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Welcome to the National Hemophilia Foundation

NHF is a Member of The National Health CouncilThe National Hemophilia Foundation is dedicated to finding better treatments and cures for inheritable bleeding disorders and to preventing the complications of these disorders through education, advocacy and research.

4th Annual Spring Soiree

HemAware Now Online!

The National Hemophilia Foundation helps consumers:

NHF's Programs and Services include:

Steps 4 LivingVirctory for WomenNYLI

There's a wide range of resources for Researchers, Medical and Healthcare Professionals, including:




NHF's public policy efforts are intended to ensure those affected by bleeding disorders have access to the quality care they require.  For information on NHF's state and federal priorities and up to date information on issues that may affect your healthcare coverage
click here.


Advocacy Website

Our research, education and advocacy initiatives are made possible with your involvement and generous support.

Here's how you can help:

Inhibitors can be a serious problem for certain people with bleeding disorders. Inhibitors are a type of antibody produced by the body's immune system in response to factor concentrate. By neutralizing the effect of the factor product, they can prevent the formation of blood clots.

Read more about Inhibitors >>

NHFs 66th Annual Meeting

Hemophilia Walk

Mark W. Skinner, JD, Appointed as a Member to PCORI’s New Advisory Panel on Rare Disease

Former Bayer Interns Share Insights from BHLDP Experience

My Life Our Future

Free Genetic Testing Initiative to be Available Nationally at Hemophilia Treatment Centers

Medical Advisory #416
Voluntary Recall Issued for Certain Lots of Monoject (TM) Prefill Flush Syringes


Managed Care Hemophilia

Take the Patient Attitude Study!