The National Hemophilia Foundation helps consumers:

• Bleeding & Clotting Disorders Facts
• About Blood & Product Safety
• Locate Clinical Trials (new)
• Find support & health information
• HANDI Publications Catalog
• HTC Directory
• And more ...

NHF's Programs and Services include:

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

• Fellowships and Grants
• Working Groups for Nurses, Social Workers and Physical Therapists
• MASAC Treatment Recommendations
• Rare Bleeding and Clotting Disorders Resource Center
• MASAC Recommendations Concerning Products Licensed for the Treatment of Hemophilia and other Bleeding Disorders

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

• NHF Insurance & Reimbursement Conference 2013
• Healthcare Reform!
• Personal Health Insurance Toolkit
• NHF Position Statements
• State & Federal Comment letters
• Tell Your Story

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

Here's how you can help:

• Make a Donation
• Memorial/Tribute
• Planned Giving
• Hemophilia Walk
• Donate your Car
• NHF 2012 Keepsake
• V4W Scarf
• Support Research & Medical Info
• Spring Soiree
• Donor Bill of Rights
• Participate in Clinical Research Trials
• CONNECT Membership

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 >>