Category: Cooper Rice-Brading Foundation

Australian media heavywieght and Nova radio host Michael “Wippa” Wipfli and highly accomplished media public relations executive Cathrine Mahoney came into Cooper’s life at a time when he was not keen on letting the outside world in.

He had very little time for anyone outside his inner sanctum of precious few people beyond immediate family.

Cooper’s condition had been deteriorating swiftly and savagely, and the outside world, even those closest to him throughout his brief life, were shut out. He did this to protect his friends. He wanted their memories of him to be positive, and not what he had become at the hands of sarcoma.

The exception to the rule were ‘Cath’ and ‘Wippa.’ Both very quickly became part of Cooper’s circle of trust and an extension of family.

Coop had a strong nose for genuine people and throughout the 18months from diagnosis to treatment, he ran his own race. He did not want to become the “boy with cancer” that elicited pity, he was hellbent on being the survivor, so becoming a token cancer patient for someone else’s personal gain, was never on the cards. He had avoided those who sought his company for pity, causing offence to some, but always sticking to his moral compass. He learned very early in the piece – Cath and Wippa were the real deal.

Both made Cooper laugh and times spent with them individually or together, were highpoints for Coops. Quality time spent with him away from cameras and media, resulted in a surprisingly strong bond and swift bond forming between the three. Unique as it was special. Each brought unbridled joy to his life when little else could.

Unsurprisingly, Cath and Wippa’s lives were impacted greatly with the news of Cooper’s passing, and from where our family stood, we couldn’t have blamed them for closing the door, and moving on. But neither chose to.

Instead, both continued with unwavering love and support for our family, at a time when we were at our lowest ebb. As a special aside, it wasn’t long before their respective families also became part of our lives, extending that very special bond, and providing enormous comfort through a myriad of highs and lows.

As we fast approach four years without Coop, Cath, Wippa and their families remain firmly by our sides. These remarkable friends continue to step up and do what they can to preserve Cooper’s legacy.

We have called on Cath and Wippa so often to assist with various projects along the way, and never once have they faltered.

Last year, both participated in the ground-breaking podcast series “Lets talk about sarcoma”, incepted and produced by Cath, giving up hours of their time and expertise to craft a finished product that resulted in a global distribution, and a meaningful tool for patients and families. Neither would accept payment in any form. Yet another labour of love, but one that held so much gravity.

Only two weeks ago, Cath and the highly talented Sarah McGilvray, who appears side by side with Wippa on the highly rating Fitzy and Wippa breakfast show, together with her role as co-creator of the very successful Nova production, “Not another parenting podcast’ performed for our guests at the annual CRBF Mother’s Day Breakfast, braving the Covid issues at the time, delivering a flawless and hysterical segment on parenting.

Which brings us to the announcement tonight.

Late last year, an unexpected call from Wippa advised us, albeit confidentially, he was going to take the Foundation with him onto the forthcoming Celebrity Apprentice Australia as his charity of choice. We were simply lost for words, and deeply humbled. We are a relatively new charity (4 years registered) and despite the high-profile charities Wippa could have chosen, he opted to choose the Cooper Rice-Brading Foundation, providing us with the opportunity of a life-time.

Filming for the Celebrity Apprentice Australia was incredibly rigorous over six days, and Wippa continued to burn the candle at both ends while filming took place, continuing is turning up each morning for a 6am start on his highly successful breakfast show, whilst also creating pilots for his production company.

This unspeakably difficult schedule did not only impact Wippa, but his wife Lisa, who was unwavering in her support. So many sacrifices were made by this family over the many weeks of filming, and for this reason, it is nigh on impossible to express our gratitude to Lisa, who at the time found herself juggling two children under the age of 5 and a new baby.

Tonight we have all watched on as Wippa’s dedication to advancing sarcoma, his bloody mindedness to ensure a win at all costs attitude, and never ending perpetuation of his very special friendship with Cooper, resulting in a win of enormous proportions. Funds that will make a quantifiable difference in the lives of the patients who are currently living without further treatment options.

