Finlee Bremners Road to recovery
Helping our great friends navigate Finlee's long journey with kidney disease.
Alexandra, Otago
On the 2nd October 2024, Kayla, Michael and Arlo welcomed a beautiful baby girl into the world, Finlee Anne Bremner.
Within a short 3 weeks, wee Finlee and her family were back in Dunedin due to some swelling in her face. 5 days later, Kayla and Finlee were flown to Starship hospital where they underwent further testing in which Finlee was diagnosed with Congenital Neprotic Syndrome which effects the function of her kidneys.
Since Thursday 23th October and just 18 days old, Finlee has been receiving daily albumin infusions and lots of antibiotics to help her kidneys retain the protein needed to function properly. Congenital Neprotic Syndrome effects around 1 in 10,000 babies.
With such a long road ahead of them, we as a friend group along with a few others in our small community thought it would be a good idea to set this page up to help with any financial burdens they may face while on this journey with Finlee
Kelsey McLean's involvement (page creator)
Close friends
Use of funds
All money received will go towards on going costs while Kayla and Michael are away from home with Finlee.
Latest update
Finlees Progress 9 December 2024
First of all we would like to thank each and everyone of you for supporting our family. It means the absolute world to us.
Finlee is progressing really well. We thought we were coming home a few times, but each time Finlee has had a wee set back, which has been mentally tough. She is stable, her meds are doing their jobs and she’s growing like a weed.
The drs are aiming to get us home by Christmas but we know that’s not guaranteed.
Hope to see you all soon.
Love the Bremner family x
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