Submission 3159 — Name Withheld — NDIS Future Generations Bill

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National Disability Insurance Scheme Amendment (Securing the NDIS for Future Generations) Bill 2026

Submission 3159

To: Senate Community AƯairs Legislation Committee

Thank you for the opportunity to provide a submission on the proposed NDIS legislation. I

am writing as a parent who experiences every day the reality of trying to parent multiple

children with disability, while balancing employment, and navigating multiple government

systems. I am a single mother living in regional Queensland, raising three young children

who are NDIS participants and have a range of disabilities including autism, ADHD, anxiety,

and Development Coordination Disorder. I also work part time as a health researcher.

The cumulative impact of raising multiple neurodivergent children is diƯicult to appreciate

unless you have lived it. My children’s disabilities and the challenges that accompany them

aƯect every aspect of our lives. Like many parents of neurodivergent children, I also

recognise that there is a higher likelihood that parents themselves are neurodivergent (even

if undiagnosed), further increasing the cognitive load required to simultaneously coordinate

multiple services and appointments and navigate complex government systems. Families

like mine are already operating well beyond capacity.

My children rely on the NDIS to access therapies and supports that enable them to function,

participate in education, develop independence and reduce the likelihood of future crisis.

These supports are not luxuries. They are evidence-based supports recommended by

treating  professionals  to help my  children communicate,  regulate  their emotions,

participate in education and community life and build independence over time. I am deeply

concerned that reforms primarily focused on reducing expenditure risk overlooking the

cumulative impact on families with multiple neurodivergent children. Decisions that appear

minor in isolation can fundamentally change whether a family is able to keep functioning.

The cumulative impact of multiple neurodivergent children means supports cannot simply

be viewed on an individual basis. Supports that enable one child to attend therapy or school

often enable the whole family to function.

Support workers have been transformative for my family. They have significantly reduced

school refusal by helping with stressful morning routines, enabling my children to arrive at

school and kindergarten ready to learn. They make it possible for my children to attend

therapy appointments and enable my oldest child to participate in an extracurricular activity

that develops his gross motor skills and coordination, which are aƯected by Developmental

Coordination Disorder. They also provide practical assistance that allows fundamental

National Disability Insurance Scheme Amendment (Securing the NDIS for Future Generations) Bill 2026

Submission 3159

household functioning to continue. These supports strengthen my capacity as their primary

carer to embed evidence-based therapy strategies into everyday family life. These have been

meaningful improvements in quality of life and reduce the likelihood of more intensive and

expensive interventions later.

I also encourage the Committee to recognise the vital role played by family carers. Parents

are not passive recipients of government assistance. We coordinate therapists, attend

appointments, implement strategies at home, advocate within schools, manage paperwork

and provide countless hours of unpaid care. Policies that increase administrative burden or

uncertainty ultimately reduce the capacity of carers to remain employed, maintain their own

wellbeing and continue providing that care.

Even with the current supports, as primary carer, I spend considerable time coordinating

services, travelling to appointments and managing administrative requirements. These

responsibilities limit my capacity to work increased hours. It has also contributed to burnout

as my physical and mental health have deteriorated significantly. This reduces my capacity

to support my children. If my children’s disability supports are delayed, as has been

indicated by this bill and in interactions with NDIS delegates, the eƯects will extend beyond

my children. It is likely that I will need to exit the workforce; their schools will carry increased

support load; and we will rely more heavily on community and public health services.

In considering these reforms, I ask the Committee to carefully assess not only immediate

fiscal impacts but also the broader social and economic consequences. Investment in

appropriate  early  intervention and  family supports helps  children develop  greater

independence and participation over time. It also supports parents to remain engaged in the

workforce and reduces pressure on other government systems.

Finally, I ask that the voices of participants and families continue to be central to any future

reforms. Those living with disability every day have valuable insights into what works, what

does not, and where unintended consequences may arise.

Thank you for considering my submission and for taking the time to hear directly from

families who rely on the NDIS.