Courtney Cebalo and son Roman have come out the other side of the five-year-old having a rare form of leukaemia. Photo / Merle Cave
Courtney Cebalo and son Roman have come out the other side of the five-year-old having a rare form of leukaemia. Photo / Merle Cave
Roman Cebalo, a 5-year-old boy, celebrated his birthday after overcoming a rare leukaemia diagnosis.
His recovery was supported by the Child Cancer Foundation, which provided crucial assistance and resources.
The Foundation’s Street Appeal seeks donations to support families facing childhood cancer, aiming to raise $6.5 million annually.
Judea boy Roman Cebalo celebrated an extra special birthday on March 10.
The 5-year-old was diagnosed with a rare form of leukaemia at 11 months old but is now running about like a normal kid, his mother Courtney Cebalo said
“He is into Hot Wheels and Minions, andenjoys swimming, athletics and playing with his friends.”
She said navigating her son’s cancer journey was only made bearable by support from the Child Cancer Foundation – which had its annual nationwide Street Appeal today and Saturday.
“We’d later learn he was allergic to antibiotics he was being given but at the same time he was developing this full-body rash,” Cebalo said.
A week before Christmas 2020 a paediatrician requested Cebalo take Roman to Starship children’s hospital in Auckland for a bone marrow biopsy.
“No-one could figure out why he was getting this rash.”
Discharged Christmas Day, Roman and his mother returned home.
“But he was still sick and we didn’t know why. It was awful. Looking back now he was lethargic, pale, snotty and chesty.”
Courtney Cebalo and son Roman’s live were turned upside down when he was diagnosed with a rare form of leukaemia at 11 months old. Photo / Supplied
The family was recalled to Starship and Roman, then aged 11 months, was diagnosed on February 23, 2021, with Juvenile Myelomonocytic Leukemia. It was later discovered he also had an under-developed airway, called Tracheobronchomalacia.
After diagnosis, Roman had two rounds of chemotherapy, followed by a round of conditioning chemotherapy to kill the body’s bone marrow; then a meticulously-timed Cord Blood Stem Cell Transplantation on June 1, 2021, to graft the new blood for it to be accepted by his body.
Roman’s donor lived in Melbourne.
Cebalo said if Roman did not have the transplant he would most certainly have died.
“It took 16 days to start seeing any signs of grafting.”
Roman Cebalo was very sick before he received a Cord Blood Stem Cell Transplant on June 1, 2021. Photo / Supplied
Thankfully Roman’s body accepted the transplant blood and his health massively improved.
Roman is no longer on medication for leukaemia and is now a “normal kid”, Cebalo said.
“The funny, smart, creative, cheeky, fun-loving, caring boy still has a million medical appointments but is living a typical 5-year-old’s life.”
Cebalo said she found Roman’s cancer journey overwhelming – especially when meeting with and being contacted by a range of health professionals.
“Post-diagnosis I’d missed quite a few calls from the Child Cancer Foundation. On the fourth I rang back and got our family support co-ordinator.
“When I met with her everything got blurted out and it was like a big relief. [It was] Like she’d just picked me up and carried me through the whole situation.
Courtney Cebalo and son Roman’s live were turned upside down when he was diagnosed with a rare form of leukaemia at 11 months old. Photo / Supplied
Roman will be four years post-transplant in June.
“He’s on six-monthly checks. Currently his donor cells sit at 96%, so as long as those donor cells keep doing what they’re doing the leukaemia should stay away.
“He’s in what’s called morphological remission, which means nothing is happening – but he’s still at that risk,” Cebalo said.
Only in the last few months had she accepted what had happened.
“Roman just has to get to five years to be deemed cancer-free as such.”
Cebalo said she used to donate to CCF but never thought she’d need them.
“Back then I didn’t know what they did. Now, being on the side of receiving their support, what they offer is just so incredible.
“Just having the check-ins, support, the practical help, mental support…they are a special bunch of people.
“They are just there – even when you don’t know you need them, they are there. Whatever you need, they will find a way to help you.”
Foundation chief executive Monica Briggs said she urged Kiwis to donate to the March 14-15 street appeal.
“Every week in Aotearoa, three more families receive the devastating news that their child has cancer. Our support is ongoing, often spanning years, as families navigate treatment and recovery.
“The cost to deliver our vital services is $6.5 million per year, and we receive no direct government funding.
