I have had messages from several of you about what a bad, bad blogger I have been. During the summer Tim is gone a lot with the church youth, and I am doing the single parent thing. Plus, the kids are home with me all day, which means by the time they drop into bed at night, I am to tired to process a coherent thought. I thought about writing this morning because I didn't have anything on my schedule. But then I spent an hour scheduling doctor's appointments for five different people. Good times.
Anyway, on to the point of this post. ENTs and plastic surgery. Now you may be wondering why I am talking about plastic surgery again, when I just talked about
plastic surgery two months ago.
Well, after Jack saw the Commission doctors, we saw the ENT that did Kate's first set of tubes, thinking that he would do Jack's too. Sure enough, he was willing to work with Dr. Andy to do them at the same time as the palate repair, but he was unwilling to do the sedated ABR (hearing test) the same day. He said he really preferred to do the the tubes and ABR first, and then let them do the palate repair later.
I nicely told him that if he was unwilling that I would have to take Jack to the other major hospital in town (that Kate is now a patient of) and let them do it all over there.
Suddenly he was a willing participant.
Fine. So I spent the next two weeks playing phone tag with the ENT's surgical coordinator and Dr. Andy's surgical coordinator, trying to get them to work together. They finally called me back with a date in the middle of August.
Fine. So then the next day I got a call from the Commission (remember how much I love them, she says sarcastically) telling me that Jack cannot get the sedated ABR done at this particular hospital because they (the Commission) don't have an audiologist contracted over there. They wanted me to go ahead and have the tubes and palate done, and then have a non-sedated ABR done in their office at a later date.
Fine. So I spent the next 24 hours mulling over all of this, and I realized that we were talking about something that was still more than two months away. I then I realized that this was more than enough time to research other options. Because at this point, I was fed up beyond belief at having to argue with the Commission, argue with a doctor, and play phone tag for weeks on end.
So, being me, I went into
research mode again. I go to the Rumor Queen boards. I go to the Adopt Cleft Yahoo boards. I call people I know locally. And I learned I had a couple of really excellent options at that other hospital across town (where Kate sees her ENT). So I made the call to the Commission to request an appointment with the physicians over there. Of course, they wanted me to wait and go through clinic again.
In August or September.
No, we just went through clinic in May. I am not waiting until August or September. I want to go to their offices and see them there. Now.
And so we spent last Wednesday at that other hospital seeing Dr. V, the ENT, and Dr. L, the plastic surgeon.
Dr. V was very nice. She took what little history we had and agreed that Jack probably needs tubes placed. She explained that because it is such a minor procedure and the palate repair is a much more complicated surgery, that the palate repair would be scheduled first, and then whatever ENT in their practice was at the hospital that day would do the tubes. Since we are already in there so often and I know how they work, I am comfortable with that.
Then we went downstairs to see Dr. L. Now, every time I asked for recommendations for Dr. L, people would say, "Oh, he is the fireball. You will love him." And then they would go on to tell me how he pours himself into his patients, staying on top of the latest techniques, and is just eager to do his best every single day.
He did not disappoint. We saw his student first (SOP at this teaching hospital), and then Dr. L came in without a white coat. Ie, he didn't terrify Jack right off the bat. He takes a bit of history, looks at his palate, explains to me structurally why Jack's left ear is a little different from the right one, notices the stitch that has been in his lip since that repair in March 2011. He tells me that he doesn't use no-nos on kids this old and that Jack doesn't have to be weaned from his soft-spout sippy. He notices Kate, asks if he could look at her palate repair. Kate says no, but I try to persuade her. He stops me and says, "No, that's ok if she doesn't want to." Ie, he cares about how patients feel, even when it isn't his patient.
Then he told me that his surgical coordinator was on vacation all week, but that he knew he had an opening on August 28 so if we could get it all coordinated that it would probably be that day. I am sorry, but I have never known a surgeon to have a clue what their schedule looks like a month out with a coordinator telling them. Wow.
Then he gave me his personal email address (in case I thought of any other questions) and his personal secretary's phone number (in case I couldn't get him via email). Again, never had a surgeon do that before.
Oh, and we were in and out in just over 25 minutes (not counting new patient paperwork) and spent about 20 minutes of it with him. Again, a record.
So, all that long story, just to say that we now have a new plastic surgeon and a new ENT. Still waiting on the final details, but it looks like they will do the repair, the tubes, and the ABR all at the same time, and Jack will spend the night at the hospital . I am feeling good about the whole thing, whereas I had a bad feeling about everything over at the other place, what with the arguing and such. Those other docs are good physicians/surgeons, I like the other hospital fine, but I think that this is a good place for Jack right now.
Posts (so far) about Jack's cleft/developmental/IA issues:
Posts (yet to come) about Jack's cleft/developmental/IA issues: