Our ambassadors

We are proud to have the support of our Ambassadors to help promote International Day of People with Disability (IDPwD) and share their unique experiences and perspectives.

03:54

(Maree Jenner) My big question is...

(James Parr) My big question is...

(Isabella Choate) My big question is...

(Ronan Soussa) Would you rather your disability be seen or hidden?

Oh wow!

I am a blind electrical engineer.

I do inclusion programs in schools.

I'm a model, a disability advocate, and Wiradjuri man.

My pronouns are they/them,

and I am a living experience advocate.

I want to make a difference

for all people with disabilities.

(Santiago Velasquez) And I am an ambassador.

(Isabella Choate) I'm an ambassador.

(Ronan Soussa) I'm an ambassador

for International Day of People with Disability.

- Hello everybody! - Nice to see you.

- I'm keen to get started. - Yeah.

(Olivia Sidhu) 'Would you change anything about your disability?'

That's a good question.

That's a good one.

(Santiago Velasquez) All of the experiences that I have had,

I wouldn't have had if I didn't have this disability.

(Isabella Choate) There's a narrative that people

with disability should wish to be different.

We should wish that we don't have our disabilities.

(Maree Jenner) It's given me such inherent strengths.

(Olivia Sidhu) It's just a part of who I am and who we are.

(James Parr) The only thing I would change is the perception

and the narrative that comes with having a disability.

The portrayal that disability is the worst thing

that could happen to you or it's a bad thing.

Every media that we're exposed to all builds a perception.

Every experience of people with a disability

where we're included, I think will

help rewrite the narrative.

(Santiago Velasquez) The more we can break down the perception that people

with disabilities need to be fixed,

the more we can move forward as a society.

My big question is 'for somebody with your disability,

how has the technology revolution been?'

(James Parr) 'Why do you think the media avoids

showing people with a disability

as sexual or desirable?'

(Isabella Choate) 'Can you give me an example of disabled rage

and disabled joy?'

I think International Day of People with Disability

is a really great opportunity

for the Australian community to consider how we feel

that we’re different and how we feel that we're the same.

(Olivia Sidhu) I am proud of everything that I do.

I am also pretty normal too.

(Ronan Soussa) Do you know what I like to say?

“Different isn't less. Different is necessary.”

(Maree Jenner) Disability, it's the diversity of human nature.

It's the assumptions, often the attitudes that people have.

For some reason we are less

because we are not able to do the things the same way

as everyone else,

but we bring to the table such an interesting group

of skills and talent as a result of our diversity.

My big question is,

'when you look towards the next generation,

what gives you hope for the future?'

(Ronan Soussa) More representation in media,

that's something good for the future.

(Olivia Sidhu) Exposure like this

allows people to learn

to be more inclusive

and accepting of people with disabilities.

(Isabella Choate) Young people who are proudly claiming their disability.

(Maree Jenner) They are much more inclusive and accepting.

(Santiago Velasquez) When I'm walking down the streets

and little kids are genuinely curious. I say to people,

ask questions because if you don't know, you don't know,

but don't put us in a box.

Yes, I'm blind, but some people are tall,

some people are short, some people

are different ethnicities.

We're just another mix in this massive pot

we call the world.

(Ronan Soussa) People with disabilities deserve to be seen,

heard and valued in all spaces.

(Isabella Choate) Disability is a culture.

There is a community and it's beautiful,

and I am proudly disabled.

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2025 Ambassadors

If you are interested in becoming an Ambassador, contact us at idpwd@health.gov.au.

Isabella Choate

Isabella Choate (they/them) is multi-award-winning Living Experience Advocate, passionate about community building and platforming the voices of young people with disability.

Isabella founded WA’s first Disability Pride Festival after winning WA Young Person of the Year 2024, and at 25, became CEO of the Youth Disability Advocacy Network, finalist for Young Australian of the Year (WA) and made the Forbes 30 Under 30 list.

02:19

My name's Isabella Choate.

My pronouns are they/them

and I am a living experience advocate.

I'm also an ambassador for

International Day of People with Disability.

I used to be an elite athlete on the Australian team

for canoe slalom.

I was diagnosed with a chronic illness in year 11.

I ended up being bedbound for about eight months.

It was about six years of isolation

and really, really struggling

before I even considered the disabled community.

My big question is

'can you give me an example

of disabled rage and disabled joy?'

Oh, that's a good one. That's a good question.

Yeah.

People are surprised by the things that I'm joyous about.

Seeing other disabled people out and about,

going out to lunch with my friends

and we've dressed up all of our mobility aids

and we look fantastic.

If people are going to look at me,

give them something to look at.

