Access Through Action

Access Through Action We connect, build capacity, and remove barriers โ€” increasing confidence and supporting independence through practical, person-centred solutions.

Empowering informed choices, real inclusion, and access to intelligible language and supports.

02/09/2026

Capacity outcomes matter, but can't be achieved or demonstrated while systems don't collaborate on the continuity of access across more than one task or environment at a time. Why complicate it, secure personal access first and independent ability to participate wherever possible. One well considered device, can replace multiple.

09/08/2026

When new devices are upgraded, it doesn't mean they always behave the same way.

Have you upgraded your cochlear processor lately..

If your finding that your Bluetooth connectivity drops out try this. If it helps, please like and follow our page.

To fix a Cochlear Nucleus 8 (N8) that stopped connecting to Bluetooth, forget the processor in your phone's Bluetooth settings, restart both your phone and the N8 processor by turning it off and on again, and re-pair the device through your phone's accessibility menu or the Nucleus Smart App.

Quick Troubleshooting Steps Forget the device:

Go to your phone Bluetooth settings, find your N8, tap "Forget This Device" or unpair it.

Power cycle:
Turn your smartphone completely off and back on. Turn your N8 processor off (remove battery or place on charger) and back on.

Toggle Bluetooth:
Turn your phone's Bluetooth off for 10 seconds, then turn it back on.

Re-pair fresh:
Put the N8 into pairing mode and reconnect it through your device settings or the Cochlear Pairing Guide instructions

Fingers crossed!

Getting out and about today, I look forward to catching up with people and exploring options that empower.
30/07/2026

Getting out and about today, I look forward to catching up with people and exploring options that empower.

28/07/2026

Is it really an ACCESS problem, or an APPROACH problem? ๐Ÿค”

One of the most useful questions we ask in AT Mentoring is this: when something isn't working, is the barrier actually about access, or is it about how the task is currently being attempted?

They can look identical from the outside, but they need completely different solutions.
๐Ÿ”น ACCESS barrier
The environment, equipment, or information genuinely isn't reaching the person the way they need it to.
Example: A child can't follow the teacher in a noisy classroom because there's no FM/Roger system connecting to their hearing device.
โ†’ The fix here is about removing the barrier: better equipment, better environmental setup, better connection.

๐Ÿ”น APPROACH barrier

The access is actually fine, but the way the task is being done doesn't match how this person takes in and processes information.

Example: A child has a working FM system, but instructions are still only ever given verbally and quickly, with no visual backup, no processing time, and no way to check understanding. The fix here isn't more equipment. It's adjusting the strategy: how instructions are given, paced, or supported.

Why this matters:
If you treat an approach problem as an access problem, you can end up adding equipment or funding requests that don't actually solve anything and the person still struggles, but now it looks like "the tech didn't work" rather than "the task needs to be done differently."
And if you treat an access problem as an approach problem, you can end up asking someone to "try harder" or "adapt" to a situation that genuinely isn't accessible to them.

The starting point is always the individual's profile: how they actually take in, process, and communicate information. From there, we can properly separate:
โœ… what needs to be removed or upgraded (access), and
โœ… what needs to be adjusted or taught differently (approach)

Once you know which one you're dealing with, the right strategy usually becomes a lot clearer.

If you're not sure which one is showing up for your child or yourself, that's exactly the kind of thing we work through together.

"CONNECT with us to IDENTIFY the barrier, ADJUST the approach, and ACHIEVE the outcome."

Built-In Accessibility and Apps: Tools Already On the Device...A lot of accessibility support is already sitting on phon...
24/07/2026

Built-In Accessibility and Apps: Tools Already On the Device...

A lot of accessibility support is already sitting on phones, tablets, and laptops, unused, because nobody told families it was there.

Reading (dyslexia traits)
Built-in text-to-speech (Speak Screen, Select to Speak, Immersive Reader)
Adjustable font, spacing, and background colour
Read-aloud apps that highlight text as it's spoken.

Writing (dysgraphia traits)
Built-in dictation and voice-to-text
Word prediction keyboards
Apps to plan out loud before typing.

