NOW MEANS
NOW MEANS
Senator Jordon Steele-John sharing our concerns at Federal Government. A powerful reminder that when we speak up, together, people listen.
For over 6 weeks we’ve raised concerns about what could happen if the NDIA didn’t listen,but it’s no longer a warning… this is a reality.
People on the scheme are losing essential supports, facing increased isolation, and being forced into crisis.
And the people who’ve spent their lives supporting them—providers, support workers, allied health teams—are burning out, scaling back, or walking away altogether
We’re seeing real harm play out in real time
In a mere few weeks, this campaign has grown beyond anything we could have predicted:
58,000 signatures
35,000 emails sent to MPs
National media attention
Decision-makers in the room, listening
What You Can Do
Document the harm you’ve experienced
The Harm Tracker is a new national tool to report how NDIS cuts are hurting people. It is an independent, grassroots, public interest project. It is co-designed with Disabled people, led by Disabled people and created in partnership with Allied Health workers.
The Harm Tracker is run by Nobody Worse Off; a national coalition of Disabled people, families, support workers, unions, and allies standing up against cuts to the NDIS.
The data will be used to create anonymous reports, maps, and visuals to show the real harm caused by NDIS changes , and to fight for a better system.
Read more about the harm tracker and how the data will be used here
Email your Local Member of Parliament (again)
To keep the pressure on, we’ve redeveloped our letter to MPs
Emailed them already? Email them again.
Just like you would follow up when a friend ghosts you… how much more so when the government doesn’t action your urgent pleads.
Your MP represents you, their job is to make sure that you are heard. Your priorities are their priorities .
Rally your community
We’ve come so far through our joint efforts; with national media, meetings with MPs, unity across this community.
To keep the public pressure on our government to hold the NDIA to account, we need our voices to stay strong and loud.
Send this page (www.itsnowornever.com.au) to the people you know who would care about this issue and make sure they know how they can make a difference
And, if you would like to take it a step further and rally your local community, we've put together a tried and tested step-by-step guide on how to make sure your local MP is aware of the harm it is causing their constituents, your community (coming soon)
How do the Changes Impact Me?
Click below to learn more
How are My Advocacy Groups/ Professional Bodies Representing My Concerns?
To see what your professional body/ advocacy group has been working on click here.
Frequently Asked Questions
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We’re made up of a group of people with disability and NDIS participants, families, providers, and supporters who care deeply about the future of the NDIS. Some of us work in the sector. Some of us live it. All of us are worried.
This campaign was sparked by people on the ground: those who’ve seen the impact of these changes up close. No corporate backing. No polished media team. Just people who couldn't stay silent any longer.
Want to know more about the people driving this? Meet the team behind the campaign.
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Because it’s not sustainable anymore. And it hasn’t been for a while.
Across the NDIS, people have been absorbing the true costs of support - therapists, support coordinators, plan managers and others in the sector...
We've all been carrying extra weight, hoping things would balance out.
For years, many providers’ response has been to just… figure it out.
To make it work however we could.
Many of us chose to undercharge, work unpaid hours, and stretch ourselves- because we care, and because we didn’t want to pass pressure onto the people we support.
But in doing that, we’ve also unintentionally hidden the true cost of delivering quality support. And when something’s hidden, it’s easy to undervalue. That’s what’s happened here- a system that slowly started to rely on unpaid labour.
We’re seeing the consequences now. People are burning out. Services are closing. Supports disappearing, especially in regional and remote areas.
This campaign didn’t start just because of one pricing update. It started because people have had enough, of working under pressure, of watching supports disappear, of being expected to do more with less.
We realised that if we don’t say something now, the NDIS as we know it - the support system that so many people rely on - could fall apart.
And for people with disability, who have fought relentlessly for their rights, it’s yet another moment of needing to speak up just to be heard.
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Nothing about us without us.
Disabled people have been leading the push for inclusion and equity long before this campaign began. We’re not claiming to speak for anyone, we’re standing with them.
But we know actions speak louder than words. So we’re:
Working with people with lived experience to co-create resources and messaging
Creating space for disabled voices to be heard through our story collection form.
Checking ourselves when we get it wrong, and staying open to feedback when we need to do better
This campaign is stronger because of disabled voices, and it’s our responsibility to keep listening, learning, and making room.
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These changes don’t just affect current NDIS participants and providers. The ripple effect reaches schools, hospitals, future workers, and communities across the country.
