NCA was founded in 1993 as a small group of people supporting each other with celiac disease. As we have grown into a national organization, we’ve focused on helping individuals and their families thrive by providing education and support through a broad range of programs, maintaining contacts within the medical community, disseminating current information about celiac disease, and creating a network of support throughout the nation.
1999
16-1616413
$1.277 million
This organization contributes to the following United Nations Sustainable Development Goals. See the SDG page for more information.
A program designed to help kids and teens navigate the experiences unique to their age group as they deal with celiac disease.
A program coordinating donations of gluten-free food to food pantries to address the chronic lack of GF options.
Educational webinars in collaboration with Harvard Medical School focused on managing celiac disease.
2024-12-03
A webinar discussing managing celiac and dietary needs around the holidays.
Learn More2024-12-04
Webinar on tracking progress and monitoring the patient with celiac disease.
Learn MoreCoordinates donations of GF food to food pantries addressing the chronic lack of GF options.
Learn MoreA program for kids and teens, guiding them and their caregivers in navigating life with celiac disease.
Learn MoreOverall Score
57
42
/100
Program Expense Ratio
53.82%
4
/20
Program Revenue Growth
-27.04%
2
/20
Leverage Ratio
0.1359
18
/20
Working Capital Ratio
2.546
16
/20
Fundraising Efficiency
0
2
/20
Fiscal Year:2022
Source:Source: Self-reported by organization
Category | Amount | Percentage |
---|---|---|
Contributions, Gifts, and Grants | 596K | 87.54% |
Program Services | 76.77K | 11.28% |
Investment Income | 8.042K | 1.18% |
Sales of Non-Inventory Assets | 0 | 0.00% |
Other Notable Sources | 0 | 0.00% |
Total Revenue | 680.8K | 100.00% |
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