Maths (dyscalculia traits)
Apps showing quantity visually before a written number
Visual number lines built into learning apps
Calculator access as an accommodation, not a shortcut

Working memory:
Built-in reminders, visual timers, step-by-step checklists
Apps that break instructions into one step at a time
Recording apps to replay instructions

Visualising language:
Some children don't naturally form a mental picture from words. Certain apps pair language with image, symbol, or sequence, so a picture builds alongside the words
None of this replaces a proper assessment. But most of it costs nothing and is already sitting in settings menus.

If your child is working hard just to access the task, it's worth checking what's already built in.

Reading for Life: A Program That Gives Confidence Back.I want to be clear from the start. This is not a promotion. I hav...
24/07/2026

Reading for Life:
A Program That Gives Confidence Back.

I want to be clear from the start. This is not a promotion. I have no relationship with this program beyond my own lived experience using it as a parent.

I'm sharing it because it did something for me that very few things did in those early years.
It gives confidence back.
Not confidence that things would "catch up" or fit some standard timeline. Confidence that what you're doing is actually working. As a parent, that's sometimes all you need.

You can put in the time every single day, but if you don't believe the strategies are landing, that time feels like a fight. Reading for Life changed that for us.

Here's what I noticed most. The switch wasn't really about the reading itself. It was about the sheer enjoyment of attempting the task. The moment something stops looking, feeling, or sounding overwhelming, a huge hurdle disappears before you even get to the reading part.
Reading avoidance and behavioural avoidance go hand in hand. A task that feels gruelling and exposing will be avoided every time it can be, and that avoidance so often gets read by adults as defiance, laziness, or lack of effort. It's none of those things.
It's a nervous system trying to avoid something that feels unsafe or impossible.
When a task is broken down properly, it can feel like a game instead of a test. That shift alone changes willingness to try.

One thing I've learned through this: knowing what the barrier is doesn't automatically tell you how to target it. Naming a diagnosis is not the same as knowing what to actually do at the kitchen table. Programs like this are valuable because they sit in that gap, between the diagnosis and the daily practical strategy.

If you're a parent standing in that gap right now, wondering if what you're doing is enough, I see you.

Keep looking for the tools that make the attempt feel possible. That's often the whole battle.

You may talk to your school, perhaps raise it at a P&C meeting, ask your school if they can support introducing the program which provides the tools, when schools can support these initiatives it does more than just provide tools, it creates collaboration, consolidates support across environments, provides the child structured activities and concrete manipulative tools they can build rather than have to have broken down. This feeds into further stepping stones and available programs often seeing continuity of learning and greater outcomes due to the foundations that came before.

Reading for Lifeยฎ - Learning Links

Reading for Life is a fully funded school-based program that empowers children in Years 2-4 who are having difficulties or falling behind in their literacy development.

24/07/2026

Soft AT and Hard AT: Two Halves of the Same Toolkit.

When people hear "Assistive Technology" they usually picture a device. A tablet. A piece of software.

But AT for a child with dyslexia is bigger than that.
There are two types of AT, and both matter.

Hard AT is the equipment.
Text-to-speech tools
Audiobooks
Word prediction software
Coloured overlays or reading rulers
Recording apps for lessons

Soft AT is the strategy. The human side. The way a task is set up so the child can access it at all.

Chunking instructions into smaller steps.
Reading a question aloud before a child starts independent work.
Giving extra processing time before expecting a response.
Pairing pictures with text.
Letting a child show what they know out loud, not just on paper.

Here's the part that gets missed. A hard AT tool without the soft AT strategy around it often fails. Text-to-speech doesn't help if a child hasn't been taught when and how to use it. An audiobook doesn't help if nobody has built in the time to listen.
The equipment opens the door. The strategy is what gets the child through it.

For primary-aged kids with dyslexia, the two need to work together every day, not just during reading time. Spelling, maths word problems, science instructions. All of it.
If your child's plan only lists the device, ask what's happening around it. That's usually where the real support lives.

Creating Smart Goals within an ILP, is a key foundational need to ensure the child's barriers are captured, understood with a plan to bridge the gap on ability to access the curriculum, retain information and express themselves in a way that suits them.

02/06/2026

Acoustics and your deaf child โ€” the things that actually matter.

