NORD and the Galactosemia Foundation Jointly Publish First “Voice of the Patient” Report to Help Inform the FDA and Researchers - National Organization for Rare Disorders
Por um escritor misterioso
Last updated 26 março 2025


New Patient Journey Infographic Gives A Glimpse Into The

NORD Announces #1in10 Campaign to Raise Awareness for Rare Disease

Writing the Book on Your Child's Rare Disease: Raymond's Story in

Scholarship Foundation. of Santa Barbara Report to our Community

Banding Together as Zebras: Merry's Story in Honor of Rare Disease

Scholarship Foundation. of Santa Barbara Report to our Community

New England Revolution on X: Wishing our very own Richie Williams

New England Revolution on X: Wishing our very own Richie Williams

Featured NORD Member Org: CTF - National Organization for Rare

Scholarship Foundation. of Santa Barbara Report to our Community
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