The National Organization for Rare Disorders (NORD)


Database Subscriptions

Many libraries, schools, universities, and hospitals subscribe to NORD’s Rare Disease Database for unlimited access to reports on more than 1,150 diseases.

Index of Rare Diseases

This is the list of diseases currently covered in the Rare Disease Database.

Rare Disease Database

Search this database for reports on more than 1,150 diseases.

View sample report

Index of Organizations

This is the list of organizations in NORD’s Organizational Database.

Organizational Database

Read about more than 2,000 patient organizations and other sources of help.

NORD's
Washington Office

NORD's Washington OfficeRead about events on Capitol Hill, funding for rare-disease research, and other topics of interest from NORD's office in Washington, DC.

 

Volunteers in Public Policy

NORD is looking for volunteers who will agree to write their own Senators and Representative up to four times a year about issues that touch the lives of people with rare diseases throughout the United States. Every few months, NORD provides background information on major health issues, clearly outlining arguments for and against each issue. Volunteers are encouraged to form their own views and express them in writing, even if they differ from NORD's, to their Congressional officials. The goal is to call attention to issues that affect the medically disenfranchised people with rare disorders and to encourage elected officials to take action.

If you would like to become involved in the initiative described above, contact Diane Dorman at ddorman@rarediseases.org.

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ABOUT | CONTACT NORD

Since 1983, working toward the prevention, treatment, and cure of rare “orphan” diseases.

Washington Office Contact
Diane Dorman
ddorman@rarediseases.org
Phone: 202.496.1296

Diane Dorman handles legislative and policy issues. Medical questions should be sent to RN@rarediseases.org
or Genetic_Counselor@
rarediseases.org
.

Volunteers in Public Policy

You can help NORD provide advocacy for rare-disease patients and their families. Every voice is important. Click here to submit your email address so that you can join NORD’s Volunteers in Public Policy.

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©2006 NORD - National Organization for Rare Disorders, Inc. All rights reserved.

Last modified Thursday, March 27, 2008