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.
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!
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!
Written by PCD Smiles
on October 27, 2026.
Posted in Topic Thursday
For most people, encountering bacteria in the environment is simply part of everyday life. Nontuberculous mycobacteria (NTM) are found naturally in soil, dust, and water—including sources such as...
Written by PCD Smiles
on October 26, 2026.
Posted in Topic Thursday
When people think about Primary Ciliary Dyskinesia (PCD), they often think about coughing, mucus, sinus infections, airway clearance, and bronchiectasis. Nutrition may not be the first thing that...
Written by PCD Smiles
on October 25, 2026.
Posted in Topic Thursday
For most people, breathing in a few bacteria or encountering a respiratory virus is something the body can usually handle. For someone living with Primary Ciliary Dyskinesia (PCD), the situation can...
Written by PCD Smiles
on October 24, 2026.
Posted in Topic Thursday
Primary Ciliary Dyskinesia (PCD) is a rare genetic condition that affects the structure and function of microscopic, hair-like structures called cilia. These cilia help move mucus, bacteria, and...