
PCD Foundation - Helping those affected by Primary Ciliary Dyskinesia
Working together to find a cure and improve care for those with ciliary disorders and their families by increasing awareness, research and support. Promoting education, advocacy and the search for the cure for Primary Ciliary Dyskinesia. TO PROVIDE THE LEADERSHIP AND RESOURCES NEEDED TO SUPPORT INCREASED RESEARCH, ACCELERATED DIAGNOSIS, IMPROVED HEALTH, AND ULTIMATELY A CURE FOR PRIMARY CILIARY DYSKINESIA (PCD).
200543474
EIN
2004
Founded
Rochester, NY 14612 USA
Address
pcdfoundation.org
Web
PCDFoundation
Twitter (809)
PCDFoundation
Facebook (5000)
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News

PCD Foundation Board Chair, Margaret Leigh MD.,and Board Member, Gary Joyner, are happy to welcome you to the PCDF booth @atscommunity and answer your questions about PCD! #ats2025 (fb)

Come visit us @atscommunity Booth 2332 #ats2025 (fb)

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Nearby
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About the organization
- G01, G45, G20 -
FIND A CENTER PCD FOUNDATION REGISTRY PCD FAQ DIAGNOSIS TREATMENT CLINICAL CENTERS GET INVOLVED Want to Get Involved. Join Us on our mission to improve the lives of those affected by primary ciliary dyskinesia PCD. Resources Contact Us Donate PCD Foundation is registered 501c3. All donations are 100 tax deductible.
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