austlii:cth/ARTA/2025/839
General information, not legal advice.
ARTA
2025-06-25
Original judgment source is linked above.
lifelong connective tissue disorder characterised by generalised joint hypermobility, joint instability, pain and hyperextensible skin that can lead to joint subluxations, dislocations, sprains and other injuries. Individuals with this disorder can experience both acute and chronic pain that interferes with daily life due to joint instability.[4]
(a) 52 hours of physiotherapy > > (b) Manual wheelchair and smart drive power assist - $26,047 > > (c) Electric lift recliner - $3,800 > > (d) Stair lift - $6,000 > > (e) Sports wheelchair - $12,500 > > (f) Rental equipment and repairs - $4,000 > > (g) Home modifications consultation - $612 > > (h) 8 hours support worker assistance per week (4 hours at Saturday rate and 4 hours at Sunday rate) - $45,243 > > (i) 50 hours of Occupational Therapy (OT) per year > > (j) 38 hours of house cleaning per year (2 hours per week) > > (k) House or yard maintenance totalling $2097 per year > > (l) Transport of $3,400 per year > > (m) Support Coordination level 2 totalling $5,007 per year.
(a) the Applicant > > (b) the Applicant's husband > > (c) Occupational Therapist (OT), Ms CL > > (d) Provisional Psychologist, Ms IG > > (e) OT, Ms LB > > (f) Rheumatologist, Dr Herman Lau
(a) Rheumatologist, Dr Tim Lu, > > (b) Rheumatologist and pain specialist, Dr Raj Anand > > (c) Orthopaedic surgeon, Dr Anthony Leong > > (d) OT, Ms LG > > (e) Physiotherapist, Mr JW > > (f) Physiotherapist, Ms AL > > (g) General Practitioner (GP), Dr ES > > (h) Psychiatrist, Dr RB > > (i) Previous Provisional Psychologist, Ms CO
(a) Invoice of wheelchair purchase dated 16 September 2023.[6]
(a) (b) (c) (d) (e) (f) (g) (h)
(i) the Tribunal stands in the shoes of the delegate/internal reviewer and must make the correct or preferable decision based upon the evidence and other material before it;[7] and
(j) (k) (l) (m) (n) (o) (p) (q) (r) (s) (t) (u) (v) (w) (x) (y) (z) (aa) (bb) (cc) (dd) (ee) (ff) (gg) (hh)
(ii) the scope of the Tribunal's jurisdiction is determined by reference to the scope of the internal reviewer's powers under section 100 of the NDIS Act, which is in turn informed by the scope of power under section 33(2) of the NDIS Act.[8]
[24] The fact that any applicant must face when applying for review of a decision in the Tribunal is that things that are personal to him or to her must be revealed if they are relevant to the issues raised by his or her application. This case provides a very clear example. Mr Panagiotou may well regard matters relating to his health as personal to him as do most, if not all, people. That does not make them irrelevant to the issues that must be decided on his application. Mr Panagiotou cannot control what the Tribunal regards as relevant and nor can TNT. Only the Tribunal can do that. > > [25] What the Tribunal regards as relevant when it is actually reviewing a decision may be different from what it regards as relevant when it issues a summons. When reviewing a decision, it must have regard only to evidence or material that it actually regards as relevant. When it is issuing a summons for documents or material, it requires only that they appear to have relevance to the issues to be decided. That is, it may issue a summons requiring their production if they can reasonably be expected to throw some light on the issues that will have to be decided in reviewing the decision.
Independent Medical Examination or Functional Capacity Assessment
(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 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 NDIS supports 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 NDIS supports under the National Disability Insurance Scheme for the person's lifetime, despite the variation. > > (3) For the purposes of subsection (1), an impairment or impairments that are episodic or fluctuating may be taken to be permanent, and the person may be taken to be likely to require NDIS supports under the National Disability Insurance Scheme for the person's lifetime, despite the episodic or fluctuating nature of the impairments. > > (4) Subsection (3) does not limit subsection (2). > > Note 1: The time at which a requirement in this section needs to be met is the time the matter falls to be determined. For an access request, that time is the time of considering the request (see paragraph 21(1)(c)). > > Note 2: National Disability Insurance Scheme rules may be made in relation to this section under subsection 27(1).
(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; or > > (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; and > > (d) the CEO is satisfied any early intervention supports that would be likely to benefit the person as mentioned in paragraphs (b) and (c) would be NDIS supports for the person. > > 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. > > Note 1: The time at which a requirement in this section needs to be met is the time the matter falls to be determined. For an access request, that time is the time of considering the request (see paragraph 21(1)(c)). > > Note 2: National Disability Insurance Scheme rules may be made in relation to this section under subsection 27(1).
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.
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.
(1) For the purposes of specifying, in a statement of participant supports, the general supports that will be provided, and the reasonable and necessary supports that will be funded, the CEO must be satisfied of all of the following in relation to the funding or provision of each such support:
(aa) the support is necessary to address needs of the participant arising from an impairment in relation to which the participant meets the disability requirements (see section 24) or the early intervention requirements (see section 25);
(a) the support will assist the participant to pursue the goals, objectives and aspirations included in the participant's statement of goals and aspirations;
(b) the support will assist the participant to undertake activities, so as to facilitate the participant's social and economic participation;
(c) the support represents value for money in that the costs of the support are reasonable, relative to both the benefits achieved and the cost of alternative support;
(d) the support will be, or is likely to be, effective and beneficial for the participant, having regard to current good practice;
(e) the funding or provision of the support takes account of what it is reasonable to expect families, carers, informal networks and the community to provide;
(f) the support is an NDIS support for the participant.
(a) the time at which the disability requirements or the early intervention requirements need to be met is the time the CEO decides to approve the statement of participant supports; and
(b) a participant's disability support needs arising from an impairment in relation to which the participant meets the disability requirements or the early intervention requirements may be affected by a variety of factors, including environmental factors or the impact of another impairment in relation to which the participant does not meet either of those requirements.
(2) The National Disability Insurance Scheme rules may prescribe methods or criteria to be applied, or matters to which the CEO is to have regard, in deciding whether or not he or she is satisfied as mentioned in any of paragraphs (1)(aa) to (f).
