Thirty Years of Purpose

Celebrating Andrea Alexander’s extraordinary contribution to Child Cancer Research Foundation

By Michele Dalton

1 July 2026

Some careers are measured in years.
Others are measured in the lives they help change.

Today, Child Cancer Research Foundation (CCRF) celebrates an extraordinary milestone as Chief Executive Officer Andrea Alexander marks 30 years with the Foundation.

For three decades, Andrea has dedicated her professional life to improving the lives of children, adolescents and young people affected by cancer. Since joining CCRF in 1996, she has helped shape an organisation that has invested more than $45 million into childhood cancer research while continually evolving to meet the changing needs of children and families.

Over those 30 years, childhood cancer research has changed dramatically. Survival rates have improved for many cancers. Treatments have become more effective. Research that once seemed impossible has become reality. Thousands of children who once faced an uncertain future are now living longer, healthier lives because researchers refused to stop asking difficult questions.

Andrea has had the privilege of witnessing that progress every step of the way. She has celebrated research breakthroughs alongside scientists. She has stood beside families during unimaginable heartbreak. She has worked with volunteers, thanked donors, supported clinicians, and watched generations of children grow into adults.

She has also witnessed another important change. As research has helped more children survive, it has become increasingly clear that surviving cancer is only part of the journey. Many children, adolescents and young adults continue to face lifelong physical, emotional, educational and social challenges long after treatment ends.

Recognising that need has helped shape the Foundation’s next chapter. While remaining committed to funding world-class childhood cancer research, Andrea has also helped guide CCRF’s expansion into survivorship, recognising that helping children thrive beyond cancer is just as important as helping them survive it.

Yet despite everything that has changed, one thing never has. Children and families have always remained at the heart of every decision.

Reflecting on her 30-year journey, Andrea says she has never lost sight of why the Foundation exists.

“I’m most proud that we’ve never lost sight of why we’re here. Over the past 30 years, I’ve had the privilege of helping grow CCRF from a small charity into an organisation that has funded millions of dollars in childhood cancer research and, more recently, expanded our work to support young survivors beyond treatment.

Knowing we’ve played a part in improving outcomes for children and families across Western Australia is something I’ll always be proud of. But more than anything, I’m proud of the incredible people I’ve worked with — our volunteers, donors, researchers, Board members, staff and families — who have made every achievement possible.”

For three decades, Andrea has quietly become one of the constants in the lives of countless families, researchers, volunteers and supporters. While childhood cancer research has evolved, treatments have advanced and the Foundation itself has grown, Andrea has remained a steady presence, building relationships, preserving the Foundation’s history and ensuring children and families have always remained at the heart of every decision.

Andrea would never write those words about herself. Which is exactly why they deserve to be written.

 

The custodian of a Foundation

For CCRF Chair Tracy Hollington, Andrea’s contribution reaches far beyond her role as Chief Executive Officer.

“Over the past 30 years, Andrea has become far more than the CEO of Child Cancer Research Foundation. She is the custodian of our history, our relationships and our purpose. Her knowledge of the Foundation is unmatched, but it is her unwavering commitment to improving the lives of children with cancer and their families that has truly defined her career.

Andrea has helped guide CCRF through decades of growth and change, always keeping our mission at the heart of everything we do. On behalf of the Board, I thank Andrea for three decades of exceptional service, leadership and dedication. Her contribution to this Foundation and to the countless children and families we have supported over the years is immeasurable, and we look forward to the impact she will continue to make in the years ahead.”

For Tracy, Andrea has become the thread connecting the Foundation’s past with its future. The person who has quietly carried its knowledge, protected its values and ensured that, through every challenge and every opportunity, the focus has remained exactly where it belongs. On children and their families.

“It’s about the kids.”

Andrea’s journey with CCRF began in 1996. Having recently returned to Perth from Melbourne, she was encouraged to apply for the role of Executive Officer after a chance conversation with then Board member Kim Williamson.

She remembers walking into the interview with long-serving Chair Geoff Cattach AM, Kim Williamson and John Myers. When asked what she could bring to the role, Andrea drew on her years of experience working at Princess Margaret Hospital.

