Celiac Disease Foundation has announced that it has partnered with the North American Society for the Study of Celiac Disease (NASSCD) to award a three-year, $150,000 grant to support young investigator research in celiac disease. This grant, which will begin with awards in 2016, will focus on finding cause and treatment for celiac disease sufferers.
Meet Janelle Smith, UCLA-educated Registered Dietitian Nutritionist and member of CDF’s Medical Advisory Board. Janelle specializes in gastrointestinal symptom management through appropriate nutrition and food choices, helping you adapt to living on a gluten-free diet. As CDF’s new resource to help our community live gluten-free, she is here to provide tips and tricks for Back to […]
Celiac Disease Foundation was selected in December 2014 to participate in PCORnet, the national resource designed to harness the power of partnerships and health data to allow researchers to conduct clinical research faster, more efficiently, and less expensively than is possible now. There is a 30 day period for our medical and research communities to […]
This month’s Delight Hero, Marilyn Geller has used her public health advocacy and software expertise to lead the way in celiac advocacy, research and education. As a mother to a son with celiac disease, this advocacy has become her lifelong mission.
September 30, 2015 Washington, DC – Representatives Tim Ryan (OH-13) and Nita Lowey (NY-17) introduce the Gluten in Medicine Identification Act, which makes it easier to identify gluten in pharmaceutical products. This legislation requires drugs intended for humans use labels contain a statement identifying the source of any ingredient constituting or derived from a grain […]
General Mills is voluntarily recalling several days of production of Cheerios and Honey Nut Cheerios cereal produced at its Lodi, California facility on certain dates in July of this year because of an undeclared allergen – wheat – with potential adverse health effects. Because this recall relates to an undeclared allergen, this is a Class I product […]
The Patient Centered Outcomes Research Institute (PCORI) holds its Annual Meeting October 6-8, 2015, bringing together members of the PCORI community, including Celiac Disease Foundation as a member of the PCORI Community Engaged Network for All (CENA) Patient-Powered Research Network. The two-and-a-half-day conference will update stakeholder communities on the highlights of the PCORI research portfolio, including […]
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 […]