Indigenous Football Week 2024 power to break down barriers

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Image credit: Moriarty Foundation

Indigenous Football Week 2024, running from 23 to 29 September, will bring the football community together to highlight the sport’s ability to transform the lives of Australia’s most vulnerable children and youth.

Indigenous Football Week (IFW), an initiative by John Moriarty Football (JMF) with support from A-Leagues and Professional Footballers Australia (PFA), will feature the annual Moriarty Cup, Australia’s leading charity football tournament raising funds for JMF’s ongoing programs.

The 2024 Moriarty Cup, hosted at Sydney’s iconic Allianz Stadium, will feature 14 teams from prominent Australian companies such as Paramount+, Optus, Stan, Channel Nine, MinterEllison, and Charter Hall. They will compete for football glory while supporting Indigenous children and youth in remote and regional Australia.

The theme of Indigenous Football Week 2024, ‘Breaking Barriers,’ is inspired by the life of JMF co-founder and first Indigenous Socceroo, Yanyuwa man John Moriarty, football and education transformed his life, lifting him out of poverty.

John Moriarty, Co-Founder of John Moriarty Football, explained the positive impact the initiative has on children’s faces.

“I love seeing the big smiles on the children’s faces when I visit community and join them on the football oval. Those smiles tell a story of wellbeing, resilience and opportunity. It’s why more children attend school on the days JMF runs its sessions. After our in-curriculum sessions, they concentrate better and show more positive behaviours,” he said via press release.

“More engagement with education, and improved mental and physical health – this is the power football has to change lives, just as it changed mine.”

A-Leagues and Professional Footballers Australia (PFA) will back Indigenous Football Week, celebrating alongside fans, players, and clubs.

A-Leagues Commissioner, Nick Garcia, added further comments.

“The A-Leagues is excited to see another instalment of the Indigenous Football Week, celebrating the ongoing contribution of Indigenous football players to the game. The power of football to influence impactful change is unlike any other and the A-Leagues is proud to support the John Moriarty Foundation,” he said via press release.

IFW and JMF are initiatives of the Moriarty Foundation, an Indigenous children’s charity focused on creating a thriving future for Aboriginal and Torres Strait Islander kids. Through innovative programs, the foundation is helping close gaps in education, health, wellbeing, and employment to achieve cultural, social, and economic equality for Indigenous children.

JMF’s sister program, Indi Kindi, is an early learning initiative for children from birth to five years. It combines a distinct Aboriginal teaching approach with the Australian Early Years Learning Framework. Graduates of this program are culturally strong, ready for school, and equipped with a lifelong foundation for learning.

For more information on Indigenous Football Week 2024, click here.

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Two NPL VIC clubs receive funding boost from State Budget

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Image credit: Football Victoria

Following the announcement of the 2026 Victoria State Budget, Avondale FC and Hume City FC will both receive major backing for facility upgrades.

 

Valuable support for future projects

Avondale and Hume City now have immensely valuable financial support for infrastructure and facility upgrade projects.

Avondale will see an injection of $500,000 for lighting developments at its home ground, Avenger Park. Meanwhile, Hume City FC, will receive $250,000 to further improve its home ground, Nasiol Stadium, which opened in 2009.

Both clubs expressed their delight at the funding from the State Labor Government, and what the backing may bring to club facilities and overall development going forward.

“We are incredibly grateful to the Victorian Government and Sheena Watt for their support through this $500,000 lighting upgrade investment, which will have a lasting impact on our players, families and the wider Avondale community,” said Avondale Club President, Stephen Strano.

“We have hundreds of players across all age groups utilising these facilities each week, and these improvements will help create an even strong environment for excellence, participation, and community engagement,” outlined Hume City President, Ersan Gülüm.

As a result of these respective investments, both NPL VIC outfits appear set for incredibly opportunities to modernise, develop and strengthen their club infrastructure.

 

Lighting the path to a brighter future

The investments will see features such as lighting upgrades improve facility access for men’s and women’s teams, and LED scoreboards become part of a more modern matchday experiences going forward.

For both clubs, however, lighting upgrades are about more than keeping a pitch open late at night. Improved lighting is a means to a more accessible and supportive future in which both the men’s and women’s teams can utliise local facilities, and matchdays can take place in the excitement of playing ‘under the lights’.

And as Football Victoria CEO, Dan Birrell, highlighted, the improvements made to club facilities are benchmarks for the wider Victorian football community.

“Both Avondale and Hume City are pillars in the Victorian football landscape,” Birrell stated via press release.