“I said, ‘Well, I have a history with the Foundation and with the hospital. I started working there back in 1979 in Medical Records. I know the people, and I know how the Foundation works.’ They said, ‘You’ve got the job.'”

Nearly 30 years later, reflecting on that interview together during her anniversary celebration, Andrea laughed as she asked Geoff a question she had always wondered.

“Were there any other interviews for the job?”

Geoff smiled. “Just you.”

As the conversation continued, Geoff reflected on what had always mattered most when choosing the people who would help lead the Foundation. “The most important word in life is attitude,” he said.

For Geoff, the role was never about titles, status or personal ambition. He wanted people who understood why the Foundation existed and who would always put its mission before themselves.

Reflecting on those early years, he recalled being frustrated by applicants who made the role about themselves rather than the children the Foundation existed to help. Then, in a sentence that has quietly shaped CCRF’s culture for decades, he summed up the Foundation’s purpose.

“It’s about the kids. We’re here to raise money to save kids’ lives.”

Looking back over Andrea’s 30 years with CCRF, it’s easy to see why Geoff believed she was the right person for the role. She brought exactly the attitude he believed mattered most: humility, compassion and an unwavering commitment to putting children and families first.

 

A survivor’s perspective

Few voices capture Andrea’s impact more powerfully than those of the children whose lives have been shaped by childhood cancer. For childhood cancer survivor and CCRF Ambassador Georgia Lowry, Andrea’s contribution is impossible to separate from her own journey.

As Georgia reflected on Andrea’s milestone, emotion quickly took over. When asked what Andrea has meant to her personally, she struggled to find the words.

“As a childhood cancer survivor, I honestly can’t put into words what Andrea means to me. I don’t think I ever could. People like Andrea and the incredible team at CCRF are the reason I’m here today. Knowing there are people who have quietly dedicated their lives to helping children and families like mine is incredibly comforting. It’s not just a job for Andrea. It’s her passion, and you feel that in everything she does.”

For Georgia, what stands out most is not what Andrea has achieved, but how she has achieved it.

“What I admire most is that Andrea never makes it about herself. She quietly steps out of the spotlight and works tirelessly behind the scenes, making things happen and creating opportunities that change lives.”

When asked what she would say to Andrea directly, Georgia’s voice once again reflected the gratitude of so many families.

“When I think of CCRF, I think of Andrea. Her dedication, consistency and heart have shaped the Foundation for 30 years. Congratulations, Andrea. Every day, every effort and every sacrifice has been noticed. You should be incredibly proud because we certainly are.”

Listening to Georgia speak, it became clear that Andrea’s legacy cannot be measured only in research grants funded or fundraising milestones achieved.

It is measured in trust, and in hope, and in knowing that, through some of life’s darkest moments, there has always been someone quietly working behind the scenes to help make tomorrow a little better than today.

 

More than a colleague

Few people have worked alongside Andrea for as long or as closely as Kylie Dalton. Over more than 13 years, Kylie has watched Andrea lead through periods of growth, challenge and change, seeing first-hand the quiet determination, resilience and consistency that have become hallmarks of her leadership.

When asked what has always stood out to her, Kylie didn’t mention a single campaign, event or fundraising milestone. She talked about consistency.

“I’ve worked alongside Andrea for more than a decade and what has always struck me most isn’t any single achievement. It’s the consistency. Organisations like CCRF experience incredible highs when research breakthroughs happen or a family’s story reminds us why we do this work, but they also face incredibly difficult moments where the outcomes aren’t guaranteed. Andrea has been the constant through all of it. She doesn’t waver when things get hard, and she never seeks the spotlight when things go well. That quiet steadiness is rare, and it’s exactly what an organisation supporting children and families affected by cancer needs at its heart.

People probably don’t realise what 30 years of service really represents. More than $45 million has now been invested into childhood cancer research, but that kind of impact isn’t built through one campaign or one successful year. It’s built by someone who simply keeps showing up, year after year, always putting children and families first. Even now, Andrea is helping lead CCRF into its next chapter through the AYA Cancer Survivorship Program, ensuring the Foundation continues to evolve as the needs of children and young people change. That willingness to keep growing after 30 years says everything about who she is.”

After speaking with so many people for this story, one word surfaced again and again.

Consistency.

