardening, but I was able to ask her some relevant questions and she was able to respond accordingly, with the information that she had learned about gardening. And she's obviously completed a Diploma of Bible Studies. And she was able to - I know that she completed that at a slower pace than others, but she - there's no - I noticed that the only report that I had at the time was that of psychologist Astra King, and she said that she had no specific learning disorder and all of that was consistent with my observations.
I would say that she needs additional time and she - it depends on what she's learning. If she's learning a university degree, yes. But in terms of learning day-to-day tasks, she might require them to be explained to her in simple terms, and then she would be able to learn that task and repeat it. So, they've given me numerous examples - say cooking, for example, she has learned how to cook a set number of meals, and that is by people, I understand, stepping out the steps involved and she's been able to repeat those steps and then learn it.
I consider that she is able to learn new routines and has demonstrated the ability to do so, just by looking at her daily routines. However, it will be longer and require more repetition.
Due to Mrs. Ray's sensory sensitivities and limited intelligence, she is unable to learn new routines in any timely manner. She must repeat the routine/task on numerous occasions and in a variety of settings before she is able to apply the learned material/routine. She is unable to generalise information/skills to other settings unless she has been taught to do so.
Further to this, her anxiety and panic attacks render her more vulnerable to what is best termed as an information overload causing her to cognitively shut down and not be able to listen to or process information. Anything more than three directions and Mrs. Ray becomes overwhelmed and confused, often becoming emotionally dysregulated and will begin to exhibit self-injurious behaviours.
As such, Mr. Ray is responsible for the majority of information processing within the home relating to home management, self-management and issues relating to the education of their two daughters. With regards to the latter, Mrs. Ray is unable to assist the girls with their schooling as she does not have the cognitive capacity to understand the materials being taught, thus leaving the task to her husband to manage.
Jennifer has tried so hard to cope with the academic demands of the subject, but she has fallen further and further behind in tests and examinations...She has shown exceptional courage and determination and she has tried to remain cheerful at all times...
Year One: Jenny has struggled with her academic work - but has really worked hard to achieve satisfactory results. Her input to college life has been excellent. Her simplicity of faith & her care for others have been very evident. She has been most appreciated by others in her cell group and really tries to achieve in whatever situation she encounters.
Year Two: Jenny was appreciated in her cell group for her thoughtfulness and care of other persons. Her faith is obvious and deep; and this has been an important part of her contribution to the group. Academically she struggles...
She's independent in attending to personal hygiene, and I think everyone's fairly - everyone agrees with that. I don't agree with Ms Barry's comments that she needs assistance with medications or attending to other self-care needs, because at exactly midday, or whatever time it was, she got up and made herself a sandwich and had her medications without any prompting from anyone. So the comment that she needs assistance with her medications, I've directly observed evidence to the contrary.
She has great difficulties in being able to adequately inform medical practitioners and specialists on her current state of being, be it physical, emotional, or psychological.
Ms Anderson: Can you explain to us how this impacts Mrs Ray's capacity for caring for herself?
Ms Barry: If you can't explain to someone else what's happening for yourself, how are you going to access self-care, healthcare? Being able to have that language, which is something that I had been working on with Mrs Ray, in trying to find ways to describe things, and provide her with a level of language that she could, to an extent, hopefully convey across to others what is happening internally for her, either emotionally or psychologically or physically.
Jenny does the washing for the family; they have a fully automatic washing machine. Jenny needs assistance with folding the washing and putting it away in an organised manner; the washing usually ends up on the furniture on the floor.
Jenny depends on others to do the ironing.
...
Jenny tends to hoard items like plastic bags and other potentially useful things. She finds it hard to dispose of personal items, such as her large collection of stuffed toys. Jenny is unable to organise her belongings and they usually end up on the furniture or the floor. Once others have cleared the area Jenny can vacuum and mop the floors.
...
Tony or in-home support workers assist with making and changing beds.
Jenny has her own room and sleeps on the bottom of a bunk-bed. She uses a sleeping bag and the bed is crowded with stuffed toy animals.
Clothes are hung from the top bunk, obscuring the lower bunk. Jenny was somewhat embarrassed about the state of her room and stated that she does not know where to start to tidy it up or to make it a nicer place to be.
I'd like a psychologist involved for Jenny that would help with Jenny on things that really mattered. Learning how to do things, important things, making positive changes and learning. Also medication being managed.
Tribunal: And is that because she told you that?
Ms Barry: Yes, it is, and I've also had that from Mr Ray as well, in verification. She says that she gets too overwhelmed with all the people, all the smells, all the sounds, the movement, trying to then visually take in information whilst being overwhelmed by the other senses at the same time. And then, getting stuck in that sensory input causes distress in limbic system.
