Transplant Australia FC Chairman Ante Kelic: “There is no shortage of people who need support”

In an event that has been a long time coming, Transplant Australia Football Club will hold the inaugural Transplant Football World Cup in Cervia, Italy on September 8-14, 2024.

Due to COVID-19 being a major roadblock, the tournament has not been able to lift off – however with the dedication and perseverance of Transplant Australia and the World Transplant Games Federation, it is now going to be a reality.

It is headed by Transplant Australia, which is a charity that supports transplant recipients and their families, while also lending support to people on the waiting list, donor families, living donors, healthcare professionals and everyone associated with organ and tissue donation.

Transplant Australia FC is one example of the many sports and activities on offer that encourage physical activity for an increased chance of survival in transplant recipients.

As the Chairman of Transplant Australia FC, Ante Kelic has gone through his own experience and is now the perfect role model for others in a similar position, while also managing the operations ahead of September’s tournament.

In this interview with Soccerscene, Kelic discusses his involvement with Transplant Australia, an update on the World Cup, building a community and looking ahead over the coming months.

Tell us about your background and why you are involved?

Ante Kelic: I started playing in junior competitions for St Albans Dinamo out in Melbourne’s west.

I grew up with the game very much part of my life, however around the age of 18 years I started having a few health issues and was diagnosed with a liver condition called primary sclerosing cholangitis (PSC).

There was not too much trouble apart from the initial onset symptoms and flare ups such as a headache and swelling and for the most part I did not feel the full effect of it for another 3-4 years.

In the year 2000, I also got diagnosed with Crohn’s disease which isn’t uncommon for people who suffer from PSC.

At that time, I broke  into the seniors for St Albans, but it all came to a halt when I required surgery for Crohn’s disease at the age of 20. From 80 kilograms being a fit and active player, my weight  dropped down to 54kg.

The recovery was slow and through all the medications and treatments, I was hoping to get back to playing Premier League senior football but the side effects such as weight gain as a result of  fluid retention  lead me to   player in the lower divisions.

At the age of 34 I was playing social soccer, however I was told during that time  I needed a transplant as cirrhosis was getting to a serious stage of liver failure.

It was in 2014 that I got put on the transplant list and needed to wait seven months before I was offered the lifesaving transplant. At the same time my wife was four months pregnant and thankfully my daughter Iva was born soon after without major hiccups.

How did you find out about Transplant Australia FC?

Ante Kelic: It was in 2018 that I found out about the team through the late Matty Hempstalk who established the team two years prior.

I was introduced to the team by participating in an exhibition match which was known as the Doujon Zammit Shield – this was in honour of Doujon who passed away, but his parents donated his organs to save multiple lives.

A few years later, Matt – along with the CEO of Transplant Australia – came up with the idea to create an inaugural World Cup for transplant recipients and I thought that I could give a helping hand as it was something that involved heaps of work to organise.

With Matt’s passing, coupled with the pandemic, it has taken us a bit of time to recover and get back on our feet but now it is something I will contribute towards.

You had an Expression of Interest period for participants, what are the numbers looking like?

Ante Kelic: We ran a large campaign for a couple months that saw around 50 applications from men and women all around Australia who want to join the club.

In addition, we are going to run a development camp in Sydney on March 16-17 to get people together and support each other based on their transplant journeys.

Our main purpose is to help people with ongoing health issues and encourage active participation.

The underlying reason why we are there is to create awareness and educate people on the life saving gift of organ donation and the donation sign up process.

On your role as Chairman, what are the main priorities?

Ante Kelic: There is no shortage of people who need support before and after transplant.

Peronsally I have had not only with liver transplant recipients, but also those undergoing cancer treatment and that shock of being unwell and going into hospital where your life changes from that point – that is where I am willing to offer support and advice drawn upon my health journey.

To have someone to talk to is super important and I have also reached out to people myself when there were instances I lost energy or motivation during the difficult times.

The wait time for transplants can be mentally challenging – I waited seven months but some other recipients in my support group had to wait for more than two years. If you throw in the fact that hospital call ups do not always guarantee a transplant due to an inadequate match occurring, it is not easy to comprehend – I know of someone that had received the news four times.

Unfortunately, you do not know how far you get through the waiting list in terms of pecking order, so this is a challenge that we offer support and advice for.

How is it juggling your responsibilities?

Ante Kelic: There are some challenges to fit it all in with a young family and running my own business, but we do have some staff at Transplant Australia who do an excellent job supporting the club.

Part of the reason that the development camp in Sydney is going ahead is down to the Transplant Australia team securing a grant to benefit recipients.

Particularly for us, one of the factors is the distance between team members, making it costly to hold events due to travel and accommodation costs.

There is representation Australia-wide, so we offer in some instances where possible to subsidise recipients for travel, accommodation and meals for them to be able to attend these camps and remain active

Even though recipients recover from transplants, they can still have ongoing issues with their health they need to manage which affects their work and earning capacity. As a club, and Translpant Australia, we want to build longevity and sustainability to support the recipients in every way we can.

A lot of recipients reach out stating they want to do something more regularly and having a club in local competitions would be a great milestone.

Our goal is to increase the participation numbers and generate awareness through the amazing stories shared about the life saving donations that people have received.

However, we cannot do that without government, community and corporate sponsorship support.

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Two NPL VIC clubs receive funding boost from State Budget

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

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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