Supporting the Maginn family financially while their newborn baby receives the care they require in Starship.
Southland
On 20 July 2023 at a routine anatomy scan for their 3rd child, Jamie and Chels found out that there was a potential problem with the way their baby’s heart has formed.
13 days passed between “maybe & definitely” as they made their way to Maternal Fetal Medicine in Christchurch - a diagnosis was made, which happened on 2 August.
Their baby was diagnosed with 'transposition of the great arteries' or TPA for short. This condition is fatal if not surgically repaired so baby will likely need a procedure called balloon atrial septostomy shortly after birth. Their baby will then require open heart surgery (arterial switch) within the first week or so of life.
TGA is a congenital heart defect meaning present at birth & is monitored by specialists for life. Whilst the condition itself is rare (less than 20 NZ babies a year out of 58,000), the outlook post surgery is generally positive.
Jamie & Chels and family will need to relocate to Auckland a few weeks prior to birth so baby can access the only possible care available in NZ at Starship Childrens Hospital.
They have been told to prepare for 6-8 weeks away from home, with the potential to be longer depending on many different factors.
They are my close friends.
The money is intended to cover some costs involved living away from home for 6-8wks. From lunches at the Hospital, to flights, meals, transport or even a sanity day at the Zoo for Arch and Van.
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