George was diagnosed with Severe Hemophilia A at 5 months old. Now, over a year and a half later, our lives are filled with running, climbing, reading, lego-building, and accessing his port every other day while watching Planet Earth to give him the Factor VIII infusions he needs. 

Through all the ups and downs, the Colorado Chapter National Hemophilia Foundation continues to be an invaluable organization for our family. Their programs and connections to other resources allow us to live a normal life... or as normal as it can be with a 2 year old. 


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