We have created this blog to help keep all of our family and friends updated on Pearson's progress as he begins to take his first baby steps in life. As most of you know, Pearson has a birth defect known as CDH and will have to overcome many challenges over the next several months. We thank you for visiting our blog and encourage you to leave comments as often as you would like. We look forward to hearing from you!
Sunday, March 27, 2011
Surgery Update
Today was a pretty good day! Pearson was able to rest most of the day. I'm sure these last couple of restless days finally wore his sweet little body out. Unfortunately, Pearson has come to a stand still and isn't making anymore progress. His lungs do not appear to be developing anymore so Dr. Kays plans to do surgery tomorrow. We were hoping he would be off the ECMO before the surgery but they are unable to wean him off anymore. However, just like last time, if he sees any progress between now and surgery tomorrow at 3:30 then he could very well postpone it again. We trust Dr. Kays and we know that God is working his miracle through him so whatever he feels is the right thing to do shall be done. We thank you so much for the continued prayers. We will update you tomorrow night.
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By the time you read this tonight, I pray that surgery is over and Little P is on his way to recovery and one step closer to coming home. Know that you all are surrounded by prayers today and everyday. As I told you yesterday GOD"S TIMING is perfect no matter what time schedule we prefer ourselves. I am trusting in God with no doubts that all is going according to his plan for his glory. We love you three and are so thankful and proud of all you and Matt have handled and continue to handle with your faith firmly in God. Can't wait to get back down there and see all the progress your little man has made.
ReplyDeleteLove,
Aunt Lunda, Uncle Ted & BB
Thinking of you guys today! Praying for Pearson! For a good day, whether that involves surgery or not. Keep fighting the good fight Pearson! You can do it!
ReplyDeleteHugs,
Jennifer
Mom to Dakota
We're lifting ya'll up in prayer each day, and are in this with ya'll, even though we can't be there in person. I will be down to visit in a couple of weeks.
ReplyDeleteLove ya'll,
Debbie
Matt & Brandi,
ReplyDeleteI just want to let you know that Pearson and you both are in my prayers. As you may already know, I was born with a birth defect as well. Not as rare as Pearson’s but I can still relate. So I may bring to you a little comfort, all children are miracles but some are not told as much as Pearson may be. I grew up surrounded with family telling me I was a miracle child. Just hearing my story and understanding the meaning of life and how fragile it may be, gives me the Strength, Faith, and Courage I need to make it through this life. I am a miracle and Pearson will be too. TELL HIM EVERYDAY!!!
Also, just to tell a quick story. My Mother and Father prayed and prayed for me but one day before my surgery my Mother knelt down beside my bed and cried to God and praised him for all he had done but just wanted him to know that she was giving ME to him. Whatever my fate should be would be one to Glorify Him. I was his to cure. I was HIS. Needless to say, it was ONE POWERFUL PRAYER!!!!
Sincerely,
Sarah Logan
(Donna's Daughter, Tony's Step Daughter)
Praying for Blessing for you today.... I KNOW God hears our prayers, and will work his miracles through Dr Kays... Keep the Faith...
ReplyDeletelove, hugs and prayers to you all...
Connie K
Praying for Pearson today. He has such a fabulous team that I am confident all the right decisions will be made!
ReplyDeleteLove,
Aunt Judy
Thinking of you today, please keep us updated!
ReplyDeletePraying today for you, Brandi and Matt, and for Pearson to rise through his surgery and begin healing and getting stronger. I am sad that I can't be there tonight to help take care of him, but I know that he will be in good hands. Dr. Kays is absolutely awesome, as is our entire team. I will keep praying and I know that Pearson is going to continue fighting and will keep showing us all what a true gift from God that he is. You both are amazing parents, keep doing what you're doing!
ReplyDeleteI know Pearson is in good hands because ultimately he is in His hands! Praying for you all today and always. Looking forward to hearing good news tonight!
ReplyDeleteLove,
Moose, Jill, & Bentley
I've lifted you all up in prayer all day today and will continue to do so through the evening...I believe with all of my heart that the Good Lord is going to heal Pearson!
ReplyDeleteLove,
Lindsey
Matt and Brandi-
ReplyDeletePlease know that you have people praying for Baby Pearson and both of you. I'm in tears reading your blog, amazed by how strong you are! Keep the faith, and find your peace in Him. Pearson is adorable, I love the pictures of him with his eyes open!
Kerri (Sparks) Helm
Know that he isn't doing anything so unusual for a CDH baby - though all are different too! Keep your hope and faith. Getting a whole lot of people to say prayers and praises for you all! Know that Dr. Kays is one of the very best.
ReplyDeleteSending thoughts, prayers and Lung Function Chants!
Elizabeth
Praying for your little man tonight!
ReplyDeleteDevon, momma of Camden =0)
Sending you all lots of prayers. I am thinking of you and your sweet boy.
ReplyDeleteAna, Mommy to Marco LCDH 3/2007