Just a quick update that we did get final results from Waverly's last test, and the good news is that she does not have the one neurological "pooping condition" that they were looking for (do you like those technical terms?). She just has slow motility, which basically means she will continue to need intervention to help her have a bowel movement. We are currently giving her milk of magnesia twice a day and she is to get an enema if she hasn't gone in 24 hours. Yes, lovely...
We are currently in the waiting area right now for her VCUG to assess her kidneys and bladder. This is since she's had a couple of UTIs. Sometimes kids with her condition have kidney reflux, so this will check for that.
Of course, once we got here at 6:45 this morning for her 7a.m. appointment, they told me that she's actually not scheduled till 8:00. What?!? All the info has 7:00 written on it and when we called and preregistered yesterday, they said 7:00 too. They are trying to go ahead and get us in soon but that's certainly frustrating. I'm not an early morning person...!
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