austlii:cth/ARTA/2025/2497
General information, not legal advice.
ARTA
2025-11-20
Original judgment source is linked above.
HZSG and National Disability Insurance Agency (NDIS) [2025] ARTA 2497 (20 November 2025)
Respondent: National Disability Insurance Agency
Decision: The Tribunal sets aside the decision under review and in substitution decides that the Applicant meets the access requirements in section 21 of the National Disability Insurance Act 2013 (Cth).
NATIONAL DISABILITY INSURANCE SCHEME - participant's access to the National Disability Insurance Scheme revoked - access criteria - disability requirements - psychosocial disability - National Disability Insurance Scheme (Becoming a Participant) Rules 2026 - permanence of impairments - availability of treatment - substantially reduced functional capacity - lifetime NDIS support - early intervention requirements - decision under review set aside
National Disability Insurance Scheme (Becoming a Participant) Rules 2016 (Cth)
National Disability Insurance Scheme (Getting the NDIS back on Track No.1) (NDIS Supports) Transitional Rules 2024 (Cth)
Beezley v Repatriation Commission [2015] FCAFC 165
Burrows and CEO, National Disability Insurance Agency [2025] ARTA 607
Drake v Minister for Immigration and Ethnic Affairs (1979) 2 ALD 60
Foster and National Disability Insurance Agency (NDIS) [2025] ARTA 718
G v Minister for Home Affairs [2019] FCAFC 79
Ghezzaoui and National Disability Insurance Agency [2023] AATA 2835
Holmes and National Disability Insurance Agency [2017] AATA 2750
Kelly v National Disability Insurance Scheme [2024] FCA 1462
Kilgallin and the National Disability Insurance Agency [2017] AATA 186
Madelaine and National Disability Insurance Agency [2020] AATA 4025
Mulligan v National Disability Insurance Agency [2015] FCA 544
MRLK and National Disability Insurance Agency [2021] AATA 3896
MZHQ and National Disability Insurance Agency [2019] AATA 810
National Disability Insurance Agency v Davis [2022] FCA 1002
National Disability Insurance Agency v Foster (2023) FCAFC 11
National Disability Insurance Agency v Lampard [2025] FCAFC 139
Nika and National Disability Insurance Agency [2021] AATA 2127
Re Drake and Minister for Immigration and Ethnic Affairs (No. 2) (1979) 2 ALD 634
Rooney and National Disability Insurance Agency [2021] AATA 3523
RZLV and National Disability Insurance Agency [2024] ARTA 294
Shi v Migration Agents' Registration Authority [2008] HCA 31; (2008) 235 CLR 286
Sutherland v National Disability Insurance Scheme [2024] AATA 411
Timofticiuc and National Disability Insurance Agency [2021] AATA 3015
Administrative Review Tribunal (Common Procedures) Practice Direction 2024
Administrative Review Tribunal (Expert Evidence) Practice Direction 2024
National Disability Insurance Agency, NDIS Operational Guideline, Applying to the NDIS (applicable to NDIS requests made before 3 October 2024)
National Disability Insurance Agency, NDIS Operational Guideline, Assistive Technology (equipment, technology and devices), 20 December 2023
NDIS plan for the period 18 December 2020 to 18 December 2021[2]
My name is [HZSG], and I am 37. I currently live on my own, in a unit provided by the department of housing. I have lived here for more than ten years now. I have two children aged 14 and 16 who live with my ex-husband. I do not see or have any contact with them. I have a close family friend named [K], and she helps when she can.
I will usually sleep throughout the day and only wake around 5.30pm. Due to my sleep routine, it is difficult for me to connect with services as these aren't usually available in the evening and I often cancel or miss specialist health appointments that have been booked. K will sometimes take me out to do shopping at night, when I feel up to it. I mostly spend my time at home, where I am very isolated. I find it difficult to engage with people but I would like to explore increasing my social opportunities. I have support to clean my home each week and to have someone assist me with my personal care routines and reminding me to take my medications.
NDIS plan for the period 4 August 2021 to 4 August 2023[3]
NDIS Plan for the period 13 April 2022 to 12 April 2024[4]
Further, there were some technical challenges at times with the video hearing.
The duty of the Tribunal is to satisfy itself whether a decision in respect of which an application for review is duly instituted is a decision which, in its view, was objectively the right one to be made.[22]
The Tribunal effectively 'stands in the shoes' of the maker of the decision under review.[23] In undertaking its review, the Tribunal may exercise all the powers and discretions that are conferred on the maker of the decision under review.[24] Also, the Tribunal may consider materials additional to those that were before the decision-maker.[25]
Section 21(1) [of the NDIS Act] provides that a prospective participant will meet the access criteria for the NDIS if the CEO is 'satisfied' that each of the access criteria is met. In this independent review, the Tribunal must also be so satisfied. This is a state of positive satisfaction or relative certainty which must be attained in relation to each criterion specifically. Therefore, while neither the Applicant nor the Agency bear any formal onus of proof, the Applicant does bear the practical onus of placing before the Tribunal, or pointing to material before the Tribunal, that can persuade it that each of the access criteria are met.[27]
21 When a person meets the access criteria > > (1) A person meets the access criteria if:
(a) the CEO is satisfied that the person meets the age requirements (see section 22); and
(b) the CEO is satisfied that, at the time of considering the request, the person meets the residence requirements (see section 23); and
(c) the CEO is satisfied that, at the time of considering the request:
(i) the person meets the disability requirements (see section 24); or
(ii) the person meets the early intervention requirements (see section 25).
(a) the person has a disability that is attributable to one or more intellectual, cognitive, neurological, sensory or physical impairments or the person has one or more impairments to which a psychosocial disability is attributable; 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 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.
(a) the permanence criteria under section 24(1)(b); > > (b) the substantially reduced functional capacity criteria pursuant to section 24(1)(c), in any of the six listed activities; > > (c) the requirement under section 24(1)(d) that the person's impairments affect their social or economic participation; and > > (d) the requirement of support under the NDIS for the person's lifetime, under section 24(1)(e).
(1) A person meets the early intervention requirements if:
(a) the person:
(i) has one or more identified intellectual, cognitive, neurological, sensory or physical impairments that are, or are likely to be, permanent; or
(ii) has one or more identified impairments to which a psychosocial disability is attributable and that are, or are likely to be, permanent;
(iii) is a child who has developmental delay; and
(b) the CEO is satisfied that provision of early intervention supports for the person is likely to benefit the person by reducing the person's future needs for supports in relation to disability; and
(c) the CEO is satisfied that provision of early intervention supports for the person is likely to benefit the person by:
(i) mitigating or alleviating the impact of the person's impairment upon the functional capacity of the person to undertake communication, social interaction, learning, mobility, self-care or self-management; or;
(ii) preventing the deterioration of such functional capacity; or
(iii) improving such functional capacity; or
(iv) strengthening the sustainability of informal supports available to the person, including through building the capacity of the person's carer.
