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

How More Participation in Drug Trials Can Create Medical Breakthroughs, As Featured in USA Today

The Celiac Disease Foundation (CDF) works tirelessly year-round to advance research toward treatments and a cure. Access to patient data is necessary to better target treatments for those with celiac disease. In CDF’s recent article featured in the December 2017 issue of Media Planet’s Digestive Health campaign of USA Today, titled “How More Participation in […]

Podcast on Patient and Caregiver Participation in Celiac Disease Research

On November 15, 2017, Celiac Disease Foundation (CDF) Chief Executive Officer, Marilyn G. Geller, was a guest on the podcast of the Celiac Disease Program at Children’s National Health System. This podcast episode focused on the importance of participating in celiac disease research. We often hear about clinical trials and research in the news, but […]

The Celiac Disease Foundation 2017 Year in Review

Each year, the world’s leading experts representing every aspect of celiac disease research, education, and advocacy gather at the International Celiac Disease Symposium (ICDS). As you know, there are no approved treatments for celiac disease beyond strict adherence to the gluten-free diet. And, as you know, it is estimated that approximately 30% of all celiac […]

CDF Trains Patient Advocates in Celiac Disease Research at the University of Chicago

On October 21, 2017, the Celiac Disease Foundation (CDF) held a Patient Advocacy Program workshop at the University of Chicago Celiac Disease Center’s Annual Celiac Education Day.  Historically, medical research has not tapped the expertise of patients in the design and development of new treatments, often leading to disconnects between therapeutic outcomes and real patient […]

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