I have difficulty answering questions on the spot, so I go into all of my conversations with my team with a pre prepared script and if it was to go off script I'd have a lot of trouble actually addressing what they need.[19]
So growing up, I didn't have any means to get an ASD diagnosis, but it was when I moved out of living with my dad and into my own house, and I felt like I could look into it myself. And I realized that there was a lot of similarities in what I was experiencing compared to what autistic people experience. And I just wanted to find out whether that was correct... I was really struggling at the time with becoming overwhelmed with lots of things, like from a sensory perspective or communication, and I wasn't coping well with all of that overwhelm.[20]
So I started reading into it then and then when I got my formal diagnosis, I read into it some more just so that I could understand more about the condition because I was told that it was something that I'm always going to need to manage.[25]
assessment of physical capacity, tolerance, kinesiophobia, followed by delivering a tailored pain education and developing an activity plan with aim to functional restoration, SMART goal setting, improving physical tolerances, upgrading physical activity and limit avoidant behaviours and exercise / activity plan to current physiotherapist.[27]
A more detailed letter will follow, along with recommended / suggested self-reading material to enhance understanding of the underlying mechanisms of chronic pain / fatigue and some helpful management strategies.[29]
And Dr Lau was able to give me some guidance on what sort of management I would need and also gave me some information about things that I can and shouldn't be doing. Like Doctor Tim Lu as well, for example, said that I should be avoiding high impact activities, for example.[33]
hEDS impairments and impact on functional capacity
I experience daily subluxations and joint instability, skin fragility and other Ehlers Danlos related impairments. In particular, my left hip and knee, fingers, bilateral wrists and bilateral feet/ankles have shown significant instability with impaired function since childhood.[39]
(a) has a standing tolerance of 2-3 minutes. > > (b) restricts her travel up and down stairs in her home to 1-2 times per day because "repeated stair usage results in a temporary flare up of symptoms and subsequent reduced capacity". > > (c) walks within a range of 500-800 meters at a time, after which she requires a period of seated rest for 15 minutes. > > (d) in a good week, can walk up to 2km on a flat surface or as little as 100m in a bad week. > > (e) uses a wheelchair for activities that take more than 10 minutes, such as shopping. > > (f) plays tennis once per week for one hour, with a seated break every 10 minutes. > > (g) can snowboard and requires breaks approximately every 10 minutes.[40]
(a) Because of daily subluxations and joint instability, she experiences "consistent difficulty with most day-to-day tasks" including cooking, food preparation, cleaning, shopping, home maintenance and self-care activities. > > (b) takes baths 30-40% of the time to reduce physical strain but trialled a shower chair which improved independence. > > (c) Putting on enclosed shoes strains her fingers ("hyperextension or subluxation occurs on most occasions").[41] > > (d) She relies on her partner to bring her food and drink throughout the day from the kitchen located downstairs.[42]
(a) can walk 500 meters on a flat, sealed surface, followed by 15-20 minutes of rest. > > (b) cannot walk more than 1-1.5km for the entire day. > > (c) can only walk between 50 and 200 metres on a bad day. > > (d) can stand for 2-3 minutes (or 5 minutes dynamic standing) but less than 1 minute on a bad day. > > (e) drives up to 30 minutes on an average day. > > (f) uses public transport, but due to "limited standing / walking capacity and weakness" relies on partner to accompany her. "If I am travelling with my wheelchair, I require assistance to be pushed..." [46]
I use a wheelchair for most occasions where I would need to be walking or standing for more than a few minutes. Without my wheelchair, I am significantly impaired in my ability to access the community, attend appointments, travel or socialise... A manual wheelchair has been recommended by my treating specialist, Dr Lau, and has been recommended through various engaged Occupational Therapists. My current wheelchair is not prescribed, as it was purchased privately through an online store. I have recently completed a wheelchair assessment with my OT, and a manual wheelchair with power assist has been prescribed, trialled and quoted.[47]
(a) Partner usually assists her to shower ("passing me shampoo bottles, opening containers, and assistance for me to get down to and up from my shower chair".) > > (b) Has a history of falls in the shower and bath. > > (c) Requires partner to help her dress including buttons, zippers and taking clothes off hangers. > > (d) Requires partner to "heat style" or blow dry her hair due to weakness and poor grip. > > (e) Requires partner to take her to "most medical appointments". > > (f) Cannot cut her own food. > > (g) Cannot open packaging or drinks. > > (h) Cannot open the mailbox.[48]
And so the first thing that I notice my body do is it will rock to one side, it will rock to my left side and it will put a lot of strain and weight on my left knee and hip. Within that period of time, my left hip will usually partially or full dislocate and my left knee will become wobbly. So I'm not actually able to sustain the standing for longer periods than that because I don't have, I don't have the strength to maintain that position. So I need to go and sit down.[52]
Counsel: Did anyone recommend to you 18 months ago that you use a wheelchair? > > Applicant: No, there was a conversation with Dr Dare about my wrists not being able to handle the weight of crutches after I got that [ankle] surgery. That's a time where I started using a wheelchair more because I couldn't hold my weight on the crutches. And since then and since getting my EDS diagnosis, then it became recommended that I keep using that wheelchair and eventually get something that's more suitable. > > Counsel: So is this the case, that in lieu of crutches, Dr Dare suggested that you use a wheelchair? > > Applicant: Yes. > > Counsel: Were you using a wheelchair before you had surgery under Dr Dare? > > Applicant: The timing of it, I think we had just bought it and I was using it for long days, like if we were at the zoo or going to an aquarium or like a, a big shopping trip, something like that. I was already using the wheelchair for those long days because I couldn't get through it otherwise. And then when I had that surgery, I had to use it more often because I wasn't weight bearing. And then once I recovered from that surgery, I went back to only using the wheelchair for like long distances. But over the last 18 months, I've had to increase how much I use it. And now I use it almost every time I leave the house. > > Counsel: So, so correct me if I'm wrong, September 2023 is 18 months ago. Do you agree with that? > > Applicant: Yep. > > Counsel: And no one recommended you start using a wheelchair in September 2023. > > Applicant: No > > ... > > Counsel: Leave aside Dr Dare, who first recommend you use a wheelchair? > > Applicant: Doctor Anand. > > Counsel: Is that something he said in his report? Are you able to help with that? > > Applicant: I can have a look. > > Counsel: This is the rheumatologist, is that right, [Dr] Anand? > > Applicant: Yes, that's the first rheumatologist. He's made a comment that says she would benefit from physical therapies and mobility aids to help maintain her general function and independence. > > Counsel: But I can't see any specific mention of the wheelchair? > > Applicant: But this is his shortened version of the report.