Note: In certain circumstances, a person with a degenerative condition could meet the early intervention requirements and therefore become a participant.
(1A) For the purposes of subparagraph (1)(a)(i) or (ii), an impairment or impairments that are episodic or fluctuating may be taken to be permanent despite the episodic or fluctuating nature of the impairments.
(2) The CEO is taken to be satisfied as mentioned in paragraphs (1)(b) and (c) if one or more of the person's impairments are prescribed by the National Disability Insurance Scheme rules for the purposes of this subsection.
(3) Despite subsections (1) and (2), the person does not meet the early intervention requirements if the CEO is satisfied that early intervention support for the person is not most appropriately funded or provided through the National Disability Insurance Scheme, and is more appropriately funded or provided through other general systems of service delivery or support services offered by a person, agency or body, or through systems of service delivery or support services offered:
(b) in accordance with reasonable adjustments required under a law dealing with discrimination on the basis of disability.
(a) Her impairments are not permanent, within the meaning of section 25(1)(a). > > (b) With respect to subsection (b) of section 25(1), HZSG's impairments have not been treated effectively, and could be treated through the pathway of mainstream services. > > (c) Section 25(1)(c) and section 25(3) are not met.[31]
(1) The CEO may revoke a person's status as a participant in the National Disability Insurance Scheme if:
(a) the CEO is satisfied that the person does not meet the residence requirements (see section 23); or
(b) the CEO is satisfied that the person does not meet at least one of the following:
(ii) the early intervention requirements (see section 25).
(2) The CEO must give written notice of the decision to the participant, stating the date on which the revocation takes effect.
27 National Disability Insurance Scheme rules relating to disability requirements and early intervention requirements
The National Disability Insurance Scheme rules may prescribe circumstances in which, or criteria to be applied in assessing whether:
(a) one or more impairments are, or are likely to be, permanent for the purposes of paragraph 24(1)(b) or subparagraph 25(1)(a)(i) or (ii); or
(b) one or more impairments result in substantially reduced functional capacity of a person to undertake one or more activities for the purposes of paragraph 24(1)(c); or
(c) one or more impairments affect a person's capacity for social and economic participation for the purposes of paragraph 24(1)(d); or
(d) the provision of early intervention supports is likely to benefit a person by reducing the person's future needs for supports in relation to disability for the purposes of paragraph 25(1)(b); or
(e) the provision of early intervention supports is likely to benefit a person by mitigating, alleviating or preventing the deterioration of the person's functional capacity to undertake one or more of the activities for the purposes of subparagraph 25(1)(c)(i) or (ii), or improving such functional capacity for the purposes of subparagraph 25(1)(c)(iii); or
(f) the provision of early intervention supports is likely to benefit a person by strengthening the sustainability of the informal supports available to the person, including through building the capacity of the person's carer for the purposes of subparagraph 25(1)(c)(iv).
209 The National Disability Insurance Scheme rules
(1) The Minister may, by legislative instrument, make rules called the National Disability Insurance Scheme rules prescribing matters:
(a) required or permitted by this Act to be prescribed by the National Disability Insurance Scheme rules; or
(b) necessary or convenient to be prescribed in order to carry out or give effect to this Act.
When is an impairment permanent or likely to be permanent for the disability requirements?
5.4 An impairment is, or is likely to be, permanent (see paragraph 5.1(b)) only if there are no known, available and appropriate evidence-based clinical, medical or other treatments that would be likely to remedy the impairment.
5.5 An impairment may be permanent notwithstanding that the severity of its impact on the functional capacity of the person may fluctuate or there are prospects that the severity of the impact of the impairment on the person's functional capacity, including their psychosocial functioning, may improve.
5.6 An impairment may require medical treatment and review before a determination can be made about whether the impairment is permanent or likely to be permanent. The impairment is, or is likely to be, permanent only if the impairment does not require further medical treatment or review in order for its permanency or likely permanency to be demonstrated (even though the impairment may continue to be treated and reviewed after this has been demonstrated).
5.7 If an impairment is of a degenerative nature, the impairment is, or is likely to be, permanent if medical or other treatment would not, or would be unlikely to, improve the condition.
When does an impairment result in substantially reduced functional capacity to undertake relevant activities?
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.
Unlike the NDIS Rules, the NDIS Guidelines are not made pursuant to a power conferred by the NDIS Act; they are issued in an exercise of executive power.[34] As such, the Guidelines set out the Agency's policy and provide guidance in how relevant powers are to be exercised. Ordinarily the Tribunal will apply such policy in reviewing a decision, unless the policy is unlawful, or unless its application tends to produce an unjust decision in the circumstances of the particular case.[35]
DOES HZSG MEET THE ACCESS REQUIREMENTS FOR THE NDIS?
Section 24(1)(a) - disability attributable to impairments
... The term "disability" is used in the Act, and in s 24, as a descriptive concept for the overall effect of a person's impairments on that person's abilities to participate in all aspects of personal and community life. Threshold provisions such as s 24 operate not on the concept of disability, but on the concept of an impairment, which, as the Tribunal correctly observed at [19] of its reasons, is generally understood as involving the loss of or damage to a physical, sensory or mental function.[37]
Analysis of the medical evidence provided and my assessment of HZSG has allowed for acceptance of the following assumptions regarding her medical conditions:
3.1.1 Major depressive disorder, obsessive compulsive disorder, panic disorder with
agoraphobia, post-traumatic stress disorder resulting in:
The Applicant's medical and allied health evidence
HZSG's cognitive state has been significantly and negatively impacted by her disability. Hr racing thoughts and reported auditory hallucinations render it nearly impossible for HZSG to concentrate on a task. She relies on others to remind her of and accompany her to important appointments. HZSG experiences panic attacks frequently, although they can occur without a clear trigger, many common daily problems may prompt the chest pain, dizziness and shortness of breath associated with these attacks. During assessment, HZSG demonstrated poor working memory and was unable to recall words listed to her. HZSG was also disorientated to date. Because of her paranoia and extreme distrust of others, HZSG does not have social contact outside of formal services, such as medical appointments and her friend (Z).[52]
HZSG spends most of her day sitting and 'thinking' as she is unable to leave the house without 1:1 support. HZSG has anxiety and symptoms of her mental illness prevent her from venturing from her known home environment and into the community.[53]
HZSG requires support when leaving the house. She is unable to independently participate in community activities. HZSG becomes overwhelmed quickly when in crowded spaces such as a train platform. She often feels faint and may experience a panic attack. Even with individualized and one on one support, HZSG's anxiety renders most community outings too overwhelming. HZSG's obsessive washing of her clothes and use of hot water has caused her extreme financial hardship. Her utility bills are much higher than an average family's.[54]
HZSG is a 39-years-old female with a primary diagnosis of paranoid schizophrenia
experiencing both auditory and visual hallucinations. HZSG is well known to mental health
services and has been hospitalised frequently for recurrent episodes of psychosis. HZSG has OCD and fear of germs. She suffers from debilitating anxiety and depression.[60]
