News NORD and Partners Publish Abstract Based on Web-Based Hemophilia A Educational Initiative for Patients, Caregivers and HCPs
News Research Grants for Rare Disease Research Available from National Organization for Rare Disorders (NORD)
News NORD CEO Statement on FDA Draft Guidance for the Plausible Mechanism Framework for Individualized Genetic Therapies
News Statement from Pamela Gavin, CEO, National Organization for Rare Disorders (NORD) on the Senate Failure to Approve the Give Kids a Chance Act By Year-End
