Lilly Thoresen and her parents
Lilly Thoresen and her parents

The Thoresen Family

Good times amongst challenges found at the House

“She woke up that morning and she was just really, really yellow…” says Mum Tina of her nine-week old daughter Lilly. And just like that in late 2009 their lives were significantly changed. This marked the start of what would soon become a huge part of this young family’s life; a string of medical tests and treatments at Auckland’s Starship Hospital. And this meant a lot of time staying at each of Ronald McDonald House Auckland, across its three facilities.

Lilly was first diagnosed with a rare disease (Biliary Atresia), requiring her to have a liver transplant in May 2010 (Dad Luke was the donor). As happens in 10% of liver transplant patients, (PTLD) Lymphoma cancer had devastatingly developed in Lilly’s wee body in October 2010.

Throughout this stressful, hospital-centred time, parents Luke and Tina drew strength from the House. It brought them comfort knowing that other families were going through similar experiences, “I’ve made so many new friends… I think that’s what’s kept me sane as well”.

The Thoresen’s have especially come to enjoy their stays at the new House Grafton Mews “…it’s off the hospital site…so you’ve got that normal, well, kind of normal side (to life).” And despite whatever she is going through medically, Lilly is lively and manages to enjoy her stays “she just loves coming here, absolutely loves it.“

Tina, Luke and Lilly are still frequently in Auckland while Lilly undergoes numerous follow ups and treatments. And Lilly continues to wow her parents, and the medical & House staff with her strength, spirit and tenacious recoveries at each step.
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