Saturday, August 24, 2013

A BIG Change.

In October of 2010 our life changed in a big way. We welcomed Logan John Lehi into our lives, with his birth nothing was ever going to be the same. That journey started a couple months before that with doctors tell us that he might not live through childbirth (this was around 27-30 weeks). We prayed to Heavenly Father that our son would make it and live, and we did ask for a healthy child. We had testing done (things that did not involve an amino), more Ultrasounds and even an MRI (a month before he was born) everything said he did not have what they thought he did. Deep down I wanted to believe there was nothing wrong with my unborn son, but I knew that something was different.

We set the day of the induction because they were worried about my blood pressure, I had never been fully induced before just helped along. It was long and painful. David had decided that we were going to change Logan's middle name we had set for him while I was in labor from Lockmann to Lehi, and I must say it fits him very well. Right after he was born he was taken to the table to get checked out, I did not see him and the doctor did not show him to us, at this point i knew something was not right. David followed them and took some pictures. He was cleaned and i was able to hold him for just a couple of minutes before the took him off to the NICU. David followed and I stayed in the room waiting for him to come back with any news at all. We were then told he was born with Apert Syndrome (www.apert.org). His fingers and toes were fused and so were the sutures in his skull, and he had a sunken midface. I did not know much, but it was a start. After 5 hours I was able to see my little man again. He was adorable and I could really see him, the swelling in his face had gone down and he had a full head of dark hair! He had issue with his breathing throughout our stay and they would take him to the nursery so I would sleep and they would keep a close eye on him. On the day we were going to be discharged he was taken Back to the NICU for breathing issues, and stayed there for about a week. He came home with an Apnea monitor. We had seen many doctors and he was delayed developmentally and had and still can have issues with weight gain. 

Logan is why we have learned to cherish everything big and small. He did not sit up unassisted till about 10 months, did not crawl till 15 months, and started walking at 2 1/2. The little things took longer as well and he is still at 2 years 9 months 3 weeks and 5 days old he is still not talking, he is making sounds and has been trying to say words, he know some sign language. Logan is a trooper as well his first surgery he had was at 6 months old which was 12 hours plus, he had half of his skull taken apart and put back together. He has has 2 hand surgeries both 8 hours or so, and a few other small surgeries. He wears glasses and hearing aids. At 2 1/2 he stayed still through a many CT scans. He still has a long road but he is a trooper and a fighter and can make it through the tough things all with a smile on his face. 








































Friday, August 23, 2013

A Little About Us!

This is our family! We have been married for just about 8 1/2 years. We have 5 children, our oldest is 7 1/2 and our youngest is almost 10 months old. Each of them is such a blessing and everyday we have is a blessing as well. Things may get crazy but we would not have it anyother way. Over the past 3 years we have been able to enjoy the little things and to us they are just as big and the bigger things.

David, Emma-Mae, Tami
Cheyenne, Noah, Logan, and Gabriel
Our Boys Gabriel, Noah and Logan

Our Girls Cheyenne and Emma-Mae