Whether you're newly diagnosed or looking to contribute to our mission, we've gathered valuable resources to help you connect with the PCD community.
Join our Discord community to connect with other PCD patients, share experiences, and stay updated on the latest research and events.
The US-based PCD Foundation provides support, education, and advocacy for individuals affected by Primary Ciliary Dyskinesia.
Visit WebsiteThe European-based BEAT-PCD organization focuses on advancing research and clinical care for PCD patients across Europe.
Visit Website