Cystic Fibrosis Community Advisory Committee
As someone who knows cystic fibrosis better than anyone, you have the power to make a difference. The Community Advisory Committee (CAC) is dedicated to amplifying the voices of those affected by cystic fibrosis, including individuals living with the cystic fibrosis, their families, friends, and caregivers. By participating in our forums and activities and contributing to our decision-making process when assessing support and services, you can help shape our advocacy, programs, and services. Members take part in online meetings, forums, and activities throughout the year. Every voice is heard, no matter where you live. Our current members include community representatives and the Services team. Each person plays a unique and crucial role in our mission. We encourage everyone to find their voice and contribute to the future direction of our work. Together, we can shape a stronger future for people with cystic fibrosis across Queensland, the Northern Territory, the ACT, and northern New South Wales.
If you’re interested in joining the CAC, please fill out the application form below. Our meetings take place online throughout the year, and we can’t wait to see you at our next event.
VANESSA TULENEW
Parent of a child living with cystic fibrosis
RYAN HENRY
Parent of a child living with cystic fibrosis
PENNE KADDATZ
Parent of a child living with cystic fibrosis

