Yesterday morning the oxygen saturation was not good. They decided to give him nitric oxide to see if that would help with saturation and thankfully it did. Since he cannot stay on oxygen indefinitely, the goal is to decrease his dependency on the oxygen and the ventilator. So now every two to three hours they are drawing a small amount of blood to test all of the gasses that are present in his blood. Depending on those readings they either increase or decrease the support he receives from the ventilator. Yesterday was a bit of up and down with re guard to that support. Yesterday morning the support was maxed out. As the day went on they were able to reduce the support from the ventilator. Unfortunately not all of those reductions have been permanent. They might make a reduction in support and then two hours later increase the support to the former level. As of last night he was not at the highest level of support that he was at yesterday morning but also not at the least amount of support for the day. This up and down is probably how it's going to be for the next several days and possibly weeks.
Caleb had a better night last night. Leah and Zeb wanted to thank you for your prayers.
I love you baby Caleb. Keep fighting. You are in every thought and prayer.
xoxo
Auntie Angie
Angie, thank you so much for this. We are all pulling for them. What a sweet little baby - he just fills my heart with how precious he is. Prayers will be constant. XOXO, Becca
ReplyDeletePraying even more... for strong lungs!!!
ReplyDeletePraying for you guys!
ReplyDeleteThanks for the update! Glad he had a better night. Baby steps! He will learn!
ReplyDeleteHey Leah! the Staff from Presby Rockwall would like you to know we are thinking of you and Caleb and we are praying for you and your family. We know you are strong and Caleb is a fighter!
ReplyDeletePrayers for all of you :).
ReplyDelete~ cousin Stephen
If anyone deserves a miracle it's Zeb and Leah! We're praying for Caleb and the Fish family. - Andrea & Jake Pettit
ReplyDelete