Cystic fibrosis plays a massive role in my family's life. Paige, our eldest child (11yrs) suffers from CF and has struggled with the disease from birth. She has recently just left Princess Margaret Hospital For Children after over three weeks with a lung function of 48% and having three types of IV antibiotics daily put through her Port, along with three sessions of Physiotherapy a day including nebulizer treatments. On top of this she has handfuls of oral medications daily and feeds through her PEG to assist with being able to take in enough calories.  If that wasn't enough, she also has CF related diabetes which means regular blood glucose tests and insulin throughout the day.  

Please help me to raise funds to be able to participate in the Cystic Fibrosis Largest Poker Run on the 1st of April 2016.
This week long ride to Victoria and week back to Perth will raise much needed funds and awareness of CF.
All proceeds are donated to the Cystic Fibrosis Association.