Oxford Paediatric Autism Assessments

Oxford Paediatric Autism Assessments Offering team autism assessments in a new location! Anthea Dobson (Speech) & Brooke Purslowe (Psych)

19/02/2026

About half of all parenting tip videos on TikTok are being uploaded by a creator with no expertise, according to research undertaken by The Kids Research Institute.

The Kidsโ€™ study analysed the top performing videos with tips for parents on the platform, finding that just 53.9 per cent of videos came from creators purported to have a relevant qualification or expertise in parenting.

Embrace Research Fellow and report lead author Dr Karen Lombardi said parents risk exposure to misinformation when they turn to social media for answers about their childrenโ€™s health.

๐Ÿ”’ Read the article here: https://shorturl.at/gOGze

Or our media release here: https://shorturl.at/TPBUK

17/02/2026

Itโ€™s very common for both siblings to be Autistic, but for only one to get a diagnosis early (or ever!) because they present so differently.

While this example includes two very different autism presentations, differences donโ€™t have to be this extreme. However, it is true that usually one sibling is more stereotypically autistic and has higher support needs while the later or underdiagnosed sibling is non stereotypical with lower support needs (and often diagnosed AHDH in my experience, although Autism and ADHD would be more appropriate).

15/02/2026
Transition to high school : masking : burnout.
07/02/2026

Transition to high school : masking : burnout.

05/02/2026

Part two of our episode with neurobiologist and author of The Lost Girls of Autism, Gina Rippon, is now live wherever you get your podcasts ๐ŸŸข

Picking up where part one ends, Gina traces how early brain science, diagnostic bias and cultural assumptions combined to hide autistic women in plain sight. She unpacks why autism was framed as a โ€œmale condition,โ€ how masking became a survival strategy, and the real cost of decades of late or missed diagnosis.

They explore the neuroscience behind prediction and masking, the forgotten female figures in autismโ€™s history, and why the language of โ€œover-diagnosisโ€ risks oversimplifying a much more complex history of under-recognition .

Gina also reflects on autistic bullying, and what meaningful change in diagnosis and research could look like next.

If youโ€™ve ever wondered why so many autistic women are only being seen now - or why you still donโ€™t feel seen - this conversation is for you. We hope it offers some clarity, context, and hope.

Watch or listen wherever you get your podcasts - just search 'The Hidden 20%' ๐ŸŸข

04/02/2026

Many parents have asked what the ๐™๐™๐™ง๐™ž๐™ซ๐™ž๐™ฃ๐™œ ๐™†๐™ž๐™™๐™จ / ๐™‰๐™ค ๐˜พ๐™๐™ž๐™ก๐™™ ๐™‡๐™š๐™›๐™ฉ ๐˜ฝ๐™š๐™๐™ž๐™ฃ๐™™ report could mean for families.

Kids First founder, Sonja Walker, has reviewed the 80,000-word document released today and below are some of the key areas we have raised with our local MP for parliamentary discussion.

It's important to note that the intention behind the report is a positive one. Everyone wants children to get the right support earlier and to see better outcomes over time.

Weโ€™re sharing our feedback because weโ€™re concerned that some of the recommendations rely on assumptions that donโ€™t always reflect family life on the ground, and that the real-world impact for children and parents hasnโ€™t been fully considered.

๐—œ๐—ป๐—ณ๐—ผ๐—ฟ๐—บ๐—ฎ๐˜๐—ถ๐—ผ๐—ป ๐˜ƒ๐˜€ ๐—ฟ๐—ฒ๐—ฎ๐—น ๐˜€๐˜‚๐—ฝ๐—ฝ๐—ผ๐—ฟ๐˜

The report recommends increasing access to information, resources and online programs to build parent capacity.
Many parents already know what their child finds hard. Whatโ€™s often missing is time, energy and hands-on support to turn advice into real change at home, school and in the community. Online programs can be helpful, but they donโ€™t replace skilled professionals working alongside children and families over time.

