A Book about the story behind the story Lachlan Child born with type C TOF

At the moment of birth, rather than being placed in our arms, he was immediately taken for surgery. Our suspicions of TOF had been earlier raised by our obstetrician, who noted the absence of a stomach bubble in the ultrasound scans.

Lachlan, being one of triplets, meant our attention was constantly divided, especially with his twin sisters requiring care as well.

It was/is not an easy journey – it is a time of heartache, worry, joy, sleepless nights, tests, surgeries, hidden tears, of fitting medical appointments in around therapists, work, family and being a wife and parent. Hospital is like a second home now.

A poignant memory etched in my mind occurred one day in the NICU. A young girl was meeting her seriously ill baby brother for the first time, in the incubator next to Lachlan’s. The overwhelming sight of the tubes and machines enveloping her brother left her inconsolably distressed, an image that will forever linger in my memory.

I penned “Lachlan” not only to honour my son’s remarkable determination and his relentless battle to remain with us but also for that little girl, her brother and every other child navigating medical challenges. The narrative aims to demystify the hospital environment and the intimidating machinery, highlighting their essential role in healing and recovery. I also wanted children, like my son to see themselves represented in literature- perfectly imperfect in every way.

This book is also a way to say thank you to the incredible medical staff that work tirelessly to save and look after these precious TOF children. My gratitude is yours- always.

Finally, to the tough TOF parents. I see you; I applaud you; I am you. Let’s have each other’s backs and keep teaching the world what incredible people these little TOF kids can be.

Thanks for your support

Kate