Our cleft team visit!
Yesterday was Caleb's big day at Shands with the craniofacial team. We saw at least 9 different team members plus about 25 students/residents. It was a long and overwhelming day. But a good one!
Some of the things we learned:
Some of the things we learned:
- We're in good hands at Shands- we felt very well taken care of and we are happy fo far with the information we've been given.
- Caleb is not hearing very well but it is most likely due to the fluid build up in his ears (very common in cleft kids, and kids in general for that matter). He will get tubes during the palate surgery.
- It doesn't look like the cleft is associated with any syndrome.
- He has moved from indiscriminate attachment (he used to reach out to strangers often) to insecure attachment (he's still afraid we will leave him and does not want us out of sight). This is a step in the right direction.
- He has all of the teeth he is supposed to have- this is very good news!
- His drooling is from teething, not from the cleft.
- He will need at least three surgeries. One now, one in a few years, and one in mid-late elementary.
- This surgery (Dec. 6) is to repair his palate. They will close the palate using the existing tissue.
- The palate repair will allow him to develop his speech.
- They're actually happy he is not speaking because that means he does not have bad speech habits to break.
- He will be in arm restraints for 4 weeks after surgery- Merry Christmas! Lord, help us!
- We will hopefully only be in the hospital one night for this surgery.
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Thanks for your time!
Christy Bock
tomiawithlove.blogspot.com