I know they are only doing what is best for Claire, and I appreciate that. And other than this, I have been so happy with Children's. They have toys and books for kids to play with, cartoons playing in every exam room, wagons to take them from one room to another. It is a Children's Hospital. But children have parents, and those parents are terrified to be there in the first place. Tell us what's going on with our kids!
:::focus on the positive, Gini, focus on the positive:::
Hydronephrosis does not hurt Claire. She experiences no discomfort, no pain, and I am so thankful for that. And while it may not hurt her, Mommy may have when she put the band on a little too tight!
Today, Claire received IV fludis (since she couldn't have anything to eat or drink) and let me tell you that she is not a fan of needles! Or the nurses who poke her with needles!
Then, they put in a catheder and injected dye into her kidneys. (She's not a fan of those either!) But it was all for a good reason, or that's what I have to tell myself to make it through the torture that is your child's screaming and looking at you like "mommy, how can you let them do this to me?" Under the machine she goes so that the technician can record the dye as the kindey empties it into the bladder (sort of like an ultrasound from afar).
And I had to keep her still (with the help of straps of course) for 30 minutes. She calmed down after a bit, but she was just looking for something to nom on.
And I knew Claire was trying to figure out how to get that needle sticking out of her arm into her mouth. I mean look where her hands are! So Wubbanub saved the day!
And can you see her super cool neon green bandaid to prove she's a tough kid? I just melted. And those poor eyes, red from crying make me want to cry!
According to the technician (I was supposed to see the doctor today, but he was at a different location), the right kidney is not emptying properly. It is emplying some, just not as much as it should and not as quickly as it should. The left (good) kidney is picking up the slack and doesn't appear to be hurt by the extra load.
But we have faith in our great God and His power to heal. We know that His will for us and for Claire is holy and perfect, and we are trusting in that. We'll have to wait and see what the doctor says about the results of this test (it's called a MAG3, although I have no idea what that means) and go from there.
We are so grateful for all of the prayers, support and encouraging words from our family, friends, and e-friends! It means so much to Luke and I. We are off to visit Luke's family in Knoxville but will keep you updated if we hear any news.
Happy Friday and Have a great weekend!




































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