How to apply for the NDIS
Who can apply, the five steps from first phone call to decision, what evidence actually carries weight, how long it takes, and what to do if the answer is no.
From first call to decision
- 1Connect
- 2Evidence
- 3Apply
- 4Submit
- 5Decision
90 daysis what the NDIS gives itself to decide, counted from a complete application
In short
- Access turns on functional impact, not on which diagnosis you have.
- You generally need to be under 65 on the day you apply — it is about when you ask.
- Connecting with an NDIS partner first is usually the easiest way in, and it costs nothing.
- Evidence from treating professionals is what decides most requests.
- The NDIS aims to decide within 90 days of receiving a complete application.
- A refusal is reviewable, and the internal review window is short — act quickly.
The hardest part of the NDIS for most people is the beginning: working out whether you can get in at all, and what the process actually asks of you. The criteria are more specific than they first appear, and the thing that decides most requests is not the one people expect. This guide walks through who can apply, the five steps from first phone call to decision, what evidence carries weight, how long it takes, and what to do if the answer is no.
If the scheme itself is new to you, what the NDIS is and how it works is the shorter road in. This page assumes you are past that and deciding whether to apply.
Who can apply for the NDIS
People tend to think of NDIS access as a single question about disability. It is actually a set of requirements, and all of them have to be met — the NDIA publishes the eligibility requirements in full (opens in a new tab), and they are worth reading directly rather than relying on any provider's summary, including this one:
- Age — you generally need to be under 65 on the day you make your application
- Residence — Australian citizenship, permanent residence, or a Protected Special Category Visa
- Disability or early intervention — the substantive test, covered below
The age requirement catches people out, because it is about when you apply rather than about the support you need. If someone is approaching 65 and might ever need the scheme, that is a reason to look into it now rather than later. Aged care is the pathway afterwards, and it is a different system with different funding.
What the disability test actually asks
This is the part most often misunderstood. The NDIS does not have a list of qualifying conditions that grants access automatically. What it assesses is whether you have an impairment that is likely to be permanent, and whether it substantially reduces your functional capacity in everyday life.
Functional capacity is assessed across areas such as mobility, communication, social interaction, learning, self-care and self-management. The question is not what your diagnosis is called — it is what you cannot do, or cannot do safely and reliably, without help.
Two people with the same condition can genuinely receive different answers, and that is not an inconsistency. It follows directly from a test about function rather than about labels.
The other door: early intervention
There is a second pathway that is easy to miss. Early intervention is for people where providing support now would reduce how much support is needed later — most commonly young children with developmental delay or disability, but not only them.
It matters because the reasoning is different. Under early intervention the case is not only about current functional impact but about what earlier support would prevent. For a young child in particular, a request framed this way can succeed where one framed purely around present limitation does not.
The five steps, start to finish
The process the NDIA runs has five stages, and they are the same for everyone. Most of the anxiety in an application comes from not knowing which stage you are at — whether the silence means something has gone wrong or simply that you are between two of these. The NDIS sets out how to apply (opens in a new tab) on its own site; what follows is the same path with the parts that trip people up marked.
Connect with an NDIS partner
For most people this is the easiest way in, and it costs nothing. Local Area Coordinators and early childhood partners are contracted to help people through access — it is their job, not a favour. They can explain what the criteria mean for your situation, help you complete the form, and submit the application for you. You can also phone the NDIA directly if you would rather.
Gather your evidence
This is the step that decides the outcome, and the one people rush. You need documentation from treating professionals that speaks to permanence and to functional impact. Start it early: a report you have to request from a specialist can take weeks to arrive, and the application does not move while you wait for it.
Complete your application
The form asks about age, residence, and your disability or your need for early intervention. There is a section for your treating health professional to complete, and existing reports, assessments and letters can be attached instead of starting from scratch. Answer about function throughout — what a day is actually like — rather than about diagnosis.
Submit it
Your partner can submit on your behalf, or you can send it to the NDIA yourself. Keep a copy of everything you send and note the date you sent it. If you cannot complete or sign the form, say so when you contact a partner — there are ways through that, and it is a common situation rather than an unusual one.
Wait for the decision
The clock only starts once the application is complete, which is why an incomplete submission is slower than a delayed one. The NDIA may come back asking for more information; responding promptly matters. The decision arrives in writing, and if it is a refusal the letter gives the reason — which is the thing a review has to answer.