Not because anyone had compared answers. But because everyone had experienced the same thing. Over three decades, Andrea has simply kept showing up.

 

A perspective only he could offer

Few people have known Andrea for as long as Justin Bruce. A childhood cancer survivor, Board Director and Treasurer, Justin’s connection with Child Cancer Research Foundation spans almost his entire life. His family’s involvement with the Foundation stretches back more than four decades, with his father, Phil Bruce, first joining the Board in 1982 before serving as Vice Chair from 2012. Justin continued that legacy, serving as a Board proxy from 2008, becoming a Director in 2012 and Treasurer in 2020.

Asked to reflect on Andrea’s 30 years, Justin’s words were simple, heartfelt and deeply personal.

“Well done, Andrea, on your 30-year anniversary with CCRF. You truly are a remarkable person. Your compassion, dedication, empathy and resilience are second to none.

Hundreds of children owe their livelihood to the work you’ve contributed over the past three decades. I have to help kids in need, because of my connection to childhood cancer. You don’t have to, and that’s a credit to who you are. Thank you.”

There are many reasons people dedicate themselves to helping children affected by cancer. For Justin, it comes from lived experience. For Andrea, it came from a decision she made almost 30 years ago. One that has quietly changed countless lives ever since.

 

“Just saying your name makes me smile.”

As Patron of Child Cancer Research Foundation, Justin Langer AM has stood proudly beside Andrea for many years, helping champion the Foundation’s work and encourage the Western Australian community to support children with cancer.

Rather than sending written thoughts, Justin recorded a heartfelt video message. It began with a sentence that instantly captured the affection so many people feel for Andrea.

“Andrea Alexander. Just saying your name makes me smile. I’ve always believed you judge champions in life by their longevity, and when it comes to 30 years with Child Cancer Research Foundation, you are an absolute champion. A legend.

What has always stood out to me is your kindness and your selflessness. For three decades, you’ve dedicated your life to helping others, and the impact you’ve had on so many children, families and the Foundation itself is truly inspirational.

As Patron of CCRF, I’m incredibly proud to have worked alongside you. I’m constantly blown away by everything you’ve done for the Foundation and by the quiet way you’ve gone about it.

Congratulations on an extraordinary 30 years, Andrea. Thank you for everything you’ve given to CCRF. And remember this… there are some people in life whose name alone makes you smile. You’re one of those people. You’re a legend.”

Others spoke about Andrea’s leadership. Her compassion. Her consistency. Justin reminded us of something equally important. The joy she brings to the people around her.

 

A life well spent

When asked what has kept her inspired for three decades, Andrea’s answer once again turned the spotlight away from herself. It wasn’t a fundraising milestone, or a research breakthrough. It was hope.

“Hope. Every breakthrough, every child who reaches another birthday, every family who tells us they felt supported, every researcher who shares exciting progress, it all reminds me that what we do makes a difference.”

Looking back, Andrea says it has never been about working for people. It has always been about working with them. As she reflected with Geoff during her small 30th anniversary impromptu office celebration, she smiled and said: “I don’t work for them, I work with them.”

She then looked around the room at the people who had gathered to celebrate with her: staff, board members, volunteers, survivors, friends. People who had shared different chapters of the same journey.

“I feel very privileged to work with the people that I work with… We’ve all got the same interest. We want kids to have better lives.”

When asked what she hopes people remember about her time at CCRF, her answer reflected exactly the woman everyone else had described.

“I hope they’ll remember that I always put children and families first. I hope they’ll remember someone who cared deeply, who listened, who brought people together and who never stopped believing that we could do better. If I’ve helped leave CCRF stronger, more compassionate and better equipped to improve the lives of children and young people affected by cancer, then I’ll consider that a life well spent.”

Over the past 12 years of working with Andrea, one thing has become abundantly clear to me. Andrea would probably be the most uncomfortable person reading an article like this.

She has spent three decades quietly celebrating everyone else’s achievements, rarely stopping to acknowledge her own. She’s far more interested in talking about the children, the families, the researchers, the volunteers and the supporters who make CCRF’s work possible.

That’s exactly why this story deserved to be written.

Over the past few days, I’ve had the privilege of speaking with people whose lives Andrea has touched over three decades.

