The Children’s Tumour Foundation was established in 2010 and has grown from a volunteer-based support service to become the peak body in Australia for those impacted by Neurofibromatosis (NF). Commonly inherited neurological condition, affecting about 1 in 2,500 people throughought the world, more common amongst children. They provide hope for everyone impacted Neurofibromatosis in Australia by advocating for change, advancing research and empowering this community with knowledge, connections and support at every stage of their journey. This year, Peter has made the decision raise awareness for this cause by SHAVING THE LOCKS! After 10 years of growing and many dares and bets, it’s finally time!
 THEIR GOAL: To improve the lives of individuals and families affected by neurofibromatosis (NF) and related conditions. Including advancing research, advocating for change, providing support and connection, and ultimately, ending NF. Striving to empower the NF community through education, resources, and access to care, fostering a sense of hope and community
 OUR GOAL: $5,500 - donating all funds to the Children’s Tumour Foundation. Help us reach it!