Cooper Rice-Brading Foundation

Cooper Rice-Brading Foundation Contact information, map and directions, contact form, opening hours, services, ratings, photos, videos and announcements from Cooper Rice-Brading Foundation, Nonprofit Organization, 14 Macleay Street, Elizabeth Bay.

Preserving Cooper’s legacy, and realising his vision of generating critical funding for sarcoma research; promoting awareness & early diagnosis; whilst supporting those living with sarcoma & their families

Four weeks ago today, a beautiful young woman dressed in a stunning red dress walked into our Mother’s Day event with he...
14/06/2026

Four weeks ago today, a beautiful young woman dressed in a stunning red dress walked into our Mother’s Day event with her husband proudly on her arm, turning heads.

Today, with profound sadness, we acknowledge the passing of Kirsty Bourke, a remarkable young woman, an adored wife, daughter, & sister, passionate advocate, & much-loved member of the sarcoma community.

Diagnosed in 2020 when life should have been filled with endless possibilities & dreams, Kirsty spent far too much of her young life confronting one of the most aggressive & unforgiving cancers imaginable.

Sarcoma is a savage disease. It has no regard for age or potential. It often strikes at a time when those affected should be building futures, not fighting for their lives. Far too often, it robs families of precious time & denies extraordinary young people the opportunity to discover their true potential.

Kirsty’s cancer never defined her.

Throughout her challenges, she demonstrated extraordinary courage, resilience & determination, becoming a powerful voice for young people living with cancer, sharing her experiences openly & helping others feel less alone during some of their darkest moments.

Kirsty understood that advocacy matters. She understood that every conversation, every story shared, & every opportunity to raise awareness could create change. Through her efforts, she touched countless lives and became a source of hope and inspiration.

We also recognise the incredible team at the YCS, Princess Alexandra Hospital, Bne. The special bond they shared with Kirsty was evident to all who knew her. Thank you for your outstanding care, compassion, friendship, & unwavering support. The impact you have on young people and their families cannot be overstated.

A special thank you to the remarkable team for turning Kirsty and Cayden’s trip to Sydney into a reality.

Today we remember a life taken far too soon, & send our love & strength to Cayden, Bron, Brian, Matthew and Kirsty’s close friends.

A life that inspired. A life that advocated for others. A life that made a genuine difference…

To read more about Kirsty’s advocacy go to https://www.crbf.org.au/vale-kirsty-bourke

Today, we are setting aside our usual posts to reflect on a special day and someone who means the world to us.Over the p...
13/06/2026

Today, we are setting aside our usual posts to reflect on a special day and someone who means the world to us.

Over the past nine years, our eldest son Mitch has carried a loss that no brother should ever have to endure. Yet through that grief, he has continued to honour Cooper’s memory, working tirelessly to support young people and families facing sarcoma.

He does it quietly and with the understated grace that has always been his way. He simply shows up, time and again, because he understands the importance of helping others feel supported during difficult times.

On today, his milestone 30th birthday we reflect on the years that have passed, the challenges our family has faced, and the countless moments of kindness, generosity and strength Mitch from the tender age of 20, has shown not only his own family, but countless families along the way.

In many ways, Mitch is emblematic of so many siblings who have experienced profound loss. While their grief is often less visible, they carry it every day. They learn to navigate life while holding the memory of a brother or sister close, finding a way to move forward without ever leaving them behind. We know there are many siblings walking that same path, and today we acknowledge them too.

We are incredibly proud of you Mitch, and so thankful for the love, laughter and perspective you bring to our lives and those whose lives have been affected by sarcoma.

Through the highest of highs and the lowest of lows, our love for you has never wavered, and it never will.

And while there is not a day that goes by that we don’t wish Cooper was standing beside you to celebrate this milestone, we know beyond any doubt how proud he would be of you. Proud of the way you have carried him in your heart, honoured his memory with quiet determination, and dedicated so much of yourself to helping others facing the same cruel disease.

His legacy lives on through the lives you continue to touch, and we know that would mean the world to him.

Looking at the difference you have made since Cooper’s diagnosis ten years ago, we cannot wait to see what the next ten years bring.

A Family Making a Difference.We would like to thank Stacey Walvin, Director of Generation Dance Centre in Brisbane, and ...
28/05/2026

A Family Making a Difference.

We would like to thank Stacey Walvin, Director of Generation Dance Centre in Brisbane, and her son Zac for their ongoing support of those living with sarcoma in Australia.

