This will be our 4th year walking and raising money for Congenital Heart Defect Awareness..

This year we will walk for one more heartbeat, one more heart. As many know my oldest daughter, Ellie, was born with a congenital heart defect. In simple terms she was born with half a heart and we have never let that mean half a life. There is not permit fix, but it never stops us from experiencing life to the fullest. 

6 months ago we welcomed our newest family member, our daughter Maddison. Even with the odds of not having another child with a heart defect, we learned of Madds special heart. Her defect may be surgically repairable and not cause her life long problems but her heart is just as special. 

Every 1 out of 100 babies are born with a heart defect. To many don't see their first birthdays. To many of our friends have gained their wings to soon. 

There is no cure or magic that can save our kids. Our hope is in research as since catches up to our amazing warriors.