HZSG is a 39-years-old female with serious mental illness, paranoid, and antisocial/verbally aggressive behaviours. HZSG lives alone in a DOH[61] unit and has a troubled history of psychosocial issues with her neighbours. She mostly isolates herself from all social contact in fear she is constantly watched and judged. HZSG has a fear of public places and will only go on short outings with her carer. HZSG had her NDIS plan cancelled in the past 2 months but continued to receive minimal support from her disability provider as a form of charity. HZSG has nil informal supports and truly cannot manage on her own. HZSG has a history of panic attacks and hyperventilation. She becomes dizzy and falls. HZSG stays at home without meaningful activities. She does not listen to music, does not read, or watch TV. She constantly worries and looks at her phone. HZSG has nil contact with her family due to psychosocial issues. HZSG has significant emotional regulations dysfunction. She is very labile and lashes out during conversations. This causes significant impairment in developing and maintaining meaningful social connections. HZSG has a fear of germs and has increasingly struggled with her OCD. She uses hand sanitizer wipes on all surfaces before touching then leaves them on the floor in her unit. HZSG is very argumentative and noncompliant. HZSG has increased issues with her urine incontinence. She covered a mattress with plastic and placed it in the lounge room on the floor. She sleeps on the mattress on the floor as she is convinced that her neighbours can spy on her inside her bedroom. HZSG also covered the kitchen and lounge room windows with plastic in fear her neighbours can see inside the unit. HZSG has unfortunately been living in squalor and hoards. Her unit is in deplorable state of unsanitary condition. HZSG desperately needs her NDIS plan reinstated to access supports for capacity building and daily living supports to cope with the effects of her disability.[62]
HZSG did not respond to any of my questions and was completely disengaged during the entire assessment and [Dr Alkhalayleh] answered all the questions on her behalf.[68]
... through telehealth, as HZSG was not prepared to meet me in person. [Dr Alkhalayleh] answered all the questions in her behalf and I did not hear her voice at all.[69]
She has been prescribed several psychotropic medications but it is unsure she is taking them regularly due to her severe cognitive deficit which makes her incapable to attend to her affairs.[70]
HZSG has severe mental conditions impacting on her ability to function as a normal citizen. She presents as someone who is psychotic and cannot hold a normal conversation. She has been traumatised since she was in Iraq and is highly paranoid. Furthermore she isolates herself from anyone and does not get ongoing treatment for her mental conditions which is very necessary. She is not likely to make any friends nor connect with any family members due to her present state of mind. She lacks self love and always talk about wanting to commit suicide. She would need experienced support workers who can handle people who are highly paranoid and delusional. She is non functioning and requires intensive assistance urgently.[72]
Guarded in her responses, limited engagement. She became very agitated for a brief period during the review. However she could contain her anger and apologized for her behaviour. Noted her hands slightly erythematous,[78] due to excessive washing.
Reported mood as feeling depressed and angry. However denies it being pervasive.
Affect was mostly restricted, except for the outburst as noted above.
Thought Content - Obsessions with content of contamination. Compulsive Washing. Themes of helplessness and loneliness.
Denied any suicidal ideation, intent or harm or thoughts to harm others. Stated this would be against her religion.
Perception - Auditory hallucinations, support worker has noted her responding to voices.
Limited insight into both obsessive symptoms and psychotic symptoms. However acknowledges she needs MH [Mental Health] treatment and support.[79]
Patient has history of OCD, seen washing hands multiple times, also cleaning hands with alcohol wipes - patient refusing water and paracetamol as patient believes its contaminated with germs. MHT [Mental Health team] aware.[86]
The only complaints she presented were about inability to sleep at night, carrying many worries, and having taxing chest oppressions. As I dragged the history from her with difficulty, I learnt that her first episode of a psychiatric disorder was in 2007 and that followed giving birth to a child. She could not give me a clear description of her condition at that time but she admitted that she was imagining things and was hearing voices. Most likely this was post-partum psychosis. Apparently because she was mentally ill, her husband left her and eventually took custody of her two children. She stated that she has not seen her children since 2012. I also learnt that she was admitted to [a] Hospital and was also an outpatient at [another] Hospital. She stated that she was prescribed Lexapro which "gave me strength" (possibly elevated her mood). She was then prescribed Effexor which she currently takes at a dose of 75mg + 37.5mg daily. She stated that she has been on that dose for the last one and a half months.
At the interview I found her mood rather unstable. She certainly was not depressed or melancholic but in fact she could at times laugh warmly. I got the impression the most likely diagnosis is either bipolar disorder (mixed type) or schizoaffective disorder. As I found her contented with the Effexor, I maintained her on that dose but added Seroquel[91] 25mg one tablet at night.
'because this is her life, she rely on the NDIA so much. I convinced her to come today by sending someone to pick her up from there, bring her here and then they will take her back home because she does not catch public transport. So for her this is do or die, and she understands this.'
It is a big worry for me, a great concern for me if the woman[96] stops coming ... because I'm very tired ... I have no one, I feel like there's no one with me in this world but God.
HZSG's psychiatric history and current symptoms have been outlined above.
She has a complex psychiatric presentation that is marked by multiple developmental stressors, including being a refugee as both a child and again as an adult, a victim of family and intimate partner violence, isolation from her family of origin and children, and a person from a culturally and linguistically diverse background.
It is unlikely that she experiences a primary psychotic disorder such as schizophrenia. Current symptoms such as fear of harm and auditory hallucinations are more likely the result of being subject to past trauma, as noted above. It is likely that she experienced an episode of Major Depressive Disorder with Psychotic Features after the birth of her second child.
There is no evidence that she has a Personality Disorder.[101]
Given the severity and chronicity of her symptoms, HZSG would require intensive and long-term care from both a psychiatrist and a clinical psychologist.
A treatment program delivered by mental health professionals, to target each of the diagnoses above, would consist of both
(i) pharmacotherapy, namely the combination of an antidepressant medication, with possible augmentation by an antipsychotic medication, and
(ii) psychological therapy, both trauma focussed and cognitive behaviour therapy.
Medication strategies that may be considered include increasing the dose of venlafaxine to 150-225mg daily, switching to duloxetine 60-120mg daily or to sertraline 50-100mg daily, and augmenting with aripiprazole 10-15mg daily.[104]
Notwithstanding the complexity, severity and in particular the duration of her symptoms, the past and current absence of a co-ordinated specialist program of pharmacological and psychological therapy must lead to the conclusion that her impairments are not permanent.[107]
As a result of past trauma, HZSG has difficulties with trusting and therefore engaging with people which may impede the provision of psychological therapy. However, her engagement with [her accompanying female support worker] does suggest that there is the potential for her to engage with a female, Arabic speaking therapist.
The main weakness is her very limited ability to speak, read or write in English which is a potential barrier in engaging independently with health and care providers. An interpreter will be necessary in any situation not involving another Arabic speaking person.[113]
A note was made by [HZSG's physiotherapy practice] on 18th January 2023 that HZSG contacted their office to state she could not attend her appointment. She responded aggressively when the cancellation policy was explained, and continued to yell when the practice was unable to accommodate her request for an appointment later that day. This vignette indicates her inability to negotiate appointment times independently.
