Welcome!

Welcome to my blog! This is mainly the story of my son, Brayton Cade Moak. His life is a testimony to me, and many others. I hope this blog encourages those of you who are going through difficult times, who have sick kids, who are lacking faith, and who need a reason to believe in miracles. I never thought that I would see a miracle, much less give birth to one. My son, my precious angel, is my miracle. His story, as well as his father's and my story, will hopefully fill your spirit with love! God is good!

Thursday, January 23, 2014

Power of Prayer

Prayer. Something so simple, yet amazingly powerful. For over 2 years, people from all over the country have been praying for my little boy. Although we are not out of the woods completely yet, prayers have been answered!

I am still amazed that I found this wonderful hospital and amazing doctors. For those of you who do not know, I found out about Dr. Cotton on Moms of Trach Babies on Facebook. I googled him, found his e-mail, and sent him an e-mail. in 24 hours, he had written me back and given me the name and number of his office. A few months later, we were visiting the Aerodigestive team at Cincinnati Children's hospital. July 2013, Brayton had a double stage airway reconstruction surgery. It was a success, but there was still a place that needed fixing. So people continued to pray for perfect and complete healing.

This last trip has been a nerve racking one! Never in the entire 2 years had I been more nervous than this past month. The closer this trip got, the more nervous I became! The first scope last Tuesday showed that the place that needed fixing wasn't very big. The doctors planned to use thyroid cartilage instead of rib cartilage (a true blessing that resulted in ONE incision instead of a painful rib incision too!) We left after the scope feeling positive, but still anxious.

Friday, January 17th, was the surgery day. What was scheduled as a 3 hr surgery lasted an hour and a half. We were told that Brayton would be intubated (put on a breathing machine) for 4-7 days. However, the doctors decided that he would only be intubated 24hours! Brayton was slightly sedated while the tube was in helping him breathe. Being LIGHTLY sedated means that every time nurses touched him, he woke up fighting! That first night was LONG! My little fighter was talking over the breathing machine which shocked a lot of people. He woke up kicking and saying, "dada" and "mama!" We ran to his side, calmed him down and he slept until the nurses would come in again (every 2 hrs).

Saturday morning, Brayton was extubated (got the breathing tube out) and was talking immediately. That evening he was able to eat and drink! Prayers answered! On Sunday, Brayton moved to a regular room and out of PICU. Nurses brought snow to his room in a bath bucket and for the first time ever, he got to play in the snow and build a snowman (complete with fruit loop eyes and a graham cracker nose)!!! He was able to run around the room and climb on and off the bed. The nurses even gave him a trach out party complete with a song, presents, and cake!

A follow up scope was performed on Tuesday and the doctors seemed really excited that all was well. I loved seeing the doctors smile and give thumbs up to us!

We were discharged from the hospital yesterday morning and spent the first night ever without hospital machines hooked up to Brayton, TRACH FREE!!!! I would love to say that I slept well. However, I found myself waking up and listening for breathing sounds. My son now snores and talks in his sleep! Prayers answered!

One of my favorite things has been hearing Brayton giggle. It is by far the most angelic sound I have ever heard in my life! His voice is perfect in my eyes! :)

So for those of you who have been praying, God has listened. Please continue to pray for Brayton as he continues to heal and as he grows. I am blessed that God has allowed me to be Brayton's mom and I pray that He helps me be the mom I need to be.

Prayer. Talking to God. Simple. Powerful. Our God is an awesome God!

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