ELISE CASSIDY

Nominee for what Award/s

Amplifier of Good Award

Amplifier of Good Award


1.       What cause or mission lights you up the most?


For over 20 years I’ve had a fire up my backside and a passion in my heart for making a difference to the lives of kids with dyslexia. Helping bright, creative kids with dyslexia to finally see themselves the way we see them. Not as broken, or behind, or difficult, but as whole, capable, and full of potential.

I’m a speech pathologist and run a clinic to assess and teach kids with dyslexia. There’s something heartbreakingly common in the stories I hear every week. A child who once loved learning begins to shut down. A parent who’s done everything they can still feels lost and unheard. A school meeting ends in more confusion than clarity. And somewhere in the middle of it all is a child, trying harder than anyone realises, who starts to believe they’re “just not smart.”

That’s what lights a fire in me.

Because it’s not that these children can’t learn. It’s that they haven’t been taught in a way that works for them. And more than that, they’ve often absorbed the message that their struggle is a reflection of their intelligence or worth.

It’s not. And it never was.

My mission is to change that.

I want every parent to walk into a school meeting with confidence and clarity, not fear and overwhelm. I want every child with dyslexia to understand how their brain works, not just so they can learn to read, but so they can believe in themselves again. And I want to be part of shifting the system, from one that waits far too long to act, to one that sees, supports, and celebrates neurodiversity from the start.

So while my work began as teaching kids with dyslexia how to read and write, this work is now so much more than that. It’s about identity. It’s about protecting a child’s sense of self. It’s about giving families answers, hope, and a plan.

That’s the mission that lights me up every single day. And I don’t think I’ll ever stop fighting for it.

 

2.     How have you used your platform or business to create positive change?

 

At its heart, my business has always been about creating change. Not just for individual children, but for families, schools, and the broader conversation around dyslexia in Australia.

As a speech pathologist with nearly 30 years of experience, I’ve worked with hundreds of bright, creative kids who were falling through the cracks. Kids who were trying harder than anyone realised, but who still couldn’t seem to make sense of the letters on the page. Kids who’d started to believe they were stupid because no one had helped them understand how their brain works.

My clinic, Little Voices Speech Pathology, exists to change those outcomes. Through one-on-one therapy, school visits, and family education, we don’t just teach reading, we rebuild belief. We help kids feel capable again. And we equip parents with the tools and understanding they’ve so often been denied.

Outside the clinic, I’ve used my voice online to reach thousands of families who may never step into my therapy room. Through Instagram, newsletters, and a growing library of free resources and webinars, I offer practical, compassionate support to parents who are often overwhelmed, exhausted, and unsure who to trust.

I also created my signature course, Navigating Dyslexia, to walk families through the journey step-by-step, because access to clear, evidence-based guidance shouldn’t be about where you live or what you earn.

But creating change means more than helping the families who find me. It also means working to change the system itself.

I’m also proud to be a founding member of the Code Read Dyslexia Network—a volunteer organisation fighting for a future where all kids are screened for dyslexia early, taught with proven methods, and seen for who they really are.

Through Code Read, I’ve spoken at conferences, manned information stalls, and stood alongside other passionate advocates to raise awareness and push for better policy. Because every child deserves to be understood, and every parent deserves answers, not roadblocks.

Everything I do, through my business, my courses, my volunteer work, and my content, comes back to this:

Changing the story for children with dyslexia.

And I won’t stop until that change is real, lasting, and nationwide.

 

3.     Tell us about a moment you saw your "good work" ripple outward.

It’s so hard to pick just one moment. There are dozens.

Like the day Sam, a funny and sporty 10-year-old who’d been labelled the “naughty kid,” finally read a paragraph aloud, and believed he could do it. He told me he used to get sent to the principal’s office on purpose, he chose to be the naughty kid, just so no one would find out he couldn’t read. He said, “If I’m the bad kid, no one thinks I’m the dumb kid.” That moment where he saw himself differently was so powerful. But it was what happened next that showed me the ripple.

His mum called me weeks later to say, “He’s reading signs in the street. He wants to read menus now.” His confidence had begun to touch every corner of his life.

