Thursday, February 26, 2009

Weston


We've been up at Primary Children's Hospital this week seeing some specialists about Weston's head. He's had a ridge down his forehead and no soft spot for several months now. His pediatrician wanted him to be seen by a specialist, so here we are. Turns out he has metopic synostosis, meaning the suture down his forehead, along with his soft spot, has prematurely closed. This wasn't a huge surprise to us, we've suspected it for a while now, and have done plenty of research on the subject.
The picture above is him getting a CT scan. I was trying to keep him happy and still long enough for them to get a good picture. Luckily it was successful. Otherwise, he would have had to be sedated.
We still are waiting to see the neurosurgeon on Monday, but from what we've been told so far, it looks like he'll need surgery. It's quite an extensive surgery, taking 4-5 hours. They cut from one ear to the other to expose the skull. Then they'll cut what needs to be open and reconstruct the skull. Sounds horrible to me, but apparently it's a fairly routine surgery. This condition is present in about one in every one thousand babies.
While it's certainly not going to be fun, there could be worse things. I'm grateful that we caught it early enough and that it can be corrected. If left untreated, brain damage or developmental problems could occur, as well as the head deformity.
I'll post any updates as they occur. Please keep him in your prayers.

9 comments:

  1. I'm so sorry! That sounds a little scary to me too. Isn't it amazing though what technology can fix! we'll keep him in our prayers, and keep you in our prayers too.

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  2. We will definitely be praying for Weston. That's not fun for anyone but especially for someone who has no idea what is going on. Tell Jason to send the boys over whenever he wants. I am here most of the time and we have lots of kids movies that no one is watching...

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  3. You are in the best of hands where you are. Please let us know if you need anything. We will keep you all in our prayers

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  4. Wow! I had no idea...I know you said something to me but I didn't realize it was going to require surgery. He as well as all of you are in our prayers. Keep us updated.

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  5. We will certainly be praying for you guys. We love you all.

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  6. How did they take the CT with your head in the way?
    Let me know what happens on Monday. I'll be checking my email in AZ.
    See you in week.

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  7. Cindy we wish you and your family the best of luck and you will be in our prayers. Please call if you need anything.

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  8. I told you about the little girl that was having the same surgery last week. I don't know if you found them off of my blog, so here is a link to theirs. http://allaboutthebenjaminsbabies.blogspot.com/
    Everything went very smoothly and she is doing well and recovering quickly. You have an awesome attitude, what an inspiration you are.

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  9. Cindy!
    That is crazy! Ryan had this surgery when he was 11 months old.
    Crazy!
    we will keep him in our prayers.

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