Returned to normal shoes > > Still feels like R ankle is unsteady/weak > > Still experiencing a mild limp with ambulation > > R scar sensitivity > > Returned to swimming with flippers > > Going snorkelling over the weekend.[62]
-Main complaint is minor sensitivity and pain in the surgical site when taking shoes on and off. > > -Apart from this, recovery has been good with no other issues reported. > > -Plans to go snowboarding in about a month.[63]
(a) No falls history. > > (b) Normal gait pattern. > > (c) Can negotiate stairs however the left knee/hip hurts and she relies on handrail to assist. > > (d) Uses wheelchair when required to walk long distances, for example, at the zoo, museums or theme park. > > (e) Independent with all transfers. > > (f) Showers every evening and washes hair every second night. > > (g) Completes all dressing tasks. > > (h) No incontinence issues. > > (i) Independent with eating. > > (j) Able to cook and taught partner to cook who now does all cooking.[70]
Participant does not wish to submit a CoC (change of circumstance) and Secondary Diagnosis Request, as she is currently at AAT for her previous review that didn't include the supports she required. Participant disclosed that she is part of groups that support other with gaining access to the NDIS or EDS (sic). She noted that she is aware of others meeting access for EDS, and therefore is wanting to continue pushing this request.[71]
Applicant: So, a partial one, I can still bear some weight through the joint. It's like a click, like quite a big click and you can feel that it's out. And then I'm not able to bear my full weight through the joint when those happen. I can normally click it back into place, but it's not that strong. > > When a full dislocation happens, I can't bear any weight through the hip and it's quite obvious that it's out. It protrudes and it's very uncomfortable and it's a bit harder to get back into place. And when that happens, I need to sit down straight away, even if it's on a dirty floor. > > Tribunal: And how do you manoeuvre it back into the joint? > > Applicant: Normally I find something raised like a step and I can put it back into place because my parents weren't the best at getting me treatment for that growing up. I had to learn how to deal with those myself at quite a young age. So, I've been putting them back in myself for a quite a number of years. But it's just a little bit more force required and putting my foot up on a step for a full dislocation. > > Tribunal: And how, how often would you say you have to put it, put your left hip back in? > > Applicant: Multiple times a day. I try and avoid activities that I know will cause a full dislocation. So, for example, if I tried to push myself beyond that 3 to 5 minutes, I would probably experience a partial dislocation within that range. But if I kept pushing, it would then become a full dislocation. (Tribunal's emphasis)
I don't have a medical answer for why, why it has been dropping for many years. My understanding of EDS is that it does affect the walking capacity, and my physiotherapist has provided a report quite recently also commenting on the drop in walking capacity just in the last year. It's probably a question that Doctor Lau would be able to answer much more than I can, but from my observations it's something that I've noticed steadily dropped for at least the last five years, but probably a little bit more.[72]
(a) She can't do any cooking. > > (b) She can't do any cleaning. > > (c) She can put clothes in the washing machine and hang out a small load of washing over a clothes horse / airing rack. > > (d) She ensures sufficient funds are in the relevant account each month to pay the mortgage. > > (e) She can water the garden, pick tomatoes, and prune a branch with secateurs if it's at waist or chest height. > > (f) On a good day, she could bend over to knee height, however that causes instability, particularly in her left hip. > > (g) She must bend her knees to pick up something lower than knee height because she doesn't have flexibility up the back of her legs. > > (h) She uses stretching techniques, resistance bands and body weight as part of daily exercise. > > (i) She goes to the gym once a week to use seated weight machines (utilising a pin, rather than free weights). > > (j) She can comfortably lift a 1.25kg free weight dumbbell above her head. She can raise a 2.5kg free weight dumbbell in each hand to chest height (shoulder raise movement) a couple of times and do bicep curls using a regular bench to sit on.[76]
So by attending fortnightly, I'm able to learn strategies from the psychologist and then have the two weeks to practice them in real life situations and then have that review with the psychologist 2 weeks later to actually talk through my experience and any difficulties I've had, or talk about different way I can handle difficult scenarios.[83]
So this was in conjunction with what [the Applicant's] reporting and viewing her as she was standing for, for components of the assessment at home... She was standing next to the dining table having a conversation with myself and then I noticed leaning, placing a hand on the table, leaning on the table.[89]
[The Applicant] previously played tennis with her friends. Due to the fatigue associated with Ehler's Danlos Syndrome she is no longer able to stand and run for the ball for the required length of time to play a social game of tennis. [The Applicant] is however, learning how to play wheelchair tennis. It is recommended [the Applicant] continue with the wheelchair tennis due to the benefits of social interaction and physical activity which positively impacts both emotional and physical wellbeing.[96]
ASD& ADHD related symptoms: > > • Impaired cognitive processing, including processing speed, problem-solving, memory, and executive functioning > > • Reduced expressive language and associated impact on social interaction with others > > • Poor social skills with difficulty making and sustaining friendships > > • Difficulty recognising emotions and reading social cues > > • Difficulty managing change and transition > > • Sensory preferences and behaviours that impact day-to-day functioning > > • Reduced vision > > • Thermal dysregulation > > • Sleeping difficulties > > • Anxiety.[104]
It says on page 5 that she reported that her speed of responding to questions is slow and she also has difficulty making spontaneous conversations due to her disability. When she mentioned that to me, I also observed that during the assessment.[105]
When I said in my report that she has impaired cognitive processing, including processing speed, I observe that I need to rephrase the questions for her to be able to understand and give me appropriate responses... she mentioned to me that if there is something that she could not understand, she would do self-research, especially if it is work related.[106]
Counsel: Ok, so for example, if you look on page three of your report, you talk about [the Applicant's] literacy. Did you watch [the Applicant] reading anything? > > Ms CL: I can't remember. > > Counsel: Ok. If you didn't administer any of those assessment tools sitting down with her during the interview, do you agree it's unlikely that you observed her doing any reading? > > Ms CL: Yes. > > Counsel: So where you say under literacy, '[The Applicant's] able to read and write at a competent level, but she struggles to understand and comprehend lengthy written or printed texts' and you go on to say she needs to reread things several times. Is the Tribunal to understand that is something [the Applicant] told you? > > Ms CL: Yes. > > Counsel: This is based on her reported capacity at the time of the assessment. Is this how the Tribunal should understand your report - it's largely based on what [the Applicant] told you? > > Ms CL: Yes.
EDS-related symptoms: > > • Reduced gross motor skills > > • Widespread joint pain > > • Chronic pain in left hip and knee > > • Hypermobility of joints > > • Subluxation of left hip and knee joints > > • Reduced bilateral lower limb strength > > • Reduced fine motor skills due to muscle weakness and hypermobile fingers affecting grip > > • Poor sitting and standing tolerance due to muscle weakness, joint pain and instability > > • Diminished mobility due to fatigue, joint instability and subluxation > > • Poor exercise tolerance and physical activity tolerance > > • Gait abnormality - pigeon toe gait > > • Difficulty performing functional transfers > > • High risk of falls > > • Decreased balance, coordination and proprioception > > • Extreme fatigue, which impacts activities of daily living > > • Reduced level of independence with activities of daily living and increased reliance on informal carers > > • Occasional urinary incontinence > > • Constipation.[109]
So during our conversation, during the assessment, she mentioned physical pains, she mentioned instability, and with instability comes falls. > > ... > > I verified to her that when she was diagnosed, what are her symptoms. And she told me that she has joint instability. Sometimes her knee would buckle. And from there I would, I would need to assess whether she is at risk of falls.[121]
Tribunal: Just on that, Ms [IG], in your letter, you say [The Applicant] presents to therapy with significant challenges relating to her comorbid diagnosis of autism and ADHD. These include very high levels of distress and significant difficulties with emotional regulation, interpersonal skills and executive functioning. So if we take the interpersonal skills, what's your understanding of what those challenges look like in daily life? > > ... > > Ms IG: So because of her autism, she can be really prone to misunderstanding social cues, which is obviously really highly distressing. So here she struggled with picking up on nonverbal responses. > > Tribunal: I understand that as a symptom or an impairment. But in terms of what's reported to you...what's a recent example of that happening in daily life? > > Ms IG: ... So I guess if we're talking about examples that have come up, unplanned conversations, like when they go off track can be really distressing for [The Applicant]. > > Tribunal: So again, I just need you to be very specific Ms [IG]. What was the unplanned conversation and what happened in that conversation. > > Ms IG: So I guess like when she's spoken generally about difficulties when conversations go off script, if that makes sense. > > Tribunal: Yep. And so where's that happening, those conversations? > > Ms IG: So that could be, I guess with anyone, like for any conversations, she's not prepared for any sort of reciprocal conversation. > > Tribunal: Do you remember an example that she spoke to about a particular conversation where that happened? > > Ms IG: I can't remember a very specific example, but it's been something she's spoken about as a difficulty. > > Tribunal: And what about executive functioning. What's an example of that? > > Ms IG: Yeah, so I guess a specific example might be at work, like she would really struggle with last minute schedule changes, like the heavy workload and things like that. > > ... > > Tribunal: Can you remember an incident where [the Applicant] came and described that happening on a particular occasion? > > Ms IG: Not a specific one from memory, but in the context of work, it's come up as something that can be difficult.
