Tuesday, December 2, 2008

Day 44: Weight up, machine down, food out

Today Loki weighed 1143 grams. That's over 2 + 1/2 American pounds! He still has not lengthened much, and thus has quite a double chin growing. That's good! Babies should be tubby.

The SiPAP breathing machine was turned down to 10 cycles per minute. After this, the next step is constant pressure, with no cycles. In fact, he was removed from the machine entirely for a bit, and he did fairly well. He did not desaturate for a few minutes.

Loki's new habit is some reflux after eating. That's when some food spills out. I am not sure what this means.

Mom held him for a long time today. Loki liked it, but after more than on hour, Mom had to go pee.

3 comments:

Anonymous said...

Weight up, machine down, fout out. Mood up, thoughts down, worries out. That's the way (ah ha) I like it. Frits en Heleen

Anonymous said...

Loki- you are doing great. You are so strong and courageous just like your parents. I read about you each day religiously. Treat each day as if it were Thanksgiving...eat and sleep well my little man.

Janet said...

Reflux is a common occurence in premies. We hope it goes away on its own, If it worsens or continues, Loki would receive two types of medication which are similar to adult antacid medications. Now that Loki's lungs are maturing nicely, we go onto the next hurdles: growth and feeding issues. So far, Loki is doing very well. I can't believe how far he has come in such a short period of time(to me.)
BIG HUGS!!
Nurse Janet

About Loki Sky

Loki Sky is a special little man. He was a very early micropreemie, weighing only 610 grams (1 lb, 5 oz) after 24 weeks, 3 days gestation, born to an American Father and a Dutch Mother in Berkeley, California on October 18, 2008.

On January 11, 2009, while still in the hospital NICU, his one kidney stopped working. It was repaired after three surgeries. After spending time in three hospitals in three cities, Loki came home on February 17. He struggled with eating, and then stopped in July, leading to 8 days in the hospital, a failure-to-thrive diagnosis, and a NG feeding tube. On October 10, a minor surgery installed a G feeding tube. Another procedure replaced it with a new one, and then again with a Mic-Key button in Jan. 2010.

In August 2010, he and his parents moved to the Netherlands.

Read about his first name.
Read & hear about his middle name.
See photos.
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