Ellis has had a good week with lots of visitors. Pictures will be coming soon. She has enjoyed meeting some more of the very special people in our lives. And she got lots of good snuggle time with her Grandmother Robin and Ken this past weekend!
Ellis continues to make progress in most areas, and her doctors are very happy with how she is doing. She is over ten pounds now and is cooing, smiling, reaching for toys, and interacting with us even more. The one area in which she is still having problems is her breathing. Some tests earlier this week showed that she is not handling her
oxgyen levels like she should and is having apnea episodes very frequently, especially as she sleeps. This would be very dangerous for her when we take her home, and she is not getting any restful sleep. So her doctors are recommending a tracheotomy on a temporary basis. Greg and I are not very happy about this, but we know it is the best thing for her. She will be able to breathe comfortably on her own for the first time. The muscles that control her airway are just not developed enough yet to handle opening and closing on their own, which is the same problem that caused a need for the feeding tube. But in the same way, her doctors are very hopeful that as she grows these muscles will get stronger and she will not need the
trach for very long. She might have it for a few months, or even up to a few years. But she has done so well in so many other areas we are hoping for only a few months. In the mean time, we will be learning some baby sign language to help her communicate with us and will keep teaching her words and sounds to help her language skills develop even though she will not be able to vocalize.
Ellis will have surgery for the
trach next week, but we don't know which day yet. This will add several more weeks to our hospital stay, but if all goes well we might be able to come home by the end of the month. We appreciate your continued prayers for her healing and safety.