Basically, it's your brain stem getting overwhelmed. And the next level up in the brain is your limbic system, and then you get to the top level, which is the cortex, the cerebral cortex, which is the thinking and logic. And she gets stuck between the brain stem and the limbic system, and that's where we start to see meltdowns.
I think that in terms of my clinical observations, she was able to manage the domestic environment to the extent that she's required to with current division of labour in that particular household.
Jenny is disorganised, she doesn't put things away, everything is untidy, Jenny can't appear to organise or tidy, she tries to but it gets more messy instead, I end up doing it or fixing what she's done.
Jenny is like a third child.
Ms Crick: Do you involve Jenny in the day-to-day decision-making processes, in terms of her daily routines?
Mr Ray: We do talk about things, definitely, but I make most of the decisions, only because, really Jenny doesn't want to make those decision. She'd rather me do it.
...
Ms Crick: You'd say that Jenny's activities are all decided and planned by you?
Mr Ray: No, she just mostly gardens, she loves to garden and she likes to do - just to keep up with a few of her friends. So, I can get her to her friends of course.
Mr Ray: ...With her garden, if you look at her plants when she plants things, she just can't work out distances. She always - I told her I need 2 metres for the mower. The lawn has been, like, 1 foot or 2 foot or maybe a metre if I'm lucky. So she just doesn't get it at all. Doesn't know what to do. She just - she'll end up getting it mixed up. Don't ask me how she does it, I don't - don't understand it. I guess I'm not autistic I that sense, but she just can't work out those sort of things.
Ms Crick: But once Jenny's had somebody say to her how far plants should be grown apart, she's quite capable of then following that in planting those plants, isn't she?
Mr Ray: No. No, she always gets it wrong and then I end up having to move things or end up getting stuck into her about not planting them where I told her to plant them. It's like she just can't seem to work it out.
Ms Crick: But that doesn't mean to say that - you don't have to correct her work very often, do you?
Mr Ray: Most of the times I don't correct it because again it'll be just ongoing battles and that's just not worth it. You've got to work out where you toe the line and where you're going to battle all the time, and I end up just giving in most of the time because she just doesn't get it right. It's just like when we planted a whole heap of plants and I used to work at a campsite, and I got help in to do those plants, but the trouble is I found out that she'd actually put them in the ground. I dug all the holes and everything, and I noticed only a year later they all started dining, and I thought, what on earth's going on, and then I realised she'd planted them all too deep, and they're all natives so they die. And I showed her how to plant them, but she still planted them all too deep, like she's got to overcompensate.
Occupational Therapist X: Okay, so self-management. She - as I said before, so the cognitive skills underlying self-management she has to a basic level. The division of labour in her home is that her husband undertakes the finances but I see no reason, based on both my results and the results of Ms Barry, that she would be able to learn this skill if required. There may be some need for augmentation such as sue of Centrepay or direct deposit, but she could learn - easily learn those skills now if she needed to. The home environment was cluttered. But I'm quite skilled in performing squalor assessments, and I didn't even pull out my assessment form because it wouldn't have met the criteria for squalor. So it was just cluttered. There was a lot of stuff. But it didn't - there was no rotting food. I understand that Ms Warden had been undertaking some de-cluttering with her, but that was based - I don't believe - on Ms Ray's request. It was something that Ms Warden suggested. And she, as I said before, in terms of self-management, she recognised that she needed to take a break a couple of times. She also recognised that she needed to take her midday medications. She was able to explain in detail the evening meals that she prepared. And at the end of the assessment, she took out some frozen chicken, or something like that, and explained what she was cooking that night. So that shows some planning as well. So I think that she - she said that she'd swept the floor. I think that in terms of my clinical observations, she was able to manage the domestic environment to the extent that she's required to with current division of labour in that particular household.
Ms Crick: Does she usually require assistance from other people to self-manage?
Occupational Therapist X: No. She undertakes those tasks as part of a routine. And I know that it's been mentioned before, by myself and by others, routine's important to her. She said she didn't enjoy it. But, you know, that's okay. She did have respite workers who came in and did some things for her. I didn't quite understand that, whether that was related to her or Mr Ray, or why that was in situ. Because, from what I could tell, she was able to do it, if she'd been provided with, as I said before, the kind of routine structures that would assist her. So, yes. She likes things done a certain way and her daughters do it differently. So I think that there's certainly some conflict with family members, and that would benefit from further psychological intervention.
Now, just to go back to your response, how would she cope without that support, at no point in my report, or today, have I suggested that she doesn't need support, and I've just detailed how professional support, as I've talked about, the 16 sessions through a mental health care plan, plus five sessions through a chronic diseases plan, would be more than enough to deal with those variances in routine that can come along.
Ms Anderson: Could you give us some examples of what you have seen yourself in relation to planning, organising and prioritising?