We are thoroughly delighted to announce, Wippa’s outstanding efforts will be directed to supporting patients and families living with a sarcoma diagnosis, and toward the funding of a pivotal paediatric phosphoporteomic sarcoma specific clinical study through the Zero Children’s Cancer Programme, which will be named the Wipfli Family Sarcoma Research Grant.  This funding will support the Sarcoma Research Laboratory of Dr. Emmy Fleuren at Children’s Cancer Institute. Funds will be allocated to identify activated (phosphorylated) targets in sarcoma patients not covered in any other project, and will build the laboratory evidence needed to ultimately transform research findings and clinical recommendations.

It is impossible to articulate our thanks to Wippa, his beautiful family, for an opportunity which is rarely granted to a charity in its formative phases. This funding will provide the very real possibility of saving young lives, and will start a much needed conversation about sarcoma.

How blessed are we that Cooper left us the gift of friendship with his two special friends and their extended families?

We wish to thank the profound generosity of our Mother’s Day Breakfast donors for making this event possible.

We would ask that if you have the opportunity to support these individuals and corporations, we would urge you to do so.

Our deepest gratitude to Robin Todd for sourcing these beautiful prizes, and to each of the businesses that appear on this page, who have supported the funding of sarcoma research in Australia

Young adults living with incurable illnesses will have access to respite care when Australia’s first hospice for young people opens on Sydney’s northern beaches next year.

NSW Premier Gladys Berejiklian together with major funders of the project, two of Australia’s leading philanthropists Kay and Greg Poche, today turned the first sods of soil at the site of the adolescent and young adult hospice, which will provide palliative care for 15 to 24-year-olds and their families.

The facility is the first of its kind in Australia, and will lead the way for similar facilities across the country for young people, who are currently forced to seek respite care in aged care facilities.

The facility cannot come soon enough. Young adolescents are over the age of 18, are currently no longer able to use the Bear Cottage paediatric respite facility.

The $19.5 million development is the result of combined state and federal government funding, community fundraising and philanthropy, supported by a very generous contribution from Kay Van Norton Poche and her husband Greg Poche.

Ms Van Norton Poche, who has supported Bear Cottage for many years, decided to back the project after learning young people were often seeking respite in nursing homes and rehabilitation centres.

“I just thought, we’re better than that. Dignity begins with life, and each life has it. So let’s give it to people that we can, when we can,” she said.

Member for Manly James Griffin said the facility would provide care for young people across NSW, including from rural and regional areas.

“This is a wonderful example of what happens when government, community and philanthropy come together to unite behind a single cause,” he said.

Because today is Mother’s Day it is one of three days each year we can use the CRBF social media platform for a post with a personal twist.

Those who know me, know I love our children Mitchell and Cooper to the moon and back, and together with CRBF co-founder & long-suffering husband Colin, & errant French Bulldog Betty, (not necessarily in that order) they are put very simply, my life.

On Friday, Mitch, delivered a flawless segment at the Covid ravaged CRBF Mother’s Day Breakfast. He roamed the room & thanked our key guests. Others were not quite so lucky.  I was one of them.

For those of you who didn’t attend this event Mitch informed our guests I “incessantly hounded the event organisers to have the venue serve alcohol @ 7am”  for our hallmark CRBF breakfast function –  in particular “a brick of Bundaberg Rum”, I sat for two minutes with the words to “killing me softly “, playing in my mind, eyes roaming the room looking for imaginary thought bubbles. “Where is she keeping that hip flask?” “Did the staff actually serve her coffee in that cup?”

Mitch I know you choose my retirement home, but you skipped a step – I choose where your inheritance goes.

There is a more serious note for today’s post.  CRBF would like to wish all the remarkable mother’s and significant others, joy, peace of mind, time with your loved ones, and a special day making special memories.  It is a day when we remember and honour those whose Mother’s Day will never be the same, as their child or indeed their mother no longer walks beside them.

To those mums, this day will always be met with a multitude of mixed emotions. A stark reminder of a perfect life forever altered.  Mother’s Day is a day to surround yourself with those who matter most, to do something simple that brings joy, or to simply march to the beat of your own drum. There is a no size fits all solution to these special days in the calendar.

Whatever form Mother’s Day takes for you, we send our love to each of our mums, & thank you from the bottom of our hearts for the difference you make in our lives.

IMG_7317

IMG_7316

IMG_7315

IMG_7313

IMG_7312

IMG_7310

IMG_7307

IMG_7306

IMG_7305

IMG_7304

small FourHotChips_Banner4[1]

OLYMPUS DIGITAL CAMERA

IMG_6547

Karen Simpson and Jo Capp are remarkable mums with equally remarkable sons.

