Welcome to our team page!
Dear Friends and Family,
This year is the 50th anniversary of the Central California Hemophilia Foundation and it is also our 50th wedding anniversary. So much has changed in those 50 years and living with a bleeding disorder is so much better than it was 50 years ago. But we still have a long way to go.
Our son was diagnosed with severe hemophilia A at 7 days. When he was one year old we were referred to the UC Davis Hemophilia Treatment Center and he was then correctly diagnosed with type 3 or severe von Willebrand disease.
Did you know that 1 in 100 people have von Willebrand disease? Many of them go undiagnosed and untreated.Did you know that 1 in 4,500 boys is affected by a bleeding disorder like hemophilia. There are 475 thousand people living with bleeding disorders in the world. Bleeding disorders like hemophilia and von Willebrand disease don't discriminate and people of all races and genders are affected.
I have volunteered with the Central California Hemophilia Foundation for over 46 years and my husband, Orville and our children, their spouses and our grandchildren are all doing their part to give back to the bleeding disorder community by volunteering at the various events.
There have been many amazing strides related to bleeding disorders, however there is no cure even though the scientists are working on better treatments and eventually a cure.
The funds raised at this walk will stay in this area. CCHF funds things like summer camp for children with bleeding disorders, scholarships, life long learning scholarships, emergency assistance, educational programs, and fun activities that allow families to network with other families.
Thank you in advance for our support and together we will make a difference.