“Professional level facilities like Avenger Park and Nasiol Stadium are critical for the development of Victorian football and Football Victoria welcomes the news that they will continue to improve thanks to the support of the Victorian State Government.”

 

More must follow

While the investments from the State Government come as welcome updates for these two clubs, there is still plenty more to be done to evenly develop facilities and infrastructure across Victoria’s football landscape.

Indeed, Avondale FC and Hume City FC are two fantastic community clubs who will no doubt put the funding towards impactful improvements.

But there are plenty more who still need external backing to build infrastructure not just for now, but for future seasons to come.

Football Community Supports Ange Goutzioulis Following MND Diagnosis

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Image Credit: One Nil Media

At just 52 years old, former National Soccer League player Ange Goutzioulis stood in front of a packed room at the Chisholm United launch night in Oakleigh and spoke about something no one ever expects to hear: a diagnosis of Motor Neuron Disease.

But rather than retreat into silence, Goutzioulis chose to speak openly. He spoke not just about the disease itself, but about the reality of living with it, the uncertainty ahead and why awareness matters more than ever.

 

Early stages

For years, football was part of Goutzioulis’ identity. Coaching, movement and routine were all things that once felt natural. Then slowly, something changed.

“I couldn’t even stand properly… I was losing my balance,” he explained.

At first, the signs were confusing rather than alarming. A couple of falls. Difficulty moving. Hospital visits and tests.

“They said, ‘You haven’t got cancer, you haven’t got MS and you haven’t got MND,’” he recalled.

But the symptoms continued worsening. Eventually, further neurological testing revealed the diagnosis: Motor Neuron Disease (MND).

The confirmation came quickly.

“They called it after two or three minutes… they saw the machines and basically said, ‘Yeah, you’ve got MND.’”

The shock was immediate.

So too was the reality.

 

Understanding Motor Neuron Disease

Motor Neuron Disease is a progressive neurological condition that attacks the nerves controlling movement, gradually taking away the ability to walk, speak, swallow and eventually breathe.

There is currently no cure.

For many Australians, awareness of MND remains limited until it touches someone close to them. Goutzioulis now finds himself confronting not only the physical decline, but the emotional weight of understanding what lies ahead.

“There’s no way to stop it… it’s going to kill me,” he said honestly.

Even breakthrough treatments tomorrow, he acknowledged, may come too late for him personally.

Yet despite the enormity of that reality, his focus has already shifted beyond himself.

 

Fighting for awareness while fighting the disease

What stood out throughout the evening was not despair, but resilience.

Goutzioulis spoke candidly about refusing to surrender mentally to the disease. Against medical advice centred around conserving energy and managing fatigue, he continues trying to stay active.

“I keep walking,” he said.

“I’ve got a theory in life that if you work out and keep moving, maybe [your] muscles won’t waste away as quick.”

Whether medically proven or not, the mentality reflects something deeper: a refusal to let MND define every remaining moment.

There was also optimism in the small victories.

Doctors believe he may have already been living with the disease for three years — longer than expected given his current condition.

“That’s a positive,” he said. “So, I’ll take it day by day.”

Image Credit: One Nil Media

Football’s power beyond the pitch

The event itself quickly transformed from a club launch into something more profound: a reminder of football’s ability to rally around people during their hardest moments.

As speakers addressed the room, one message became clear — Goutzioulis is not facing this battle alone.

“There’s probably 100 people here,” said Bill Kosmopoulos, who was hosting the discussion,

“I guarantee there’s 100 people cheering for you, 100 people that would do anything to find a solution for MND.”

In community football, conversations are usually dominated by results, signings, tactics and ambition. But nights like this reveal another side of the game entirely.

Connection.

Humanity.

Support.

By speaking publicly, Goutzioulis gave a deeply confronting disease a human face. Not statistics. Not headlines. A person. A father. A football figure. Someone trying to process what it means to slowly lose control of their own body while still showing up for the people around them.

That vulnerability is precisely why awareness matters.

Because awareness drives conversation.

Conversation drives funding.

And funding drives research that could one day change outcomes for future families facing the same diagnosis.

Image Credit: One Nil Media

“We’re behind you”

As the night closed, the room rose behind him.

Showing admiration for someone willing to confront unimaginable news publicly in the hope it helps others understand the devastating reality of MND.

“On behalf of everyone… thank you so much mate,” one speaker told him.

“We’re behind you.”

Support and raising awareness for the disease is what matters.

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