I detected atrophic scars on her back, piezogenic papules on her heels, mild skin hyperextensibility, abnormal striae over her pelvis and under her breasts, and absence of aortic root dilatation or valvular disease on echocardiogram. She has dental crowding... She reports a family history of joint hypermobility... > > She has a degree of joint hypermobility which is manageable with paracetamol and anti-inflammatory. She does not want to go on onto stronger analgesia. > > She has NDIS support for ASD and ADHD, and will have an occupational therapist assessment next week to focus on her musculoskeletal condition. > > Her joint discomfort and instability does affect her day-to-day activity. She was under the care of a physiotherapist in the past and has not needed to see her physiotherapist for the last 8 months because of recurrent issue of left pain. > > ... > > I have asked her to prepare a functional Impact statement together with the occupational therapist report and a physiotherapy/exercise physiology report. I have asked her to email them to me once available so I can draft a medical report to help her through NDIS application. She will then make an appointment to see me so we can go through the application report and the process.[124]
[The Applicant] has been diagnosed with Ehlers-Danlos Syndrome (EDS), a life-long connective tissue disorder that primarily affects the skin, joints, and blood vessel walls. There is no cure for this condition and it results in permanent physical impairments and disability, which are not reversable or treatable. This condition has a significant impact on [the Applicant's] life, causing joint hypermobility, joint pain, skin fragility, fatigue, and various other impairments. > > ... > > The condition primarily affects her left hip and knee, fingers, bilateral wrists, and bilateral feet/ankles, leading to impaired function since childhood... > > ... > > Despite these challenges, she remains committed to maintaining her joint strength and function to continue participating in these activities [snowboarding and tennis], which provide significant mental and physical health benefits. > > ... > > There is no further intervention that would improve her functional capacity. Her condition is stabilised and has reached maximum medical improvement".[125]
[The Applicant] is under the care of a physiotherapist who recommends weekly physiotherapy, focusing on developing a graduated exercise program, proprioception training, posture awareness and correction. Her occupational therapist has recommended various interventions, including assistive technology, daily adaptive aids, and psychological support. [The Applicant] requires assessment for an appropriate wheelchair, as recommended by her Occupational Therapist.[129]
[The Applicant's] disability is from joint instability, muscle weakness from deconditioning as per my previous assessment report. She has expected level of pain from joint hypermobility and she uses simple analgesia, anti-inflammatories as required when she suffers an injury. She does not have chronic pain syndrome that requires pain clinic management.[130]
(a) Achieved a Beighton score of 8 (which assesses generalised joint hypermobility) (Criterion 1). > > (b) Had the following features (at least 5 of 12 features must be present) > > > (i) Mild skin hyperextensibility > > > > (ii) Unexplained striae distensae or rubae (stretch marks) without history of significant weight gain or loss > > > > (iii) Bilateral papules of the heel > > > > (iv) Atrophic scarring > > > > (v) Dental crowding > > (c) Positive family history > > (d) Musculoskeletal pain or two or more limbs, recurring daily for at least 3 months > > (e) Recurrent joint dislocations or instability, in the absence of trauma.[137]
even if a person doesn't have the name hEDS, if they have a lot of systemic features with a strong clinical suspicion, then the management is the same. I'll watch the person very closely as if the person has hEDS and the management is also exactly the same. Joint strengthening, proprioception training, physiotherapy, conditioning, devices, it's the same management.[141]
So in my impression of [the Applicant], the first thing I asked her, I want to suss out whether she's got pain seeking or pain behaviour or pain syndrome. And she was very honest. She said, 'look, pain is not a thing, I don't want more painkillers'... And then she goes to work, she tries her best to fulfil he work requirement. She tries to engage with various sports and activities. She tries to manage on her own health with various interventions or physiotherapist exercise, self manage program.[142]
So if a person has chronic pain behaviour or pain avoidance behaviour or because they are avoiding activities because of pain, then we need pain psychologist involved.[143]
So I don't think she'll need a wheelchair for the rest of her life because she's engaging in physical strengthening and I want her to continue to do that. But if she requires a wheelchair for a trip that her body doesn't tolerate, I think that's reasonable.[145]
(a) Prepares her clothes in piles for the week ahead (and stored in the room next door). > > (b) Wakes her up with the dog. > > (c) Gives her medication to her with a glass of water. > > (d) Prepares a cooked breakfast, such as eggs benedict or hash browns, sausages, eggs, toast and sometimes cereal. > > (e) Helps to pull down a sports bra or join the clasp on a traditional bra. > > (f) Runs the bath for her and gets her pyjamas. > > (g) Retrieves her clothes from the neighbouring room and puts them on the bed for her. > > (h) Packs her bag for work including laptop, sensory toy, umbrella, water bottle and make-up. > > (i) Pushes the Applicant in the wheelchair onto the train and then pushes her from the station to her office in Sydney about every 3 weeks, spends the day in Sydney and then returns home with her on the train. > > (j) Prepares all meals, such as sandwiches and salads for lunch and nachos or pasta for dinner. > > (k) Serves all meals to the Applicant in her office upstairs or at the dining table downstairs. > > (l) Cuts up the Applicant's meal because her index finger hyperextends if she uses a knife for anything harder than an omelette. > > (m) Drives the car whenever they are together. However, she can drive herself to some local appointments and he doesn't attend all medical appointments. He nominated, for example, attending an orthodontist appointment.[153]
(a) The Applicant cannot use a knife and fork together. > > (b) She doesn't have the strength to hold a pot or pan and to stand or bend in the kitchen to cook. > > (c) She cannot get her own clothes ready in the morning because of textures and the time needed to stand/walk to retrieve them from the room next door. > > (d) She cannot hold a fork or pen in a regular manner. Rather she grasps the fork or pen (much the way a small child does) because she doesn't have grip or pinch strength. > > (e) She cannot retrieve snacks or meals from the cupboard or fridge herself because it involves walking downstairs. > > (f) She cannot carry a plate of food from the kitchen to the dining table. > > (g) She cannot get up off the ground without assistance. > > (h) She will not eat if he's not there to prepare and deliver food to her. > > (i) She generally only uses the stairs once per day, appearing slow, wobbly and as though her legs will buckle - "I mean pretty typically it's just once down, once up every day". > > (j) She has a fall or near fall on average twice per week. > > (k) They bought a wheelchair in 2023 for about $200. > > (l) She was playing able-bodied doubles tennis until 8 months ago (approximately September 2024). > > (m) She plays wheelchair tennis once or twice a week. > > (n) She sees a friend about every 2 weeks and communicates online with a friend who lives overseas. > > (o) The Applicant introduced him to snowboarding after she was introduced to it by a previous boyfriend. > > (p) They went snowboarding together in Perisher ski resort for 5 - 10 days in July/August 2024. They also snowboarded during the Australian winter in 2022 and 2023 but have not purchased a season pass this year. A season pass costs about $1000 per person. > > (q) They went snowboarding in Whistler, Canada in January/February 2024. They spent 8 days at the resort and snowboarded on about 5 of those days. > > (r) They spent 10 - 15 days in New York as part of the Whistler trip and the husband pushed the Applicant around in a wheelchair. > > (s) The Applicant can snowboard for about 2 minutes at a time before requiring a rest of 5 to 10 minutes, sitting on the snow. She could also walk about 50 meters in snow boots in the snow without wobbling. The Applicant uses wrist, ankle braces, a bum pad and helmet. > > (t) The Applicant spent 2 - 3 hours on a bus from Vancouver to Whistler. > > (u) He was not sure whether a shower chair had been requested at the hotel where they stayed in New York stating: "No, because I mean, yeah, she's as far as I know, she's happy to sit on the floor" [of the shower recess]. > > (v) She can use a SLR camera that weighs between 1 - 2kg. > > (w) The Applicant stopped going to the gym last year. When the husband was informed that the Applicant told the Tribunal she attends the gym each week, he indicated she might do some gym exercises as part of her wheelchair tennis session with her coach on Mondays. > > (x) She can't concentrate watching a tv program but can concentrate on a puzzle for up to 1.5 hours.[154]