– A past Chairman who entrusted her with the future of the Foundation.
– A Chair who describes her as the custodian of its history, relationships and purpose.
– A childhood cancer survivor who couldn’t find the words to explain how much Andrea means to her.
– A Patron whose face lights up simply by saying her name.
– A Board Director and survivor who reminded us that while he helps because childhood cancer became part of his own story, Andrea simply chose to.
– A colleague who has watched her quietly lead with consistency for more than a decade.

Not one of them spoke first about Andrea’s title. Not one spoke first about fundraising. Or awards. Or achievements.

Every one of them spoke first about her heart.

Andrea, my greatest hope is that through these reflections, perhaps for the first time, you’re able to see yourself through the eyes of the people whose lives you’ve touched.

I hope you see what we all see. Because after 30 years of quietly celebrating everyone else…

It’s finally your turn.

Thank you for an extraordinary 30 years.

Perhaps no words capture Andrea’s journey better than her own.

“Thirty years ago, I joined CCRF hoping to make a difference. Looking back, I’ve realised that it’s the children, families, supporters and colleagues I’ve met along the way who have made the greatest difference to me.” — Andrea Alexander

 

CCRF Chair Tracy Hollington Brings Lived Experience Voice to National Childhood Cancer Forum

Child Cancer Research Foundation (CCRF) Chairperson Tracy Hollington has represented both Western Australia and the lived experience community today at the inaugural Children’s Cancer CoLab Forum 2026 in Melbourne.

Held at the Peter MacCallum Cancer Centre, the national forum brought together researchers, clinicians, advocates and lived experience representatives from across Australia to explore the future of childhood cancer research, treatment and survivorship care.

Tracy was invited to speak as part of a clinical research session examining how real-world evidence and patient experience can help improve outcomes for children and adolescents diagnosed with cancer. The session explored topics including financial toxicity, equitable access to care, survivorship, supportive care, precision medicine and long-term treatment impacts.

Drawing on her family’s own experience following her son Angus’ diagnosis with Ewing Sarcoma and later treatment-related Acute Myeloid Leukemia (AML), Tracy spoke openly about the lifelong effects childhood cancer can have on young people and their families long after treatment ends.

“We know the drill. Chemotherapy is damaging. It’s chemical warfare against cancer,” Tracy said during her presentation.

“But chemo is often the best we have, and that’s why we are here. Because our kids deserve better.”

Angus was just 11 years old when he first complained of pain in his leg. What initially appeared to be a simple ache soon became a diagnosis that would change the course of his life and his family’s future.

Over the years that followed, Angus endured surgeries, chemotherapy, extended hospital stays and complex limb salvage procedures. More than four years into remission, routine blood tests revealed another devastating diagnosis — treatment-related Acute Myeloid Leukemia caused by the chemotherapy used to treat his original cancer.

“The chemotherapy he had caused another, more deadly cancer,” Tracy said.

Angus ultimately underwent an amputation followed by a stem cell transplant during the height of the COVID-19 pandemic. Today, he lives with significant long-term health impacts including cardiomyopathy, infertility, neurocognitive challenges and disability resulting from treatment.

Tracy’s presentation highlighted the growing national conversation around survivorship and the reality that while childhood cancer survival rates have improved significantly, many survivors continue to face lifelong physical, emotional, educational and psychosocial challenges.

“Survival isn’t the end of the story,” Tracy said.

“We need better treatments that cause less fallout. We need stronger psychosocial support and systems that recognise the lifelong impacts childhood cancer can have on young people and their families.”

Her presentation also explored the often-overlooked impact childhood cancer has on siblings, family stability, education and future employment opportunities.

“I could talk about the impact on my daughter, and how siblings become the forgotten ones in this experience,” Tracy shared.

“How they suffer the same loss and grief with very little support, and how as parents we are in constant crisis and barely able to meet their needs let alone our own.”

CCRF is proud to see Tracy representing both the organisation and the lived experience community on a national stage, helping ensure the voices of survivors and families remain central to the future of childhood cancer research and care.

As Australia continues to improve survival outcomes for children diagnosed with cancer, forums such as the Children’s Cancer CoLab Forum play an important role in driving conversations around not only cure, but quality of life, survivorship and long-term wellbeing.

