Genotyping for Progress in Hemophilia

 
 

resource center

learn more about My Life, Our Future

We encourage you to learn more via our informational videos,  and to sign up to receive updates from NHF.

You may also contact the staff members at HANDI, NHF's information resource center, who are available to answer live requests from Monday through Friday, 9:00 am to 5:00 pm Eastern Time, at 800.42.HANDI. Requests can also be sent by fax to 212.328.3799 or email to handi@hemophilia.org. Information requests made through HANDI are always kept confidential.

learn more about genotyping

There are many resources available on the benefits of genetic testing. For more detailed information, we invite you to visit:

HANDI: NHF's robust resource center on hemophilia and other bleeding disorders.

Genetic Alliance: A health advocacy organization committed to transforming health through genetics and promoting an environment of openness centered on the health of individuals, families, and communities.

About Health Information Privacy: Background information from the U.S. Department of Health and Human Services on federal laws and regulations designed to protect your privacy.

About the Genetic Information Nondiscrimination Act (GINA): Background information from the National Human Genome Research Institute of the National Institutes of Health on a federal law that protects against genetic discrimination in health insurance and employment.