Counsel: Describe how it happened? > > Husband: So she's just washing, you know, washing herself and her, her lower, lower body couldn't take, you now, standing up any longer. And she sort of gave out beneath her, I suppose her legs just like gave out. > > Counsel: [Mr Husband], can I suggest to you, it doesn't sound like you're describing what you saw, but rather a series of things you imagine happening. So you said she's washing herself and her lower body couldn't take the strain or words to that effect and she fell...Are you able to describe what you saw happen? > > Husband: ...She has to get up to wash a particular part of her body. She gets a bit wobbly and she's struggling to hold herself up. So she's like trying to grasp something on the side of the wall...like a recess, I should say on the side that she tries to hold onto. That's not very effective. And yeah, she falls to the floor sort of mainly sliding down with her back down the, the back of the shower in between the shower chair and the corner of the shower...[155]
Her ASD is also sort of yeah, the impairments, I suppose, or you know, the symptoms that I've observed have gotten worse as well.[156]
Tribunal: But you'd agree with the point that 2 minutes of - and I've never snowboarded - but I imagine 2 minutes of physical stamina, bracing, concentration...doing that down a run that you're not particularly familiar with in a foreign country is more effortful than walking to the fridge to get a snack? > > Husband: Yeah, so this is probably best answered by [the Applicant]. But what I can say, I mean just right off the bat, I mean the fridge is downstairs. So she already has to walk down the stairs, I know that I can see what you're saying just at a base level...but we, I am talking about in the context of ASD and how overwhelming going from task to task and, you know, the physical side of it as well with the EDS and going up and down the stairs, all of that combined.
[62] The starting point in construing a statutory provision is its text, considered in the light of its context and purpose. It is necessary to strive to give meaning to every word of the provision. > > [63] Context includes the surrounding statutory provisions because the meaning of a statutory provision must be determined by reference to the language of the statute viewed as a whole. It is necessary to construe the provision so that it is consistent with the language and purpose of all the provisions of the statute... > > [64] In some circumstances - such as where a statute is part of a wider legislative scheme - context may include reading a statute together with other statutes so that, together, those statutes are construed as a combined statement of the will of the legislature.
(a) the time at which the disability requirements or the early intervention requirements need to be met is the time the CEO decides to approve the statement of participant supports;
...
Item 46 inserts an additional criterion (new paragraph 34(1)(aa)), which provides that the supports must be necessary to address the needs arising from an impairment that meets the disability requirements (in accordance with section 24) or early intervention requirements (in accordance with section 25). Item 48 makes consequential amendments to subsection 34(2) to ensure that NDIS rules can be made for the purposes of new 34(1)(aa). > > This amendment clarifies that the NDIS only funds supports for impairments that meet the disability or early intervention requirements, as per the Scheme's original intent. This amendment reflects the Agency's current operational guidelines and will provide clarity to participants and other service systems about what supports will be funded through the NDIS. It will not require participants to repeatedly prove their disability.[160] (Tribunal's emphasis).
(a) Is the requested support necessary to address the need of a participant? In other words, there must be a clear link or nexus between a participant's need, for example improved mobility, and the support requested, for example, a piece of assistive technology to aid mobility.
If another participant living with psychosocial impairments had a need for increased social participation in the community but requests support was for personal care, then it would be difficult to conclude that the support was required to address the need for increased social participation.
(b) Does the need arise from an impairment? For example, a participant may need a mobility device because of an injury to their leg. The injury caused the impairment which prevents the participant from moving around their home or accessing the community.
Another participant may want transport to attend the supermarket because they don't own a car or don't like using public transport. In the latter case, the need (or want) does not arise because of the participant's impairment.
(c) Does the same impairment meet the disability or early intervention requirements? For example, if a participant's leg is amputated, the impairment is permanent and substantially reduces their functional capacity in the domain of mobility. However, if the participant's ankle is broken, it will probably not result in a permanent impairment once they undergo treatment and a period of rehabilitation.
Substantially reduced functional capacity re 'ASD' impairments
[68] The Agency also submits that the term 'substantially' in the context of reduced functional capacity carries a 'high threshold'. I am satisfied that this is the correct interpretation and my considerations are as follows: > > The recommendation of the Productivity Commission was that the scheme provide supports only to a sub-category of persons within a much larger category of the persons who have a disability. > > The Productivity Commission also recommended that the scheme provide these supports 'judiciously rather than routinely'. This recommendation is logical and central to the operation of the scheme and ensures its financial sustainability. > > The scheme was never intended to provide support to 'every person with a disability'. > > Rather, as part of one of its functions the scheme was intended to support persons with disability to receive supports outside of the scheme through mainstream services. This would of course include persons with a disability who do not fall within the sub-category of persons for whom the scheme was intended. > > The scheme was not intended to respond to shortfalls in other mainstream services, including those provided by relevant State and Territory governments. > > The intention of providing supports to only a subcategory of persons with a disability is reinforced by the ability of the legislature to prescribes rules in relation to access to the scheme. By way of example Rule 5.8 of the Access Rules operates to categorise certain persons 'into' the category of persons with a 'substantially' reduced functional capacity. > > The concept of prescribing rules in relation to a category of certain persons who would be mandatorily 'excluded' from the category of persons with a 'substantially' reduced functional capacity is an unrealistic if not impossible task. Notwithstanding, the Access Guidelines assist the decision maker with an informed approach by way of practical examples and circumstances in which access will not be granted. > > I am satisfied that the Tribunal's satisfaction of what constitutes 'substantially' reduced functional capacity for an applicant seeking access to the NDIS scheme requires a high threshold. This decision will therefore be made on that basis.
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. > > ... > > 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.[162]
Well day-to-day, I rely on [husband] to speak on my behalf as much as he can. It's obviously really difficult in this environment where I have no choice but to speak in these settings. But if there's things like phone calls or booking appointments or even speaking to someone at the door or dealing with the cashier at the supermarket, I don't engage in any of those communications because that would need me to script and prepare for those conversations ahead of time, which is very overwhelming.[163]
The Tribunal accepts that the Applicant has a relatively small social circle. However, the Tribunal finds the Applicant has maintained a working relationship with her manager, who she worked with at a previous company. Despite some reported difficulties, the Applicant continues to manage staff as part of her full-time job and her employer has not formalised any reasonable adjustments for the Applicant in the workplace. The Applicant had a boyfriend prior to meeting her husband who taught her how to snowboard. She met her husband online 4 years ago, with the couple marrying last year. She has maintained at least two friendships since school, one who she sees in person and the other who she communicates with online. There was some evidence the Applicant doesn't particularly like socialising with other people.[169] The Applicant previously played able-bodied tennis and now interacts with a coach and other players at wheelchair tennis each week. The Applicant also gave evidence she catches up with immediate family members for birthday and other family occasions.
