Wednesday, December 30, 2009
Latest news
Thanks to all of those who have written comments and offered prayers for William. He has shown improvement since Christmas Day and we are thankful for that. The comments make us smile, laugh, remember you, and provide encouragement.
Following are some notes I took after Dana and I spoke with one of the doctors yesterday.
*Consistently stable-to-better lung x-rays. The doctor was going to review his x-rays to see if any trends appear, but on the whole the last few days have shown that the lung collapse is focused on the upper right side.
*Please pray for increased digestion so that his feedings can be increased. Currently he is on a three-hour feeding schedule where after about 2 hours or so they pull out the contents of his stomach via his feeding tube. (It's somewhat of a vaccum, so it's really pretty simple.) After examining the contents and the volume, they determine whether to increase feedings, check for infection, etc.
*He was to have another brain scan today. Please pray for no bleeding in the brain. This has probably already happened but Dana and I have yet to communicate with the NICU staff today. We are heading up there soon so I will update this later today.
*He started receiving hyrodrocortisone Tuesday morning. It is a steriod to improve his lung development. The course will be at low doses and last for about two days. This is a somewhat new methos of treatment so please pray that it works and that no side effects appear.
*It looks like his movement, muscle tone, and motor skills are developing well.
We love you all and thank you for your prayers.
Following are some notes I took after Dana and I spoke with one of the doctors yesterday.
*Consistently stable-to-better lung x-rays. The doctor was going to review his x-rays to see if any trends appear, but on the whole the last few days have shown that the lung collapse is focused on the upper right side.
*Please pray for increased digestion so that his feedings can be increased. Currently he is on a three-hour feeding schedule where after about 2 hours or so they pull out the contents of his stomach via his feeding tube. (It's somewhat of a vaccum, so it's really pretty simple.) After examining the contents and the volume, they determine whether to increase feedings, check for infection, etc.
*He was to have another brain scan today. Please pray for no bleeding in the brain. This has probably already happened but Dana and I have yet to communicate with the NICU staff today. We are heading up there soon so I will update this later today.
*He started receiving hyrodrocortisone Tuesday morning. It is a steriod to improve his lung development. The course will be at low doses and last for about two days. This is a somewhat new methos of treatment so please pray that it works and that no side effects appear.
*It looks like his movement, muscle tone, and motor skills are developing well.
We love you all and thank you for your prayers.
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Mark and Dana, I can only imagine how hard this must be for you. I am keeping you and little William in my thoughts and prayers.
ReplyDeletePlease let David and I know if you need us to bring you some comfort food from Moonshine!
Hugs,
Laura
Thanks for the update!
ReplyDeleteMark and Dana, thank you for keeping us posted on William. Your lives are so encouraging to me.
ReplyDeleteOn behalf of the 23+ people with us in Tennessee for Christmas who are praying for you, may God grant you great healing and growth. May He protect your body and make it strong. May He give the doctors and nurses great wisdom and compassion. May He bless your parents with peace and comfort that only He can give. We are pulling for you, Will!
ReplyDeleteKelly & David & crew
You are in my thoughts just about every day. Praying for little Will! Praying Will won't have any chronic lung issues but if he does I know some absolutely incredible pulmonologists at Dallas with great training at Riley Children's in Indianapolis and Boston Children's they know how to take excellent care of preemie babies with chronic lung disease/bronchopulmonary dysplasia. During the three years I worked in the Pulmonary Division they and their families became very close friends of mine. Can't recommend them enough. Tanya Martinez-Fernandez and Yadira Rivera-Sanchez they are some awesome lung doctors.
ReplyDeleteBeth A. Coleman