Has anyone dealt with the surgery department at Children's?
I haven't had to deal with a surgery yet (and hopefully won't have to) - but I've been in contact with the neurosurgery department for the past week due to possible fusing on Baby A's skull. All I can say is that everyone I've come in contact with thus far in that hospital has been outstanding.
That is what my son has. The top part of his skull has fused and therefore his head is growing oblongated (I think is what it is called) and they are gonna go in and take part of his skull out to give his brain room to grow. I liked the doctor we met today and plan on calling him back on Monday and going ahead with it. I wanted to see though what other people thought.
That is what my son has. The top part of his skull has fused and therefore his head is growing oblongated (I think is what it is called) and they are gonna go in and take part of his skull out to give his brain room to grow. I liked the doctor we met today and plan on calling him back on Monday and going ahead with it. I wanted to see though what other people thought.
I'm sorry to hear that. I hope everything goes well with his surgery.
How are your little ones doing? Any progress since the last update? They sound like they are fighting hard, they will be fine.
Has anyone dealt with the surgery department at Children's?
They're doing awesome!! I just got back from visiting with them and how I hate leaving!!! Yesterday I got to hold both of them for the first time and next week I get to start Kangaroo Care. Baby A is still on atrophic feeds of 2 cc's every 3 hours and Baby B is up to 18 cc's every 3 hours. They're both on the nasal canula - Baby A is down to 3 litres and Baby B is at 4. The doctor on rounds today said that they were textbook great and the best babies on the unit! They both have minimal issues with apnea and brady's - and each time they recover on their own. Baby A will have another ultrasound of his head on Monday to look at the fusing - some doctors say they feel the bones moving independently and suspect just overlapping and some don't and suspect fusing.
I'm having a baby shower - that's been planned for over a month now - tomorrow. That seems funny to me.
I hope your little one does well with the surgery - I will be anxious to hear that it all goes well.
My kids have never had surgery there but I have dealt with Childrens many times. They are the greatest! Your son is in the best place and in the best hands. One of my best friends son had surgery there and she had everything good to say about them. Best of luck to you and I will keep your son in my prayers.
I might have overlooked but is this surgery soon?
Has anyone dealt with the surgery department at Children's?
Has anyone dealt with the surgery department at Children's?
They're doing awesome!! I just got back from visiting with them and how I hate leaving!!! Yesterday I got to hold both of them for the first time and next week I get to start Kangaroo Care. Baby A is still on atrophic feeds of 2 cc's every 3 hours and Baby B is up to 18 cc's every 3 hours. They're both on the nasal canula - Baby A is down to 3 litres and Baby B is at 4. The doctor on rounds today said that they were textbook great and the best babies on the unit! They both have minimal issues with apnea and brady's - and each time they recover on their own. Baby A will have another ultrasound of his head on Monday to look at the fusing - some doctors say they feel the bones moving independently and suspect just overlapping and some don't and suspect fusing.
I'm having a baby shower - that's been planned for over a month now - tomorrow. That seems funny to me.
I hope your little one does well with the surgery - I will be anxious to hear that it all goes well.
Has anyone dealt with the surgery department at Children's?