๐—˜๐˜…๐—ฝ๐—ฒ๐—ฐ๐˜๐—ถ๐—ป๐—ด ๐—ฝ๐—ฎ๐—ฟ๐—ฒ๐—ป๐˜๐˜€ ๐˜๐—ผ ๐—ฑ๐—ผ ๐—บ๐—ผ๐—ฟ๐—ฒ

The report suggests that parent capacity can be expanded indefinitely through access to education and online programs.
In reality, many parents are already carrying a heavy load. Between work, siblings, appointments, school meetings and daily challenges, families are doing their best with limited reserves. Expecting parents to absorb even more responsibility without enough professional support risks burnout and could leave children without the help they need.

๐—จ๐˜€๐—ฒ ๐—ผ๐—ณ ๐—น๐—ฎ๐—ฏ๐—ฒ๐—น๐˜€ ๐—น๐—ถ๐—ธ๐—ฒ โ€œ๐—บ๐—ถ๐—น๐—ฑโ€ ๐—ผ๐—ฟ โ€œ๐—บ๐—ผ๐—ฑ๐—ฒ๐—ฟ๐—ฎ๐˜๐—ฒโ€

The report relies on terms such as โ€œmild to moderateโ€ developmental delay or autism to guide decisions.
These labels donโ€™t always match daily life, and they do not reflect clinical practice. Children described as โ€œmildโ€ can still struggle significantly with learning, friendships, behaviour, sleep, toileting or emotions. When decisions rely on labels rather than how a child functions day to day, some children miss early support at the point it could make the biggest difference.

๐—ฃ๐—ฟ๐—ฒ๐—ณ๐—ฒ๐—ฟ๐—ฒ๐—ป๐—ฐ๐—ฒ ๐—ณ๐—ผ๐—ฟ ๐—น๐—ฎ๐—ฟ๐—ด๐—ฒ ๐—ผ๐—ฟ๐—ด๐—ฎ๐—ป๐—ถ๐˜€๐—ฎ๐˜๐—ถ๐—ผ๐—ป๐˜€

The report often refers to large Non-Government Organisations (NGOs) as the primary voice of best practice and service delivery.
Many of these organisations hold charitable status, which gives them access to funding structures, tax exemptions, grants and pilot program opportunities that smaller providers simply donโ€™t have. This allows them to trial new models, absorb financial risk and operate at scale in ways that are not possible for most local services.

However, many of these organisations no longer operate consistently within local communities. (The NGO that Sonja once served as a Board member, Lifestart, moved out of the northern beaches years ago to redirect supports to other areas of Sydney.) When this kind of thing happens, families rely heavily on smaller, local services that know their child, their school and their area, and who can respond flexibly as needs change. These relationships are built over time and are central to effective support. If local services that are dedicated to their community disappear, that trust and knowledge canโ€™t be replaced quickly or easily.

๐—™๐—ฟ๐—ฎ๐—บ๐—ถ๐—ป๐—ด ๐—ผ๐—ณ ๐—ฝ๐—ฟ๐—ถ๐˜ƒ๐—ฎ๐˜๐—ฒ ๐—ฝ๐—ฟ๐—ฎ๐—ฐ๐˜๐—ถ๐—ฐ๐—ฒ

The report implies that private or unregistered providers are more 'transactional' or higher risk than NGOs.
In reality, private practice clinicians are regulated by exactly the same professional bodies and bound by the same strict codes of conduct as NGOs. Many experienced therapists choose not to register with the NDIS because of cost and complexity, not because of poor or unethical practice. This distinction matters to families who depend on these services. We encourage the Thriving Kids committee to ask the question: 'If 92% of NDIS providers are unregistered, why is this so?'

๐— ๐—ฎ๐—ป๐—ฑ๐—ฎ๐˜๐—ผ๐—ฟ๐˜† ๐—ฟ๐—ฒ๐—ด๐—ถ๐˜€๐˜๐—ฟ๐—ฎ๐˜๐—ถ๐—ผ๐—ป

The report supports mandatory registration without clearly outlining a timeframe or how services will transition safely. There are insufficient resources in the sector to allow this to happen, even with a January 2028 floated as a 'done by date'.
If changes are introduced too quickly, some local services may be forced to close. Families wonโ€™t simply move elsewhere, because there often isnโ€™t anywhere else to go. Once local services are lost, rebuilding them is extremely difficult.

