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The Celiac Disease Foundation provides educational resources about celiac disease, including symptoms, diagnosis, treatment, and gluten-free living, and connects people with healthcare practitioners, school resources, and virtual education. It supports research through the iCureCeliac patient registry, clinical trials, research awards, and data resources to advance understanding and therapies. It also leads advocacy and public policy efforts, awareness campaigns, events, and fundraising to support policy changes and community needs.
AI named Celiac Disease Foundation in February 2026.