Our aim is to raise awareness and ultimately help find a cure for Cystic Fibrosis. This page is dedicated to Jessie. Jessie was diagnosed with Cystic Fibrosis at 5 weeks, there is currently NO CURE.
Cystic Fibrosis [CF] is the most common, genetically acquired, life-shortening chronic illness affecting young Australians today, yet most of us wouldn't have a clue what it is. Unless a cure is found Cystic Fibrosis will eventually take your life. A successful lung transplant only buys you time, it does not cure you of Cystic Fibrosis.
It's never easy putting these posts up of Jessie and one day when she's older, she may not like or want her photo's being plastered all over social media. Until that time, we will continue to raise awareness whenever and wherever we can.