In July 2015, four and a half year old Amber had woken up from her sleep complaining of a sore stomach – which was very out of the ordinary for her as she always sleeps right through the night. Peter, Amber’s dad, tells us their story,

The next day she was still not well and sore in her stomach, so her parents Peter and Sarah decided to take her to their closest hospital (in Gosford) to get her checked out. Once there, she was given some medicine and started to feel better however, she still needed to go for further tests to get to the bottom of her concerns.

After getting a scan on her stomach it was made apparent that Amber was very unwell. The radiologist had seen scans like hers before and believed she had the rare childhood cancer neuroblastoma.

At the John Hunter Hospital in Newcastle, Amber underwent a mass of tests, ultrasounds and surgery with the results confirming Peter and Sarah’s fears – their precious little girl had stage 4 high risk neuroblastoma.

Amber with her sister in hospital

Amber immediately commenced treatment, which consisted of chemotherapy every 10 days for 70 days. Initial tests after this time had shown improvement, however more still needed to be done. Since then, Amber has undergone further rounds of chemotherapy, radiation therapy and a stem cell transplant.

She went on to undergo autoimmune therapy – a very painful and intense treatment that unfortunately needed to be continued for the next 5 – 6 months to help diminish Amber’s aggressive cancer.

Amber’s father Peter says that they have been very lucky to have such great support from their families, as it allowed them to give everything they had, to support their beautiful daughter through this difficult time.

There is a lot more to this situation than just having a sick child. Before this happened to us, I would hear the story of another child with cancer going through a rough time, but never really understood what it meant for the parents, or siblings of that child, and what they go through too.

Peter, Amber’s Dad

Peter is now more aware that, on top of his daughter’s illness and the day to day juggling of appointments and treatments, there are many additional pressures to manage such as financial and relationship stress and depressed periods for all concerned.

In May 2017 Amber unfortunately relapsed, and very sadly she passed away on April 18, 2018.

Your help can change lives...

Neuroblastoma Australia has raised over $4 million for innovative research, funding 17 early stage projectsfocused on changing the future for children with neuroblastoma – one of the most aggressive childhood cancers. Behind every dollar raised are children and families facing the devastating impact of this disease, like the story shared here.

Donate now to help fund potentially life-changing medical research that gives hope to children diagnosed with neuroblastoma. Donations are secure and you’ll receive an immediate tax-deductible receipt. Thank you.

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