For more than four decades, CCRF has funded childhood cancer research while continuing to advocate for improved outcomes for children, adolescents and survivors affected by cancer.

Professor Nick Gottardo recognised for advancing childhood cancer treatment in WA

The Child Cancer Research Foundation (CCRF) congratulates Professor Nick Gottardo on being named a finalist for Western Australian of the Year 2026, recognising his significant contribution to childhood cancer treatment and research.

Professor Gottardo is Clinical Director of the WA Comprehensive Kids Cancer Centre and a leading paediatric oncologist whose work has helped improve outcomes for children facing cancer, particularly children diagnosed with brain tumours.

According to reporting by The West Australian, Professor Gottardo has led the Australian and New Zealand AIM BRAIN project, which uses advanced molecular profiling to improve diagnosis and personalise treatment pathways for children with brain cancers. The program has helped move childhood cancer care away from a “one size fits all” approach and toward more precise, targeted treatment based on the individual biology of each child’s tumour. Importantly, the work also focuses on reducing the long-term impacts many survivors experience following treatment.

“The goal is not only to cure more children, but to do it with kinder, less toxic treatments,” Professor Gottardo told The West Australian.

That focus strongly aligns with the growing recognition across the childhood cancer sector that survival alone is not enough. Today, around 80 per cent of children diagnosed with cancer survive, but many continue to face lifelong physical, cognitive and emotional impacts from treatment. Research that improves both survival and long-term quality of life is critical.

At CCRF, we know progress in childhood cancer happens because of researchers, clinicians, families and supporters all working together to improve outcomes for children and young people. Recognition like this highlights the importance of continued investment in childhood cancer research, innovation and survivorship support here in Western Australia and across the country.

We congratulate Professor Nick Gottardo and the wider childhood cancer community on this well-deserved recognition.

Source: The West Australian, Kirsty Lichtenstein, 22 May 2026.

Survivors Are Speaking Up About Life After Childhood Cancer

Childhood cancer survivorship is no longer a quiet conversation. Survivors and families across Australia are increasingly speaking up about what happens after treatment ends, and the challenges that follow.

Recent national coverage, including reporting by The Canberra Times, reflects a growing call for better long-term support. Survivors are describing the ongoing reality of managing their health, navigating complex systems, and carrying the responsibility of coordinating their own care well into adulthood. This shift is being driven by lived experience.

A recent story shared by the Children’s Cancer CoLab highlights the experience of Maryjo, who was diagnosed with cancer at 12 after losing vision in her left eye. Her treatment involved intensive chemotherapy, radiation, and multiple surgeries. While she reached remission, the need for ongoing care did not stop.

Now 27, she continues to attend regular scans and medical appointments, while managing her own care across multiple providers. Her experience also reflects the broader impact on families, including the loss of her younger brother to the same disease. Her story is one of many now contributing to a broader national conversation.

Child Cancer Research Foundation Chair, Tracy Hollington, has seen this firsthand. Drawing on her own experience as a parent, she has spoken about the period after treatment as a “free fall”, where the structure of hospital care ends and families are left to navigate ongoing needs without a clear pathway.

For many, the challenge is not the absence of services, but the lack of connection between them. Survivors and families are often left to piece together support across health, education, and community systems, creating an ongoing burden at a time when stability is critical. As more survivors share their experiences, a clear pattern is emerging. The system has made significant progress in treatment, but is still catching up when it comes to long-term care.

At Child Cancer Research Foundation, this shift is shaping future priorities. Alongside funding research into improved treatments, there is a growing focus on survivorship and the need for more coordinated, accessible support that reflects the realities families are describing.

The conversation is changing. Survivors are making that clear. The question now is whether the system can respond.

Read the Articles:
Angus and Tracy Hollington

Surviving Childhood Cancer Is Not the End of the Story

More children than ever are surviving childhood cancer. It is a significant medical achievement. But survival comes with a cost.

A recent ABC News article has highlighted a growing concern across Australia’s childhood cancer sector. Many survivors are now living with long-term and chronic health conditions caused by the treatments that saved their lives. These impacts can include heart damage, infertility, cognitive challenges, and ongoing mental health needs.

For families, the end of treatment is not the end of the experience. It is the beginning of a new and often complex phase.

