The Living Rare Study® is the first large-scale, long-term U.S. study tracking the evolving experiences of individuals and caregivers impacted by rare diseases.
Sharing your story can help shape NORD programming, inform policy decisions, and improve access to resources that enhance quality of life.
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Missed NORD's Rare Disease Scientific Symposium? Explore expert presentations, breakthrough insights, and key research and regulatory discussions shaping the future of rare disease.
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Rare disease policies vary by state. See where your state stands in the 2025 NORD State Report Card.
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Shop exclusive NORD merchandise that helps raise awareness, spark conversations, and celebrate the strength of the rare disease community.
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Get help with access to medication, diagnostics, caregivers support, and other needs.
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Learn more about 1,200 rare diseases through our comprehensive database.
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NORD® Rare Disease Centers of Excellence are diagnosing and treating thousands of rare disease patients.
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Assist researchers throughout the world better understand and treat rare diseases by enrolling in our registry and sharing your experiences.
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Adults living with rare disease and caregivers share their lived experiences to help drive positive change
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Discover how your rare experiences can help researchers and lead to a brighter future.
Learn MoreYou or a loved one has received a diagnosis. Now what? Gaining knowledge, connecting with advocacy organizations, and learning about treatment at places like the Centers for Excellence are the next steps.
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We help inform and advocate for legislation and policies that reflect the needs of rare disease patients and their families.
We provide information about rare diseases, patient organizations and other resources. We also promote awareness of rare diseases among physicians and other medical professionals.
We pioneered Patient Assistance Programs in 1987. Today, NORD programs include free drug, co-pay and premium assistance, travel/lodging assistance for clinical trials, expanded or emergency access, and more.
Disease-specific patient organizations are crucial partners in our mission to serve rare disease patients and their families. That’s why we provide capacity building and mentorship services to start-up and established organizations.
Our grant programs have resulted in numerous published advances and at least two FDA-approved therapies.
NORD believes in the power of collaboration. It is the foundation upon which NORD was built. NORD works with partners in the patient community, government, academia, and industry who share the ultimate goal of identifying, treating, and curing rare diseases. In addition to the partnerships listed below, NORD works with many national partners to achieve its advocacy goals.
The mission of NORD is to improve the health and well-being of people with rare diseases by driving advances in care, research and policy.
NORD helps drive more effective government policies by elevating the voice of the rare disease community.
Patient advocacy organizations play a vital role in helping people with rare diseases live their best and fullest lives. We can help you find one or even start your own.
