The Hemophilia Act of 1973 allows federally funded comprehensive hemophilia treatment centers to be established
The act provided funding for hemophilia treatment centers, which were established to provide specialized medical care and education for individuals with hemophilia and their families.
In addition, the Hemophilia Act of 1973 established a federal program to provide financial assistance for the purchase of clotting factor therapies. This program was intended to ensure that individuals with hemophilia had access to the costly clotting factor treatments they needed to manage their condition.
The Hemophilia Act of 1973 was significant because it was one of the first federal laws to provide specific support for individuals with a genetic disorder. It recognized the unique challenges faced by individuals with hemophilia and provided resources to help them manage their condition and improve their quality of life. The law has been amended several times over the years to reflect changing medical and financial circumstances.
In 1973, NHF launched a two-year campaign to establish the creation of a nationwide network of hemophilia diagnostic and treatment centers. The goal was to provide a range of comprehensive services for patients and families within one treatment facility. Today, there are about 141 federally funded treatment centers and programs across the country. Source
