Hi everyone! If you’re here, you know that I’m an open book about my heart story. I was born with congenital heart defect, tetralogy of Fallot. It’s 4 different defects. 15 years ago, I had pulmonary valve replacement at Rochester Mayo. I get annual check ups and had my usual check up today (7/8/21). It was revealed that I need a new valve. Thanks to medicine, technology and the amazing cath lab, I will hopefully be getting it replaced without open heart surgery! This will be where I will update how things are going and how I’m doing. Thanks for joining in my journey.