Central California Hemophilia Foundation (CCHF) has served individuals and families affected by inherited bleeding disorders in 27 counties of northern and central California since June 1969. Founded by Will and Gloria Curtis, the parents of a young man with hemophilia, the mission of CCHF is to improve the quality of life of those impacted by bleeding disorders through education, advocacy, and support. People with inherited bleeding disorders have trouble stopping their bleeding because their blood does not clot properly. They live with the danger of life-threatening bleeding as well as spontaneous bleeding in their joints, which can result in painful arthritic joints, joint damage, and limited mobility.
CCHF currently serves approximately 450 households of affected individuals and families. Many people with severe bleeding disorders receive intravenously infused clotting factor replacement medication, often several times per week and in some cases, daily. At the time of a new diagnosis, this can be overwhelming for parents. As one mom said, "CCHF means a family that understands what we are going through... It's a family that gives you strength when you wouldn't have it on your own."
As the only nationally affiliated bleeding disorder nonprofit in our service area, CCHF creates opportunities for individuals to meet others with rare disorders, while providing educational materials and programs that help them advocate for themselves and support others. Services include Youth Programs, Education Day, Camp Hemotion, emergency assistance, Lifelong Learning, and scholarships. Currently we are developing a new Life Skills Series to assist adults and teens with expanding their opportunities.
CCHF works in cooperation with her sister chapters in San Diego, Southern California, the San Francisco Bay area, and with the Hemophilia Council of California, the National Hemophilia Foundation, and the Hemophilia Federation of America.