Or Lucy’s mum, who walked into my clinic with a notepad filled with every missed word and spelling mistake, convinced she was doing something wrong. After our sessions, she told me, “I finally feel like I understand her. I can actually advocate for her now.” The next school meeting? She went in calm, clear, and grounded. And she walked out with the support her daughter deserved.

Then there are the teachers.

One emailed me after a masterclass: “I’ve been teaching for 20 years and no one ever explained dyslexia to me like that. I used your strategies with a student today, and she finally got it. Her face lit up.”

Those are the ripples.

When a child starts to believe in themselves again…
When a parent goes from confused to confident…
When a teacher changes their approach and unlocks learning for a whole classroom…

That’s how change spreads.

It starts small, in therapy rooms, Zoom calls, school staffrooms, but it doesn’t stay there.

The good work echoes. In kids’ voices. In parents’ advocacy. In classrooms across Australia.

And that’s the most rewarding part of all.

2.     What obstacles did you face while amplifying others?

 

One of the hardest things about advocating for children with dyslexia, and the families who love them, is facing the walls that shouldn't be there in the first place.

Time and time again, I’ve walked alongside parents who are doing everything right. They’re listening to their child, following their instincts, seeking support, only to be told by schools, “There’s nothing we can do without a diagnosis,” or worse, “We don’t have funding for that.”

 

And they’re not wrong.

In Australia, there is no specific funding, not from health or from education, for children with dyslexia. None. They don’t get NDIS despite it being a disability, and they’re not included in the Disability funding schemes in education in any state.

If a child is struggling to read, there’s no automatic support plan. No early screening. No funded intervention. To even begin the process, parents are often told they need a formal diagnosis. But a diagnosis typically costs upwards of $1000. This is a barrier that makes help completely inaccessible for many families. So they wait. And while they wait, their child continues to fall further behind.

So many of the families I support have been stuck in that loop - schools saying they can’t do anything without a diagnosis, but no pathway for how to get one. And children, caught in the middle, quietly losing confidence in themselves day after day.

I’ve had schools push back when I suggest evidence-based intervention, claiming they don’t have the staff, the training, or the budget. I’ve had parents tell me they feel gaslit. Told they’re overreacting, or worse, imagining the problem.

And yet, we keep going.

Because I’ve seen what happens when a parent understands dyslexia and finds their voice. I’ve seen teachers shift from “I don’t have time” to “What can I do differently?” because someone gave them the tools and the language to act.

The obstacle is the system. The solution is information, empathy, and relentless advocacy.

That’s what I try to offer every day, because these kids can’t afford for us to give up.

3.     What’s your bigger vision for making an even greater impact?

My bigger vision is simple.

I want to live in a country where no child ever believes they’re “dumb” because reading is hard. Where dyslexia is recognised, understood, and supported from the start, not after years of struggle.

Where families don’t have to fight tooth and nail just to be believed, let alone get help.

Where support isn’t a privilege for those who can afford a $1000 + diagnosis but a right for every child, regardless of postcode, income or parent’s education level.

That’s the future I’m working toward.

I dream of a world where every teacher is trained to recognise the signs of dyslexia early, and knows exactly what to do next. Where schools don’t wait for a label before providing intervention. Where early screening is standard practice in every Prep classroom across the country.

I want every parent to feel confident walking into a school meeting, not anxious or afraid, and every child to see themselves not as a problem to fix, but as a person with strengths worth celebrating. Where every child knows their worth.

And I believe we can get there.

Through my clinic, I’ll keep supporting kids one-on-one, because change starts with individual transformation. And I’ll keep educating schools and teachers about what these kids need, to help them to see it as a human rights issue. Every child deserves the right to learn to read.

Through my online course, I’ll keep educating and empowering parents, because an informed parent is a powerful force.

Through my content, I’ll keep reaching families who haven’t been heard yet, because they deserve to know they’re not alone.

And through my advocacy with Code Read Dyslexia Network and beyond, I’ll keep pushing for policy change, because until the system shifts, too many children will be left behind.

My bigger vision is a system that sees every child clearly.

That acts early.

That teaches differently.

And that never lets a learning difference define a child’s potential.

That’s what I’m here to build. And I won’t stop until it’s real.