Featured News

As we head into fall, I am happy to share that our 2023 Virtual Turkey Trot is right around the corner – and our team is gearing up for a terrific event! As our biggest annual fundraiser helping move us toward treatments and a cure for celiac disease, the Turkey Trot offers our community a wonderful opportunity to promote our shared mission.

At CDF, we deeply value hearing stories from our patient community. Your stories are a pivotal part of our efforts to build awareness and fight for research funding. 

Research is pivotal to the mission of the Celiac Disease Foundation, and so I’m excited to provide you with an update on the groundbreaking findings of a recent study conducted for the European Union’s Joint Research Centre (JRC).

During the month of May, the Celiac Disease Foundation is taking the opportunity to honor the advocacy efforts of our dedicated, inspiring celiac disease patient community.

This week I will be traveling to attend an international symposium hosted by the Celiac Disease Center at Columbia University. This event is a valuable opportunity for leaders and influencers in celiac disease research to connect, share, and learn.

2023 promises to be a year full of robust research, advocacy, and education efforts on behalf of our patient community.

The Celiac Disease Foundation is pleased to announce the establishment of two international celiac disease research prizes to inspire a new generation of researchers whose work in celiac disease will be invaluable.

The Celiac Disease Foundation is in discussion with a team at the University of Colorado, Denver to develop the first-ever, FDA-approved pediatric PRO (patient-reported outcome tool).

On April 8 and April 9, the Celiac Disease Foundation is sponsoring the Columbia University Celiac Disease Center International Symposium on Celiac Disease.

To share with you some insight into our advocacy work, I recently interviewed Mark Van de Water, Senior Advisor at Baker Donelson.