Here’s what’s at risk:
Our Education Systems
Teachers and schools rely on NDIS-funded supports to help students regulate, communicate, and stay engaged. Without this support, students may be excluded, or left behind entirely, leaving our already overloaded and under-resourced educators to pick up the slack.Future Therapists and NDIS Workers
Students studying allied health, support work, or looking to join the NDIS workforce are watching these changes and reconsidering their career paths. Poor placement experiences, reduced supervision, and burnout are turning people away before they’ve even entered the field.Public Infrastructure
When people can’t access the support they need through the NDIS, they’re often pushed into systems not built for long-term care, like emergency departments, child protection, or crisis services. That means already overstretched systems become even more saturated. Emergency waiting rooms are somehow even more packed. Triple-zero is off the hook, and child protection cases grow.
These are structural impacts, and they affect all of us.The question isn’t if this impacts you, it’s when.
Read more about the impact here.
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Until recently, a formal Parliamentary Petition wasn’t possible. Following the election, Australia was operating under a caretaker government. Key ministerial roles, and the Standing Committee on Petitions, weren’t yet up and running.
Without that structure in place, no petitions could be accepted.
Now, though, things are getting back on track. We expect the new ministry and committee to be fully in place by August. Once that happens, a national petition might be on the cards 👀
In the meantime, we’ve been using every tool we can (Change.org, media, advocacy…) to make sure our message is already loud and clear.
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On its own? No. A petition won’t rewrite the Price Guide or overturn legislation.
But a petition with over 100,000 voices? That’s something. That’s momentum. That’s pressure.
And this campaign isn’t stopping there. We’re:
Creating resources to educate participants, providers, and supporters
Engaging directly with MPs, peak bodies, and media to keep the conversation going
Building connections across this space so this momentum turns into real, lasting advocacy
Signing the petition is about more than a signature, it’s about proving to people that this issue; the rights and access of people with disabilities is something that we all back. That enough is enough. That it’s now or never.
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Phase 1 was our push in the lead-up to the 2024- 25 NDIS Price Guide.
We knew decisions were being made behind closed doors, and this was our last real chance to speak up before they were locked in.We focused on:
A national Change.org campaign
MP letter-writing tools
Open letters and data-gathering across the sector
And it made an impact.
Minister Jordan Steele-John responded directly to the petition—acknowledging the pressure and concerns raised. It also brought together thousands of voices across the country—providers, families, and community members—many of whom had never been connected in this way before. For the first time, people across disciplines, roles, and regions came together to say the same thing: this matters. -
Phase 2 was a rapid, final push in the days just before the 2024–25 NDIS Price Guide was released. It was the 11th hour. We knew decisions were close to being locked in.
We launched a social media campaign focused on visibility and action.
People were encouraged to:Share their stories about how the changes would impact them
‘Paint the town purple and orange’ to show solidarity
Tag and email MPs, post online, and
Challenge 11 others to sign the petition and do the same
This stage was about using every channel we had to make the real-world impact on people with disability impossible to ignore, right before the final decision was made.
And it reached far.
We saw national media coverage, and a wave of public attention.For a few crucial days, the conversation couldn’t be ignored.
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If NDIA leadership and government don’t respond by 31 July, We move to our next big national movement in August
Together, we’re growing louder and stronger.
We will not be silenced.
Now means now. -
A lot of advocacy happens behind the scenes - through meetings, submissions, and policy work. Many peak bodies have been doing this for years, often balancing complex relationships and priorities.
Each professional body represents an entire profession or community, including people working both within the NDIS space and outside of it. That means their advocacy might look different, and their decisions around involvement often reflect a broader scope of responsibility to their discipline.
Some peak bodies have their own strategies or things to consider before backing a grassroots campaign like this. That doesn’t mean they support the NDIS changes, it just means they’re advocating within the responsibilities of their boards, the needs of their broader membership, and the sector relationships they’re navigating every day.
And whether or not they’re officially involved in the It’s Now or Never campaign, we believe we’re all pushing for the same thing: a fairer, more sustainable NDIS that works for the people it was built for - in whatever ways we can.
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There are plenty of ways to support the campaign, big or small, loud or behind the scenes:
Sign the petition and explore resources
Share your voice
Volunteer your time or skills
Join the mailing list for updates
Follow along on Instagram
Connect with our team
We’re in this together, however you show up, you are a part of the change, and we are so grateful to have you join us.
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Absolutely, we know how confusing this can get.
That’s why we have a dedicated page for resources to support NDIS Participants in understanding and navigating the changes. Click here to be redirected to it
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Fair question. As a grassroots group made up of people volunteering time outside of their usual 9–5s, we know things don’t always update at lightning speed. Sometimes, details slip through the cracks.
We’re working hard behind the scenes to keep everything as current and accurate as possible, while juggling advocacy, media, events, and life. If you spot something that’s no longer relevant or could be clearer, please let us know. It helps more than you think. 💙
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