February 17 marks the launch of the CDF and Children’s National Health System program to educate healthcare providers about celiac disease and the psychological factors related to living with this chronic disease. Register today for this free seminar, underwritten by a generous grant from the Resnick Family.
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 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, […]
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 […]
On November 9, 2015, Celiac Disease Foundation (CDF) sent a letter to Congressman Chairmen and Ranking Members of the House and Senate Subcommittees on Agriculture, Rural Development, Food and Drug Administration, and Related Agencies. This letter urged the FDA to increase the FY16 budget to $2.8 billion dollars, which is $200 million more than the […]
Celiac Disease Foundation is pleased to announce its pledge of support for the Teal Pumpkin Project™, an international initiative that promotes safety, inclusion, and respect of individuals managing food allergies by encouraging households to display a teal pumpkin and provide non-food treats for trick-or-treaters. The Teal Pumpkin Project™ launched as an international campaign last year […]
In 2013, Representative Tim Ryan (D-Ohio) introduced legislation that would apply gluten labeling requirements on all medications, both prescription and over-the-counter. We strongly endorsed this legislation when it was first introduced in 2013, but it never made it to a vote. This year, we pledge to re-double our efforts, along with other celiac disease organizations, […]
In a rare moment of bipartisan cooperation in Washington, D.C., the landmark 21st Century Cures legislation passed the U.S. House in early July, 2015, by a vote of 344-77. The bill seeks to bring new drugs and treatments to market faster by encouraging medical innovation in research, and streamlining some FDA requirements.
This year, the CDF Southern California Chapter has provided education on celiac disease and gluten sensitivity to more than 500 nurses in Southern California through the CDF School Nurse Awareness Program (SNAP). From February 12-14, 2015, Janelle Smith, RD, and Kris Ledesma, RN, attended the California School Nurse Organization Annual […]
CDF is committed to advancing the delivery of personalized health solutions emerging from the rapidly developing fields of genomics and data collection and analysis. We are a lead institutional participant in the Community Engaged Network for All (CENA), a ground-breaking initiative to create a massive national patient-driven cohort for disease research. The White House has launched […]