Ms Barry: A good example would be the planning and organising of meals. I worked with her in an attempt to try to expand the family's diet to include slow cooker meals that did not require her to be at a stovetop continuously and have to maintain concentration, so that she could plan those.
Initially, we started off with recipes that had multiple ingredients. And she attempted those, but became extremely overwhelmed by being able to follow step-by-step instructions, even for slow cooker recipes, which are really fairly simple. It got to the point where she was having difficulty in being able to follow a list of ingredients, to be able to purchase those, just to put together the slow cooker meal, which is basically a buy-and-dump kind of idea.
Even that, trying to follow the steps of that became very difficult for her. We got to the point where we would break the meals down into two, three, maybe four ingredients, and being able to plan and organise at that level, because it was just otherwise too overwhelming for her, all the different steps. With regards to the impulsivity, anywhere she goes that has stuffed animals, she wants to buy all of them, specifically relating to Australian animals in particular.
Her husband has had to put in place a rule that she has to - I think it was either two or three, she has release control of, release hold of, to purchase one more, because she will just continually - to the point that her whole bed is covered, and there's barely any space for her, which shows a lack of awareness of her own physical space requirements.
On that test alone it says that it's adequate visual perceptual skills, yet her planning and organisation was noted to be weak. So it is not just the visual perceptual nature, it's also the planning and organisation that's measured in the Bender.
Jenny Ray is a very friendly and caring lady with complex issues and significant care needs.
Jenny requires assistance with all daily living activities and participation in social interactions and community events.
She can follow short and simple instructions when a clear outline of the steps to follow has been provided and demonstrated.
She does not have the capacity to develop her own processes and is easily overwhelmed.
Jenny relies heavily on familiar/ well practiced activities and routines designed and reinforced by other people.
Jenny requires more assistance than family and informal networks can be expected to provide.
She needs daily, consistent and on-going help with organisation, establishing routines and completing them in a timely manner.
Ms Anderson: You talked a lot about (indistinct) web site, about occupational therapy, about skilled professionals setting up routine and structures, doing things repetitively. And then you've stated that the most appropriate place for this to be funded is through mental health or chronic disease plans. Are you familiar with this document ... about mainstream interface with mental health?
Occupational Therapist X: I have read it a while ago.
Ms Anderson: And so where it says: "Supports funded by the NDIS includes: assistance with planning and decision-making and household tasks; assistance to build capacity to live independently or achieve their goals; supports to participating in community activities". These are supports to be funded by the NDIS and not the health system. How would you separate those out from all of the suggestions you've made today about what would be useful for Mrs Ray? Are these not exactly the types of supports that she needs?
Occupational Therapist X: I think that things are - what they're talking about here is that they're lifelong needs. I don't think that she needs lifelong needs. As I said, she needs intermittent assistance with developing these new routines, and once they're set, they're set. So I think that she does need a little bit of input now, but I don't think it needs to be ongoing. I think it's a matter of setting up her system and walking away, and that's what I have done with other clients, and it has been successful. It's particularly successful with people who like routine. And I don't think that this kind of support is necessarily required lifelong.
Ms Anderson: In terms of the documentation you've reviewed, has there ever been a time when Mrs Ray hasn't required?
Occupational Therapist X: There's a difference between required and received. So she didn't receive support prior to her children being born, for example. That's my understanding, until after they were born. So she was able to function, get a job, get a diploma, finish grade 12, be employed in a part-time capacity - - -
Ms Anderson: I will just correct you there. She didn't finish year 12. She failed year 11. She had a job for a very brief period, if at all. So those - - -?
Occupational Therapist X: Okay, I must - I think that I did draw that from another report, which was obviously incorrect. But I do understand that she didn't get a Diploma of Bible Studies. Yes? I do understand that she worked part-time with Mr Ray early on. Is that correct?
Ms Anderson: (indistinct)?
Occupational Therapist X: That's my understanding, is that she did have a job and that she was able to maintain a part-time job. All of that without support. So the answer to that question is that really the factor that has changed her need for support has been her children, and particularly children that were born with ASD. And that's why I believe that once the children are independent, which should be in a couple of years, then her need for support will go back to what it was before. In fact it should be less than it was before because she has had the benefit of all of this intervention over that time. My understanding is that the preponderance of all of that support was directed towards her care of her children and not her care of herself.
Ms Anderson: Okay. But isn't having children and raising children a very normal life [stage] for somebody? This is not something that only Mrs Ray has done?
Occupational Therapist X: No, it's not - - -
Ms Anderson: So the fact of needing support because life got harder and her skills were not at the same level, it doesn't necessarily mean it's not lifelong support, just that there are some periods which are more stressful than others. Is that not correct?
