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.
Saturday, June 11, 2011
ECMO Wean Attempt
Lincoln responded well to the changes the doctors made yesterday. They were able to wean him every hour from 8am until 3 pm, when he hit a plateau. He was still doing well, but his stats had begun to drift down, so the docs decided to just hold steady through the night. By morning, Linc had brought his numbers back up. His morning x ray looked great. He even has breath sounds on the right side too now. So the plan for today is to continue the wean as long as Lincoln can tolerate it. Undersandably, he has been pretty sleepy yesterday and today, but that is a-okay. He is doing a great job!
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