The National Organization for Rare Disorders (NORD) in New York, NY, is a leading resource for patients, caregivers, clinicians, and researchers in the rare disease community. With a focus on advocacy, education, and support, NORD offers a wide range of services including patient assistance programs, clinical trial exploration, and rare disease awareness initiatives.
Through their extensive network of partnerships and programs, NORD is dedicated to advancing research, improving clinical care, and driving policy changes to benefit those affected by rare diseases. With a strong emphasis on community support and empowerment, NORD strives to make a meaningful impact in the lives of individuals facing rare medical conditions.
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