In this very special interview, Kate Boshammer shares her family’s story and the journey they have travelled with their baby girl, Zara.

Zara was born with a rare chromosomal condition called Pallister Killian Syndrome and at almost seven months, she passed away peacefully, surrounded by her loving family.

“Our beautiful baby Zara was with us for nearly seven months, and we hold a deep gratitude for the blessings she brought to our lives,” says Kate. 

Kate’s courage, love and resilience will astonish you as she shares with me the precious time Justin, Kate and Theo spent with Zara.  

Following her passing, Justin and Kate organised ‘Zara’s Day’.  They raised an incredible $150,000 for the Royal Flying Doctor Service in Queensland and the Steve Waugh Foundation (SWF supports children and young people living with rare conditions).  They also funded two high-flow oxygen facilities for their local hospital.

This year, the family have chosen to once again host Zara’s Day and are currently running an on-line raffle for the RFDS (QLD).  

Friday, October 29th is officially Zara’s Day, and an online auction will commence with funds again supporting the Steve Waugh Foundation.

To assist the Boshammer family and their incredible legacy to Zara, head to 
https://zarasday.com.au/

You can also follow Zara’s Day on Facebook and Instagram.

Many thanks to Isaac Regional Council and the QLD Government for bringing this interview to you.