Supporting Nala and her family as they navigate her cancer diagnosis, helping ease the burden so they can focus on being by her side.
Nationwide
Mil and Steve are facing every parent’s worst nightmare, following the devastating cancer diagnosis of their beautiful four-year-old daughter, Nala.
The three of them have now relocated to Starship Children’s Hospital and Ronald McDonald House in central Auckland to begin the journey ahead, with little Soraia joining them in the near future when the time is right.
This means being away from home, work, and daily routines, and their new reality will likely have an impact on their collective work situation, along with the anticipated and unexpected expenses that will no doubt start to accumulate rapidly.
This Givealittle page has been set up to help provide practical and tangible support during the challenging and uncertain times ahead.
After learning of the proposed creation of this page, Mil and Steve have humbly accepted the offer for it to be set up and expressed their intention to be thoughtful stewards of any funds generated as much as possible.
If you’re in a position to make a contribution, it would mean heaps to them, but simply sharing the page can also make a real difference.
Thank you for keeping this lovely family in your thoughts and sending them strength and love.
Friends
Donations will provide vital support with living costs to help Nala’s family manage the challenges ahead and stay by her side throughout her cancer journey.
The latest from Ward 27B 13 October 2026
Hi all, a wee update on our darling Nala.
After surgery we had nearly three weeks at home to recharge. Between clinic visits and tests, Nala got to just be a kid: a fairies and pirates festival, lighting the Sky Tower gold, playcentre, giggly chases with Soraia, pancakes, and screaming “Up the Wahs” out the car window on the way to the Warriors’ last game!
The big news: her oncologist confirmed a “complete response” to induction. No visible tumour, no disease on the MIBG scan or in her bone marrow, and normal urine markers. That puts her in the top 20% globally, a strong predictor of long-term survival. Huge hope! The cost is some high-frequency hearing loss from chemo, which may need managing at school.
We’re now 2.5 weeks into the first of two transplant cycles: intense chemo, then her own stem cells returned. It’s been brutal, with mucositis (sore mouth, tummy and bottom, constant phlegm), a rash, and she’s very knocked around. The team are managing her pain and nausea well. We’re in isolation, and it’s tough on us too. But like the long wavy grass in We’re Going on a Bear Hunt, we can’t go over or under it. We have to go through it.
All going well, we’re out in 1.5 weeks, then four weeks off before cycle two, ending just before Christmas: the summit of the hardest stage.
She still springs back at times, hiding under the bed, giving nurses spicy directions, and doing song and dance shows for staff.
Thanks for all your good vibes and support!
Steve and Mil
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