In 1958, HFNC began as an effort to raise awareness for a small group of hemophilia patients. Today, we provide advocacy, support, and resources to over 3,000 Northern California families (in 47 counties) with a myriad of inherited and acquired blood related conditions.
WE ARE DEDICATED TO HELPING
HFNC membership is free. New families will gain valuable support from programs such as Family CAMP and Dad's in Action. We are also here to help suggest a Hemophilia Treatment Center!
HFNC Children's programs include a week long Camp HEMOTION for patients and siblings, our holiday party to see friends, and the Hemophilia Walk to name a few!
Our teen programs focus on developing leadership skills with programs such as B Leaders and advocacy awareness with Legislation Day and a trip to our state capital.
Valuable affiliations with other national foundations provide advocacy and awareness. HFNC support groups include inherited and newly acquired disorders.
The Hemophilia Foundation of Northern California (HFNC) serves the needs of people impacted by bleeding disorders through enhancing quality of life by providing support, education, outreach, advocacy and research through our affiliated national foundations.
HOW WE HELP
AMONG THE COUNTIES WE SERVE
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