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NHF's HANDI

HANDI, the information service of the National Hemophilia Foundation (NHF), provides up-to-date resources on bleeding disorders. Information specialists are available to answer questions, conduct library searches, and refer individuals to other agencies when necessary. Each HANDI request is customized to meet the individual’s needs through the use of the latest information available. Some common topics requested:
Hemophilia
von Willebrand Disease
Gene Therapy
Hepatitis
Sports and Exercise
Blood Safety

HANDI also offers fact sheets that provide easy-to-read references on the following topics:

Inheritance of Hemophilia
  Also available in Spanish–
  Informacion sobre la Herencia de Hemofilia

Women with Bleeding Disorders
  Also available in Spanish–
  Informacion sobre Desordenes de Sangrado en Mujeres

von Willebrand Disease in Women

Hemophilia B Leyden

Prophylaxis
  Also available in Spanish–
  La Profilaxis: Un Guia para Padres

NHF’s HANDI offers an array of publications on topics of interest to the bleeding disorders community. Click here for a complete listing.

Contact HANDI at (800) 42-HANDI,
e-mail: handi@hemophilia.org,
or fax: (212) 328-3799.

If you have any questions or need information on health coverage, insurance matters, or managed care, please send them to Nava Rahmanim at nrahmanim@hemophilia.org. When e-mailing a request for information, please be sure to include your name, mailing address, and telephone number.


Disclaimer
The information contained on the NHF web site is provided for your general information only. NHF does not give medical advice or engage in the practice of medicine. NHF under no circumstances recommends particular treatment for specific individuals and in all cases recommends that you consult your physician or local treatment center before pursuing any course of treatment.
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