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NORD’s Living Rare Forum and Rare Impact Awards Highlight Powerful Patient Stories and Community Rock Stars

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NORD CEO Statement on Rare Cancer Day

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April Showers Bring May Flowers: Christine’s National Volunteer Month Story

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Congress should protect the intent of the Orphan Drug Act and pass the RARE Act

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NORD Named Charity of the Week By The Week Magazine

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HLRCC Family Alliance

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The Undiagnosed: Orphans of the Rare Disease Community

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NORD Publishes Guide to Promote Physician Awareness of Rare Lung Disorder

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Creating Your Medical Advisory Board

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Cutis Laxa Internationale

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National Brain Tumor Society

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Be a Hero-Help NORD Help Patients Obtain Life-Saving Treatments

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NORD Developing 20 Natural History Studies for 20 Rare Diseases

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Undiagnosed: When Your “Depression” Isn’t Depression

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Rare Disease Artists’ Work Traveling Globe to Raise Awareness

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Today is Rare Disease Day®

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NORD Announces 2016 Rare Impact Award Recipients to be Honored on May 17

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Delaware Enacts Law to Address Needs of Rare Disease Patients and Families

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NORD CEO Welcomes FDA Leadership Appointments, Emphasizes Stability and Innovation for Rare Diseases

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NORD Statement on Dobbs v. Jackson

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Kiera’s Rare Disease Journey

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Together, we can be stronger for those that need us.

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Nominations for the Rare Impact Awards Close Friday, January 12

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NORD Rare Action Network® 2018 State Report Card

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NORD Reaction to Recently-Enacted Government Spending Bill