National Organization for Rare Disorders

Non-Profit - Danbury, CT, US

National Organization for Rare Disorders Details

The National Organization for Rare Disorders, a 501(c)(3) organization, is an independent patient advocacy organization dedicated to helping individuals with rare diseases and the organizations that serve them. NORD, along with its 280 patient organization members, is committed to the identification, treatment, and cure of rare disorders through programs of education, advocacy, research, and patient support services.NORD serves all stakeholders in the rare disease community, including patients and their families, patient organizations, researchers, medical professionals, medical students, and companies developing orphan products. NORD also works closely with many government agencies, most notably the National Institutes of Health (NIH) and the Food and Drug Administration (FDA). All NORD programs are focused on one ultimate goal -- to improve the lives of individuals and families affected by rare diseases. NORD is the official sponsor of Rare Disease Day in the U.S., an observance day held on the last day of February each year worldwide. Its goals are to raise awareness for rare diseases and improve access to treatment and medical representation for individuals with rare diseases and their families. To learn more, visit rarediseaseday.us.To learn more please visit the NORD website at www.rarediseases.org. You can also follow NORD on Twitter at @RareDiseases.

National Organization for Rare Disorders logo, National Organization for Rare Disorders contact details
Website: rarediseases.org
Employees: 100 - 249
HQ: 203-744-0100
Location: Danbury, CT, US
Revenue: 10 - 20 Million
rare diseases patient assistance patient support rare disease information advocacy information for medical professionals research online communities orphan diseases Non-Profit Nonprofit Organization Management
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