SAVE THE DATE: Rare Disease Day 2025
Rare Disease Day is the official international awareness-raising campaign for rare diseases observed annually on the last day of February. With over 300 million people globally living with a rare […]
Rare Disease Day is the official international awareness-raising campaign for rare diseases observed annually on the last day of February. With over 300 million people globally living with a rare […]
2025 INDUSTRY FORUM The purpose of Industry Forum is to present information on new and pipeline products that treat rare bleeding disorders. Often the presentations are given directly by pharmaceutical […]
We want to share an important update about Washington Days from the National Bleeding Disorders Foundation (NBDF). NBDF has announced changes to their Washington Days registration process including a shortened […]
Panda Express will donate 28% of sales to the Hemophilia Foundation of Southern California in support of those living with and who are affected by inherited bleeding disorders in Southern […]
We invite you to learn more about the Hemophilia Foundation of Southern California, explore bleeding disorders, and connect with your community. Open to families who are new to Southern California […]
Women’s bleeding issues continue to present specific challenges with diagnosis, treatment and access. Heavy menstrual bleeding can lead to anemia (low red blood cell count/low blood iron levels), with symptoms […]
HFA Symposium 2025 is coming to San Diego in 2025! Connect with your community at one of America's most beautiful locations! Valuable educational sessions for severes, milds, rares, and more. […]
Join us for a celebration of our unbreakable bond. The bleeding disorders community may be tied together by a diagnosis, but the connections go even deeper. Our 2025 One Family […]
Join us for a celebration of our unbreakable bond. The bleeding disorders community may be tied together by a diagnosis, but the connections go even deeper. Our 2025 One Family […]
Join Sanofi for a dinner to explore the treatment of hemophilia A and B, with or without inhibitors, and to discuss how shared decision making with your healthcare provider can […]
Please join us for HFSC’s annual event where the community comes together to learn about updates and strategic goals of the foundation and exciting issues that span medical, psychological, and […]
Please join us for an educational lunch, where we will hear from patient speaker, Daniel, on "My Kovaltry® Conversation | Kovaltry® Antihemophilic Factor (Recombinant)." This event is for men and […]