Elijah is doing well from his second dilation today. They were able to stretch the esophagus to 10mm, up from 8mm last week. He is resting comfortably. The Speech Therapists were impressed with him yesterday, as he continues to do well and move along. Dr. Hess mentioned this morning he is still working on the end of the month to get us out of here. We are saying by Thanksgiving, just to be safe. And if we are earlier than that, it is gravy. If all goes well overnight, he will probably move to the floor tomorrow. It is good news, but it kinda splits us up again. Please pray for that as it will be hard on us, especially the boys, as Tammy will be spending most of the time with Elijah. But hopefully, it won't last too long. We are missing the 'Bluegrass State' and hope it won't be long before we return.
God Bless..
Bad Day for the Cut sledování filmů online 2017
5 years ago
2 comments:
My son also has esophageal atresia he was born 10 months ago he has e.a down syndrome tracheomalacia and bronchomalacia, larangomalacia, and also atalectsis of the lungs. I would love to talk some time. I have a site at kaylapearson.com and also a site at bornwithea.com. It is very nice to meet you and i hope all is going well with your little one and god bless!
Hi, I don't know if you remember me but my son Ian was in the NICU at UK with Elijah, and I just wanted to say hi, and I am very happy to read that he is doing better and you guys are getting closer to going home. I know what the hospital feels like and I am so thankful to be home. I just wanted to say hi and see how you guys are doing. I hope he gets better soon, and I will keep your family in my prayers.
Stephanie Pilarski
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