(Ronan Soussa) Paralympics, wheelchair basketball, is like joy,

because it's not just about the disability,

it's what people can actually do.

(Maree Jenner) Joy for me was when I first connected

with the Short Statured People of Australia.

When we go out, it's pretty joyful.

Disabled rage is an experience that is unique

to people with disability.

It is a human right that people

with disability should be allowed in any space.

It's okay to be upset when you are discriminated against.

(Santiago Velasquez) My rage comes when somebody says,

"Trey can't come in."

I can be refused and you feel powerless.

But my joy is the opposite,

when people realise I'm just another person.

International Day of People with Disability

is a really great opportunity

for the Australian community to consider how we feel

that we are different and how we feel that we're the same.

Like many, many Australians, I didn't have anything to do

with disability, or so I thought.

Disability is a culture.

It's not a look, it's not just a definition.

It's not just a way to access different benefits.

There is a culture, there is a community, and it's beautiful,

and I'm proudly disabled.

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Maree Jenner

Maree Jenner (she/her) is a long-time advocate of participation and engagement in her community. She facilitates the Social Futures school inclusion program, ‘Same but Different & Champions for Change’, which aims to remove social barriers and encourage inclusion for people with disability.

Beyond the classroom, she drives community change through her roles with the Central Coast Council’s Access and Inclusion Reference Group, Accessible Arts NSW, and Short Statured People of Australia.

02:04

A young girl said to me one day, she said,

"You've grown up little,"

and her father was like, "Oh!"

And I went, "Your daughter's brilliant."

'Cause I have, I've grown up,

and I am little.

My name's Maree and I live on the wonderful Central Coast.

I love to travel, but I also like to get out

and about and riding my bike.

I'm a disability advocate and I'm an ambassador for

International Day of People with Disability.

My big question is,

'when you look towards the next generation,

what gives you hope for the future?'

I'm the only person with short stature in my family.

Going to school, that was hard.

Some of the children at school decided that it was okay

to mock and laugh at me.

I had to learn early to stand up for myself,

and that's the part of my living with disability.

It's given me the strength to be an advocate, to speak up

and challenge people's thinking.

(Isabella Choate) Something that gives me hope for the future

is our younger generations

who are proudly claiming their disability.

(Ronan Soussa) More representation in media

to raise awareness as well.

(Santiago Velasquez) When I'm walking down the streets

and little kids are genuinely curious.

(James Parr) Having the next generation advocate for us and with us.

I love their thinking.

Now, I tell them when I apply for a job,

"Do you think I wrote, I had short stature or dwarfism?"

And they said, "No, it doesn't matter."

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James Parr

James Parr (he/him) is an award-winning model, speaker, content creator, writer, athlete and advocate. He is a proud Wiradjuri man and uses his role to talk about inclusivity and diversity in the modelling industry.

James won the GQ Model of the Year Award in 2023, was included on the Forbes 30 Under 30 list for 2024 and is a TedX speaker on intersectionality.

02:01

I acquired my disability when I was 21.

I remember when I woke up from surgery,

everyone's attitudes around me,

the doctors’ and the nurses’, instantly changed.

I was just like constantly hearing people tell me

that they felt sad for me and sorry for me,

and I didn't really connect with that.

I'm James. I'm a model, a disability advocate

and Wiradjuri man.

And an ambassador for

International Day of People with Disability 2025.

Being an ambassador is really important to me

to challenge and keep rewriting the narrative

of what it's like to have a disability.

My big question is why do you think the media

avoids showing people with a disability

as sexual or desirable?

We're all humans, we all have desire,

and a part of desire is also to be sexual.

(Isabella Choate) There is an ongoing issue where the general public

seems to infantilise people with disability.

(Maree Jenner) It's the lack of representations.

People think we live life with a deficit,

where it's exactly the opposite.

(Ronan Soussa) I truly agree with you

because like you just think of yourself

as a regular person.

Going back into dating after acquiring a disability

was like a whole different experience.

And, in that, what I did find is a narrative there

that they're like going to be a helper or a caregiver.

I think having more people with disability in media

and in mainstream spaces is probably the most important.

And when I first started modelling,

actually it was my first runway,

and I remember a kid, I think he was about five or six,

and he was using a prosthetic,

and to be able to watch him and his reaction

when he saw me up on the screen,

he probably had never seen someone like him before.

My hopes for the future is just have people with disability

as characters or within media, just there as people,

just showing us living life as someone else would.

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Ronan Soussa

Ronan Soussa (he/him) is an Autistic advocate, performer and piano player. He is mostly known for his appearance on the second season of ‘Love on the Spectrum’ on ABC and Netflix. Ronan’s mission is to encourage people with disability to be their authentic selves.

