Yesterday Kaylin met with her orthopedic surgeon. We've been with the same doctor since she was 1.5 years old, and it's been so nice to have him remember us, remember her condition, remember what is going on.
We did the usual x-rays. Kaylin used to smile when they'd x-ray her hips, but not anymore. She now realizes they aren't really taking her picture. The same x-ray tech was there, "move your biscuits over a little"--super sweet lady.
Then we waited over an hour in the same small exam room. Ever been in a super small exam room with 2 kids, with no toys or TV? Not fun. It was all I could to keep them from climbing the walls. They read a couple baby books and generally annoyed me and each other.
The surgeon came in and met with us about the x-rays. Long story short, it was good news, bad news. The hip itself, in the socket where he fixed it a long 6 years ago, is healing nicely with cartilage forming around it like it's supposed to. It doesn't seem to cause her pain or restrict her range of motion. He was pleased with that. He's not pleased with the the way the top of the bone is forming around the top of the ball socket. It appears to be curving up instead of laying flat. He showed me on the x-rays where over the last 4 years, it has made that progression. He said several times "no surgery, but..."
So we wait another 2 years to see what that bone will do. He's not a rush into anything doctor, which I appreciate. We'll wait 2 years to see if it has flattened out or still continuing to curve. I'm guessing at that time, some sort of decision will have to be made. I couldn't get a sense of what that decision was going to be--surgery? Meds? No idea. I'm praying it will not be surgery and another spica cast. The spica cast was hard enough to handle when she was 1.5 years old; cannot imagine her being 9 in one.