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Formerly know as the Annual Meeting, the National Hemophilia Foundation’s Bleeding Disorders Conference enables the bleeding disorders community to come...Get Details
Register for the Alliance Virtual Hill Day! Only One Day Left! Hemophilia Alliance is excited to be planning a virtual...Get Details
HFA is pleased to announce new dates for our previously-postponed Symposium. The 2020 Symposium will be held Aug. 24-29, 2020....Get Details
Update: Due to the COVID-19 pandemic, NHF has decided to host the 2020 Rare Bleeding Disorders Conference virtually. By creating a virtual environment, we will make the experience consistent with the top-level education you are used to receiving from NHF. Please continue to check this page for further updates.
In the bleeding disorder community, the “rarest of the rare” (those with rare factor deficiencies and platelet disorders) often struggle with similar symptoms and challenges compared to more common bleeding disorders (hemophilia and VWD). The resources available to those consumers living with rare bleeding disorders are quite limited. This conference is an opportunity for families affected by these rare bleeding disorder to attend rare-specific educational sessions and meet other families in the bleeding disorder community.