The National Fragile X Foundation empowers families affected by Fragile X syndrome through community support, education, and research. They provide resources for families to help navigate the challenges of living with Fragile X while advocating for patients' needs. Their ongoing efforts focus on advancing research and improving treatments for individuals with Fragile X-related conditions.
2001
84-0960471
$2.775 million
Join a panel discussion about navigating challenging behaviors in children with Fragile X.
Celebrate Friendsgiving with the Sibling and Self-Advocate Network virtually and participate in fun activities.
Join families, caregivers, and advocates for the NFXF Advocacy Day to support the Fragile X community.
2024-11-20T19:00:00Z
Join a panel discussion with experts as they discuss how to navigate challenging behaviors.
Learn More2024-11-23T14:00:00Z
Join us for a Thanksgiving celebration with games and fun activities.
Learn More2024-12-16T13:00:00Z
Discussion about community surveys on gene therapy for the Fragile X syndrome.
Learn More2025-02-24T00:00:00Z
Annual event gathering families, self-advocates, and researchers to discuss and advocate for the Fragile X community.
Learn MoreFacilitates research activities to advance knowledge about Fragile X syndrome.
Learn MoreA multi-day event showcasing the latest in research and support for Fragile X.
Learn MoreConnects families with researchers for improved participation in studies.
Learn MoreOverall Score
68
66
/100
Program Expense Ratio
81.41%
14
/20
Program Revenue Growth
162.69%
20
/20
Leverage Ratio
0.1097
18
/20
Working Capital Ratio
1.181
12
/20
Fundraising Efficiency
0
2
/20
Fiscal Year:2022
Source:Source: Self-reported by organization
Category | Amount | Percentage |
---|---|---|
Contributions, Gifts, and Grants | 2.563M | 79.08% |
Program Services | 665.9K | 20.55% |
Investment Income | 1.762K | 0.05% |
Sales of Non-Inventory Assets | 0 | 0.00% |
Other Notable Sources | 0 | 0.00% |
Total Revenue | 3.241M | 100.00% |
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