Zadie (on the right) with her brother,
Jonathan, and sister, Beatrix
In the fall, we started noticing that she wasn't hearing very well. At first, we thought it was a "listening" problem, but then we realized it was more likely a hearing problem. We took her to the doctor and found out that she had a terrible ear infection along with lots of fluid in her ears. Interestingly enough, even with a raging ear infection, she never once complained about her ear. She failed a hearing test and was put on some meds to help clear up the infection and fluid. After a few more visits to the ENT, and the fluid wasn't clearing up very well, as well as another failed hearing test, we were able to get her an appointment with one of the pediatric ENTs from CHOP, but at their satellite office in Princeton. Princeton is a whole lot closer than Philly!
We were basically expecting to hear that the fluid was still there and that she'd need tubes again. She's only had tubes put in once, at the same time as her palate repair at 11 months. Kids with Pierre Robin Sequence often need tubes throughout their life. Because of the way their anatomy is, they're more likely to have fluid buildup. Zadie's been pretty lucky in that she has only had tubes put in once.
The ENT looked in her ears and right away said they looked great. He didn't see any fluid. After we saw him, she was given a hearing test. The test went great! There were slight issues, but nothing of major concern, and the issues could have been just because she was on the tail end of an infection/fluid problem.
Next up, some dental issues, but nothing major yet. And she has a follow up appointment with her pulmonologist in a few weeks. I'm going to ask him about a sleep study for her. She hasn't had one since before she was decannulated and she does snore sometimes, so I want to make sure she's sleeping ok.