18/06/2026
At the final hearing of the Senate inquiry into the NDIS Bill, NDIS Quality and Safeguards Commission Assistant Commissioner Alisa Chambers noted that providers had reported participants being affected by service changes and provider viability issues, but that this had not been reflected in the Commission's complaints data.
That is not particularly surprising.
When a trusted provider closes, withdraws services, reduces supports or decides they can no longer operate because NDIS pricing does not cover the cost of delivering services, participants often do not blame the provider.
They blame the policy settings that made the service unsustainable.
Why would a participant lodge a complaint against a provider for something outside that provider's control?
Many want to report the impact of NDIA pricing decisions, market settings, funding changes and policy decisions.
But where is that information recorded?
The Commission's complaints system is designed to receive complaints about providers.
It is not designed to systematically capture participant reports about harms arising from Agency decisions, pricing settings, market failure, service withdrawal or the cumulative impacts of reform.
So when we are told that provider viability concerns are not showing up in complaints data, we should ask a second question:
Is the system collecting the information that would allow those impacts to be seen?
Because data can only tell us about the things we have chosen to measure.
If participants are angry at the Agency rather than the provider, and there is no mechanism to systematically record those reports, then the absence of complaints does not demonstrate the absence of harm.
It may simply demonstrate the absence of a dataset.
That is one reason the Nobody Worse Off Coalition created the Harm Tracker.
Professionals Australia is a proud member of NWO, supporting the critical work done to protect the NDIS for Disabled people now and into the future. We work alongside Disabled People's Orgs, Disabled individuals, families of Disabled people and all NDIS focused workers who believe that Disabled people have the right to equality in this country.
If participants are losing supports, trusted providers are disappearing, families are entering crisis, and nobody is systematically recording those impacts, then somebody needs to.
If the system cannot see the harm, we will document it ourselves.