James and I began this blog at the very beginning of our pregnancy with Wyatt to share and update our new adventures as we became pregnant and start the new season of parenthood. Sixteen weeks into pregnancy, I had to go into surgery to ensure our son would not come too early and shortly after, we found out Wyatt has Congenital Diaphragmatic Hernia (CDH). This is our humble attempt at being transparent and hopefully sharing the joys and love of Christ through this roller coaster ride we're on. And now to share even more with the new miracle on the way.

Saturday, October 20, 2012


Day ONE HUNDRED: It's hard to believe its been 100 days. The teacher in me wants to have a party with lots of "100" things!! And maybe some balloons!
There weren't any real changes today. They did change the settings on his nasal cannula to resemble what it'll look like at home again, 100% oxygen with a pressure of 0.2. He's been doing some spitting up, more than before his surgery but that can happen and were hoping it lessens. Also, his heart rate was a little high today, praying that's not a sign he needs blood again!!! James and I enjoyed just getting to hang out with him tonight. Praying he's ready to come home in a week!!! (now I've got to make sure we're ready at home!!!)

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