The PCD Foundation is a 501(c)(3) patient advocacy organization dedicated to serving individuals affected by Primary Ciliary Dyskinesia (PCD). Founded by a parent and a patient, the foundation aims to address unmet needs in the PCD community, including improving diagnostics, treatment accessibility, and generating research. The foundation collaborates with various partners to create a clinical center network and to further research on inherited ciliary disorders.
2004
20-0543474
$3.346 million
This organization contributes to the following United Nations Sustainable Development Goals. See the SDG page for more information.
The PCD Foundation has established a network of clinical centers aimed at improving diagnostic capabilities and treatment accessibility for individuals with PCD.
The foundation is developing a registry to collect data on PCD, facilitating research and improving patient care.
The 'PCD on the Move' conference gathers PCD experts to share the latest research and developments.
November 8, 2024
A gathering to highlight future plans for individuals with PCD and honor the impact of the PCD community.
Learn MoreA registry to collect clinical data on PCD to support research and improve patient outcomes.
Learn MoreA network aimed at providing high-quality diagnostic and treatment options for individuals with PCD.
Learn MoreOverall Score
58
50
/100
Program Expense Ratio
76.01%
10
/20
Program Revenue Growth
-0.45%
2
/20
Leverage Ratio
0.09469
20
/20
Working Capital Ratio
3.662
16
/20
Fundraising Efficiency
0
2
/20
Fiscal Year:2022
Source:Source: Self-reported by organization
Category | Amount | Percentage |
---|---|---|
Contributions, Gifts, and Grants | 1.094M | 98.65% |
Program Services | 10.01K | 0.90% |
Investment Income | 5.86K | 0.53% |
Sales of Non-Inventory Assets | -884 | -0.08% |
Other Notable Sources | 0 | 0.00% |
Total Revenue | 1.109M | 100.00% |
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