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.

ELIZABETH JACKLIN

Services Administration

services@cfqld.org.au

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KIM HOLLEY

Community Advisory Committee Coordinator

Parent of a child living with cystic fibrosis

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Connie Arundel

CONNIE ARUNDEL

Cystic Fibrosis Queensland Board Member

Adult living with cystic fibrosis

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Brooke McCarthy

VANESSA TULENEW

Parent of a child living with cystic fibrosis

Brooke McCarthy

ASHTON GREAVES

Adult living with cystic fibrosis

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Brooke McCarthy

JESSICA CAESAR

Adult living with cystic fibrosis

RYAN HENRY

Parent of a child living with cystic fibrosis

Brooke McCarthy

PENNE KADDATZ

Parent of a child living with cystic fibrosis

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