You are here: Home / Rare Disease Information / Patient Organizations Database

Search Patient Organizations

Enter organization name or disease name to search for organizations that help people with rare diseases.

0-9 - A - B - C - D - E - F - G - H - I - J - K - L - M - N - O - P - Q - R - S - T - U - V - W - X - Y - Z

**IMPORTANT**

The information contained in the Organizational Database (ODB) is provided for informational purposes only. There is no implied endorsement by NORD. NORD does not promote or endorse participation in any specific organization. The information is subject to change without notice. Every effort is made to ensure that the details for each entry are as current as possible.

National Hemophilia Foundation

a/k/a: NHF

Address

116 West 32nd Street, 11th Floor
New York, NY 10001
USA

Phone

212-328-3700

Fax

212-328-3777

800 Number

800-424-2634

TDD

--

Email Address

handi@hemophilia.org

Chapters

48

Website

http://www.hemophilia.org

Founded in 1948, the National Hemophilia Foundation is a national, non-profit organization dedicated to the treatment and cure of hemophilia, related bleeding disorders and complications of those disorders, including HIV and HCV. NHF also strives to support people with bleeding disorders, their families and healthcare professionals; increase public awareness of bleeding disorders; and advocate on behalf of affected individuals. NHF is also committed to disseminating current information on bleeding disorders; raising funds for medical research; and promoting legislation beneficial to affected individuals and family members.

0-9 - A - B - C - D - E - F - G - H - I - J - K - L - M - N - O - P - Q - R - S - T - U - V - W - X - Y - Z

NORD's Rare Disease Information Database is copyrighted and may not be published without the written consent of NORD.

 
Copyright ©2013 NORD - National Organization for Rare Disorders, Inc. All rights reserved.