As Generation Dance Centre approaches its 30th anniversary, Stacey continues to inspire her students and community with remarkable resilience. After experiencing shoulder pain for six months, she initially believed she had suffered a work-related injury. Instead, she was diagnosed with chondrosarcoma, a rare and aggressive bone cancer.

Stacey’s story is a powerful reminder that recognising when something is not right and seeking medical advice early can be lifesaving. Early diagnosis matters.

Despite facing the daily realities of living with chondrosarcoma, Stacey remains committed to making a difference. Through Generation Dance Centre’s annual Mid-Year Showcase, Stacey, her students and their community have now raised more than $15,000 for sarcoma awareness and support.

What makes this even more remarkable is that Stacey has continued these fundraising efforts while facing significant personal adversity herself, a true reflection of her generosity, resilience and commitment to helping others.

Son Zac, a very talented competitor in motorsport has proudly added the CRBF logo to his race car, helping raise awareness wherever he competes. Since beginning his motorsport career at Brisbane’s iconic Lakeside Park in 2014, Zac has gone on to win multiple championships and today races for Team NorthRock in the national Toyota Gazoo Racing Australia Scholarship Series. An electrician by trade, Zac is also raising funds through his workplace with the support of the ETU.

Together, the Walvin family are helping raise awareness of sarcoma, highlighting the importance of early diagnosis, and supporting vital research and the Jack Gibson Sarcoma Patient & Family Support Programme.

Our deepest thanks to Stacey, Zac, the Walvin family, Generation Dance Centre, and Zac Walvin Motorsport for their unwavering support of the sarcoma community.

Please visit the link in our bio if you would like to support this remarkable effort.

For nine years, the Cooper Rice-Brading Foundation has operated with a simple philosophy, every possible dollar raised s...
20/05/2026

For nine years, the Cooper Rice-Brading Foundation has operated with a simple philosophy, every possible dollar raised should go to where it is needed most.

We recognise that, for those living with sarcoma, there is simply not enough funding reaching the areas of greatest need. That reality is one of the reasons our Foundation has always chosen to operate through voluntary expertise and support wherever possible. We are certainly not alone in doing this, and we acknowledge the many charities and organisations across Australia that also rely on volunteers and donated professional expertise to maximise their impact.

Ou work is powered by volunteers who generously give their time, skills, experience and professional expertise to support Australians living with sarcoma. From governance and administration, to events, fundraising, marketing, finance, social media, patient support and strategic advice, our Foundation exists because of people willing to contribute their knowledge and energy for a cause bigger than themselves.

During National Volunteer Week, we want to acknowledge and sincerely thank every person who has helped us over the past nine years. Your contribution has enabled us to fund over $4.4m of vital research, provide meaningful supportive care through the Jack Gibson Patient & Family Support Programme, provide national awareness, and continue fighting for better outcomes for those impacted by sarcoma across Australia.

Quite simply, we would not exist without our volunteers.

To everyone who has given up their time to help our Foundation and our sarcoma community, thank you. Your generosity, compassion and expertise continue to make a genuine difference in the lives of others.

Another extraordinary evening with at the Tour de Qure Canberra Ball. Thank you for once again bringing together a comm...
17/05/2026

Another extraordinary evening with at the Tour de Qure Canberra Ball.

Thank you for once again bringing together a community so passionate about changing the future of cancer research in Australia, and for creating a space where we were able to bring together the most extraordinary people from the sarcoma community in Canberra for the event.

Through your incredible work, more than $160 million has been raised, supporting over 1,228 projects and contributing to 250 major research breakthroughs. Beyond research, Tour de Cure continues to make a real impact through regional cancer support programs and school initiatives promoting cancer awareness across Australia.

We are especially grateful for your generous commitment to sarcoma research, with more than $500,000 contributed over the past three years toward groundbreaking advancements that are giving hope to families facing this devastating disease.

An unforgettable night with extraordinary people, united by purpose, hope and determination.

in

13/05/2026

The superb once again hosted our annual Mother’s Day event, this year, a High Tea overlooking Sydney Harbour.

The sun was shining, skies were blue, & Sydney Harbour provided a spectacular backdrop. More importantly, the room itself was filled with extraordinary generosity, compassion & love, helping raise $50,000, for those who need it most.

It was an afternoon defined by passion, purpose and hope. In the midst of a challenging economic climate, we are humbled by the kindness & generosity shown by our guests in support of a disease that, for many, may never personally touch their lives.