Accordingly, the Tribunal finds rule 5.8 does not apply because the Applicant does not require assistive technology, equipment, home modifications or assistance from another person to participate effectively in the domain of socialising.
Her report talks about the struggles with tasks and them being broken down into many steps and the sensory issues around those tasks and trouble with transitions and rigid behaviours are all addressed in her report.[171]
[The Applicant] reported persistent major problems with relationships [and] poor performance with activities of daily living such as shopping and meal preparation. [The Applicant's] hypervigilance, hyperfocus, poor emotional and behaviour regulation and adherence to rigid routines with difficulty adapting to changes in circumstances is significantly affecting her daily life resulting in increased burnout and meltdowns.[176]
[25] The term 'impairment' is not defined in the NDIS Act. However, the Agency's operational guidelines define it to mean "a loss of or damage to your body's function". I note that this conceptualisation of impairment for the purposes of s 24(1) was specifically approved by the Court in Davis.[178] That definition is a simple rendering of the definition of impairment[179] used in the application of the International Classification of Functioning Disability and Health (ICF), which is "a problem of body function or structure such as a significant deviation or loss as compared with typical or expected function or structure".[180] (Tribunal's emphasis)
[24] In the context of s 24(1)(a), and Chapter 3 of the NDIS Act more generally[186], the term "disability" has a specific meaning, being a functional outcome that is attributable to specified categories of impairment. The concept of impairment is distinct from the concept of 'disability', and from a diagnosed health condition. Care needs to be taken not to conflate these separate concepts or use them interchangeably. Failure to maintain this conceptual distinction may lead to a misapplication of the access provisions.[187]
The Tribunal accepts that skin fragility may be a symptom of hEDS, however there was no evidence indicating how this could properly be considered an impairment in the Applicant's case. While her skin may be thinner or more fragile than most people, and as such, it 'deviates' from the norm, the Tribunal cannot be satisfied as to the degree of the deviation or how this affects her in daily life.
(b) Pain
The Tribunal understands pain is also a symptom of hEDS. Dr Lau did not quantify the scale of pain usually associated with this condition. There was inconsistent evidence about the degree, type and location of pain experienced by the Applicant however the Tribunal will address those issues under section 24(1)(b). The Tribunal accepts that the Applicant has a disability attributable to the physical and/or sensory impairment of pain.
(c) Hypermobility / joint instability
The Tribunal understands from Dr Lau's evidence that hypermobility and joint instability are also symptoms of hEDS and other hypermobility spectrum disorders, suggesting there is a continuum of mild through to severe hypermobility/joint instability. The Applicant scored 8 on the Beighton's score which is a screening tool used to confirm hypermobility. The Tribunal accepts that the Applicant has a disability attributable to the physical impairments of hypermobility and joint instability.
(d) Loss of strength / muscle weakness & fatigue / reduced flexibility
Loss of strength, muscle weakness/fatigue and reduced flexibility are also said to be symptoms of hEDS. They are also clearly attributable to other conditions including deconditioning or muscle wasting. It is a question of degree whether these symptoms could also be classified as impairments, however the Tribunal will proceed on the basis that they rise to the level of physical impairments.
(e) Subluxations and Dislocations
Subluxations refer to a partial dislocation of a joint, where the bones are misaligned, whereas a full dislocation, for example, in the case of hip, refers to the ball joint coming out of its socket. Both subluxations and dislocations are symptoms of hEDS or hypermobility. The Tribunal accepts that the claimed frequency and degree of subluxations and dislocations would be a physical impairment.
However, besides the Applicant's self-reports, there was no medical or allied health practitioner who observed a subluxation or directly reported on the occurrence of a subluxation, including details of when it occurred, how it happened, what it felt like and how it was corrected. This was despite the Applicant claiming she could effectively induce a subluxation in her hip by standing for longer than 3 minutes (and which reportedly did not cause significant pain).
Further, the Applicant's description of a full hip dislocation, which she claims occurs multiple times per day, was plainly at odds with Dr Lau's explanation that it is "horrible" and would usually require attendance at the Emergency Department. The Applicant described it as uncomfortable and something she routinely resolved herself by using a step to put it back in.
The Tribunal cannot be satisfied that the subluxations and/or dislocations are impairments in circumstances where it is unclear whether they occur. For reasons noted above, the Tribunal has concerns about the reliability of the Applicant's evidence and the Husband's written evidence was lacking in detail regarding the occurrence of subluxations and dislocations. If they are occurring, they can be properly assessed as part of a medical review, which is considered below.
(f) Pigeon toes and altered gait.
Ms CL and Mr JW were the first practitioners to mention the Applicant having pigeon toes. Mr JW said the Applicant had internally rotated femurs.[189] There was no medical explanation for this change in the Applicant's legs or feet, which was not reported prior. Several practitioners reported the Applicant had normal gait. The Tribunal will proceed on the basis that it could be an impairment however further medical review will likely be required.
(a) Pain > > (b) Hypermobility / joint instability > > (c) Loss of strength / muscle weakness & fatigue / reduced flexibility > > (d) Pigeon toes and altered gait.
[85]...In my opinion, the correct meaning of "permanent" in s 24(1)(b) is "enduring". This meaning reflects the purpose and context of the legislative scheme, as a scheme intended to deliver lifelong support to persons with disability. > > [86] The critical point is that "permanent" is used as an adjective in s 24(1) to the noun "impairment" (or in the plural, "impairments"). The focus of the text, consistently with the purposes of the scheme, is on 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. > > ... > > [130] ...I explained ...above my view about the correct construction of "permanent" in s 24(1)(b). The phrase "permanent impairment" in s 24(1)(b) means an impairment which is of an enduring nature. In other words, the question for the decision-maker is whether the impairment(s) experienced by an individual (rather than the cause of the impairments or the specific diagnoses made about a medical condition) has or have an enduring quality so as to require supports funded and/or provided under the NDIS Act on an ongoing basis..[190]
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. > > ... > > 5.6 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). > > ...[191]
(a) the word 'remedy' should be understood to mean something approaching a removal or cure of the impairment';[193] > > (b) the word 'known' connotes a treatment which can be identified by Australian medical practitioners as a suitable treatment for the person's particular impairment';[194] > > (c) the word 'appropriate' 'connotes a treatment which has a capacity to "remedy" the impairment and is suitable for the particular individual concerned to undergo';[195] and > > (d) the word 'available' should be understood as directed at what treatments an individual can, in reality, access'.[196]
To meet the disability requirements, we need to know that your impairment is permanent, or likely to be permanent. Permanent under the law for the NDIS means enduring. This means we need to know whether your impairments are enduring so that you require NDIS supports on an ongoing basis. > > We will focus on your impairments, and not on the cause of your impairments, or your diagnoses. 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, or if there are known, available and appropriate evidence-based clinical, medical or other remaining treatments options that are likely to remedy the impairment. > > Generally, we'll consider whether your impairment is likely to be permanent if all available and appropriate treatment options are pursued. > > ... > > When we look at what treatments are available to you, we think about whether the treatment is suitable for your personal situation. The word treatment should be understood in a broadest sense and may include changes to your diet and lifestyle. > > If you're still undergoing or have recently had treatment, we may not be sure you have a permanent impairment if that treatment could remedy the impairment.
