Featured News

Otorhinolaryngological (ORL) – better known as ear, nose, and throat – complaints in celiac disease are considered rare and are often overlooked by physicians. A recent international narrative review analyzed the latest evidence on the association among celiac disease, ORL, and esophageal symptoms. 

The Celiac Disease Foundation today announced its Board of Directors re-appointments for 2024. The Board represents a diverse mix of professionals, patients, and caregivers who are deeply committed to advancing the Foundation’s mission of accelerating diagnosis, treatments, and a cure for celiac disease.  

The Celiac Disease Foundation is expanding its operations with the appointment of three senior-level staff. These roles are aligned with the Foundation’s latest strategic plan and ongoing work to accelerate diagnosis, treatments, and a cure for celiac disease – one of the world’s most prevalent genetic autoimmune diseases.

On behalf of the entire celiac disease patient community, thank you for your participation in the Celiac Disease Foundation’s 2023 Gift of Hope campaign! Our annual year-end initiative to raise awareness and funds for celiac disease research was extraordinary – all thanks to YOU.

This month's story comes from Dan Gibbons, a patient advocate who also happens to be the Foundation's newest board member!

The Celiac Disease Foundation, a global leader in celiac disease patient advocacy, today announces its new relationship with Mark Cuban Cost Plus Drug Company (Cost Plus Drugs) to provide resources for celiac disease patients and all consumers concerned about potential gluten in the company’s medications. 

The Celiac Disease Foundation and Celiac Cruise are pleased to announce an innovative partnership to offer safe and delicious gluten-free travel experiences, provide educational opportunities, and foster philanthropy within the celiac disease community.

The SynCeD Study is looking for adult volunteers with celiac disease to join a phase 2a clinical trial. Your participation could make a difference. 

Each November the Celiac Disease Foundation hosts our annual Turkey Trot to raise funds for celiac disease research to accelerate treatments and a cure. On November 11 and 12, more than 1,200 supporters from 38 states and countries around the world laced up to move 3.1 miles (5K) for a cure.

This month we hear from Sonia, the mother of a young celiac disease patient. Thank you, Sonia for sharing your family's story!