Fill out our survey on the effect of COVID-19 on people with PCD
About Us
Who We Are
-
The Faces of PCD
-
Our Stories
Resources
-
Technipro PulmoMed
-
Bronchiectasis Toolbox
-
Physiotherapy
-
Livewire
Contacts
-
Contact PCD Australia
-
PCD USA
-
PCD UK
-
Medical Directory
Member
You Can Help
News & Events
FAQ
Donate
Join Mailing List
Join our 55km Ride/Run/Walk/Swim Challenge this October!
Get your family and friends to sponsor your challenge
Help us raise much needed funds for PCD Australia!
55km Ride, Run, Walk or Swim for PCD Australia
Download Printable Pledge
Download Poster
What is PCD? How it is diagnosed? How do you live with it?
These are stories told by people affected by PCD
The faces of PCD
Real People. Real Stories
Catherine Kruljac
Born a month early, I was taken to intensive care where an incubator was my home for a number of weeks.
Read Catherine's Story
Yasmine Krahge
For the first five years of my life, the doctors had no idea what was wrong with me.
Read Yasmine's Story
Casey Brennan
My lungs collapsed when I was only 24 hours old and spent 2 weeks in neonatal intensive care.
Read Casey's Story
Fiona McBeath
After a very normal delivery at the Elliston Hospital in SA, Casey’s lungs collapsed day one.
Read Fiona's Story
Bill March
Bill was born in late November 2014. Five hours after his birth we became concerned something was not right.
Read Bill's Story
Jackie & Lucy
I was diagnosed with bronchiectasis in the 80s and specialists suspected I had some “sort of ciliary dysfunction”.
Read Jackie's Story
Bridget Bourke
After a bad episode when I was 11, I ended in the Emergency Department at the Royal Children’s Hospital.
Read Bridget's Story