Monday, November 1, 2010
Welcome back to Noah's blog! Thank you for following us through our journey and for your continued thoughts and prayers!
I know it has been a long time since we have updated Noah's blog. We will be updating on a more regular basis for a while from here on out.
A week from today, our sweet baby boy will be undergoing his 4th major surgery. This one being the most complex surgery thus far. His heart surgeon came to talk with me the other day about the procedures will be done. It is a TON of information and I will do my best to write as much information about it as I can.
The main and most important step with his heart repair is closing the VSD (the whole between his right and left ventricles). The way he described that procedure is he will kind of make it a tunnel to Noah's pulmonary artery instead of patching the hole and rerouting his PA. He said that in Noah's case, the VSD location makes it easier to do that then in other DORV patients. His next step, he will do a left PA plasty. Basically, manipulating his left PA to open it up, with either a stent or ballooning it open. (There was something else... kind of lost track of my thought... umm....)
He also talked about his right PA and whether or not he will be doing anything with it, seeing as Noah's right lung is so small. Changing the right PA would be extremely extensive and would change the amount of blood flow significantly. He said that he may just leave his right lung alone and focus more on his left 'good' lung and make it as strong as possible. The only thing, he said later down the road, his right lung may start to cause problems, in which case, he would take part of his lung out.
The last step to Noah's repair is his airways. Back in January, Noah had his airway pexy surgery. For his heart repair, Dr. Mitchel will be cutting down the old sutures in order to get to his heart. After the heart is done, they will do a broncoscopy and he will redo the pexy and make adjustments so his trachea and left bronchus are more open. But, if his chest cavity is too swollen after they are done with the heart, Dr. Mitchel will have to leave his chest open and do the pexy and close him up a few days later.
I think that is all the info... that I can remember anyway :)
Noah is the first surgical case that day. And his surgery will pretty much be all day. Dr Mitchel said the heart will be asleep for approximately 3 hours and he will be on bypass until they restart his heart. That is after the 2 to 3 hour prepping of the heart (i.e. cutting the pexy down and opening his chest). Then even longer work on the PA and then the redo of the pexy.
This past week, Noah has been super happy and wanting to play and go on walks ALL day long! It is going to be VERY difficult to "hand him over" to the surgical team and get him back sedated and intubated with a fresh cut down his chest and bed ridden for a while. But I know this must be done so we can continue to have our happy sweet boy running circles around us!
I know it has been a long time since we have updated Noah's blog. We will be updating on a more regular basis for a while from here on out.
A week from today, our sweet baby boy will be undergoing his 4th major surgery. This one being the most complex surgery thus far. His heart surgeon came to talk with me the other day about the procedures will be done. It is a TON of information and I will do my best to write as much information about it as I can.
The main and most important step with his heart repair is closing the VSD (the whole between his right and left ventricles). The way he described that procedure is he will kind of make it a tunnel to Noah's pulmonary artery instead of patching the hole and rerouting his PA. He said that in Noah's case, the VSD location makes it easier to do that then in other DORV patients. His next step, he will do a left PA plasty. Basically, manipulating his left PA to open it up, with either a stent or ballooning it open. (There was something else... kind of lost track of my thought... umm....)
He also talked about his right PA and whether or not he will be doing anything with it, seeing as Noah's right lung is so small. Changing the right PA would be extremely extensive and would change the amount of blood flow significantly. He said that he may just leave his right lung alone and focus more on his left 'good' lung and make it as strong as possible. The only thing, he said later down the road, his right lung may start to cause problems, in which case, he would take part of his lung out.
The last step to Noah's repair is his airways. Back in January, Noah had his airway pexy surgery. For his heart repair, Dr. Mitchel will be cutting down the old sutures in order to get to his heart. After the heart is done, they will do a broncoscopy and he will redo the pexy and make adjustments so his trachea and left bronchus are more open. But, if his chest cavity is too swollen after they are done with the heart, Dr. Mitchel will have to leave his chest open and do the pexy and close him up a few days later.
I think that is all the info... that I can remember anyway :)
Noah is the first surgical case that day. And his surgery will pretty much be all day. Dr Mitchel said the heart will be asleep for approximately 3 hours and he will be on bypass until they restart his heart. That is after the 2 to 3 hour prepping of the heart (i.e. cutting the pexy down and opening his chest). Then even longer work on the PA and then the redo of the pexy.
This past week, Noah has been super happy and wanting to play and go on walks ALL day long! It is going to be VERY difficult to "hand him over" to the surgical team and get him back sedated and intubated with a fresh cut down his chest and bed ridden for a while. But I know this must be done so we can continue to have our happy sweet boy running circles around us!
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About Me
- Pray For Baby Noah
- Welcome to Noah's blog! We thank you for following us on our God-led journey and thank you for all your thoughts and prayers! Noah was born June 22, 2009 with many anatomical birth defects and underwent his first major surgery when he was just 4 days old. He has been in and out of the hospital since day one and has had a total of 4 major surgeries to date, with his latest one being the most extreme and difficult - his first open heart surgery on November 4 and December 17th, 2010. He is a warrior and this is his journey...
Double Outlet Right Ventricle Tracheoesophageal Fistula Scimitar Syndrome Dextrocardia
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2010
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- Things look promising...
- Round 1....
- Things are speeding up a little...
- Happy Thanksgiving (a couple days late) EVERYONE!!...
- Right this moment, Noah is getting an ultrasound d...
- Rough seas ahead...
- Yesterday had been a great day, but towards the ev...
- Noah has pooped TWICE today!!!!!!!!!!!!!! This is ...
- Today, they are not going to change much on his dr...
- Extra, extra!! Read all about it!! There's GOOD NE...
- Noah's chest has been closed for 24 hours now! PRA...
- Noah's chest is closed!!!!They took him down to th...
- The Silver Lining....
- Still need focused prayers on Noah's kidneys and b...
- There was no update yesterday because things are p...
- Psalm 41:1 The LORD sustains him on his sickbed; i...
- Today, they did a short trial run of turning down ...
- For those who have been asking.....
- Noah had a relatively good day today. His ECMO dre...
- No real changes in his recovery plan. He is doing ...
- The excessive bleeding has slowed, if not, stopped...
- URGENT!!!!!!!!! NOAH IS BEING CUT OPEN!!!!!!!!!! W...
- A BIG scare........
- 12 hours post-op
- 8:15pm CT
- 7:30pm CT
- updates 5:30pm AND 6:30pm CT
- 4:30pm CT
- 3:30pm CT
- 2:30pm CT
- 1:30pm CT
- 12:30pm CT
- And now it is all a waiting game.
- How is THAT for some shock value?!?!
- Welcome back to Noah's blog! Thank you for followi...
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He is getting so BIG!!!!
My handsome men!
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4 comments:
I will pray everyday for strength for your stress and Noah's Strength.
Greg H.
Praying for you guys and for complete healing in Noah - - may you and Aaron know the presence of Christ and His peace as you walk through the weeks to come.
In His love
Cole
Wow...I have no idea how you are as strong as you are b/c I would be falling apart. That poor baby boy! Our prayers are w/ you!
Astrid
praying for you guys. praying for a miracle, healing, strength, peace, wisdom and guidance for the doctors and God's glory to be revealved through all of this.