She is not able to travel to appointments independently given agoraphobia.
... such teams are certainly available within the [relevant State] public health public mental health system, but I think we're all aware that there are significant resource issues with such services. So in reality, it's unlikely that the kind of presentation that HZSG has would lead to that level of care being delivered by a multidisciplinary mental health care team.
... theoretically be available, with the caveat that resourcing certainly varies from area to area within [the State] and also that her presentation with a depressive disorder and trauma may not take precedence over patients who present with so-called severe mental illness such as schizophrenia or bipolar disorder.
But I think the whole point is that she would require the assistance of a support worker to take her to these appointments, whether it's late in the afternoon or whether she needs prompting to go earlier in the day ... that is what's an important use of the support worker.
And it may be that her health literacy is such that she is more open to, for instance, pharmacological medication, whereas she is less familiar with the importance of psychological therapy, which frankly can also carry with it a certain level of distress, for instance, when past traumas are discussed. So that will be an example of something that she would need to be educated about the importance of engaging in.
The main concern would be ... she may well have a sense of hopelessness in that this is someone who on the one hand has experienced these symptoms of depression, obsessive compulsive disorder and post-traumatic stress disorder for a long time and has experienced these symptoms without remission for a long time, so there might be a sense of hopelessness in that she doesn't feel the symptoms will ever resolve.
... obviously hypothesising here, apart from the sense of hopelessness related to the chronic, unremitting nature of the symptoms, I guess the other aspect that we need to be potentially mindful of is the fact that she's essentially lost everything. She has no access to her two children, she has no contact with her father, mother or siblings. That too may bring with it a sense that she has little to get better for.
Finally, the evidence is that she's been the victim of verbal emotional abuse from her family for many years and for instance, I note in my report ... that her family repeatedly called her crazy and incompetent, so I think that would mean it may well be that she internalises her symptoms and disability as her own fault or result of her inability or incompetence.
What we characterise as medical disorders, they [HZSG's family] have characterised as personal failings.
HZSG has not engaged in regular therapy for some years.[116] This seems to be due to a combination of lack of funds and lack of readily available and consistent transport.
HZSG said that her current treatment involves reviews with GP as needed. These are in person. She is transported and accompanied by a support worker.[117]
[D]ue to the effects of her medical conditions, HZSG experiences difficulties undertaking tasks that involve:
HZSG presented as exceedingly anxious. She stood with her arms folded across her stomach. Her eye contact with poor. She looked down as she spoke. She presented as distrusting of others. There was a degree of irritability. Rapport was difficult to establish. She appeared to keep her distance from myself and the
She declined to sit. Her preference was to stand. She stood several metres away when communicating. She stood for the majority of the 2.5-hour assessment.
She removed herself from the conversation (without warning) at times to go into the bathroom. She appeared to be washing her hands. Her hands were visibly red and raw.[119]
[HZSG] was asleep at my arrival for the assessment and appeared unaware of my role and the reason for the assessment, an indication of her impaired capacity to plan and manage her appointments.[120]
HZSG does not drive. She does not hold a driver's licence. To leave her unit, she is totally dependent on her trusted support workers ... HZSG is unable to utilise public transport. Her restrictions associated with her psychiatric impairments are simply too great.
She is totally dependent on her support workers to transport and accompany her to GP reviews and any specialist appointments, of which she schedules at night to account for her poor day-time sleep routine.[123]
... requires transport and accompaniment support to leave her unit and access her community. She requires this support to engage in social and community-based activities as well as essential services such as medical and therapy consultations.[125]
... critical in ensuring that HZSG can access all her medical appointments and essential services. The provision of this support will ensure that she attends all her medical appointments, and the risk of missed or avoided appointments is minimised.[126]
I'm unsure if the typical short duration of the SASH program would be able to accommodate that. That's something that would need to be assessed on an as needs basis.
Ms Sale noted that a SASH package, while designed to provide short term assistance to help somebody improve their level of function so that the degree of care and help needed is no longer required, she was aware of instances where the usual program length of six weeks had been extended to months and in some cases two years.
... there is insufficient evidence to establish that the Applicant has explored all known, available and appropriate evidence-based clinical, medical or other treatments that would be likely to remedy the psychosocial impairments.
As such, the Tribunal cannot be satisfied that there are no known, available and appropriate evidence-based clinical medical or other treatment that would be likely to remedy the impairment, per r 5.4.[137]
In that case Mortimer J rejected an argument advanced by the NDIA that permanent meant "irreversible" or "untreatable" (at [77]). Her Honour instead held (at [85]) that the correct meaning of "permanent" in s 24(1)(b) is "enduring", noting that > > ... This meaning reflects the purpose and context of the legislative scheme, as a scheme intended to deliver lifelong support to persons with disability.[140]
"The focus of the text, consistently with the purposes of the scheme, is whether the impairments experienced by individuals (rather than the cause of the impairments or the specific diagnoses which might be applied to a medical condition) have an enduring quality so as to fit within the conceptual emphasis of the scheme." [141]
In this context, "remedy" should be understood to mean more than just relieve or improve. That is because r 5.5 recognises that an impairment may be permanent notwithstanding the severity of its impact on a person may fluctuate, or there are prospects for improvement. These changes in the impacts of an impairment may occur because of, amongst other matters, treatment. Therefore, in r 5.4 the word "remedy" should be understood to mean something approaching a removal or cure of the impairment. That is consistent with the meaning I consider should be given to the statutory phrase "permanent impairment", as an impairment which is enduring and, while its impacts on a person from time to time might fluctuate, is not an impairment which is likely to be removed or cured.[142]
One key word that appears in the legislation and the rules [that] does not appear to have been addressed in the authorities is 'likely'. The Macquarie Dictionary defines likely as: 'probably or apparently going or destined (to do, be, etc.)'_. Likewise, the Oxford English Dictionary defines the word as '_probable' _in the sense of '_having a high chance of occurring'. Accordingly, where this word plays a role in helping to determine permanence, I consider it to be indicative of probability rather than possibility, and certainly not mere speculation.[144]
We need evidence that you'll likely have your impairment for your whole life.
You might have some periods in your life where there is a smaller impact on your daily life, because your impairment may be episodic or fluctuate in intensity. Your impairment can still be permanent due to the overall impact on your life, and the likelihood that you will be impacted across your lifetime.
Even when your condition or diagnosis is permanent, we'll check if your impairment is permanent too. For example, you may not be eligible if your impairment is temporary, still being treated, or if there are remaining treatment options.
Generally, we'll consider whether your impairment is likely to be permanent after all available and appropriate treatment options have been pursued.
Your impairment will likely be permanent if your treating professional gives us evidence that indicates there are no further treatments that could relieve or cure it.