๐—”๐˜€๐˜€๐˜‚๐—บ๐—ฝ๐˜๐—ถ๐—ผ๐—ป๐˜€ ๐—ฎ๐—ฏ๐—ผ๐˜‚๐˜ ๐—ฐ๐—ถ๐˜๐˜† ๐˜€๐—ฒ๐—ฟ๐˜ƒ๐—ถ๐—ฐ๐—ฒ๐˜€

The report focuses heavily (and rightly so) on the challenges that are experienced by families living in Australia's regional and rural areas - however it also assumes that children in metropolitan areas have enough services and capacity.
City families face the same workforce shortages, waitlists and burnout as regional areas. Many parents already ration therapy or go without support because services are stretched.

๐—ช๐—ผ๐—ฟ๐—ธ๐—ณ๐—ผ๐—ฟ๐—ฐ๐—ฒ ๐—ฐ๐—ฎ๐—ฝ๐—ฎ๐—ฐ๐—ถ๐˜๐˜†

The report assumes the workforce can expand quickly to support new models of care.
Therapists take years to train, and many experienced clinicians are leaving the sector due to workload and uncertainty. New systems canโ€™t succeed unless there are enough skilled people available to deliver care.
Switching responsibility to educators, teachers and schools is not the answer to these challenges. Educators are already stretched and are not trained or resourced to provide disability-specific assessment or intervention. Expecting them to fill workforce gaps risks pushing people beyond their scope, increasing pressure in classrooms, and leaving children without the specialised support they need.

๐—ง๐—ต๐—ฒ ๐—ฏ๐—ถ๐—ด๐—ด๐—ฒ๐—ฟ ๐—ฝ๐—ถ๐—ฐ๐˜๐˜‚๐—ฟ๐—ฒ

Support for children isnโ€™t just about programs or policy frameworks. ๐—œ๐˜ ๐—น๐—ถ๐˜ƒ๐—ฒ๐˜€ ๐—ถ๐—ป ๐˜€๐—ธ๐—ถ๐—น๐—น๐—ฒ๐—ฑ ๐—ฝ๐—ฒ๐—ผ๐—ฝ๐—น๐—ฒ, ๐˜๐—ฟ๐˜‚๐˜€๐˜๐—ฒ๐—ฑ ๐—ฟ๐—ฒ๐—น๐—ฎ๐˜๐—ถ๐—ผ๐—ป๐˜€๐—ต๐—ถ๐—ฝ๐˜€ ๐—ฎ๐—ป๐—ฑ ๐˜€๐—ฒ๐—ฟ๐˜ƒ๐—ถ๐—ฐ๐—ฒ๐˜€ ๐˜๐—ต๐—ฎ๐˜ ๐˜„๐—ฎ๐—น๐—ธ ๐—ฎ๐—น๐—ผ๐—ป๐—ด๐˜€๐—ถ๐—ฑ๐—ฒ ๐—ณ๐—ฎ๐—บ๐—ถ๐—น๐—ถ๐—ฒ๐˜€ ๐—ผ๐˜ƒ๐—ฒ๐—ฟ ๐˜๐—ถ๐—บ๐—ฒ. ๐—œ๐—ณ ๐—ฒ๐˜…๐—ถ๐˜€๐˜๐—ถ๐—ป๐—ด ๐—ฐ๐—ฎ๐—ฝ๐—ฎ๐—ฐ๐—ถ๐˜๐˜† ๐—ถ๐˜€ ๐˜„๐—ฒ๐—ฎ๐—ธ๐—ฒ๐—ป๐—ฒ๐—ฑ ๐—ผ๐—ฟ ๐—น๐—ผ๐˜€๐˜, ๐—ถ๐˜ ๐—ฐ๐—ฎ๐—ป๐—ป๐—ผ๐˜ ๐—ฏ๐—ฒ ๐—ฟ๐—ฒ๐—ฝ๐—น๐—ฎ๐—ฐ๐—ฒ๐—ฑ ๐—พ๐˜‚๐—ถ๐—ฐ๐—ธ๐—น๐˜†.

