Just wanted to give an update on Kaitlyn and her UAB appointment from yesterday. I know most of my blog readers already know all of this but a few do not :)
We saw Dr Wellons on Monday (the pediatric neurosurgeon) down at UAB and overall things went well. Originally we were told Kailtyn had a form of Spina Bifida called lipomyelomeningocele, but yesterday he told us she has Spina Bifida Occulta. She definitely has a tethered cord and he'll have to do the surgery to untether it along with removing the growth on her back. We were told the growth was most likely fatty tissue at HH NICU but he seems to think its more fluid than fatty tissue but I think she is considered to still have it, because she does have the growth and the spinal cord is attached inside of it.
We got to see her MRI and it does show the tethered cord but it also showed that her nerves were still attached which is why she can move her legs/feet so well right now. There is a chance that the surgery could result in leg weakness and/or Kaitlyn not being able to walk depending on if he has to cut the nerves or not.
We go back on 6/16 for an appt with the Urologist and also for her to get a CT Scan. Her surgery is scheduled for 6/22, but we have to be back on 6/21 for the Pre Op appt with Dr Wellons and then we'll stay there for the week.
The CT scan is being done to see if she has any fluid in her head, called : Hydrocephalus right now he doesn't think so but he wants to verify before surgery. If she does they will have to place a shunt to drain the fluid back down, and there is a chance she will need it even if there isn't currently fluid there, due to the surgery (since the growth may be fluid filled).
The surgery is expected to take about 4 hours (if no complications) and the recovery time is atleast 3 days, and she has to be flat on her back the entire time. So we'll be down at UAB from 6/21 thru 6/25 or 6/26 at the very least.
Thank you all again for your thoughts and prayers and please continue to pray for us and Kaitlyn.
We saw Dr Wellons on Monday (the pediatric neurosurgeon) down at UAB and overall things went well. Originally we were told Kailtyn had a form of Spina Bifida called lipomyelomeningocele, but yesterday he told us she has Spina Bifida Occulta. She definitely has a tethered cord and he'll have to do the surgery to untether it along with removing the growth on her back. We were told the growth was most likely fatty tissue at HH NICU but he seems to think its more fluid than fatty tissue but I think she is considered to still have it, because she does have the growth and the spinal cord is attached inside of it.
We got to see her MRI and it does show the tethered cord but it also showed that her nerves were still attached which is why she can move her legs/feet so well right now. There is a chance that the surgery could result in leg weakness and/or Kaitlyn not being able to walk depending on if he has to cut the nerves or not.
We go back on 6/16 for an appt with the Urologist and also for her to get a CT Scan. Her surgery is scheduled for 6/22, but we have to be back on 6/21 for the Pre Op appt with Dr Wellons and then we'll stay there for the week.
The CT scan is being done to see if she has any fluid in her head, called : Hydrocephalus right now he doesn't think so but he wants to verify before surgery. If she does they will have to place a shunt to drain the fluid back down, and there is a chance she will need it even if there isn't currently fluid there, due to the surgery (since the growth may be fluid filled).
The surgery is expected to take about 4 hours (if no complications) and the recovery time is atleast 3 days, and she has to be flat on her back the entire time. So we'll be down at UAB from 6/21 thru 6/25 or 6/26 at the very least.
Thank you all again for your thoughts and prayers and please continue to pray for us and Kaitlyn.
2 comments:
We will be praying!!! God is a mountain mover so don't loose faith. He's got her right in the palm of His hand.
Erica from NJM
Thanks Erica! :)
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