Once more, the incredible , one of the most genuine & authentic women in Australian media, hosted the afternoon with professionalism & grace, accompanied by the at-times mischievous Mitch Rice-Brading, whose humour & energy kept the room smiling.

Our speakers were simply remarkable. The Hon Trish Henry - CRBF Chair, , Professor(s )David Thomas & Mandy Ballinger , Prof Richard Boyle, & shared powerful insights & reflections that resonated deeply with all in attendance. Guests were deeply moved by the story of resilience & hope shared by Kaela Graham-Bowman , alongside the incredibly heartfelt words of Mark Mathot, devoted father of Jac. All speakers left a lasting impact.

Sincere thanks to for providing our AV, & the amazing Pariscomino & & for their tireless behind the scenes work leading up to & on the day of the event. Thanks also to the superb performances by and throughout the event.

To every guest, donor & supporter who joined us, thank you for making the afternoon so meaningful. Your generosity & support continue to bring hope and connection to families impacted by sarcoma.

A heartfelt thank you also to the individuals and organisations below whose ongoing support helped make this event possible. We encourage our community to support them whenever possible, as events like this would not happen without their kindness & commitment.

For the full story and photos head to link in our bio.

Last night we had the privilege of attending the Australian premiere of Permanent Scar, a deeply moving film by New York...
12/05/2026

Last night we had the privilege of attending the Australian premiere of Permanent Scar, a deeply moving film by New York-based filmmaker Ally Betker, dedicated to the memory of the remarkable Sophie Kyprianou.

Sophie Kyprianou was no ordinary young woman. Her story truly defies words. Sophie was just 14 years old when she was first diagnosed with osteosarcoma in March 2014. In 2016, she was diagnosed with Myelodysplastic Syndrome, which led to a diagnosis of Acute Myeloid Leukaemia in February 2017. A subsequent diagnosis of B Cell Lymphoma in April 2017, followed by a recurrence of osteosarcoma in October 2022, seems to most of us more than any one person should ever be expected to endure. Yet in December 2022, Sophie was further diagnosed with a brain tumour. Sophie’s family sadly lost their precious daughter/sister in May of 2024.

The Kyprianou family, mother Cathy, father Paul, sister Jessie and brother Sam, together with aunt Susan and were nothing short of extraordinary as hosts for the evening, with each family member playing a pivotal role in bringing Sophie’s legacy, Smiles Don’t Lie, to life with honesty, grace and immense courage. The fundraising initiative was established to support an osteosarcoma programme through Professor Emmy Fleuren through , continuing Sophie’s impact and determination to help others facing this devastating disease.

Permanent Scar is a powerful reflection on the unique nature of grief and the many ways it manifests within all of us. Told through the eyes of a family member, the film offers an intimate and relatable interpretation of love, loss and the enduring impact of losing a loved one.

It was an evening filled with emotion, vulnerability and immense admiration for a family who continue to honour Sophie in such a meaningful and beautiful way.

Forever part of my world, forever held in my heart....Mother’s Day looks different for everyone.For some, it is filled w...
09/05/2026

Forever part of my world, forever held in my heart....

Mother’s Day looks different for everyone.

For some, it is filled with love and treasured moments. For others, it can quietly bring sadness, memories, and deep longing.

Those who shape our lives never truly leave us; they remain part of every heartbeat and every memory.

Sending our love today to all mothers, to those who have loved and cared with a mother’s heart, and to the families who carry them always.



For more than nine years, the , the Magiros family, and Phillip Fikkers, licensee of , have stood alongside us in supp...
05/05/2026

For more than nine years, the , the Magiros family, and Phillip Fikkers, licensee of , have stood alongside us in support of those impacted by sarcoma. Our connection with the Magiros family, through our son Cooper, makes this support especially meaningful.

Their long-standing commitment to our annual Mother’s Day event reflects a deep and enduring belief in the importance of this wor. helping us honour lives, support families, and keep momentum behind sarcoma research and support.

We are sincerely grateful for their continued partnership and the difference it makes, year after year.

Visit the link in our bio to purchase a ticket in this year’s raffle and help make a meaningful difference in the lives of those living with sarcoma.

Address

14 Macleay Street
Elizabeth Bay, NSW
2011

Opening Hours

Monday 9am - 8pm
Tuesday 9am - 8pm
Wednesday 9am - 8pm
Thursday 9am - 8pm
Friday 9am - 8pm
Saturday 8am - 5pm
Sunday 8am - 5pm

Telephone

0412239020

Website

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