Your treating professional will tell us or be asked to certify if there are medical, clinical or other treatments that are likely to remedy your impairment. We need to understand whether there are treatments that are:
The word treatment should be understood in a broadest sense and may include changes to your diet and lifestyle. So, for example, conditions such as obesity are unlikely to be found to be permanent.
If you're still undergoing or have recently had treatment, we'll need to wait until you know the outcome of the treatment before we can decide your impairment is likely to be permanent.
In some situations, it may be clear your impairment is likely to be permanent while you're still undergoing treatment or rehabilitation. For example, you may still need treatment and rehabilitation for a spinal cord injury, but it's clear you'll have a permanent impairment.
You might still have a permanent impairment, even if its effects may change over time.
For degenerative impairments, or those that get worse over time, we consider them permanent if treatment isn't likely to help or improve the impairment's effects.
The executive has chosen to use three descriptors, each of which must be given work to do. See Commonwealth v Baume [1905] HCA 11; 2 CLR 405 at 414, Griffith CJ; Project Blue Sky v Australian Broadcasting Authority [1998] HCA 28; 194 CLR 355 at [71], McHugh, Gummow, Kirby and Hayne JJ; Wilkie v Commonwealth [2017] HCA 40; 263 CLR 487 at [146]; District Council of Streaky Bay v Wilson [2021] FCAFC 181; 287 FCR 538 at [63]. On the application of principles of statutory interpretation to delegated legislation, see Collector of Customs v Agfa-Gevaert Ltd [1996] HCA 36; 186 CLR 389 at 398; Master Education Services Pty Ltd v Ketchell [2008] HCA 38; 236 CLR 101 at [19]; ADCO Constructions Pty Ltd v Goudappel [2014] HCA 18; 254 CLR 1 at [28]. See also Berenguel v Minister for Immigration and Citizenship [2010] HCA 8; 264 ALR 417; Acts Interpretation Act 1901 (Cth) s 46(1); Legislation Act 2003 (Cth) s 13(1).
The chosen descriptors must also be construed consistently with the other language used in this section of the rules, and in r 5.4 in particular, including the requirement that the treatment "would be likely to remedy the impairment".[146]
As a general observation, in my opinion each of the adjectives must be construed as referring to circumstances in Australia. In r 5.4, the word "known" connotes a treatment which can be identified by Australian medical practitioners as a suitable treatment for the person's particular impairment. The word "appropriate" connotes a treatment which has a capacity to "remedy" the impairment and is suitable for the particular individual concerned to undergo. The capacity of individuals with an impairment to undergo certain treatments may vary depending on their physical and psychological capabilities, other aspects of their physical and mental health, on their personal circumstances in terms of where they live and who they live with, and who cares for them.
The word "available" should be understood as meaning available to a particular individual. If it were to be construed as meaning "exists in Australia", then it would have little different work to do from the word "known". The Macquarie Dictionary defines "available" as meaning:
"adjective 1. suitable or ready for use; at hand; of use or service ... "
Assuming as I do the validity of r 5.4, and on the premise any given treatment is "known" and "appropriate" as I have explained those terms, in my opinion the adjective "available" should be understood as directed at what treatments an individual can, in reality, access. Whether a person can afford a treatment will form part of the factual circumstances a decision-maker may need to examine in deciding if a treatment is one that an individual can in reality access.
Affordability may not be the only feature of a treatment affecting whether an individual can access a treatment. For example, whether a known and appropriate treatment for an impairment for a person in a remote Aboriginal community in Australia is "available" to that person is likely to involve considerations of whether that treatment can be delivered in that community, or whether a person has to travel to a major city or regional town to receive that treatment. So too the personal circumstances of a person, and the combination of impairments they might have. If a person has severe agoraphobia, but also has an impairment for which there is a known and appropriate treatment that can only accessed at a busy public hospital, a decision-maker may need to consider whether, as a matter of fact, that treatment is "available" to that individual, even if it might be "available" to a person without agoraphobia. [147]
... prescribe circumstances where, if the repository of the power is satisfied on the evidence of the applicability of either of those rules, a person's impairment will be excluded from meeting the permanency criterion in s 24(1)(b).[148]
Section 24(1)(c) - substantially reduced functional capacity
Does your impairment substantially reduce your functional capacity?
Your permanent impairment needs to substantially reduce your functional capacity or ability to undertake activities in one of the following areas:
• Communicating - how you speak, write, or use sign language and gestures, to express yourself compared to other people your age. We also look at how well you understand people, and how others understand you.
• Socialising - how you make and keep friends, or interact with the community, or how a young child plays with other children. We also look at your behaviour, and how you cope with feelings and emotions in social situations.
• Learning - how you learn, understand and remember new things, and practise and use new skills.
• Mobility, or moving around - how easily you move around your home and community, and how you get in and out of bed or a chair. We consider how you get out and about and use your arms or legs.
• Self-care - personal care, hygiene, grooming, eating and drinking, and health. We consider how you get dressed, shower or bathe, eat or go to the toilet.
• Self-management (if older than 6) - how you organise your life. We consider how you plan, make decisions, and look after yourself. This might include day-to-day tasks at home, how you solve problems, or manage your money. We consider your mental or cognitive ability to manage your life, not your physical ability to do these tasks.
Your impairment substantially reduces your functional capacity if you usually need disability specific supports to participate in or complete the above tasks.
To help us decide if you're eligible, we need to know your capacity and where you need more help. We get this information from you when you apply to the NDIS.
If you have more than one permanent impairment, we will consider them together, to see if they substantially reduce your functional capacity.
We consider how you're involved in different areas of life like home, school, work and the community, and how you carry out tasks and actions. We also consider any other factors that may impact your day-to-day life.
Your needs might go up and down each day or each month. Progressive Multiple Sclerosis (MS) can be a good example of this. We consider your ability over time, taking into account your ups and downs.
HZSJ is 'independent with her basic day to day communication needs. She does not require formal support worker assistance in this domain.
Ms Sale made some recommendations to improve and maximise HZSG's functional capacity in this domain, being input from a psychologist to provide support and education to improve her communication skills and address barriers.[157]
To improve and maximise HZSJ's functional capacity in this domain, Ms Sale recommended HZSG be provided with supports, in the form of transport and accompaniment support to meaningful and well-suited activities within her community, and professional supports (such as an occupational therapist or social worker) to help HZSG engage with local community based social groups and activities. It is noted that HZSG expressed interest in engaging with a particular support group for Muslim women in her community.[158]
Ms Sale concluded that HZSG 'has significant restrictions in this domain,' noting HZSG has 'significant difficulties leaving her unit, accessing her community and engaging in social activities due to her psychiatric impairments ... '[159] Ms Sale also noted that the support services recommended by her 'are critical in increasing HZSG's level of socialisation, face-to-face interaction and exposure to the community'.[160]
Ms Sale recommended supports in the form of transport and accompaniment of HZSG for all medical reviews and essential services; psychological intervention and occupational therapy engagement, to help improve and maximise HZSG's functional mobility in the context of her difficulties in leaving her home and accessing the community.[163] As noted above, Ms Sale considered the support services recommended by her to be critical in ensuring HZSG can access all of her medical appointments and essential services.[164]
Ms Sale commented that HZSG experienced 'considerable difficulties' with meal preparation and access to a nutritious diet, noting that HZSG reported that she:
Ms Sale observed that there were very limited food items in HZSG's fridge or kitchen at the time she conducted her assessment (some boxes of tea, one avocado, a pack of six eggs and a packet of Jatz biscuits) noting '[H]er cupboards were either completely empty or filled with cleaning products. The pantry was empty.'
