PCD Foundation - Helping those affected by Primary Ciliary Dyskinesia

FIND A CENTER

Access to PCD-specific diagnostic tests and treatment is available throughout the US and Canada.

PCD FOUNDATION REGISTRY

One of our primary areas of focus is to develop and maintain a North American PCD Registry.

PCD FAQ

You’ve got questions? We’ve got answers! Here is your one-stop shop for a crash course in everything PCD.

NEWS & BLOG

Vertex Announces FDA-Approval of New Triple Drug Compound Effective for the Most Common Mutation in Cystic Fibrosis

October 24, 2019 BY Michele Manion

Vertex Announces FDA-Approval of New Triple Drug Compound Effective for the Most...

Next 5 Year Round of PCD Research Re-funded

October 9, 2019 BY Michele Manion

We are delighted to announce that the Genetic Disorders of Mucociliary Clearance...

Global PCD Connections: Collaborating in Israel and Palestine

September 12, 2019 BY Lynn Ehrne

Collaborating with international PCD doctors and researchers is crucial for diag...

PCD Foundation Partners with Prometheus Research to Develop an Innovative Platform to Advance Research, Diagnosis, Care and Cures for PCD

August 23, 2019 BY Lynn Ehrne

Read the Press Release

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BECOME A VOLUNTEER OR ADVOCATE

Join us on our mission to improve the lives of those affected by PCD. Find out how YOU can make a difference today!