๐—™๐—ฎ๐—บ๐—ถ๐—น๐—ถ๐—ฒ๐˜€ ๐—ป๐—ฒ๐—ฒ๐—ฑ (๐—ฎ๐—ป๐—ฑ ๐—ฑ๐—ฒ๐˜€๐—ฒ๐—ฟ๐˜ƒ๐—ฒ) ๐—ฐ๐—น๐—ฎ๐—ฟ๐—ถ๐˜๐˜†, ๐—ฐ๐—ผ๐—ป๐˜๐—ถ๐—ป๐˜‚๐—ถ๐˜๐˜†, ๐—ด๐—ฒ๐—ป๐˜‚๐—ถ๐—ป๐—ฒ ๐—ฐ๐—ต๐—ผ๐—ถ๐—ฐ๐—ฒ ๐—ฎ๐—ป๐—ฑ ๐—ฎ๐—ฐ๐—ฐ๐—ฒ๐˜€๐˜€ ๐˜๐—ผ ๐—ฒ๐˜…๐—ฝ๐—ฒ๐—ฟ๐—ถ๐—ฒ๐—ป๐—ฐ๐—ฒ๐—ฑ ๐˜€๐˜‚๐—ฝ๐—ฝ๐—ผ๐—ฟ๐˜. Without careful planning, broad consultation and agreement across systems, there is a real risk that well-intentioned changes could unintentionally make things harder for the very children they aim to support.

21/01/2026

While the I-CAN assessment tool (The Instrument for the Classification and Assessment of Support Needs) is a validated and tested assessment tool, we are concerned about its potential use in the context of the NDIS as a standalone tool.

This change by the NDIA undermines the ability for psychologists โ€“ and other professionals โ€“ to work with participants to ensure that NDIS supports are appropriate and best placed to contribute to building a person's capacity, and increasing their independence and participation in the community.

The NDIS assessment process needs to be fit for purpose and consistent with the principles of the Scheme, which is to promote participantsโ€™ choice and control.

Any assessment process that attempts to be a โ€˜one-size-fits-allโ€™ solution often overlooks details which can be very important for individual NDIS participants.

We are continuing to call on the Government to engage actively, meaningfully and transparently with psychologists, the APS, and other allied health professionals in designing and implementing reforms to the NDIS.

Read more from APS President Dr Kelly Gough in The Guardian: https://ow.ly/qOC850Y0rkz

09/01/2026
OPAA are taking a short break to rest and recharge with our families. We wish you all a happy and healthy festive season...
20/12/2025

OPAA are taking a short break to rest and recharge with our families. We wish you all a happy and healthy festive season. Thank you for your ongoing support this year. We will be returning to work on the 5th of January 2026!

17/12/2025

The Child Development Services team is seeking young volunteers (aged 6 months to 5.5 years) to help train Paediatric Registrars in developmental assessments.

This is a great opportunity for your child to engage in a relaxed, informal session while helping doctors develop their skills.

When:
โ€ข 2 โ€“ 4 February 2026

Where:
โ€ข Murdoch Community Hub

During the session, your child will take part in activities that assess motor skills, hearing and speech, eye/hand coordination, social development, and more, all guided by Paediatric Registrars.

Parents are welcome to join, ask questions, and enjoy the experience together!

Places are limited, so donโ€™t wait โ€“ sign up now via our online form:
https://forms.office.com/r/z1JQTPAjgc

Wonderful road map for those wonderingโ€ฆ what next?
10/12/2025

Wonderful road map for those wonderingโ€ฆ what next?

25/11/2025

We are seeking expressions of interest from parents and youths to participate in a two-hour online workshop to better understand the experiences of Western Australian students with learning differences.

Your insights will guide the development of a statewide survey that will be launched in 2026.

What participation involves:

You will be invited to join one two-hour online workshop focused on shaping the design, content and priorities of the statewide survey.

To ensure everyone feels safe and able to share openly, workshops will be held separately for:

1๏ธโƒฃ young people aged 15 to 24 years who can speak to their current or recent experiences in Western Australian schools;

2๏ธโƒฃ parents and caregivers of children with learning differences.

No formal diagnosis is needed to take part.

This project is inclusive of students with experience in any education setting in WA: public schools, independent and Catholic schools, distance education, home education or unschooling families.

Your voice can help highlight what is working and what needs to change.

Submit an expression of interest today: https://redcap.link/ImpactforLearningDifferences

This research is focused on learning differences that are supported by the WA Department of Education's Educational Adjustment Allocation (EAA).

Address

250 Oxford Street, Leederville
Perth, WA

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