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Ava's story will be told by one of the two people who know it best-Ava's Mama. My name is Chessie Vetter and I'm Ava's Mama! My husband and I, collectively, would like to raise awareness of Congenital Heart Defects. Prior to Ava's diagnosis, we had minimal knowledge of any CHD. Yet, 1 in every 100 babies are born with some variety of a CHD. I cannot fathom that statistic. It does not seem fair. Nonetheless, it cannot be changed and the only option is to become educated. I'm going to take you, as the reader, through Ava's journey from start to now. If you are reading this then you have shown interest and for that we are thankful and appreciative!

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