Lincoln was born with a rare diaphragm defect known as right-sided Congenital Diaphragmatic Hernia (CDH) on May 26th, 2011. We were told that Lincoln had little more than 50% chance of survival. Linc fought hard for his life in the beginning, coming very close to losing his life. After 83 days in the NICU, Lincoln came home to us. He remains strong and stubborn, and is now a happy, healthy one year old. This blog documents his life.
Wednesday, June 8, 2011
ECMO day 8
Lincoln's morning x-ray showed no improvement from yesterday. We are still waiting for his lungs to clear. The repeat echocardiogram done yesterday showed that Linc has some fluid accumulation around his heart. The surgeon said that it was expected since he is accumulation fluid all over. He said it will be something to watch, but no intervention needs to be done now. Too much fluid around the heart can make it difficult to beat, but since Linc is on ECMO, his heart doesn't need to work that hard anyway. Once they start to wean him, they will reevaluate it then. Lincoln also got an ultrasound of his head to check for bleeding. Linc has to be on blood thinners while on ECMO, so he is at an increased risk of bleeding. The results showed no signs of bleeding. So for now, "stay the course" as the docs say. "An uneventful day on ECMO is a good day."
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