02:08

You know what I like to say?

“Different isn't less.

Different is necessary.”

I'm Ronan. I'm 26 years old,

and I'm an ambassador

for International Day of People with Disability.

Creative arts have been such a big part of my life.

I love to sing, act, dance, model,

and I'm very passionate about motor racing.

All of these creative arts that I do,

it gives me a lot of confidence inside me.

My big question is,

'would you rather your disability be seen or hidden?'

Oh, wow.

That's cool.

(Olivia Sidhu) Being seen

because it shows what I can do

in the community.

(Isabella Choate) For me, whilst I wouldn't change my disability,

I think it would be easier to navigate the world

with people understanding that I do have a disability.

And I think that's why I do things like, you know,

wearing a sunflower lanyard

or pins, you know? - You know what?

You guessed it.

So, the sunflower lanyard represents hidden disabilities.

Many times autism can be like known as invisible

or a hidden disability,

and I really like to raise more awareness because of this.

If people saw me wearing a sunflower lanyard,

that way they will know, just try to be patient.

I want others to think of the things that they can do.

Like, I'm a black belt in karate.

People with disabilities deserve to be seen,

heard and valued in all spaces.

It's all about acceptance

and embracing diversity, for a more inclusive future.

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Santiago Velasquez Hurtado

Santiago Velasquez Hurtado (he/him) is the CEO and founder of two companies, an accomplished innovator, designer and the first blind electrical engineer in the Southern Hemisphere.

Santiago utilises his lived experience and degree in electrical engineering to invent solutions to make the world more accessible. As a UN panellist, Churchill Fellow and TedX speaker, he is determined to change the way the world perceives people with disability.

02:14

Yes, I'm blind, so what?

I love listening to music, cooking,

trying new, unusual things.

I flew a plane last weekend, like an actual real plane.

That's not a joke.

Hi, my name is Santiago.

Everything that I always wanted to do,

I have always given it a go.

And now I'm a blind electrical engineer

and I am an ambassador for

International Day of People with Disability 2025.

My big question is 'for somebody with your disability,

how has the technology revolution been, good or bad?'

I run a company called Hailo, and I started it

because I was frustrated by buses leaving me behind.

And if I fix that or if I fix the problem

of being dropped off at the incorrect stop, in a way

that benefits me but benefits everybody else,

we can improve public transport for everybody.

(Maree Jenner) For me personally, I think

Siri and Alexa is fantastic.

For light switches and things,

I can turn lights on with it.

(Olivia Sidhu) Technology is good

because it helps us to travel,

to use transport.

(Isabella Choate) The creative solutions that tech

or tech companies are coming up with, I think a lot

of them are coming from people with disability.

When the people who need it the most

are either developing it

or right there from the beginning,

technology is brilliant.

But it's when people

that are designing it have no lived experience,

getting to this mindset of technology is

going to fix my life,

that we get into trouble.

The more we can break down the perception that people

with disabilities need to be fixed,

the more we can move forward as a society.

Everybody has to play an equal part

for getting rid of this idea that we are a burden.

I'm not a second class citizen

and I'll be damned if somebody's going to tell me otherwise.

Yes, I'm blind, but some people are tall,

some people are short, some people are

different ethnicities.

We're just another mix

in this massive pot we call the world.

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Olivia Sidhu

Olivia Sidhu (she/her) is a health ambassador for Down Syndrome Australia and has represented Australia as a civil society delegate at the United Nations in 2023.

02:00

My family is my everything.

I have three brothers

and they are loud and crazy.

I love spending time with them.

I can travel, I can have a normal life,

and live the best life.

Hi, my name is Olivia Sidhu

and I have Down syndrome.

I love makeup and fashion

because it makes me feel trendy.

I am also an ambassador for

International Day of People with Disability.

For me, there is no challenges in my disability.

I work at the Down Syndrome New South Wales

as an inclusion support officer.

I go and present to medical students.

It is important to include us in our own health

and speak to me and not to parents,

so that we are informed about our own health.

So my big question is

'would you change anything about your disability?'

Oh, that's a good one.

(James Parr) I wouldn't change anything

about my disability within myself.

The only thing I would change is the perception

and the narrative that comes with having a disability.

(Ronan Soussa) Different isn't less, different is necessary.

(Maree Jenner) It's given me such inherent strengths.

I wouldn't change anything about my disability.

It's just a part of who I am and who we are.

I want to make a difference for all people with disabilities

and making a voice for them.

I am proud of everything that I do.

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