What is cystic fibrosis?
Cystic fibrosis (CF) is a genetic condition that affects how salt and water move across cell walls. In the lungs this makes mucus thick and sticky, so it traps bacteria and is hard to clear. The result is repeated chest infections and inflammation over time.
How respiratory physiotherapy helps
- Airway clearance: teaching and refreshing techniques as you grow and your needs change.
- Devices: reviewing and fitting PEP and oscillating PEP devices.
- Exercise: programs to support lung health, fitness and bone health.
- Extra support when unwell: more clearance help during chest infections or after hospital admissions.
- Posture and muscles: musculoskeletal care, which is often overlooked in CF.
We are happy to communicate with your CF team so your community care matches your hospital plan.
Your first visit
- 40 minutes: a full assessment of your breathing, your chest and how you manage with activity.
- A plan from day one: we agree goals with you and start treatment on the day.
- No referral needed: Medicare GPCCMP, DVA, NDIS and HICAPS accepted.
Frequently asked questions
Do you see children with CF?
Yes. We treat children and adults, and involve parents in learning home routines.
Do I need a referral?
No. You can book directly. A GP referral is only needed if you want to claim a Medicare rebate through a GP Chronic Condition Management Plan (GPCCMP), or if you are a DVA client.
Can I claim on Medicare or my health fund?
Yes, in most cases. With a GP Chronic Condition Management Plan from your GP, Medicare pays $63.40 back for each visit, so a first visit costs you $45 and a follow-up $25. Private health extras are claimed on the spot with HICAPS. See our fees page.
Trusted information: Lung Foundation Australia