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.
Friday, June 10, 2011
Happy Friday
Lincoln had a good night last night. His x ray this morning looks about the same as yesterday afternoon ( still the best since being put on ECMO), but his breath sounds are improved from yesterday meaning his lung is opening more. The doctors want to challenge him this morning by making changes to push him toward getting off of ECMO. They are going to turn down the flow on the machine slowly and increase his ventilator settings to see if he will he able to oxygenate himself more using his lung, instead of the machine. They are also going to bring back the nitric oxide he was on before ECMO, which helps him to absorb the oxygen they are giving him. He will also go on a med to help his heart work better as they make his body work harder. It is great news that Lincoln is doing better and the docs feel comfortable making changes. Of course, it is a little scary too since he has been so stable the past few days on the same settings, but he has to work towards coming off if he is ever going to come home! Hopefully Linc will remain strong and be accepting of the changes this morning. We are cheering for him with everything in us!
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We are definitely rooting for Little Linc. I think he and Aubrey look a little alike - definitely can tell they are cousins. We're glad to see the ECMO is beginning to work. He's so cute and such a Fighter and we sure do love him!
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