The countdown to PCD Awareness Month begins now! Be sure to click, like, join, follow, and share!
Are you ready to help make PCD a household name?
Here we come!
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Our Mission
Our mission at PCD Smiles is to bring smiles to hospitalized primary ciliary dyskinesia, no mater their age; through the gift of a cheer package. Currently serving only The United States and Canada. -
Request Cheer Package
Know of a hospitalized primary ciliary dyskinesia patient? Please visit our “Request a Cheer Package” link and fill out our secured form to submit them for a cheer package today! -
Donations
Our cheer package program runs on donations. To see how you can help PCD Smiles, visit our donations section today! -
The PCD Artist Project is a collaborative effort by artist to raise awareness for PCD & support the PCD Smiles cheer package program. Visit our exhibits today!
Random Fact Friday 2024.138
Primary ciliary dyskinesia (PCD) is a congenital motile ciliopathy, associated with chronic...
Random Fact Friday 2024.131
Did you know that olfactory dysfunction is common in chronic rhinosinusitis (CRS); indeed, it is...
No Magic Bullet; Primary Ciliary Dyskinesia & COVID-19 in North America
The United States PCD Foundation held its very first town hall meeting on 30 March, 2020 with one...
Will this cough ever go away?
I’m often get asked if this PCD cough will go away, or what’s the best things to use to get my...
Things Not to Say to a Person with PCD or their Caregivers
For Rare Disease Day 2018 we asked the PCD (Primary Ciliary Dyskinesia) community, “What are your...