NHF launches Research Journal Club to bring researchers and community members together to discuss the latest science and innovative breakthroughs

NHF refocuses its mission statement to reflect a renewed emphasis on research and an expanded scope to include inheritable blood disorders.

NHF hosts a launch party for Super Seven, its new children’s book for kids with rare bleeding disorders.

NHF announces that its newest fellowship, named in honor of Jeanne Marie Lusher, will prioritize diverse researchers.

An NHF survey found that 86 percent of all registered voters surveyed believe the government should require copay assistance to be applied to a patient's out-of-pocket costs.

NHF enters another five-year cooperative agreement with the CDC to provide educational programming.

MyBDC -- NHF's patient dashboard -- rebrands to Community Voices in Research (CVR).

NHF partners with local HTCs to provide support to the bleeding disorders community in Puerto Rico after the island is devasted by Hurricanes Irma and Maria.

The NHF and CDC conducted a survey, completed in March 2000, aimed at ascertaining knowledge about, attitudes toward, and behaviors associated with key prevention activities among people with hemophilia.

In 2000, NHF launched Project Red Flag with program partners from the the Centers for Disease Control and Prevention. The national campaign had the aptly phrased tagline, “real talk about women’s bleeding disorders."