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The National Organization for Rare Disorders (NORD) is dedicated to advancing meaningful change for individuals affected by rare diseases. They provide a comprehensive range of resources for patients, caregivers, and healthcare professionals, including educational materials, support programs, and opportunities for community involvement.
NORD also plays a pivotal role in research advocacy, policy development, and raising awareness about rare diseases. Through partnerships and initiatives, they aim to enhance clinical care, promote patient-focused drug development, and support organizations dedicated to rare diseases.
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