Many libraries, schools, universities, and hospitals subscribe to NORD’s Rare Disease Database for unlimited access to reports on more than 1,200 diseases.
Read about more than 2,000 patient organizations and other sources of help.
NORD's
Washington Office Read about events on Capitol Hill, funding for rare-disease research, and other topics of interest from NORD's office in Washington, DC.
Programs & Services
How to be an Effective Fund-Raiser
Building Local Awareness
A presentation given by Jean Campbell, NORD Vice President for Development, at a Sturge-Weber Foundation Conference in July 2005
Finding the Funding
A presentation given by Jean Campbell at the NORD Annual Conference in 2004
Finding the Funding II
A presentation given by Jean Campbell at the Medtronic Foundation's Patient Link Conference in 2005
Over 1200 Disease Reports
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Since 1983, working toward the prevention, treatment, and cure of rare
“orphan” diseases.
NORD Resource Guide
The new and expanded NORD Resource Guide
(5th edition) is now available. It lists more than 1,300 organizations helping
people with rare disorders.
Travel Assistance
For information about free or low-cost travel to treatment facilities or sites
of clinical studies, NORD refers patients and families to the National Patient Travel Center.