Hollington FamilyChild Cancer Research Foundation Chair, Tracy Hollington, contributed to this national conversation as part of her role on the Children’s Cancer CoLab Patient and Family Advisory Committee. Tracy brings both professional expertise and lived experience. Her son was diagnosed with Ewing Sarcoma at age 11 and later developed secondary Acute Myeloid Leukaemia as a result of treatment. While now cancer-free, he continues to live with the long-term effects of that treatment.

Her experience reflects what many families face. When treatment ends, support often reduces significantly, leaving families to manage ongoing health concerns, education disruption, and emotional recovery with limited coordination between services.

As Tracy has shared, the transition out of hospital care can feel like a “free fall”. There are services available, but accessing and coordinating them is complex. For families already carrying the trauma of treatment, this adds another layer of pressure.

This is where the gap sits. The current system is heavily focused on acute treatment, but not designed to support the long-term realities of survivorship. As survival rates improve, this gap is becoming more visible and more urgent.

At CCRF, this is a key area of focus. Our work continues to fund research into better, less harmful treatments. At the same time, we are increasing our focus on survivorship, including improving understanding of late effects, advocating for coordinated long-term support, and ensuring lived experience informs future solutions.

Survivorship is not a single moment. It is a lifelong experience. Children who survive cancer deserve the chance to live well beyond it, with a system that supports them not just through treatment, but through life. Read the full ABC News article

Read the article

Run for a Reason: Join Team CCRF & Help Fund Childhood Cancer Research

Perth’s biggest running event is back! On Sunday, 25 May 2025, thousands of West Australians will take to the streets for the HBF Run for a Reason, and you can be part of something bigger by running for the Child Cancer Research Foundation (CCRF).

This is your chance to run, walk, or roll to support vital childhood cancer research—ensuring better treatments and brighter futures for kids facing cancer. Sign up now!

Why Choose Team CCRF?

By joining Team CCRF, you’ll be making a real difference for WA kids battling cancer.

💙 100% of funds raised go directly to childhood cancer research in WA
💙 Support ground-breaking research that improves treatment options
💙 Raise awareness and be part of a community fighting for better outcomes

Choose Your Challenge

🏃‍♂️ CommBank 3km – A great option for families & first-timers
🏃‍♀️ Specsavers 12km – The perfect middle-distance challenge
🏅 Brooks Half Marathon – Take on the ultimate test of endurance

How to Get Involved

1️⃣ Register for the event at the official HBF Run for a Reason website
2️⃣ Select Child Cancer Research Foundation (CCRF) as your chosen charity when setting up your fundraising page
3️⃣ Start fundraising and training – Every dollar you raise supports life-changing research

🔥 Don’t miss out! Early bird pricing ends 4 March – sign up today! 🔥

Not a runner? You can still make a difference!

Even if you’re not taking part in the run, you can still support Team CCRF by donating or spreading the word. Every contribution brings us closer to better treatments and outcomes for children fighting cancer.

👉 Join Team CCRF & Start Fundraising Today

Together, we can take steps towards a future where every child with cancer has a chance to survive and thrive.


Consulate Court Residents Light Up to Beat Child Cancer

The residents of Consulate Court, Thornlie are once again lighting their houses for Christmas and in turn helping raise vital funds for child cancer research.

Each December the residents of Consulate Court ‘light up’ their street to celebrate the Festive Season, spreading joy amongst the community and bringing smiles to the thousands of visitors the street attracts throughout the month.

Consulate Court, Thornlie is a well-known Christmas Lights Street in Perth. Residents have been ‘lighting up’ on 1 December each year for the past 30 years.  Nine houses in the Cul-de-sac are lit with each home adding new features in 2023. The displays are interactive with musical toys, laser light shows, bubble machines and giant reindeers, designed for kids and adults alike to leave with a smile on their faces and an appreciation of the community spirit.

Decorated homes carry donation collection points for those visitors wishing to show support to the chosen charity partner.  Last year $27,235 was donated to the Child Cancer Research Foundation (CCRF), helping to fund vital research and support families that have been affected by a child cancer diagnosis.  CCRF will again be the charity partner in 2023.