Where are you up to?
Pick the stage you are at, and see what usually happens next.
You are deciding whether to apply
What is happening
Nothing is lodged yet. This is the stage where a Local Area Coordinator or early childhood partner is most useful, and they cost nothing.
What usually goes wrong
Waiting until you feel "ready". Working out what ready looks like is part of what a partner is contracted to do.
What you can do today
Phone a partner or the NDIA and ask what evidence a situation like yours usually needs.
You are waiting on reports
What is happening
Your treating professionals are writing about two things: whether the impairment is likely to be permanent, and what it stops you doing day to day.
What usually goes wrong
A letter that confirms a diagnosis and says nothing about function. It is the most common reason a request fails.
What you can do today
Give each professional the NDIS evidence page, plus a plain list of what you cannot do unaided on an ordinary day.
The application is in front of you
What is happening
The form covers age, residence and disability or early intervention, with a section for your treating health professional to complete.
What usually goes wrong
Answering about diagnosis rather than about function, and starting from scratch when existing reports could be attached.
What you can do today
Write about a day, not a condition — and attach the assessments you already hold.
It is with the NDIA
What is happening
Either you or your partner has lodged it. The decision clock is tied to a complete application, not to the date you first made contact.
What usually goes wrong
Submitting a pack that is still missing something. An incomplete application is slower than a delayed one.
What you can do today
Keep a copy of everything you sent, note the date, and check the contact details the agency has for you.
You are waiting on the decision
What is happening
The NDIS says it will tell you within 90 days of receiving a complete application. It may come back asking for more information first.
What usually goes wrong
A request for further information sitting unanswered. That is the usual reason an application "submitted months ago" has not moved.
What you can do today
Answer any request the day it arrives. If the answer is no when it comes, the review window is short — read the reason and act on it.
Why the evidence decides it
Most unsuccessful requests fail on evidence rather than on eligibility. What carries weight is documentation from treating health professionals that speaks specifically to permanence and to functional impact — not a letter confirming a diagnosis. The NDIS describes what evidence it is looking for (opens in a new tab) and it is worth handing that page to the professional writing your report.
The distinction is worth being blunt about. "This person has X condition" tells the NDIA very little. "This person cannot shower unassisted, cannot prepare a meal safely, and requires prompting to take medication, and these limitations are expected to be lifelong" tells them what they are required to assess.
- Reports from specialists, GPs, occupational therapists, psychologists or other treating professionals
- Statements about whether the impairment is likely to be permanent
- Concrete description of functional impact across daily activities
- Evidence of what has already been tried, and its result
- Recent documentation — older reports carry less weight
Most requests that fail do not fail on eligibility. They fail on evidence.
How long the decision takes
The NDIS says it will tell you whether you are eligible within 90 days of receiving your application and all of your supporting evidence. The second half of that sentence is the important one: the clock is tied to a complete application, so evidence still being gathered is time that has not started counting yet.
If the agency asks for more information, the decision waits on your answer. That is the most common reason an application people describe as "submitted months ago" has not been decided — not that it was lost, but that something in it was still outstanding.
90 days
is what the NDIS gives itself to decide
Counted from when your application and all supporting evidence have been received, not from when you first made contact. A request for further information pauses the practical clock. Timeframes and rules change — check the current NDIS guidance before relying on this.
If you are approved: the planning conversation
If access is granted, the next step is planning: a conversation about your goals and needs that produces your first plan. That plan is where funding is decided, and preparing for it properly is worth as much effort as the access request was. Our guide on preparing for a plan review applies to a first planning meeting as much as to a later review.
What if you are not eligible?
A refusal is not the end, and a good proportion of decisions change on review. You can ask for an internal review of the decision (opens in a new tab), and the window for doing so is short — generally a matter of months from the decision — so the single most important thing is not to sit on it while gathering perfect evidence.
A review is strongest when it addresses the specific reason given. If the decision said the impairment was not established as permanent, more detail about daily impact will not help; what is needed is evidence about permanence. Read the reason carefully and answer that. If an internal review does not resolve it, there are further external avenues beyond the agency.
