On May 15, 2026, the Fédération Nationale de la Maladie Cœliaque (FNMC) was officially launched in France, bringing together several patient associations to strengthen advocacy for celiac disease. The federation aims to improve diagnosis rates, support research, and enhance the quality of life for the estimated 1% of the French population affected by this autoimmune disorder.
According to the FNMC, celiac disease remains underdiagnosed in France, with many cases going undetected for years. The federation will work to raise awareness among healthcare professionals and the general public, as well as push for better access to gluten-free products in schools, hospitals, and restaurants.
Key founding members include the Association des Intolérants au Gluten (AIG) and the Association Française des Intolérants au Gluten (AFDIAG), which have long advocated for patients. The FNMC plans to coordinate national campaigns and provide a unified voice in discussions with policymakers.
Dr. Sophie Martin, a gastroenterologist at Hôpital Saint-Antoine in Paris, commented: 'This federation is a crucial step forward. It will help standardize care pathways and ensure that every patient receives a timely diagnosis and proper dietary support.'
The FNMC also intends to collaborate with European celiac organizations to harmonize labeling regulations and promote gluten-free options across borders. For more information, patients can visit the federation's website at fnmc.fr.
