Today is the day.

Later this morning Ava and I will be at her evaluation. By this evening we should know if we'll continue to receive services after her birthday or if we'll be on our own. Wish us luck.

I'm trying to keep a win-win outlook about this situation. If she doesn't qualify, that'll be because she's made more progress than I could have possibly imagined a year ago. Now that we have a good rhythm going with therapy at home, I can probably handle working with her myself for a while. We also have the advantage of working with a local apraxia expert twice a month who is guiding me on what to work on in between sessions with her. So even if we don't qualify, I have a plan. And it is a plan I can live with.