This blog was created to keep family and friends informed of our baby's progress through his journey with Congenital Heart Disease. All prayers and good wishes are welcome. I never dreamed that this little blog would go so far!
Tuesday, March 2, 2010
Got the update call a few minutes ago..They are now attempting to balloon his pulmonary artery...we are hoping that the artery responds and doesnt' shrink back too small after the balloon is removed. If it shrinks too much they will place a stint. We are starting hour 4 for surgery now...but should have another update within the hour...