In addressing domestic activities, Ms Sale observed that HZSG does little cleaning of her unit, beyond her obsessive use of single-use wipes on benchtops and touched items. Ms Sale observed there were piles of wipes and tissues scattered throughout the unit (her report contained photographs reflecting this), and several bags of rubbish outside the door (apparently awaiting the support worker to take these to the unit bins area). Ms Sale also noted that HZSG depends on her support worker to wash her clothes. Again, this is because of lack of motivation and fatigue.
HZSG said that bed sheets are changed by her support workers, every few weeks. She said she uses a plastic mat over her mattress as she is fearful of mould developing on the mattress and sheets. She sleeps on top of her quilt and blankets (rather than underneath) for fear of contaminating the bed sheets. She places tissues around her head to avoid touching the blanket. She worries about germs (from her scalp) on the blankets.
Ms Sale was of the opinion that HZSG has 'considerable difficulties' with attending to 'nearly all her self-care tasks', with her limitations arising from her psychosocial impairments. Further, Ms Sale stated in her report that:
HZSG frequently neglects, avoids or attends to self-care activities at an inappropriate level (i.e. handwashing and teeth brushing) due to her psychiatric impairments and resulting restrictions.
She requires professional support and services to ensure consistent and appropriate attendance to her self-care tasks.[167]
In responding to a specific question posed by the Agency in briefing her, Ms Sale advised that HZSG could not, in Ms Sale's opinion, increase her functional capacity for self-care with the use of commonly used items, strategies, modifications to the way that she undertakes tasks, pacing and/or planning of her day/week, because the restrictions arising from her psychosocial disability are too great.[168]
[HZSG] requires input and assistance with any decision-making and problem-solving tasks beyond that of a basic level of complexity.[169]
The threshold requirements to achieve functional capacity in relation to activities of mobility are "relatively modest"; a person has functional capacity if they can, for example, move about their home, get in and out of beds and chairs, leave home, and mobilise in the community.[178]
While the Applicant's level of functioning, particularly with respect to accessing the community, suggests a reduction in functional capacity, the Applicant appears otherwise capable of functioning across each of the domains. While aspects of her self-care and attending to household tasks are obsessive, these are matters which might be addressed by the combination of psychological therapy and pharmacology recommended by A/Professor Wijeratne to be provided by the mainstream medical system. The Respondent's view is that the high threshold of substantially reduced functional capacity is not met in any of the domains.
Noting that the Applicant's impairments as a result of her diagnosed medical condition cannot be said to be permanent, the Respondent is of the view that a finding of substantially reduced functional capacity (s24(1)(c)) is not open on the evidence. This is due to fact that all available and appropriate treatments have not been trialled by the Applicant, therefore it is impossible to determine the severity of the reduction in the Applicant's functional capacity.[184]
Rule 5.8 of the Rules defines the circumstances in which a person must be taken to have "substantially reduced functional capacity" for the purposes of s 24(1)(c) of the Act.
Rule 5.8 operates expressly by reference to each of the activities in s 24(1)(c)(i) to (vi). It requires the decision-maker to look, as a matter of factual assessment, at the outcome or effect of a person's impairment on the performance of each, and any, of those six activities. If the outcome or effect is any of the outcomes or effects specified in r 5.8(a), (b) or (c), the deeming effect of r 5.8 operates_.[185]_
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 meaning 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.[186]
[55] Using the concept of impairment enables assessment of the severity and permanency of a person's condition, and of the effects of that condition through not only the evidence of an applicant, but also medical and clinical evidence. The legislative scheme contemplates a relatively high degree of precision by decision-makers (see, for example, the six activities in s 24(1)(c)) in assessing what a person can or cannot do. The assessment to be undertaken is avowedly functional, and multi-faceted. > > [56] That being the case, no arbitrary limits are placed on access to the NDIS. No decision-maker need be satisfied a person's impairment is "serious", or more serious than another person's. No qualitative judgments in that sense are called for. Rather, the legislative scheme is based on a functional, practical assessment of what a person can and cannot do. Critically, the scheme makes detailed provision for that assessment, and it is sufficient for a person to have substantially reduced functional capacity in relation to one activity. That, in my opinion, recognises the spectrum of impairments which can be experienced by persons with disabilities, and accommodates different abilities within one person in terms of her or his daily activities. That is why a detailed functional assessment is so important.[188]
The World Health Organisation has a universal definition of assistive technology.
Assistive technology is equipment or devices that help you do things you can't do because of your disability. Assistive technology may also help you do something more easily or safely. Assistive technology will reduce your need for other supports over time.
This could be small things like non-slip mats, or special knives and forks. It could be big things like wheelchairs and powered adjustable beds. It also could be technology like an app to help you speak to other people if you have a speech impairment.
Not all equipment or technology you use is assistive technology. Many people use some equipment as part of their lives, for example, a radio to listen to music, or a standard microwave oven to cook food.
Assistive technology is only the equipment you need because it helps you do things that you normally can't do because of your disability.[191]
Social interaction as referred to in in 24(1)(c)(ii) doesn't, in our view, mean social interaction with the whole of the community. It means social interaction with elements of the community, sections of the community.[206]
... is limited to tasks associated with making and keeping friends, interacting with other people in the community, and maintaining behavioural and emotional regulation in a social context.
I note that this bundle of tasks, as identified, does not incorporate any reference to social interaction with immediate family, which is often referred to as evidence of functional capacity for social interaction in access cases ... It is to be noted that represents a departure from the ICF/WHODAS[208] assessment framework. However, upon reflection, it appears to me that this is a deliberate departure that is consistent with the objects of the NDIS Act, with its emphasis on the independence and social and economic participation of persons with disability, beyond their immediate family.[209]
... consistent with the ICF, the assessment of a prospective participant's functional capacity is based upon the 'naked' person; that is, it seeks to determine the person's capacity without personal assistance or use of assistive devices. That is the case, except to the extent that this principle is modified by Rule 5.8(a) to require commonly used item of equipment, such as glasses, to be discounted. In my opinion, given that Rule 5.8(a) should be taken to evince a legislative intention, the same approach should be taken in relation to the assessment of functional capacity for the purposes of s 24(1)(c) other than when Rule 5.8 is applicable.[210]
... a prospective participant's inability to perform these tasks results in squalor or malnutrition, for example. In such circumstances these tasks may be considered as related to 'health care' in the self-care activity area.[215]
... are limited to cognitive tasks associated with personal organisation, planning, decision-making, self-care, problem-solving and financial management.[217]
Section 24(1)(d) - social and economic participation
Section 24(1)(e) - likely need for lifetime NDIS support
The focus of s 24(1)(e) is on whether a prospective participant is likely to require support under the NDIS, or whether those support needs are most appropriately met by other systems ... The answer to that question depends on whether the support is required in respect of substantially reduced functional capacity to participate in an "activity", as assessed in accordance with s 24(1)(c). In the present case, there is another system that provides support to Mr Foster, albeit that it does not cover the full costs of his catheters.
