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.

U.S. Food and Drug Administration (FDA)

List of Orphan Product Designations and Approvals

Experiences of the Rare Disorder Community

In 1989, a Congressional committee released a report on the ways in which having a rare disease affects patients and their families. Now, NORD and a Sarah Lawrence College graduate student have conducted a similar, but smaller, study to update the findings. Read the full text of the report.

NORD Member Organization Events and Requests for Proposals

NORD’s Member Organizations host many conferences and scientific meetings. Read about important upcoming events on the Member Organization Events page and Member Organization RFPs page.

NORD Nonprofit Resource Center

Helpful advice for establishing and growing a patient organization

Dr. Brady to Receive
One of Nation's Top Awards

Dr. Roscoe Brady September 3, 2008 — Roscoe O. Brady, MD, a member of NORD's Medical Advisory Committee, has been named a recipient of the nation's highest honor for innovative achievement in science and technology. On September 29, President George Bush will present Dr. Brady with a National Medal of Technology and Innovation.

Read our news release.

Social Security Administration
Seeks Input From Physicians

People with rare diseases who apply for Social Security disability assistance are often turned down at first because their diseases are not on the approved list. To help the Social Security Administration address this problem, NORD is asking physicians with expertise on various rare diseases to help establish criteria related to those diseases. Read about a survey for medical professionals.

PNH Support Meetings

September 16, 2008 — NORD is hosting a series of regional support meetings for patients and families affected by paroxysmal nocturnal hemoglobinuria (PNH).

The Northeast Regional PNH Support Meeting will be held in New York, NY on Saturday, September 27th. The PNH Research and Support Foundation's Third Annual Walk for PNH is taking place September 28, 2008 in New York City. This event is the biggest annual U.S. fundraiser dedicated to raising money to help fight PNH disease by funding much-needed medical research and patient support programs.

What Is PNH? (Presentation by Dr. Wendell Rosse, Professor of Medicine, Emeritus, Duke University Medical Center)

FDA Approves First
Bone Marrow Stimulator

August 22, 2008 — The Food and Drug Administration (FDA) today approved romiplostim (Nplate), the first product that directly stimulates the bone marrow to produce needed platelets in patients with chronic immune thrombocytopenic purpura (ITP). Platelets are the blood components that help with clotting, and people with ITP have too few of them.

Survey Being Conducted in Argentina

A research project is being conducted in Argentina to determine problems experienced by people with rare diseases.  This project could potentially lead to public policy changes to address these problems.  NORD has been helping Moira Liljesthrom, president of Fundacion FOP (fibrodysplasia ossificans progressiva) get the word out about this survey. People who live in Argentina who are interested in learning more about this project, may visit www.fundacionfop.org.ar or write to info@fundacionfop.org.ar.

FDA Approves First Drug
For Huntington's Disease Chorea

August 15, 2008 — The Food and Drug Administration approved tetrabenazine (Xenazine) for the treatment of chorea in people with Huntington's disease. Chorea is the jerky, involuntary movement that occurs in people with this disease. This is the first drug approved in the U.S. for any symptom of Huntington's disease. The manufacturer is Prestwick Pharmaceuticals, Inc.


President Ronald Reagan signed the Orphan Drug Act in 1983, bringing new hope to the 25 million Americans with rare diseases. Throughout 2008, we’ll be celebrating the 25th anniversary of this very successful legislation and of the founding of NORD.

No Fall Conference This Year
Because of the special activities related to NORD's 25th anniversary celebration, there will be no fall conference this year.� However, watch this space for announcement of a major event in 2009.

Read our news release.

Read About NORD’s
Patient Assistance Programs

NORD administers various programs to help people obtain certain medications. These include medication assistance programs for uninsured patients, Medicare and insurance co-pay programs, early or expanded access to investigational products, travel and relocation assistance for clinical trial participants, and emergency or limited access to products in short supply. Click here to read about the patient assistance programs currently being administered by NORD.

NORD Gets 4-Star Rating
for Sound Fiscal Management

For the fifth consecutive year, NORD has been awarded a top (4-star) rating for sound fiscal management by Charity Navigator, a leading charity evaluator. The evaluation shows that NORD spent slightly over three percent of its revenues on fundraising and administration. All the rest went directly to programs and services. Details.

NORD supports National Family Caregivers Month.

NORD Celebrates
25 Years of Progress

Peter Saltonstall, Nancy Harris, Montel Williams, Carolyn Asbury

More than 500 people attended a recent gala at Washington's Union Station in honor of the 25th anniversary of NORD and of the Orphan Drug Act. As a result of the Orphan Drug Act, more than 320 new drugs have been brought to market for rare diseases.

         

         

View NORD's 25th Anniversary Gala video



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ABOUT | CONTACT NORD


Help NORD improve the lives of people with rare diseases.

Make an online donation in honor or memory of a friend or loved one.

Who We Are

NORD is a unique federation of individuals and organizations working together to build a better world for people affected by rare diseases. Read about NORD.

NORD Member Organizations

NORD Board of Directors

NORD Medical Advisory Committee

NORD Corporate Council

Our Online Community

Visit the Community

NORD has partnered with Inspire to create a free, unique online community service for rare-disease patients, their families, and caregivers. It will be a place where people can find and support one another, share stories, and build a network of online friends.

Please Help US Raise Awareness

Please Help Us Raise Awareness

Do you have a newsletter, community bulletin board, or other place where this ad might be placed to raise awareness of rare diseases and to encourage support for NORD's programs and services? If so, please write to Mary Dunkle (mdunkle@rarediseases.org) or call her at (203) 744-0100 and she will send a copy to you.

NORD's Washington Office

Read about NORD's advocacy on current issues, and learn how you can become involved. Click for details

Looking for Help?

You can contact NORD's Nurse or Genetic Counselor with questions or concerns. Call (800) 999-NORD or write to RN@rarediseases.org or Genetic_Counselor
@rarediseases.org
.

Newsroom

Quick facts, FAQs, and other information for members of the press. Click for details.

Travel Assistance

For information on charitable, long-distance, medical air transportation, visit the National Patient Travel Center's Web site or call their Helpline at 1-800-296-1217.

What's new?

Read about new drug approvals and other recent developments on NORD’s News Briefs page.

Free Booklets for Physicians

NORD provides free booklets on rare diseases to physicians and other medical specialists. (Go to story)

Medical Assistance Programs

NORD’s Medication Assistance Programs provide specific prescription drugs to people who cannot afford them. (Go to Article)

NORD is a participant in the Combined Federal Campaign: #11992 in the CFC brochure.

Raise pennies for NORD when you search the Internet.

Order flowers here, and 20% of the purchase price will be donated to NORD.

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©2008 NORD - National Organization for Rare Disorders, Inc. All rights reserved.

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