National Organization for Rare Disorders
U.S. nonprofit organization / From Wikipedia, the free encyclopedia
Dear Wikiwand AI, let's keep it short by simply answering these key questions:
Can you list the top facts and stats about National Organization for Rare Disorders?
Summarize this article for a 10 year old
SHOW ALL QUESTIONS
For other uses, see Nord (disambiguation).
The National Organization for Rare Disorders (NORD) is an American non-profit organization aiming to provide support for individuals with rare diseases by advocating and funding research, education, and networking among service providers.[2] It was founded in 1983 by Abbey Meyers, along with individuals and rare diseases leaders of rare disease support groups, and it is a 501(c)(3) tax exempt organization.[2][3][4]
Quick Facts Founded, Legal status ...
Founded | 1983 |
---|---|
Legal status | 501(c)(3) nonprofit organization |
Headquarters | 55 Kenosia Avenue, Danbury, Connecticut[1] |
Services | provide support for individuals with rare diseases by advocating and funding research, education, and networking among service providers. |
President and CEO | Peter Saltonstall |
Website | rarediseases |
Close