Both Karen and Jo-Ann stood by their son’s sides every step of the way, from the day of  their respective sarcoma diagnoses, throughout savage treatment regimes, and beyond.  Neither missed a beat.

With Mother’s Day fast approaching, it is timely to remember those mums whose lives have been impacted by tragedy of varying degrees, and to hold them in our thoughts and in our hearts.

Jake’s story

In the words of his mum, Karen Simpson

Jake Simpson was a normal sport mad young man living a normal life, when his life changed irreversibly.  Jake was diagnosed with cancer on 12th December, 2012.   On Christmas Eve in a further bitter blow, that cancer diagnosis was confirmed as Ewing Sarcoma.

Jake commenced treatment on Boxing Day, and was given the daunting prognosis of a 25%chance of survival.

The cancer was first located in Jake’s spine, hip and chest plate when the initial cancer diagnosis was made, and by Boxing Day,  it had metastasised to his collar bone, shoulder, and throughout his skull and bottom.

Chemotherapy initially worked, and in August Jake had a stem cell transplant and by October the family were informed he was in remission. For 15 months he lived normally celebrated his 21st birthday and continuing to reach all medical milestones.

Early January 2013, he complained of a sore back and on Australia Day it was confirmed the cancer had returned, this time no chance of survival unless a cure was found.

November we were told he wouldn’t see his 23rd birthday after chemo and radiation it just wasn’t working. 12 weeks later on the 17 February he closed his eyes.

Jake never once complained  and never asked why?  He started a bucket list,  and those last 10 weeks he had adventures with his family. Unfortunately the sarcomas on his spine paralysed Jake and he was bed ridden for the last few weeks of his life, which according to his mum Karen, “annoyed him”.

Jake fought courageously, but that cure just didn’t come.

Today these woman honour their sons with the tireless work they each do to advance sarcoma awareness and funding, despite the hand of cards they have each been dealt.

Reid’s story 

In the words of Jo-Ann Capp, Reid’s mum

Reid’s diagnosis of Ewing’s Sarcoma came when he was a month off turning 6 and it was incredibly life changing for all of us. Occasionally he complained of a sore leg. We put it down to growing pains.

On May 21 2007  we were told he would be facing massive doses of chemotherapy, perhaps some radiation on his lungs, the loss of his right tibia with only a 30-60% chance that he would live.

We got through all the treatment then due to having his tibia removed and replaced with his left fibula Reid went on to break this leg 14 times over the next 10 years. He spent his entire childhood until he was 16 in either a cast or with an Illarzarov frame attached to straighten or lengthen his leg.  He is a pretty resilient little bugger, and not too mention a demon on crutches!!

He is now 19 (nearly 20) and enjoying everything a young man his age can do!  He is at University in Brisbane studying to be a teacher and loving his freedom living away from the watchful eyes of his parents!

As if this process was not enough?, Jo-Ann went on to write a book, Four Hot Chips – “One family’s story of childhood cancer, love and how they survive, and how they nearly didn’t”. The book is now available through Audible, by following the link below:

https://www.audible.com.au/pd/Four-Hot-Chips-Audiobook/B086WQ7368

CRBF and the sarcoma community wish to extend our sincere gratitude to both Karen and Jo-Ann for their courage, and for their unwavering dedication to funding a cure for this insidious cancer.

International Childhood Cancer Day (ICCD) is a global collaborative campaign on the 15th February, to raise awareness about childhood cancer, and to express support for children and adolescents with cancer, the survivors and their families. (ICCD, 2021)

Every year, more than 400,000 children and AYA’s are diagnosed with cancer, with Sarcoma accounting for up to 20% of these diagnoses.

As the sun sets on the 2021 ICCD, we recognise and silently support those young patients and their families walking this road, and cherish the memory of those whose lives have been lost.

We thank those remarkable individuals and organisations who are immersed in childhood cancer. From the dedicated paediatric, and adolescent and young adult, nurses, specialist support staff, and medical oncology teams, to the passionate researchers working tirelessly towards a cure, the state and federal governments for their ongoing commitment to advancing children’s cancer research, and finally, the not-for-profit organisations, often driven by personal and devastating loss, which help support the research into a cure.

Each of these bodies and individuals has an equally important role to play, as we strive collaboratively to find a cure for all childhood cancers.