Celiac Disease Foundation drives diagnosis, treatment and a cure for celiac disease through advocacy, education and research to improve the quality of life for all people affected by gluten-related disorders

Happy Gluten-Free Holidays

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A diagnosis of celiac disease or non-celiac gluten sensitivity not only changes what we eat, but how we celebrate. Gluten-free holidays certainly take planning and coordination to ensure that you or your loved ones can be safe while eating and enjoy the experience with some of your regular traditions! Here are some of our recommendations […]

Infant Feeding and Risk of Celiac Disease: Systematic Review and Meta-Analysis

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In a recent article, “Gluten Introduction to Infant Feeding and Risk of Celiac Disease: Systematic Review and Meta-Analysis,” published in the Journal of Pediatrics, researchers, including three members of the Celiac Disease Foundation Medical Advisory Board, Joseph Murray, MD, Stefano Guandalini, MD, and Peter H. R. Green, MD, set out to compile and analyze data […]

CDF Secures Co-Sponsor for H.R. 3648: Gluten in Medicine Disclosure Act

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After a long fight, in 2014 the FDA finally implemented regulations for the labeling of gluten-free foods. In 2012, Representative Tim Ryan (D-Ohio) introduced legislation that would require that gluten be identified on all medication labels, both prescription and over-the-counter. Celiac Disease Foundation (CDF) strongly endorsed this legislation when it was first introduced in 2012, but […]

CDF Urges Rapid Confirmation of Dr. Robert Califf as Head of FDA

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CDF has joined with a coalition of disease advocacy organizations led by FasterCures in urging the U.S. Senate to quickly confirm Dr. Robert Califf as the new Commissioner of the U.S. Food and Drug Administration. We have focused considerable resources in recent years on making the voice of the celiac disease community heard among decision makers in Washington, […]

CDF Attends Digestive Disease National Coalition Public Policy Forum in Washington, D.C.

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On October 27-28th, 2015, Talia Hassid, Celiac Disease Foundation’s Community Coordinator, attended the Digestive Disease National Coalition Public Policy Forum held in Washington, D.C.  The forum gathers representatives from digestive disease organizations across the U.S. together to arrive at a common agenda to influence healthcare policy in the United States. Talia met with Members of Congress and […]

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