Rare Disease Day is observed on the last day of February each year. Share your story, participate in global awareness, or find an event in your community to build support.
Join NORD’s signature charity running program to raise awareness for rare diseases, fundraise for NORD programs for undiagnosed patients, and contribute to a team of individuals seeking to make a meaningful difference.
We work with student organizations across the country to facilitate opportunities for the next generation to learn about rare diseases and the patient experience. Join a Students for Rare chapter today.
NORD hosts many events, webinars, and conferences throughout the year that you can attend, elevate, or lend your support to. View our interactive calendar.
The Rare Action Network (RAN) is the nation’s leading advocacy network working locally to improve the lives of the 30 million Americans living with a rare disease. Join more than 18,000 rare community members to get involved in raising awareness, advocacy, fundraising, participating in local events, sharing your story, and creating a lasting impact.
Connect with a patient organization for resources, community, and opportunities to lend or gain support.
Sign-up for our mailing list for a variety of newsletter options! Keep up to date on what is happening at NORD and in the rare disease community.
NORD supports medical professionals and researching working in the rare disease field with critical information, continuing education, research support, and networking opportunities. Learn more.
NORD elevates research and companies working towards treatments and cures for rare diseases through grants, translational research, patient-focused data collection, and our IAMRARE Registry Program, and other key initiatives.
Join over 330 peer organizations as part of the NORD network! Access up-to-date resources, critical opportunities, and take the next step in research or advocacy.
Become part of a select group of leading companies working alongside NORD who are committed to helping people with rare diseases.
