Submission to the Senate Community Affairs Committee Inquiry into the National Disability Insurance Scheme Amendment (Securing the NDIS for Future Generations) Bill 2026

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

Submission 2645

Submission to the Senate Community Affairs

Committee Inquiry into the National Disability

Insurance Scheme Amendment (Securing the NDIS

for Future Generations) Bill 2026

From: Anonymous parent and sole carer, NSW

Date: 1 June 2026

I am a sole parent of a young child with autism and ADHD with high support needs. I am

concerned this Bill will make the NDIS less responsive to children whose needs change quickly

and whose families are already under significant pressure

My son started school this year. He still needs ongoing speech therapy, occupational therapy,

psychology, behavioural support, and school related capacity building supports to help him

participate safely, manage transitions, regulate emotions, and stay engaged in learning. His

needs do not stay the same across home, school, holidays, illness, fatigue, and developmental

change. A system that is slower and narrower will not reflect the reality of childhood disability.

One of my biggest concerns is the change to parental responsibility. The Bill would define

substantial care and support in a way that captures supervision, personal care, transport,

emotional support, behavioural support, and help with daily living, regardless of the child’s

disability, and it also says supports should not be funded where the main purpose is to reduce

parental burden below what is reasonably expected. For families raising children with significant

disability, this risks shifting more disability related care back onto parents and treating very high

support needs as ordinary parenting.

This matters in real life. My child can become highly distressed during transitions. I can be hit,

scratched, bitten, and headbutted while trying to leave the house or get him safely into the car.

We have been stuck on the street many times for hours, unable to get him home safely. These

are not ordinary parenting demands. They are disability related support needs that affect safety,

health, work, and school attendance. The Bill does not appear to properly recognise that reality.

I am also concerned about the move away from the established reasonable and necessary

framework. According to public explainers, the Bill changes how support decisions are made and

leaves more detail to rules and later determinations. That creates uncertainty for participants and

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

Submission 2645

families. The core test for what supports can be funded should stay clear in the Act, not be

narrowed over time through rules.

The Minister is also given broader powers in important parts of the scheme. The government fact

sheet says the Bill enables the Commonwealth Minister to make determinations to reduce funding

for groups of supports, and also makes the Minister the decision maker on NDIS pricing. Those

are significant powers. Decisions that affect the supports available to disabled children and the

value of those supports should not be made with so little protection for participants.

I am concerned about the tighter rules for unscheduled plan reassessments. The government fact

sheet says reassessments will only be possible where there have been significant and ongoing

changes in support needs or in living, education, work, or informal supports. Children can change

quickly. Families should not have to wait for matters to become severe and prolonged before

support can be reconsidered.

I am also concerned about the changes to permanence. The Bill says access will only be granted

when all appropriate treatment to remedy or alleviate an impairment has been undertaken, no

other treatment is likely to materially improve the impact of the impairment, and the impairment is

likely to be lifelong. This creates a risk that children may be denied access or face greater

barriers because of debates about what treatment should have been tried, even where access to

that treatment is limited by cost, location, waiting lists, or the child’s actual circumstances.

This Bill should be amended so it does not expand parental responsibility for disability related

care, does not weaken the established reasonable and necessary framework, and does not hand

such broad power to the Minister to shape the scheme through rules and determinations.

Children with disability need a system that is flexible, transparent, and responsive to their actual

support needs at home and at school.

Kind regards,

A concerned parent and voter.