Mr Foster submitted that question was not to be approached by asking what supports he was presently requiring but also what supports he might need to be funded through the NDIS once he was a participant in the scheme. That submission cannot be accepted. Section 24 is the gateway provision. The "likely" support referred to in s 24(1)(e) can only be referable to the result of the impairment the subject of the application to gain access to the NDIS.[223]
There is no scope for support to be partially funded under the NDIS. Once the CEO has formed a state of satisfaction about whether a support is "reasonable and necessary", and not more appropriately funded or provided through other general systems of service delivery or support services offered by a person, agency or body" (s 34(1)(f)), it must be fully funded: McGarrigle v National Disability Insurance Agency [2017 FCA 308; 252 FCR 121 at [94] per Mortimer J.[224]
You must be likely to need support under the NDIS for your whole life.
NDIS supports are investments that help you build or maintain your functional capacity and independence, and help you work, study or take part in social life.
Even if your needs go up and down over time, or happen episodically, we may still consider it's likely you'll need lifetime support under the NDIS.
We consider your overall situation to answer this question.
When we decide if you'll likely need support under the NDIS for your whole life, we consider:
For example, you may have an impairment which is caused by a chronic health condition. Many chronic health conditions are most effectively managed or remedied through medical management through the health system. If this is the case, we may decide that you don't have a lifetime need for support under the NDIS.
... would benefit from engaging with mentorship programs for adult learners to increase her independence and support her choice and control of wanting to boost her practical life skills which is best met through mainstream supports.[225]
Such change in support needs occur not infrequently for participants of the NDIS and is anticipated by the legislative provisions for plan variations and reassessments.[230]
[1] Hearing Bundle, Document H1, Agency's Statement of Facts, Issues and Contentions, 6 January 2025, (the Agency's SFIC), pages 1-21, [5].
[2] Hearing Bundle, Document T13, NDIS Plan 18 December 2020 - 18 December 2021, pages 144-158.
[3] Hearing Bundle, Document T14, NDIS Plan 4 August 2021 - 4 August 2023, pages 159-174.
[4] Hearing Bundle, Document T15, NDIS Plan 13 April 2022 - 12 April 2024, pages 175 - 190.
[5] Hearing Bundle, Document T8, First Eligibility Check Letter from Agency to HZSG, 17 November 2022, pages 118-123.
[6] These reports were in the Hearing Bundle; Document T6, Report of Waren Berger, Occupational Therapist, 2 May 2021 (relating to an assessment conducted on 8 April 2021), pages 84-99; and Document T7, Report of Waren Berger, Occupational Therapist, 2 February 2022 (relating to an assessment conducted on 28 January 2022), pages 100-117.
[7] Hearing Bundle, Document T5, Report of Bernadette Beary, Occupational Therapist, 10 December 2019, pages 71-83.
[8] Hearing Bundle, Document T3, NDIS Access Request Form, Dr Joseph Di Silva, dated 15 August 2019, pages 55-62.
[9] Hearing Bundle, Second Eligibility Check Letter from Agency to HZSG, 9 February 2023, pages 124-130.
[10] Hearing Bundle, Document T10, Revocation of Access Letter, 15 May 2023, pages 11- 136.
[11] Dr Alkhalayleh is a Director of a Sydney based support service. He appeared as an advocate for HZSG at the hearing of this review.
[12] Hearing Bundle, Document T12, Extract of NDIA interaction record - Request for Review, dated 29 May 2023, page 143.
[13] Hearing Bundle, Document T1A, Internal Review Decision, 31 May 2023, pages 29-40.
[14] Hearing Bundle, Document T11, Report of Dr Alfred de Robillard (Psychologist), dated 19 May 2023, pages 137-142.
[15] Hearing Bundle, Document T1, Application for Review of Decision, 6 June 2023, pages 25-42.
[16] Hearing Bundle, Document R3, Agency's Targeted Questions for HZSG's treating practitioners, 22 November 2023, pages 403-405 (relevant to Dr Younan).
[17] Hearing Bundle, the Agency's SFIC, pages 1-21); Document H2, Applicant's Statement of Facts, Issues and Contentions, 22 January 2025, pages 22-24 (the Applicant's SFIC).
[18] Hearing Bundle, Document A2, Occupational Therapy Independent Living Options Assessment report of Waren Berger (Occupational Therapist), 13 July 2023, pages 294-313 (Mr Berger's third report)
[19] Hearing Bundle, Document R1, Report of Associate Professor Chanaka Wijeratne, Consultant Psychiatrist, 8 April 2024, pages 333-347 (A/Professor Wijeratne's report); Document R2, Functional Capacity Assessment Report of Ms Melissa Sale, Occupational Therapist, dated 26 July 2024, pages 348-400 (Ms Sale's report).
[20] Administrative Review Tribunal (Common Procedures) Practice Direction 2024, Part 6.
[21] This and some following sections of this decision dealing with the applicable law have been adapted from prior NDIS access decisions of this Tribunal Member.
[23] Shi v Migration Agents' Registration Authority [2008] HCA 31; (2008) 235 CLR 286 (Shi), 324-325, 327 (Kiefel J).
[25] Shi 300-301 (Kirby J); 314-315 (Hayne and Heydon JJ); 327-328 (Kiefel J).
[26] Beezley v Repatriation Commission [2015] FCAFC 165 [68], as applied in Sutherland v National Disability Insurance Scheme [2024] AATA 411 [53].
[27] National Disability Insurance Agency v Lampard [2025] FCAFC 139, per Bromwich, Neskovcin and Vandongen JJ, [31].
[29] The following excerpts reflect how these provisions read prior to 3 October 2024.
[32] Again, these excerpts relate to the Rules as they were before 3 October 2024.
[34] G v Minister for Home Affairs [2019] FCAFC 79, [18].
[35] Re Drake and Minister for Immigration and Ethnic Affairs (No. 2) (1979) 2 ALD 634, 645 (President Brennan J).
[36] Hearing Bundle, Document T4, NDIS Access Request Form, page 56.
[37] Mulligan v National Disability Insurance Agency [2015] FCA 544, [51] (Mulligan)
[38] Hearing Bundle, Document H1, Agency's SFIC, [42].
[39] As listed in Ms Sale's report, page 396.
[42] Hearing Bundle, Document A9, HZSG's statement of lived experience, 23 February 2024, pages 331-332.
[43] A/Professor Wijeratne's report, page 335.
