National Fragile X Foundation Logo

MIP Score

68

Med Research
Hereditary Disease Research

National Fragile X Foundation

Mission

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.

Basic Information

Tax-Exempt

Address

1012 14th St NW, Washington, District of Columbia, 20005

View all Washington charities

Founded in

2001

EIN

84-0960471

Total Assets

$2.775 million

At a Glance

Webinar: Navigating Challenging Behaviors

Webinar: Navigating Challenging Behaviors

Join a panel discussion about navigating challenging behaviors in children with Fragile X.

Virtual Friendsgiving Celebration

Virtual Friendsgiving Celebration

Celebrate Friendsgiving with the Sibling and Self-Advocate Network virtually and participate in fun activities.

Advocacy Day 2025

Advocacy Day 2025

Join families, caregivers, and advocates for the NFXF Advocacy Day to support the Fragile X community.

Upcoming Events

NFXF Webinar Series: Navigating Challenging Behaviors 2024

NFXF Webinar Series: Navigating Challenging Behaviors 2024

2024-11-20T19:00:00Z

Join a panel discussion with experts as they discuss how to navigate challenging behaviors.

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Virtual – SSAN Friendsgiving Celebration

Virtual – SSAN Friendsgiving Celebration

2024-11-23T14:00:00Z

Join us for a Thanksgiving celebration with games and fun activities.

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NFXF Webinar Series: Gene Therapy & the FXS Community

NFXF Webinar Series: Gene Therapy & the FXS Community

2024-12-16T13:00:00Z

Discussion about community surveys on gene therapy for the Fragile X syndrome.

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NFXF Advocacy Day 2025

NFXF Advocacy Day 2025

2025-02-24T00:00:00Z

Annual event gathering families, self-advocates, and researchers to discuss and advocate for the Fragile X community.

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Our Programs

NFXF Research Readiness Program

Facilitates research activities to advance knowledge about Fragile X syndrome.

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Community Support Network

Volunteer-led support groups for families affected by Fragile X.

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Fragile X MasterClass

Educational series for professionals and families about Fragile X.

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NFXF International Conference

A multi-day event showcasing the latest in research and support for Fragile X.

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MyFXResearch Portal

Connects families with researchers for improved participation in studies.

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Impact Reports

MIP Score (Beta)

The MIP Score is in beta! We'd love any feedback you may have.

The MIP Score and it's methodology is purely used as a way to visualize how a nonprofits public financial data compares against others. It doesn't reflect the unique circumstances and impact that a nonprofit has.The MIP Score should never be used to say one charity is better than another.

Overall 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

Latest Filing Data: Form 990

Fiscal Year:2022

Source:Source: Self-reported by organization

Financial Details

Revenue

CategoryAmountPercentage
Contributions, Gifts, and Grants2.563M79.08%
Program Services665.9K20.55%
Investment Income1.762K0.05%
Sales of Non-Inventory Assets00.00%
Other Notable Sources00.00%
Total Revenue3.241M100.00%