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Accelerating diagnosis, treatments, and a cure for celiac disease and non-celiac gluten sensitivity through research, education, and advocacy.

The Celiac Disease Foundation Expands Partnership with Children’s National Celiac Disease Program

In honor of May Celiac Disease Awareness Month, the Celiac Disease Foundation is proud to announce our expanded partnership with the Children’s National Health System Celiac Disease Program, dedicated to improving the way pediatric celiac disease is diagnosed and treated. The Program recently developed the Celiac Disease and Gluten-Free Diet Digital Resource Center to house […]

The Celiac Disease Foundation Attends FDA Engagement Workshop

Patients and caregivers have unique perspectives on the burdens and benefits of various treatment options. As such, their input is invaluable to the drug evaluation process. On April 3, 2018, Celiac Disease Foundation Legislative Analyst, Alana Broe, attended the FDA’s Public Workshop on Keys to Effective Engagement with the Center for Disease Evaluation and Research […]

Marilyn G. Geller Joins Gluten-Free Living Magazine Advisory Board

“I look forward to working together to spotlight celiac disease and gluten-free champions in our community, and to our shared commitment to advance celiac disease research. Gluten-Free Living provides a unique platform to reach the many people following a gluten-free diet who so often feel alone and who struggle to find a supportive community and credible information.”

The Celiac Disease Foundation Submits Comment to the Centers for Medicare and Medicaid Services on Proposed Rule: Short-Term, Limited Duration Insurance

On February 21, 2018, the Centers for Medicare and Medicaid Services (CMS) released a proposed rule to modify the definition of short-term, limited duration insurance to exclude it from individual health insurance coverage. Short-term, limited duration plans (STLDPs) are not required to meet Affordable Care Act (ACA) requirements, as they are currently only intended for […]

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