We invite you to join the quarterly board of directors meeting for the National Hemophilia Foundation on Thursday, August 19th at 7:00 PM EDT. This meeting will discuss NHF business operations and decisions and is…
Raring for Rares? Join us for Part 3 of Living Rare: 2021 Rare Bleeding Disorders Series at the 2021 Virtual Bleeding Disorders Conference. If you have a rare bleeding disorder or support someone with a rare bleeding disorder connect with…
If you are a person with hemophilia A or B with an active or tolerized inhibitor or support a person with one, join us for Part 3 of the 2021 Inhibitor Education Series at the 2021 Virtual Bleeding Disorders Conference. The Inhibitor Track…
Cuando vive con hemofilia con un inhibidor, usted y su familia tienen preguntas e inquietudes que merecen una atención especial. La serie Viviendo con Inhibidores 2021 proporcionará precisamente eso: educación de calidad y apoyo significativo…
NHF is excited to remind attendees of the 2021 Virtual Bleeding Disorders Conference that a series of E-Poster Abstracts, including some with a video presentation, will be on display for the duration of the program from Wednesday, August 25 –…
NHF is pleased to announce that two new resources have been added to the Nurses’ Guide to Bleeding Disorders (NGBD), both of which were developed to be practical guidelines for the preparation and administration of bleeding disorders therapies.…
NHF requests members of the inheritable blood disorders community be informed of a recent FDA recall involving Monoject™ Flush Prefilled Saline Syringes. Please see the below and discuss with your physician for more information. Patients who would…