There is no cure for this condition and it results in permanent physical impairments and disability, which are not reversable or treatable. This condition has a significant impact on [the Applicant's] life, causing joint hypermobility, joint pain, skin fragility, fatigue, and various other impairments.[202]
[The Applicant's] physiotherapist recommends ongoing physiotherapy to manage her symptoms related to hypermobility. She will require a graduated exercise program, proprioception training, posture awareness and correction. These interventions aim to improve joint stability, and to maintain [the Applicant's] functional abilities.[207]
(a) The Tribunal accepts Dr Lau's evidence that ongoing muscle strengthening is important for managing impairments arising from hEDS. > > (b) The Tribunal is not satisfied on the evidence that the Applicant has engaged in regular strength-based exercise programs, either at home or in a gym, as recommended by Dr Lau and Ms LG. > > (c) The Tribunal is not satisfied on the evidence that the Applicant has engaged in regular physiotherapy as recommended by Dr Anand and Mr JW. This is particularly concerning given the claimed level of physical impairment and associated functional decline over the past 2 years. > > (d) The Applicant did not provide any explanation or evidence for not engaging in regular physiotherapy except that she couldn't afford it. For the reasons mentioned above, the Tribunal does not accept that regular physiotherapy treatment is not available to the Applicant. > > (e) The letters/reports provided by Mr JW were brief. They did not provide the level of detail and explanation that one would expect from a physiotherapist who was treating a 27-year-old woman who had gone from playing tennis and snowboarding to being unable to walk beyond 3 - 5 minutes in the space of less than 2 years and who was transitioning to daily wheelchair use. > > (f) The Applicant continued to snowboard contrary to Dr Lu's medical advice to avoid high impact activities. By not making appropriate changes to her lifestyle, the Tribunal cannot be satisfied that this activity has not aggravated her physical impairments. > > (g) Due to the inconsistencies in evidence regarding the issue of pain, the Tribunal cannot be satisfied that the issue of unmanaged pain is not contributing to the Applicant's other physical impairments and/or that her pain has been optimally treated. > > (h) Due to the evidence regarding the Applicant's underlying mental health issues, the Tribunal cannot be satisfied that her psychological conditions are not contributing to the Applicant's physical impairments. Further, there was no evidence that her longstanding diagnosis of depression and anxiety have been optimally treated in recent years. The Applicant's symptomology, found to be consistent with PTSD has not been reviewed by an appropriately qualified practitioner and therefore treatment options have not been recommended.
However, Rule 5.6 is also relevant. As set out above, this provides that an impairment may require medical treatment and review before a determination can be made as to permanence, and:
"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".
As already canvassed above, I consider there is further treatment available to Mr Richardson, namely participation in the RNSH Pain Clinic program, which is likely to substantially relieve the impairment attributable to his chronic back pain. I accept it is unlikely the program will completely cure or eliminate Mr Richardson 's pain. However, as explained by Dr Gorman, there is a good prospect the program will substantially reduce the pain experienced by Mr Richardson, and the limitations resulting from that pain....
Having regard to this evidence, I have concluded Mr Richardson 's chronic pain impairment does require further treatment and review before an accurate determination can be made as to its permanence or likely permanence. On the evidence, participation in the RNSH Pain Clinic program is likely to have a dramatic impact on this impairment and reduce it substantially. Given the degenerative changes in Mr Richardson's back are not particularly unusual for his age, it is even possible the program may result in something approaching a cure. In these circumstances, in my view it is premature to attempt to assess the permanency or likely permanency of the impairment. Accordingly, I am also not satisfied this impairment is permanent within the meaning of the Act and the Access Rules.
For completeness, I should add that even if Rule 5.6 had not operated to exclude permanency, I would not have been satisfied that Mr Richardson 's chronic back pain had the "enduring" quality necessary to establish permanency within the meaning of the Act. While the physical degenerative changes in Mr Richardson's back will not change, it is clear on the evidence the same cannot be said for the chronic back pain he is currently experiencing. Both doctors agreed that in circumstances such as this, pain is a complex and multifaceted phenomenon, moderated and affected by many factors. It can also be influenced and ameliorated by many of the modalities deployed by chronic pain programs.
While an impairment can be permanent notwithstanding fluctuations or positive changes in its impact on a person's functional capacity, it is not tenable in my view to regard an impairment as permanent in circumstances where treatment offers the possibility of a dramatic and lasting improvement which will substantially increase a person's functional capacity. Where this is the case, in my view it is simply not accurate to say that the person's current impairment is permanent. The concept of 'impairment' has both a qualitative and a quantitative dimension. Even where it is likely a person's impairment will persist but at a much lower level, it would not be accurate, or consistent with the aims and objectives of the Act, to regard their current impairment as permanent.[231]
(a) Reviewing all relevant medical records and reports. > > (b) Re-assessing, and if necessary, obtaining a second-opinion regarding a relevant diagnosis, particularly where important information was previously unavailable or not considered. > > (c) Undertaking any necessary screening, testing or assessment for any disease or disorder (including mental health conditions) likely to be contributing to a sudden, significant and/or unexplained change in presentation. > > (d) Consulting with independent and suitability qualified allied health practitioner(s) trained to assess certain impairments and/or functional capacity. > > (e) Reviewing previous treatments undertaken, including compliance and efficacy (supported by clinical data where possible). > > (f) Reporting conclusions and making recommendations.
(a) Pain > > (b) Hypermobility / joint instability > > (c) Loss of strength, muscle weakness/fatigue, and reduced flexibility > > (d) Pigeon toes and altered gait.
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.[233]
Your impairment substantially reduces your functional capacity if you usually need disability specific supports to participate in or complete the above tasks. > > These disability-specific supports include: > > • a high level of support from other people, such as physical assistance, guidance, supervision or prompting. > > • assistive technology, equipment or home modifications that are prescribed by your doctor, allied health professional or other medical professional.[234]
[68] In any case before a merits review tribunal (or a first instance decision-maker), a decision can only be made on the basis of relevant and probative material. The material must be probative of the matters for which the statute provides: see Minister for Immigration and Ethnic Affairs v Pochi [1980] FCA 85; 44 FLR 41 per Deane J. If an applicant does not provide evidence and information sufficient to meet the statutory requirements, an applicant is unlikely to have the statutory power exercised in her or his favour. And unless and until a decision-maker is satisfied, or persuaded, that the requirements are met, then no occasion to exercise the power in favour of an applicant arises. In that sense, as a practical matter, it is not incorrect to say that a person "must satisfy" the requirements in the statute. To say that is not to impose an onus of proof on an applicant, but rather to recognise the operation of the legislative scheme under which the person seeks a benefit or interest: see generally, McDonald v Director-General of Social Security [1984] FCA 59; 1 FCR 354 at 356-357 and 358 (per Woodward J), 366 (per Northrop J) and 369 (per Jenkinson J); Ward v Western Australia [1996] FCA 1452; 69 FCR 208 at 215-218; and Evans v Secretary, Department of Families, Housing, Community Services and Indigenous Affairs [2012] FCAFC 81; 289 ALR 237 at [18] and the cases there cited. (Tribunal's emphasis).
