About the National Hemophilia Foundation

When the National Hemophilia Foundation was established 50 years ago, people with hemophilia were known as "sufferers," and their life expectancy was less than 30 years. People with hemophilia had no formal means of communication, and no one advocated for research money, better healthcare, or improved insurance coverage. Families were not connected with other families. People had very little way of knowing if they were all alone or if there was anyone in their neighborhoods facing the same problems.

Today, the National Hemophilia Foundation makes an important difference in the lives of people and families with bleeding disorders. With its strong national presence, chapters throughout the country, and an intricate communications network bringing healthcare professionals and consumers the latest news and information about bleeding disorders, the National Hemophilia Foundation has a proven track record of improving the quality of life of people with bleeding disorders and their families.

To find out more about the National Hemophilia Foundation, visit their Website at www.hemophilia.org