Occupational Therapist X: That is correct, but I would like to point out that she had two children with ASD. That is an incredibly difficult thing for anyone. Any parent who is neurotypical needs support and gets support for children who have ASD. That's not related to their disability necessarily, it's related to the disability of their children. And that is what has consistently come through, and it's an important point that you raise, and I've raised it in my report. I do believe that she needs support with those girls, without having met them or having a deep understanding of their difficulties. But it is not to say that it's a typical requirement in terms of raising children. Raising children with ASD is a completely different kettle of fish, and it would not be regarded as a normal life stressor.
Ms Anderson: Okay. Finally, the NDIS Act is about giving people with disability a quality of life that is more equivalent to the rest of the community. It's about the right to access supports to provide them with equal opportunity to engage with the community. Do you consider that Mrs Ray at this point in time has the same quality of life, the same opportunities as other members of the community?
Occupational Therapist X: Yes. She's engaging with the community in a rich and varied way. She's volunteering at the local nursing home, she's participating in a craft group, she's actively engaged with her church community both on Sundays and on another day of the week. I think that she has a very rich life and that she is participating in the community more than most people I know. And she seems to be very happy. I don't know if anyone has actually asked her, but she indicated to me that she was happy with her life. Her only difficulty was the communications that she was having with her daughters and the difficulty collating all of the information that's being thrown at her from all directions. So her quality of life I think is good. She's contributing to the household, she's maintaining independent personal care....
Ms Anderson: We have heard a very different version of that this morning, but I understand that you had three hours and that that was what you were told, so I will leave it there.
Mr. Ray is the sole "adult" in the house and is required to manage all aspects of daily living within the family. He is at great pains in his attempts to provide a "normal" home for his wife and daughters, even with his wife's disabilities and those also of his daughters.
Mrs. Ray has the developmental and cognitive style age of a young adolescent who is extremely easily led, excited, agitated, and stimulated. As such, her behaviours make it extremely difficult for her to engage in social settings and activities that would be expected of someone of her age.
Section 24(1)(d) - the impairment or impairments affect the person's capacity for social or economic participation
Section 24(1)(e) - support required for the person's lifetime
(a) Mrs Ray meets the disability requirements under s 24(1) of the Act and therefore, she meets the "disability" access criterion under s 21 of the Act; and
(b) Mrs Ray meets the "age" and "residence" access criteria under s 21 of the Act.
I certify that the preceding 157 (one hundred and fifty seven) paragraphs are a true copy of the reasons for decision of Member K. Parker.
Date of final closing submissions: 27 July 2020
Solicitors for the Applicant: Villamanta Disability Rights Legal Service Inc
[1] Refer paragraph [7] of the NDIA's Statement of Facts, Issues and Contentions dated 27 March 2020 (NDIA's SFIC).
[2] Refer Exhibit T1, Tab A26 - academic transcript issued by RTO.
[4] Refer paragraph [11] of Ms Ray's Closing Submissions dated 6 July 2020 (Ms Ray's Closing Submissions).
[5] Refer paragraph [33] of Mrs Ray's Closing Submissions.
[6] Refer paragraph [38] of Mrs Ray's Closing Submissions.
[7] Refer paragraph [43] of Mrs Ray's Closing Submissions.
[12] Refer paragraph [1.1] of the NDIA's Closing Submissions dated 27 July 2020 (NDIA's Closing Submissions).
[13] Refer paragraph [17] and Annexure A of the NDIA's SFIC.
[14] Refer Annexure A of the NDIA's SFIC.
[15] As specified in List A - reproduced at paragraph [24] of these Reasons for Decision.
[16] Refer [3.1] to [3.4] of the NDIA's Closing Submissions.
[17] Refer [4.1] of the NDIA's Closing Submissions.
[18] The Tribunal has omitted the name of the occupational therapist in accordance with orders made by the Tribunal under s 35 of the Administrative Appeals Tribunal Act 1975 (Cth). Those orders were made following a request for such orders received by the occupational therapist after this Decision and Reasons for Decision were handed down, to which both parties to this application provided their consent.
[20] Refer [5.2] of the NDIA's Closing Submissions.
[21] Refer [5.11] of the NDIA's Closing Submissions.
[22] Refer [5.3] of the NDIA's Closing Submissions.
[24] Because the Tribunal is so satisfied, it was not necessary to consider whether Mrs Ray also met the "early intervention" access criterion.
[25] Refer Transcript P-28, lines 40 to 44.
[26] Refer paragraph [75] in Mulligan.
[28] Refer Transcript at P-100, line 35; P-102, line 25 and P-102, line 5 respectively.
[43] Refer Exhibit "T1, Tab A25".
[60] Refer Transcript P-98, line 5 and Exhibit "T1" at page 100.
(2015) 233 FCR 201