(a) Inconsistencies with evidence and behaviour > > (b) Limitations of functional capacity assessments > > (c) An unexplained dramatic reduction in functional capacity without supporting medical evidence or explanation.
Limitations of OT functional capacity assessments and reports
Dramatic reduction in functional capacity without supporting medical evidence
The Tribunal, pursuant to section 105 of the Administrative Review Tribunal Act 2024 (Cth) sets aside the decision under review and remits the matter for reconsideration with the following order:
1. 12 hours of psychology support in relation to impairments arising from the Applicant's Autism Spectrum Disorder (ASD) is not a reasonable and necessary support and is not to be approved for inclusion in her statement of participant supports (SOPS).
2. Any additional psychology support is not reasonable and necessary and is not to be approved for inclusion in her SOPS.
3. The Applicant does not meet the requirements of ss 24 or 25 of the National Disability Insurance Scheme Act 2013 (Cth) in relation to impairments arising from Ehlers-Danlos Syndrome (EDS) - Hypermobility Subtype (hEDS) and the supports requested in relation to these impairments are not reasonable and necessary supports.
[5] The names of local treating practitioners have been altered where they might tend to reveal the identity of the Applicant.
[7] See Shi v Migration Agents Registration Authority [2008] HCA 31; (2008) 235 CLR 286 at [37]- [38], [45]-[46] (Kirby J), [99] (Hayne and Heydon JJ), [143] (Kiefel J); Esber v The Commonwealth [1992] HCA 20; (1992) 174 CLR 430 at 440; Frugtniet v Australian Securities and Investment Commission [2019] HCA 16; (2019) 266 CLR 250 at [51]; QDKH, by his litigation representative BGJF v National Disability Insurance Agency [2021] FCAFC 189.
[8] QDKH, by his litigation representative BGJF v National Disability Insurance Agency [2021] FCAFC 189 at [7].
[9] The summons records are contained in JHB2 (110 pages) and JHB3 (488) pages.
[10] Explanation of the relevant law has been set out in previous decisions and is repeated here.
[11] Re Drake and Minister for Immigration and Ethnic Affairs (No 2) (1979) 2 ALD 634 at [635].
[12] Mulligan v National Disability Insurance Agency [2015] FCA 544 ('Mulligan') at [55].
[14] National Disability Insurance Agency v Foster [2023] FCAFC 11 ('Foster') at [44].
[15] National Disability Insurance Agency v WRMF [2020] FCAFC 79 at [202].
[16] For example, Beezley v Repatriation Commission (2015) FCAFC 165 at [68] (North, Tracey and Mortimer JJ).
[21] Applicant's and Husband's oral evidence.
[22] See also Dr Leong's letter dated 1 September 2023 at JHB3, p143.
[24] See Letter from Dr Lu to Dr Leong dated 31 October 2023 at JHB3, p3.
[27] JHB2, p8. The Tribunal understands the term 'kinesiophobia' to refer to the fear of movement due to injury or pain.
[34] See JV of JHB3, p457-460 confirming surgery occurred in October 2023.
[73] JHB3, pp130. See also consults on 26 July 2023 in relation to joint pain in both ankles (p134) and back and joint pain on 19 March 2024 on p138.
[78] Applicant's oral evidence. See also AA4 of JHB4.
[102] Defa and The CEO, National Disability Insurance Agency (NDIS) [2024] ARTA 34 at [36].
[159] The Pocket Macquarie Dictionary, Second Edition, 1989.
[160] Parliament of the Commonwealth of Australia, National Disability Insurance Scheme Amendment (Getting the NDIS Back on Track No.1) Bill 2024 - Explanatory Memorandum, p27-28. See https://parlinfo.aph.gov.au/parlInfo/download/legislation/ems/r7181_ems_f83281ef-0f46-4fbb-a59f-2e19439dcacb/upload_pdf/JC012589.pdf;fileType=application%2Fpdf
[161] See section 24(2) and (3) of the NDIS Act.
[162] Our Guidelines - Becoming a participant - Applying to the NDIS, 10 December 2024, p9.
[171] Applicant's oral evidence. See also T1A of JHB1.
[178] At [118] referring to [113].
[179] World Health Organisation (2002), Towards a Common Language for Disability, Functioning and Health, ICF, Geneva, WHO/EIP/GPE/CAS/0.1.3 (WHO (2002) at page 2.
[180] World Health Organisation, (2011), International Classification of Functioning, Disability and Health, Geneva: International Classification of Functioning, Disability and Health (ICF)
[181] Re Schwass and NDIA [2019] AATA 28 at [34]- [35].
[184] Convention on the Rights of Persons with Disabilities. Opened for signature 30 March 2007. 2515 UNTS 3
[188] T1G of JHB1, p58, T1D of JHB1, p44,
[189] A10 of JHB1, p313 and A13 of JHB1.
[190] National Disability Insurance Agency v Davis [2022] FCA 1002 ("Davis").
[191] National Disability Insurance Scheme (Becoming a Participant) Rules 2016 (Cth)
[192] See Davis at [75] and [131]. See also [158].
[233] Our Guidelines - Becoming a participant - Applying to the NDIS, 10 December 2024, p9.
[234] Our Guidelines - Becoming a participant - Applying to the NDIS, 10 December 2024, p9.
[236] For example, Beezley v Repatriation Commission (2015) FCAFC 165 at [68] (North, Tracey and Mortimer JJ).
[244] T1A of JHB1, p25. The Tribunal did not observe issues with poor concentration over 6 days of hearing, with the Applicant able to direct both the Tribunal and Counsel to relevant documents on several occasions.
Beezley v Repatriation Commission [2015] FCAFC 165
Burrows and CEO, National Disability Insurance Agency (NDIS) [2025] ARTA 607
Defa and The CEO, National Disability Insurance Agency (NDIS) [2024] ARTA 34
Esber v The Commonwealth [1992] HCA 20; (1992) 174 CLR 430
Frugtniet v Australian Securities and Investment Commission [2019] HCA 16; (2019) 266 CLR 250
FTXB; Secretary, Department of Social Services and (Social services second review) [2024] AATA 3021
Garcia Albiol and National Disability Insurance Agency [2024] AATA 496
McGarrigle and National Disability Insurance Agency [2017] FCA 308
Mulligan v National Disability Insurance Agency [2015] FCA 544
National Disability Insurance Agency v Davis [2022] FCA 1002
National Disability Insurance Agency v Foster [2023] FCAFC 11
National Disability Insurance Agency v WRMF [2020] FCAFC 79
QDKH, by his litigation representative BGJF v National Disability Insurance Agency [2021] FCAFC 189
Re Drake and Minister for Immigration and Ethnic Affairs (No 2) [1979] AATA 179; (1979) 2 ALD 634
Re Panagiotou and TNT Australia Pty Ltd [2011] AATA 565
Re Schwass and NDIA [2019] AATA 28
Richardson and National Disability Insurance Agency [2024] AATA 3505
Shi v Migration Agents Registration Authority [2008] HCA 31; (2008) 235 CLR 286
(1992) 174 CLR 430
(2019) 266 CLR 250
(2008) 235 CLR 286