2024 DDW Award Reception
Prize For Excellence in Celiac Disease Research
Please join us in honoring the awardees and the celiac disease medical and research community.
Register NowAttend educational webinars and meetings, lend your voice to state and federal advocacy initiatives, and fundraise for celiac disease research. Whatever your interest, we have an event for you!
Please join us in honoring the awardees and the celiac disease medical and research community.
Register NowJoin Celiac Disease Foundation partner Stanford Medicine Children’s Health Center for IBD and Celiac Disease for an upcoming community educational webinar, “IBD and Celiac Disease College Transition.” The free Zoom event will feature moderators Vicki Gainsberg, RD and Alison Kotzen, MSN, RN, C-PN.
Register NowJoin Celiac Disease Foundation partner Celiac Kids Connection for a series of webinars throughout the month of May dealing with issues in celiac disease. There will be programs aimed at reaching the needs of both medical providers and families living with celiac disease.
Register NowJoin Celiac Disease Foundation partner Celiac Kids Connection for a series of webinars throughout the month of May dealing with issues in celiac disease. There will be programs aimed at reaching the needs of both medical providers and families living with celiac disease.
Register NowHaving a structured 504 Plan in place is crucial for all students with celiac disease, especially those attending public schools or those that receive federal funding. The Celiac Disease Foundation School Support Sessions in partnership with Boston Children’s Hospital will be held monthly and open to all parents of a child with celiac disease in the United States. Each session will be led by an on expert on setting up 504 plans specific to celiac disease and will cover federal laws and regulations that govern this autoimmune disease, the appropriate type of plan to set up, reasonable accommodations, and how to get individual support for your family. This meeting is appropriate for families with a child of any age including early childhood through college.
Register NowAre you a teen ages 13-17 with celiac disease living the gluten-free life? Join our vibrant community and be part of the Celiac Teen Talk club, where your voice matters, and your favorite gluten-free products take center stage! Forge connections with like-minded teens who understand the ins and outs of navigating the gluten-free world. Each month engage in fun and interactive virtual meetups where we dive into the latest and greatest in the gluten-free world, with host influencer Gabrielle Hemond of “No Gluten Gabby” and special guests each session.
Register NowHaving a structured 504 Plan in place is crucial for all students with celiac disease, especially those attending public schools or those that receive federal funding. The Celiac Disease Foundation School Support Sessions in partnership with Boston Children’s Hospital will be held monthly and open to all parents of a child with celiac disease in the United States. Each session will be led by an on expert on setting up 504 plans specific to celiac disease and will cover federal laws and regulations that govern this autoimmune disease, the appropriate type of plan to set up, reasonable accommodations, and how to get individual support for your family. This meeting is appropriate for families with a child of any age including early childhood through college.
Register NowCamp Celiac serves children ages 9-15 years old by the date of camp who have been diagnosed by an MD with celiac disease or gluten intolerance. Register by February 14 for priority status for the in-person camp session Monday, July 15, to Saturday, July 20. Campers age 16 at the time of Camp entering 10th grade or lower may choose to register as a junior counselor or camper. Campers ages 16-17 who are entering 11th grade or higher must register as a junior counselor. There is no cost to attend other than the $25 non-refundable registration fee (waivers available by writing [email protected]).
Register February 1-14Are you diagnosed with celiac disease? Join the Celiac Disease Foundation and experts in the community for our monthly “Living with Celiac Virtual Meet-Up.” During this one-hour session, you’ll gain valuable insights from celiac experts who will provide practical tips, resources, and guidance on thriving with your diagnosis. And you’ll meet others who are navigating the gluten-free diet, share your experiences, questions, and triumphs in a supportive and understanding environment. Topics will vary by month.
Register NowJoin Celiac Disease Foundation partner Celiac Kids Connection for a series of webinars throughout the month of May dealing with issues in celiac disease. There will be programs aimed at reaching the needs of both medical providers and families living with celiac disease.
Register NowAre you diagnosed with celiac disease? Join the Celiac Disease Foundation and experts in the community for our monthly “Living with Celiac Virtual Meet-Up.” During this one-hour session, you’ll gain valuable insights from celiac experts who will provide practical tips, resources, and guidance on thriving with your diagnosis. And you’ll meet others who are navigating the gluten-free diet, share your experiences, questions, and triumphs in a supportive and understanding environment. Topics will vary by month.
Register NowDelayed diagnosis of celiac disease can result in long-term health complications and increase the risk of developing other autoimmune disorders. Early management is crucial to prevent these potential outcomes. To address this, Adelphi Real World partnered with the Celiac Disease Foundation and conducted a comprehensive analysis comparing diagnostic practices for celiac disease across the USA, Germany, Italy, and Spain. Join the Association of European Coeliac Societies (AOECS) for this insightful webinar where they will unveil the findings and discuss implications for improving early diagnosis rates globally.
Register Now