Life takes us off course and back on again. We have bad days and some good days.

But what if something happened that would change the direction of your life so much that it shatters all your plans?

What if you are a 10 year-old that found out you may not live to 30? What if you knew your end date? What if you knew your child’s end date and that they would suffer in between a short gap of life and death.

The clock is ticking for Simon, Our family and other children fighting this disease. The gap is shortening.

“It is not the observer who counts; not the person who points out how they want to help but just watch on. The credit belongs to the person who is actually taking action, who stops and helps a child with a touch of love - who has limited resources but rises to their best selves again and again; who strives to do the deeds; that elevate their own life and of those experiencing unimaginable pain. If you only choose one day or minute or second to rise to your hero self, we hope you will consider our son".

Simon was diagnosed with Cystic Fibrosis at just 17 months old. There is currently no cure but your generosity can help fund the incredible work of those fighting to give children like Simon a chance at more life.

Join us for an enjoyable evening for a worthy cause featuring exceptional entertainment, a 3-course menu and an auction of many coveted items. A night not to be missed!

All proceeds will go towards the Team Simon Foundation for Cystic Fibrosis to fund new research into a cure for this childhood genetic disease