Monday, June 14, 2010

New meds...

So Saturday night Mark picked me up and I spent the night at home while he worked the night shift. When he got home on Sunday morning he called the nurse to see how he had done throughout the night. She said that he dropped his heart rate and they had to bag him. They also had to turn his oxygen up to 4 liters. He was at 3 in Billings. We found out that right after they got off the phone with us he had a pretty bad episode. He dropped his heart rate and they had a heck of a time getting it back up. He was not a pretty pink she said. He wasn't getting much air through his airway so they decided to add quite a few medications to his list. They were trying to figure out what was done differently in Billings that may have caused this. One thing we did in Billings was feeding him his bottle. G.F. usually waits to do that until his acid reflux is under control and he is on boulous feedings vs. the continuous feedings he is on right now. Feeding him could have caused fluid in his lungs since he has acid reflux pretty bad right now. That is just great! He was weezing pretty bad when we got to G.F. with him and we asked about it and it was kind of ignored. I guess it only got worse and that they could hear him weeszing in the hallway. I just kind of wish we could be a step ahead of the game instead of waiting for him to have an episode for them to act on it. Mark was pretty frustrated with this too.

So Sunday was a decent day for him and he only dropped his oxygen level once in the night and he recovered by himself so they didn't need to do anything. While I was here last night though he has started to lift his head on his own. They have him laying on his belly (don't do this at home I am told ;) and he was lifting his head to turn it but wouldn't make it all the way and would face plant it in the mattress. So of course his oxygen levels were dropping so I just moved his head to the side so he could breath. I asked if it could be because they have the bed at such an angle (this is to help with the acid reflux) that it is giving him leverage to do that. She said no he is just getting bigger and more active. They will do that. Ok well I understand that but how about yeah he is a stinker like that but I will make sure to watch it while you are gone. Just some comfort to know that he is taken care of while I am not here is greatly appreciated some days.

1 comment:

  1. AWww he is getting big and strong! YAY!
    I had to laugh a little with the face planting it into the matress thing! I can just picture it and it is kind of funny.
    Ava (Naomi's daughter) is just starting to pick her head UP but hasn't quite got the hang of putting it back down yet without giving herself whiplash! It's pretty cute!

    I wish too that the nurses and everyone at G.F. Would listen to you guys more rather than just blowing you off. You're the parents, you know more than anyone! Because you are with him in G.F., Billings, Seattle, you see his care every step of the way!
    I hope they figure out the reasons for all these things so Ethan can get better.

    Love you guys!

    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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