The other thing worth knowing is that the NDIS is not the only door. Connecting people with mainstream and community supports — health, education, local services, carer supports — is part of what the scheme and its partners do, and a partner can help with that whether or not you end up with a plan. Not being eligible is a smaller dead end than it feels like on the day the letter arrives.
Getting help with the process
Local Area Coordinators and early childhood partners help with access at no cost to you, and for many people that is enough. Advocacy organisations also support people through access and review, particularly where a request has been refused.
Note the sequencing, because it confuses people: a support coordinator is funded *in* a plan, so coordination is not available to help you get access in the first place. Once you are in, Support Connection is the lightest level of help to turn a first plan into working supports.
What happens after you receive a plan
It is worth knowing what is on the other side. An approved plan funds reasonable and necessary supports related to your disability — which in practice can mean anything from a few hours of daily living support a week to a full roster of care, therapy, equipment, transport or help finding somewhere to live.
It is not a cash payment and it does not cover everyday costs that everyone has, like rent, groceries or utilities. What it funds is the disability-related gap: the things you need because of your disability that another person would not.
Then you choose who delivers it. You are not assigned a provider, you can use several, and you can change your mind without justifying it. The supports a provider can be engaged for gives you the vocabulary for that conversation, and where we work across Melbourne is the other half of it — a service that reads well and cannot roster reliably in your suburb is not a service.
The bottom line
Access turns on function, permanence and evidence — in that order of misunderstanding. If you are unsure whether to apply, the honest answer is that a well-evidenced request is worth making, and that the cost of not asking is usually higher than the cost of being refused once.
If you are somewhere in this process and it is not making sense, a free Meet & Greet is a conversation rather than a form. We are a provider, not the NDIA — but pointing people toward the right door costs nothing.
Written by
Somya Verma
Specialist Support Coordinator
Over 6 years in the disability sector · At Gencare since 2020
I am a dedicated and compassionate Specialist Support Coordinator with over six years of experience in the disability sector, including extensive experience in specialist support coordination.
Gencare Disability Services is a registered NDIS provider supporting participants across Melbourne and regional Victoria.
Explore the related Gencare supports
Common questions
Broadly, you need to meet three sets of requirements: an age requirement (generally being under 65 when you make your access request), a residence requirement (Australian citizenship, permanent residence, or a Protected Special Category Visa), and either the disability requirements or the early intervention requirements. All of them apply, not just the disability test.
No, and this is the most common misunderstanding. There is no list of conditions that grants access automatically. What is assessed is whether you have an impairment likely to be permanent that substantially reduces your functional capacity in areas such as mobility, communication, social interaction, learning, self-care and self-management. Two people with the same diagnosis can legitimately receive different answers.
There are five steps. Connect with an NDIS partner — a Local Area Coordinator or early childhood partner — who can help at no cost, or contact the NDIA directly. Gather evidence from your treating professionals. Complete the application, including the section your health professional fills in. Submit it yourself or have your partner submit it for you. Then wait for the decision, responding promptly if the agency asks for anything further. The evidence step is the one that decides most outcomes.
The NDIS says it will tell you whether you are eligible within 90 days of receiving your application and all of your supporting evidence. The clock is tied to a complete application, so time spent gathering evidence is not counted, and a request for further information means the decision waits on your answer. Timeframes and rules change, so check the current NDIS guidance rather than relying on a figure quoted anywhere else.
Documentation from treating health professionals that speaks to two things: whether the impairment is likely to be permanent, and what it actually stops you doing day to day. A letter confirming a diagnosis is much weaker than a report describing specific functional limitations and their expected duration. Recent reports carry more weight than older ones.
A second pathway into the scheme, for people where support now would reduce the need for support later — most commonly young children with developmental delay or disability, though not only them. The reasoning differs from the standard test: the case rests partly on what earlier support would prevent, not only on current functional impact.
Ask for an internal review, and do it promptly — the window is short, generally a matter of months, and waiting to assemble perfect evidence is a common way to miss it. Address the specific reason given in the decision: if permanence was the issue, more detail about daily impact will not help. If internal review does not resolve it, there are further external avenues beyond the agency.
No, and the sequencing catches people out. Support coordination is funded within a plan, so it is not available to help you obtain access in the first place. Local Area Coordinators, early childhood partners and disability advocacy organisations are the ones who help at that stage, generally at no cost to you.
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