tag:blogger.com,1999:blog-6860580304473971259.post1122475831770944804..comments2023-04-03T04:42:50.636-07:00Comments on Walking in Faith: My Heart.Joneshttp://www.blogger.com/profile/17884794489481411366noreply@blogger.comBlogger1125tag:blogger.com,1999:blog-6860580304473971259.post-55406489600318435932008-07-28T10:14:00.000-07:002008-07-28T10:14:00.000-07:00Hi, I'm Julie and my son Brigham has Congenitally ...Hi, I'm Julie and my son Brigham has Congenitally Corrected Transposition of the Great Arteries. He's nearly 2 and has had a pulmonary artery band put on to condition his left ventricle -- he will be having the double switch surgery sometime in the next few months. We are in the process of diagnostic tests right now to determine if the left ventricle is now strong enough to handle the switch.<BR/>I am thinking of your sweet baby. We didn't know of Brigham's defect until he was about 3 months old. It has been quite a journey, but, as you will experience for yourself, I'm sure, life has a funny way of continuing to move forward. We love our little boy so much and continue to pray he will be healthy and live a normal life. You can visit our blog any time. I don't keep a separate one for Brig's heart, but if you scroll down the sidebar, there's a label thing -- you can click on "Brigham's Heart" to see everything I've written about him.<BR/><BR/>Good luck and you're in my thoughts.Jocelynhttps://www.blogger.com/profile/13914081924660422629noreply@blogger.com