The Consulate Court displays run every night December 1-25 from 7.30-10pm each evening. The street hosts special events throughout the month, including Saturday 16th December, CCRF volunteers will be in place as the street hosts a visit from 20+ different costume characters, a Cheerleader team display and a special Santa visit on a fire truck thanks to the Gosnells Volunteer Bush Fire Brigade.  All events are promoted via social media at https://www.facebook.com/consulatecourtlights

The street has won the City of Gosnells ‘Safe City’ award numerous times and has collected for charity over the past 14 years, with approx. $250,000 being donated to charities during this time.

Win a $250k Prize!

We are so excited to announce our brand new partnership with Play For Purpose, Australia’s Community Raffle where you can win hundreds of great prizes including a $250,000 first prize pack!

The First Prize Pack includes the Audi Q5 Sportback S Line + $131K in Cashable Gold. Don’t miss your chance to win it all, with every ticket supporting our cause, to help us see more children live the long and fulfilling lives they deserve.

Raffle 21 will close at 8pm AEST 14 December 2023. Tickets are just $10.

ENTER NOW

Meaningful Christmas Gifts That Give Back!

As the holiday season approaches, the search for gifts intensifies. This year, consider spreading joy not only to your loved ones but also to childhood cancer families. Below are some great Christmas gift ideas that will help make a real difference, so you can help make this holiday season truly special.

An $8,000 Dollhouse
Want to win yourself the most amazing gift just in time for Christmas? Enter our raffle to win a stunning, custom-made dollhouse valued at $8,000. This dollhouse is all about the details, with the amazing builders spending months creating the masterpiece before kindly donating it to our foundation.

PLUS, the runner-up of the raffle will win a Keiko Designer Jewellery Set worth $530! This includes one pair of North Star Drop Earrings with White Rhodium and Colourful Cubic Zirconia and a Shimmer and Shine Wrap Bracelet in Hot Pink Cord and White Pearl.

The very lucky winners will be chosen on 18 December so don’t miss out on your chance to win big this Christmas.
 ENTER NOW!

CCRF Merch
Embrace the spirit of giving by choosing from a delightful array of merchandise available on our online shop. Whether you’re on the hunt for a Secret Santa surprise or just want to spread some holiday cheer, we’ve got you covered with unique and thoughtful gifts that give back.

From summer picnic essentials to cycling gear, you’ll be sure to find something great for your loved ones! Plus, we are offering 25% off all purchases made during the festive season! Simply use the code XMAS25
SHOP NOW

Entertainment Membership
Give the gift of experiences with an Entertainment Membership. This versatile gift opens the door to a world of savings on entertainment, activities, and restaurants. Whether your loved ones are foodies, adventure seekers, or culture enthusiasts, this membership offers a plethora of options. Plus, 20% of each sale will be donated to our foundation, making it a gift that keeps on giving.
BUY NOW

Donation in Lieu of a Gift
For those who have everything, consider making a donation on their behalf. Support a cause close to your heart and theirs by contributing to the Child Cancer Research Foundation. If you mention your donation to us (over the phone or in the notes section of our online donation form), we’ll even send you a paper Christmas Bauble that they can hang on their tree! It’s a meaningful gesture that spreads love and support during the holiday season.
DONATE NOW

This Christmas, let your gifts tell a story of compassion and generosity. Let’s make this holiday season not only a time for celebration but also a time for making a positive impact on the world.

 

Think of us when you recycle

As the festive season approaches, and you get ready to start celebrating with your family and friends, we can imagine bottles and cans might start to pile up. Why not use these empty drink containers to make a real difference?

Every container you save from landfill will not only protect our environment, but it can also help our foundation ensure the ground-breaking research into childhood cancers can continue, so less lives are cut short by the gruelling disease.

All you need to do is:

  1. Collect eligible containers
    Most aluminium, glass, plastic, steel and liquid paperboard drink containers between 150ml and 3L are eligible.
  2. Take them to a refund point
    With over 200 refund points in WA, there is sure to be one near you! 
  3. Donate your funds
    You’ll receive 10 cents for every eligible container, which you can donate to CCRF using our Scheme ID: C10285275

So, don’t let your 10c containers’ potential go to waste! Together we can keep these containers out of landfill, give them another life, and help our community while doing it.

Our Scheme ID is C10285275

News Archive
Categories