We were so excited when we arrived at Kelsons bedside today. After a few rocky days, we were greeted by an alert, happy looking little boy. Kelson was all smiles and ready to play. His temperature was normal, and he had great color.

Krista got to hold him for feeding time, and he did much better than the day before.

Even though he looked great, we were informed that the fluid on his chest had continued to build overnight, and the plan for the day was to reinsert the right chest drainage tube. This was very disappointing to hear, because we can't hold Kelson while the tube is in. Even though it is the best thing for him, it will be hard to not hold for a while.

Krista had to go meet with her employer today, so that meant Kelson and I would get some one on one time. Normally we have to space out our holding times, but I convinced the nurse to let me hold him for the 1 PM feeding before they put the new tube in. This was his first feeding on the new, special formula. I was worried he would not react well to the diet change, but he didn't even spit up. Hopefully the new formula will allow the chylothorax to heal, and the chest tube can be removed.

At about 3:30 the doctors came to put in the new tube. We had to leave the area, because it is a minor surgical procedure and requires a sterile environment. Today we learned just how tough our little man is, because he was still smiling afterwards, even without sedation! I think he was relieved to release some of the pressure that had been building on his chest. Within minutes if inserting the new tube, over 30 cc of fluid had been drained off. The X-ray tonight already showed major improvements.

Even though Kelson had to have the chest tube put back in, it still was a good day. Since the pressure has been released from his chest, he will likely tolerate the ventilator changes better, and may be able to finally get off the vent. Kelson is already trying to pull the tubes out of his throat, so hopefully it will happen soon!