<div>Xavier’s Journey
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<div>Xavier was first diagnosed with Stage IV high-risk neuroblastoma in March 2021 when he was 3.
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<div>After 18 months of intensive treatment in Australia, he completed frontline therapy in September 2022.
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<div>Since then, our family has faced three relapses.
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<div>Each time, Xavier has returned to chemotherapy — enduring powerful drugs, immunotherapy and radiation — while we’ve travelled between Australia and the United States to access specialist treatment at Memorial Sloan Kettering in New York.
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<div>The heartbreaking reality is that in Australia there are currently no curative treatment options for children in Xavier’s position. 
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<div>Accessing clinical trials here involves enormous red tape, and government funding does not extend to overseas trials.
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<div>So if we want Xavier to have access to the most advanced therapies in the world, we have to take him to them.
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<div>His care now spans two countries. And so does our fight.
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<div>Right now, things are steady — and that is something we never take for granted.
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<div>If all continues to go to plan, he has just 2–3 more cycles until we reach words we once couldn’t even imagine: end of treatment.
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<div>If we continue to see clear scans, we’ll return to the US to focus on the next steps — keeping him in remission. Forever.
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<div>We know more options are emerging if we ever need them. 
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<div>For some children like Xavier, this becomes a chronic fight — continuing treatment while searching for the cure.
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<div>Our family continues to juggle life across two countries. Andrew holds down the fort at home — running the business, doing school runs, managing cheer, carrying more than most will ever see — so that Xave can get what he needs.
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Sarah Carrick

TERESA KOVACIC

Kathleen Willie

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Bianca Edwards

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SAVE XAVE from relapsed neuroblastoma RARE childhood cancer

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