Tuesday, July 6, 2010

Another Day

So they started Ethan on medication yesterday to help him off the ventilator. We were hoping that would be today but I had my doubts (when the Dr's change plans tend to change.) So this morning they did his weekly eye exam and they gave him morphine for the first time for it. Last week he didn't do so hot with his eye test so they thought this would help him. Well it helped him but it also made him out of it for awhile so the Dr. decided to wait until tomorrow to extubate him and put him back on the high flow nasal cannula. They said that if he pulled it out himself tonight that they would put him on the high flow at that point. I asked "how about I just pull it out and hand it to you." It was hard to see him on the ventilator when he was first born but it is really hard now. He is bigger. He looks like a "term" baby. He looks like he is ready to come home. For some reason though if I tried walking out of the hospital with him I don't think it would go so well (trust me... I have thought of many ways of doing this ;) Well when I was holding him tonight he pulled at his tube and I ended up screaming for a nurse and pushing the call button. (Oh how I thought of just letting him finish pulling it out so they would put him on the cannula but I just couldn't do that!) Things like putting off being extubated for another day just gets to me. I asked why they couldn't do it later at like 5 when he would be awake from the morphine wearing off. She said no because she wanted to make sure she was there in case anything happened. Then she said "another day won't hurt." Yes, as a matter of fact another day will hurt. We are creeping up on that 100 day mark. And that hurts! I so so so badly want to go home with my baby. I know there will be challenges when we are at home (ie... getting up at night, doing daily chores, and having no nurses) but I am so up for that challenge. That challenge will be nothing compared to these last almost 100 days! Seeing Ethan take a step back and having to go back on the ventilator is very hard. Praying he gets off the ventilator tomorrow and onto the nasal cannula.

1 comment:

  1. I am so sorry that in the midst of all your good days you have to have such hard ones! I am so happy to hear how big Ethan is, and How well he is doing. Maybe these little bumps in the road are just him taking a break, so that when he does go home, he can be strong everyday! his little body is working so hard to do so much!
    Stay strong Mark and Leah! God is watching out for you and Ethan!
    Don't count the days you've been there, count the days you have been blessed to have Ethan in your life, and count the days until you go home.
    I know it's hard, hang in there!
    Love ya Lots!

    ReplyDelete

About Me

This blog started as a hobby for many reasons. It later became a way to keep the family up to date on our micro preemie baby, Ethan. Now as Ethan is nearing the 8 year mark with a little sister of 5 years I am finding a new reason to document on this blog.

Last year we were told by the school that Ethan had cerebral palsy, a blindspot and dyslexia. That is what started it all. I started taking him to doctors to find out what was going on and why this hasn't been discovered before now. In April 2017 we were told that he has executive functioning disorder. What the heck is EFD I thought?!?! After the doctor explaining it to us he basically said that if we don't start making changes now he could fall into the ADHD or possibly the autism category. Ok... so now what? What can we do?!? Well this blog is my way of documenting it all not only for me but also to help others find their way thru similar situations.

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