Hugo's Hero's

31/03/2026

We love our support from Indigicare Connect and the wonderful women at Vital Health Louisa Greste, Dianne Morris,

🧠💪 Living with Muscular Dystrophy means learning life skills that empower independence—even as your needs change. https://bit.ly/44s42Zj

💚You don’t have to do it alone. With the right support system and care team, you're capable of shaping a life that works for you.

👇 What life skill has helped you feel more independent?

31/03/2026

Please share our flyer.

If you would like to donate to our MONSTER RAFFLE, please reach out.
Raffle tickets and special coffee mugs also available to purchase with the QR Code.

28/03/2026

🧠💪 Living with Muscular Dystrophy means learning life skills that empower independence—even as your needs change. https://bit.ly/44s42Zj

💚You don’t have to do it alone. With the right support system and care team, you're capable of shaping a life that works for you.

👇 What life skill has helped you feel more independent?

21/03/2026

Sign up and join the Hugo's Hero's team and host a morning tea for a cause!

Want to make a delicious difference this April? ☕🍰

Host a morning tea for Muscular Dystrophy Queensland and help support Queenslanders living with neuromuscular conditions.

We’ll give you everything you need to get started, including optional merch to sell on the day to boost your fundraising, just ask and we’ll get you sorted.

Sign up, gather your crew and pop the kettle on: https://www.redbow.org.au/

20/03/2026

Calling all Hero's who don't live in St George!

Want to do something but can not attend the event?

You can donate directly to Muscular Dystrophy Queensland, or sign up to the cause and join our team and host a morning tea at your work, business or school!

Click on the link to find out more!

Make a donation today to support people with muscular dystrophy

20/03/2026

Coffee Mug pre-orders available now!

$20 each with all profits going to Muscular Dystrophy Queensland

https://www.eventbrite.com.au/e/hugos-heros-bottomless-brunch-tickets-1983655949343?utm-campaign=social&utm-content=attendeeshare&utm-medium=discovery&utm-term=listing&utm-source=cp&aff=ebdsshcopyurl

18/03/2026

🎀 WE WANT YOU! 🎀

Hugo’s Heroes is calling on our incredible community to help make something special happen this Mother’s Day.

We are hosting a Mother’s Day Morning Tea fundraiser in support of the Red Bow Appeal for Muscular Dystrophy Queensland, and we’re currently looking for local sponsors and prize donations to help bring the event to life.

There are lots of ways businesses and community members can get involved:

🎁 Donate prizes for our raffles or lucky door draws
☕ Support the morning tea with sweet or savoury treats
❤️ Become an event sponsor and help cover event costs

Every contribution helps us raise vital funds and awareness for families living with muscular dystrophy.

📅 Event: Mother’s Day Morning Tea
📍 Location: St George Bowls Club
🗓 Date: Saturday 9 May 2026

If you or your business would like to support this event, we would love to hear from you.

📧 [email protected]

📞 0460 364 311

You can also send us a message through the Hugo’s Heroes social pages.

Together we can make this Mother’s Day event something truly special for our community. ❤️

28/02/2026

Today is rare disease day!
Such an elite club to be apart 💪

22/02/2026

Just a little nudge… 🎀

Have you locked in 9 May 2026 yet?

Our Hugo’s Heroes Bottomless Brunch at St George Bowls Club is on its way, proudly supporting the Red Bow Appeal and raising vital funds for Muscular Dystrophy Queensland.

It’s more than brunch.
It’s community, connection and giving back. ❤️

Make sure you’re following our page so you don’t miss ticket details, raffle prizes and event updates.

Pop on a red bow. Bring your people. Let’s do some good together.

12/10/2025

🎥 New clip + quick update from Team Hugo

Hey Hugo’s Heroes family — a little update from Hugo’s mum. ❤️

Hugo’s had a few setbacks lately with his tummy, so we’ve been doing some tests and had to slowly wean him off his steroid while we figure out the next steps. We’ve got appointments coming up (big one on Wednesday) — fingers crossed we get some clear direction soon.

The clip really shows something important: Hugo and Poppy are twins, but they have different superpowers. Poppy’s a natural climber, and Hugo’s working so hard on his steps — and that contrast is exactly why we share these moments. Every small win matters, and every challenge is part of their story.

If you’ve got a kind thought, a cheer, or a tip — drop it below. Your love, messages and tiny cheers give this little family a huge boost. 💙🦎✨

With thanks,
— Hugo’s mum & Team Hugo

10/09/2025

Every hero needs the right gear!

For boys with Duchenne Muscular Dystrophy, night-time leg braces (like Hugo’s super-splints 💥) are more than just equipment, they’re a secret weapon.

✨ They fight off stiffness (contractures) while our little heroes sleep
✨ Help keep ankles strong and flexible
✨ Make walking and moving easier during the day
✨ Protect independence so kids can stay active for longer

And here’s the real superpower: early diagnosis + early intervention.
The earlier Duchenne is picked up, the sooner families can access supports like night braces, physio, and treatment plans that change futures. 💙

Together, we can help our heroes rise, run, and keep chasing adventures.

10/09/2025

Every hero needs the right gear!

For boys with Duchenne Muscular Dystrophy, night-time leg braces (like Hugo’s super-splints 💥) are more than just equipment — they’re a secret weapon.

✨ They fight off stiffness (contractures) while our little heroes sleep
✨ Help keep ankles strong and flexible
✨ Make walking and moving easier during the day
✨ Protect independence so kids can stay active for longer

And here’s the real superpower: early diagnosis + early intervention.
The earlier Duchenne is picked up, the sooner families can access supports like night braces, physio, and treatment plans that change futures. 💙

Together, we can help our heroes rise, run, and keep chasing adventures.