About the Nonprofit
Visit Our Website
Our Mission Statement
Improving the quality of life and building community for those living with inherited bleeding disorders in Southern California
History
The Hemophilia Foundation of Southern California has been serving the community since 1954, providing quality programs and services to individuals affected by hemophilia and other bleeding disorders. Like many foundations, ours began out of the vision of a few individuals who saw the need and importance of uniting in an effort to provide information, education, and improved treatments that would keep their loved ones alive.
Over the years, we have continued this mission and have grown to meet the changing needs of the bleeding disorders community. We continue, where medical treatment leaves off; in our efforts to reach all people affected by hemophilia, and other serious forms of bleeding disorders. We want them to know that there are others who understand their hardships, who are here to support them as they journey through the adventures and struggles of living with a bleeding disorder.
Who We Serve
We serve the following 9 counties: Los Angeles, Orange, Kern, San Bernardino, Santa Barbara, San Luis Obispo, Riverside, Inyo and Ventura Counties. Based on a conservative estimate, 12% of the nation’s bleeding disorder population resides in our area, an approximate 3,000 individuals with Hemophilia A and B, over 300,000 individuals with von Willebrand, as well as countless more with other types of genetic bleeding disorders.
What We Do
HFSC offers assistance in many areas such as medic alert sponsorship, emergency financial assistance, family gatherings and retreats, educational seminars, advocacy, and youth focused programs such as summer camp and teen leadership training. HFSC aims for a future where there is a cure for our members, and in the meantime, to raise awareness about bleeding disorders. Through our programs, events, and advocacy days, we hope to achieve this locally and nationally.