Hard floors, high ceilings, and bare walls don't just echo. They actively compete with every word your child is trying to hear.

Here's what makes the biggest difference:

๐Ÿ”น Rugs on hard floors โ€” the single highest-impact change. Even one large rug in the main living area reduces reverberation noticeably.

๐Ÿ”น Soft furnishings โ€” couches, cushions, curtains. They absorb sound. Hard surfaces reflect it. The more reflective the room, the harder your child's auditory system is working just to separate speech from noise.

๐Ÿ”น Talk with them, not across the room โ€” face-to-face at close distance beats a perfect acoustic room every time. Position matters more than distance.

๐Ÿ”น Turn off competing background noise โ€” TV on in another room, dishwasher running, fan overhead. These aren't neutral. They're signal killers.

๐Ÿ”น Quiet the kitchen โ€” extractor fans are loud. So are benchtops. If the kitchen is where your family talks, it's where your child is working hardest.

None of this requires renovation. It requires attention.
Your child's listening environment is something you can actually change.

29/05/2026

๐Ÿง  Just thinking out loud โ€” "Ozempic Ear" and a hypothesis I can't stop turning over
There's been growing chatter in health communities about people on Ozempic, Wegovy and similar GLP-1 medications experiencing ear symptoms โ€” tinnitus, muffled hearing, ear fullness, and pressure. It's been loosely coined "Ozempic ear" and while it's not yet an official side effect, the reports are significant enough that researchers are starting to pay attention.
I've been reading the emerging research and I want to share a hypothesis โ€” and I want to be really clear, I am not a medical professional. This is me, someone who spends a lot of time in the hearing and access space, connecting dots that I think are worth a conversation.
Here's what I think might be happening:
These medications cause rapid weight loss. That weight loss includes fat tissue around the Eustachian tubes โ€” the tiny channels that connect your middle ear to your throat and regulate ear pressure. Lose that cushioning quickly and those tubes can become structurally compromised. We already see this happen after bariatric surgery.
At the same time, GERD and reflux are among the most strongly reported side effects of GLP-1 medications โ€” across every drug in the class. And here's where it gets interesting: there's solid existing research showing that laryngopharyngeal reflux (silent reflux) can travel up to the throat, inflame the Eustachian tube openings, and cause exactly the kind of ear symptoms people are reporting โ€” pressure, fullness, tinnitus, even hearing loss.
So my hypothesis is a two-hit model:
๐Ÿ‘‰ Weight loss strips the structural support from the Eustachian tubes
๐Ÿ‘‰ Reflux then inflames those already-compromised tubes
๐Ÿ‘‰ The result is middle ear pressure disruption and the hearing changes people are experiencing.
This isn't me diagnosing anyone or telling anyone what to do. It's me saying โ€” if you're on a GLP-1 medication and you're noticing ear changes, please mention it to your GP or ENT. And if you have pre-existing silent reflux, that context matters.
The research is young. The conversation is just starting. But I think these dots are worth connecting.
๐Ÿ‘‚ Not medical advice. Always consult your treating health professional.

14/05/2026

The Cost of Self-Advocacy

There is a moment that happens in environments more than anyone documents.

A child has already said what they need. Clearly. Through the right channels. In the right meetings.

Sometimes more than once, or repeated by a trusted person.
Nothing changes.
So the child reacts. They push back, shut down, disengage, or say something in a space they should never have had to say in a space. And in that moment, the conversation changes. It is no longer about the access that was not provided. It is about the child's behaviour. Their attitude. Their ability to cope.

The access failure disappears from the record. The child's response to it does not.
This is what the cost of self-advocacy actually looks like. It is not just exhausting. It is reframing. A child who was failed by a system becomes a child who is struggling. A child who was right becomes a child who is difficult. Ability gets questioned where access should be. And the child learns something they should never have to learn.
That speaking up changes nothing except how they are perceived.

I've learnt that Self-advocacy is not a skill you can teach a child in isolation. It only works when the adults around them are consistent, when provisions are upheld without the child having to fight for them in real time, and when a child's silence is not mistaken for agreement.
When those conditions are not in place, asking a child to self-advocate is not empowerment. It is exposure.

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