We are still here at the NICU. Griffin is doing really good. He is still on antibiotics for the fever he had last week but those will be done on Wednesday. After that he will have his PICC line taken out and will be free of almost all his lines (he will still have his feeding tube). He started eating last Wednesday and has been kind of crazy with that. One day he will eat really well and then the next day he doesn't want to wake up to eat and has to have his feeding given to him through a tube. We are seeing the light at the end of the tunnel. He will be taking as much food as he should for his weight starting tomorrow morning and then all he has to do is to eat all of his feedings for 48 hours and then we can go home. We are really hoping to be home this week some time so we hope he will keep up the good work. Thank you everyone for your support and we hope to see you all at home soon.
Michelle & Griffin
Christmas Ornaments 2017
7 years ago
2 comments:
We are Greg Munk's Parents. Cathy Colville told us of your baby's surgery and about your blog. Greg, Gretchen, Brandon and Ethan will be coming to St. George for Thanksgiving. We will share your info with them. God Bless, Sandy & Mel Munk
Dalton and my son Kayden are in 2nd grade together....
Glad to hear things are looking better. Both my kids were in the NICU for being premies. The IV's, the antibiotics and the feeding tubes and oxygen. I remember they would eat really good one feeding and be too tired for the next. Hang in there...he will get the hang of it. A very stressful time for you...I pray the Lord will give you and your family comfort and that you will soon be able to bring that baby home.
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