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FDF Presents Patient Registry Poster at NORD Summit in DC

The Fibrous Dysplasia Foundation (FDF) strives to advance FD/MAS research and to ensure that the patient voice remains in the center of scientific advancements. In an effort to further both of these goals, FDF attended the National Organization of Rare Disorders (NORD’s) annual summit in Washington, DC this November. There, Teneasha Washington, FDF’s Research Programs […]