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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
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
For the first five years of my life, the doctors had no idea what was wrong with me.
Read Yasmine's Story
My lungs collapsed when I was only 24 hours old and spent 2 weeks in neonatal intensive care.
Read Casey's Story
After a very normal delivery at the Elliston Hospital in SA, Casey’s lungs collapsed day one.
Read Fiona's Story
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
After a bad episode when I was 11, I ended in the Emergency Department at the Royal Children’s Hospital.
Read Bridget's Story
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