Statement by National Organization for Rare Disorders CEO, Pamela Gavin, on Congress’s Exclusion of Critical Rare Disease Bills in the Continuing Resolution
For the last several years, the National Organization for Rare Disorders (NORD) has had the privilege of working in close collaboration with Members of Congress from both sides of the …
Continue reading "Zane’s Diagnostic Odyssey: His Mother’s Story in Honor of Undiagnosed Day"
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