[45] It is noted that Ms Sale reported HZSG speaks on the telephone to her mother 'every few weeks'; Ms Sale's report, page 358.
[46] Hearing Bundle, Document T3, Access Request Form, Dr Di Silva, 15 August 2019, pages 55-62.
[47] Hearing Bundle, Document T4, Access Request Form, Dr Aladdin Matter, 23 August 2019, pages 63-70.
[48] Hearing Bundle, Document T3, Access Request Form, Dr Di Silva, 15 August 2019, page 59.
[49] Hearing Bundle, Document T4, Access Request Form, Dr Aladdin Matter, 23 August 2019, page 67.
[50] Hearing Bundle, Document T5, Report of Ms Bernadette Beary (Occupational Therapist), 10 December 2019, pages 71-83.
[57] Hearing Bundle, Document T6, Report of assessment conducted on 8 April 2021, pages 84-99; Document T7, Report of assessment conducted on 28 January 2022, pages 100-117; and Mr Berger's third report, pages 294-313.
[60] Mr Berger's third report, page 298.
[61] A reference to Department of Housing.
[62] Mr Berger's third report, pages 298-299.
[64] A/Professor Wijeratne's report, page 337.
[65] Hearing Bundle, Document T11, Report of Dr Alfred de Robillard (Psychologist) dated 19 May 2023, pages 137-142 (Dr de Robillard's report).
[66] Hearing Bundle, Document R3, Agency's Targeted Questions for the Applicant's Treating Practitioners, pages 401-403 (relevant to Dr de Robillard).
[67] Hearing Bundle, Document A4, Responses of Dr de Robillard to the Agency's Targeted Questions, dated 28 January 2024, pages 320-323.
[68] Dr de Robillard's report, page 288.
[69] Hearing Bundle, Document A4, Responses of Dr de Robillard to the Agency's Targeted Questions, page 320.
[70] Dr de Robillard's report, page 289.
[74] Hearing Bundle, Document A4, Responses of Dr de Robillard to the Agency's Targeted Questions, page 322.
[75] Hearing Bundle, Document A5, Report of Dr Naveen Nataraj (Consultant Psychiatrist), dated 29 October 2024, pages 324-326 (Dr Nataraj's report).
[76] For clarity, it is noted that this worker was identified in Dr Nataraj's report; it was not Dr Alkhalayleh.
[78] The Macquarie Dictionary defines this term as meaning 'abnormal redness of the skin due to local congestion, such as in inflammation'. Home - Macquarie
[83] Hearing Bundle, Document R3, Agency's Targeted Questions for HZSG's treating practitioners, 22 November 2023, pages 403-405 (relevant to Dr Younan).
[89] Dr Matter's records reflect that his first consultation with HZSG, for an unrelated matter, was in that same month.
[91] Seroquel is an antipsychotic medication.
[95] Evidence of Dr Alkhalayleh, 28 April 2025.
[96] This is a reference to the support worker providing unpaid regular assistance to HZSG, as of the date she gave her evidence.
[98] A/Professor Wijeratne's report, page 334.
[99] A/Professor Wijeratne's report, page 335.
[102] Evidence of A/Professor Wijeratne, 29 April 2025.
[103] A/Professor Wijeratne's report, page 339.
[108] Evidence of A/Professor Wijeratne, 29 April 2025.
[109] A/Professor Wijeratne's report, page 341.
[115] Evidence of A/Professor Wijeratne, 29 April 2025.
[116] In her evidence at the hearing on 29 April 2025 Ms Sale confirmed that this was a reference to psychological and psychiatric therapies, and physiotherapy.
[128] Ibid, page 380, and evidence of Ms Sale, 29 April 2025.
[129] Applicant's SFIC, pages 22 and 24.
[130], Agency's SFIC, [43]; opening submissions of Counsel for the Agency, 28 April 2025; and closing submissions of Counsel for the Agency, 21 July 2025.
[134] Closing submissions of Counsel for the Agency, 21 July 2025.
[135] Agency's SFIC, [53]-[55] and closing submissions of Counsel for the Agency, 21 July 2025.
[136] Closing submissions, 21 July 2025.
[139] Lampard, [20]-[21], [23].
[140] Kelly v National Disability Insurance Scheme [2024] FCA 1462 (Kelly), [15].
[146] Mortimer J's explanation of the meaning of the word 'remedy', as already noted above, has been omitted here.
[149] A/Professor Wijeratne's report, page 339.
[152] Evidence of Ms Sale, 29 April 2025.
[153] Noting that the descriptions contained within the Operational Guidelines should be considered as providing 'non-exclusive content to the range of tasks and action' (as referred to in Rule 5.8) that comprise the activities the NDIA is required to consider, consistent with the legislative history, context and purpose.' National Disability Insurance Agency v Foster (2023) FCAFC 11 (Foster), [62].
[154] The current Practice Direction is the Administrative Review Tribunal (Expert Evidence) Practice Direction 2024.
[156] Mr Berger's third report, pages 306-307.
[175] The Agency's SFIC, [71]-[73].
[178] Ibid, [64], citing MRLK and National Disability Insurance Agency [2021] AATA 3896 at [150]- [154]; Madelaine and National Disability Insurance Agency [2020] AATA 4025 at [104]- [106]; see also Holmes and National Disability Insurance Agency [2017] AATA 2750 and MHZQ and National Disability Insurance Agency [2019] AATA 810.
[179] The Agency's SFIC, [63]-[66].
[180] The Agency's SFIC, [68]-[70].
[181] Closing submissions, 21 July 2025.
[190] Timofticiuc and National Disability Insurance Agency [2021] AATA 3015, [96].
[191] NDIS Operational Guideline, Assistive Technology (equipment, technology and devices), 20 December 2023, page 2.
[192] Ms Sale's report, pages 378-379.
[197] A/Professor Wijeratne's report, page 345.
[202] Agency's SFIC, [61], citing Rooney and National Disability Insurance Agency [2021] AATA 3532 at [22].
[205] Ghezzaoui and National Disability Insurance Agency [2023] AATA 2835, [79]; noting Madelaine and National Disability Insurance Agency [2020] AATA 4025, [87] and Nika and National Disability Insurance Agency [2021] AATA 2127, [241].
[206] Kilgallin and the National Disability Insurance Agency [2017] AATA 186, [19].
[208] International Classification of Functioning Disability and Health.
[209] Burrows and CEO, National Disability Insurance Agency [2025] ARTA 607, (Burrows)at [108]-[109].
[210] Burrows, [71] (footnotes omitted).
[219] A/Professor Wijeratne's report, page 345.
[226] Ms Sale's report, pages 377-378.
[228] As to what is an 'NDIS support', see section 10 of the NDIS Act and the National Disability Insurance Scheme (Getting the NDIS back on Track No.1) (NDIS Supports) Transitional Rules 2024.
[229] Noting the observations made earlier in this decision in Kelly as to the proper interpretation of the term 'likely'.
(2008) 235 CLR 286