“Ordinary individuals can make a meaningful difference in their communities by speaking up about issues they care about.” – Celiac Disease Foundation Advocate, Reagan Moore In 2026, updates to the…
Continue ReadingOn May 13, the Celiac Disease Foundation hosted a legislative hearing gathering advocates, clinicians, lawmakers, families, and members of the celiac disease community at the Massachusetts State House to discuss…
Continue ReadingWhen advocates from across the country spoke together, lawmakers paid attention. In an important step forward for the celiac disease community, Senator Richard Blumenthal of Connecticut led a Senate sign-on…
Continue ReadingThe Celiac Disease Foundation is proud to announce that CEO Marilyn Geller has been appointed to the Research & Programs Committee of the National Health Council (NHC). This appointment reflects…
Continue ReadingWe have an important opportunity for Massachusetts residents to contact their legislators today in support of two timely pieces of legislation. In January of 2026, the CAPE Act and the…
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