SNF Access Act Becomes Law
The Hemophilia SNF Access Act becomes law, thanks to the voices and concerns of NHF and HFA advocates.
The Hemophilia SNF Access Act becomes law, thanks to the voices and concerns of NHF and HFA advocates.
NHF becomes an endorsing partner of the first-ever Telehealth Awareness Week.
NHF hosts virtual State of the Science Research Summit to help shape the National Research Blueprint
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).