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Zach's TECosaurs
Story
Hi there!
On Sunday 26th August 2018 our 5 year old son, Zach, was diagnosed with Stage 3 Neuroblastoma and Opsoclonus Myoclonus Syndrome (OMS). After 8 rounds of chemo and a 7 hour surgery three tumours were finally removed. Thankfully he has been in remission since March 2019. Although monthly infusions and steroid pulses continue to treat the OMS.
The chemo, although effective, was brutal on our little boy. It completely broke my heart to see him suffer the way he did. There must be a better way to treat this insidious disease. Funds raised through Neuroblastoma Australia will help find a cure and a less toxic treatment for these sick kids. Please donate whatever you can.
More of Zach's story here https://run2cure.org.au/our-heroes/superheroes/zach-story
Donations made through this platform are secure and will be remitted directly to Neuroblastoma Australia. It is all tax deductible too!
Thank you from the bottom of our heart!
Thanks so much for your support!
Neuroblastoma Australia
Neuroblastoma is a devasting childhood cancer with the average age of diagnosis being just two years old. With survival of rates for aggressive neuroblastoma at only 50%, this disease claims more lives of children under the age of five than any other cancer.
We don’t need a miracle; just more research.
Neuroblastoma Australia, is a registered charity founded by families with children affected by the disease and has raised over $1.7 million for research into a cure for this complex cancer which almost exclusively affects young children.
You can make a difference. Help raise funds for research into more effective and less toxic treatments for neuroblastoma today.
To get involved, or learn more, visit our charity website: www.neuroblastoma.org.au