Madie had a CT scan Thursday morning.
and when I met Dr. Rice Thursday afternoon he said that it looked like she might be missing a half of a turn of her cochleas but that he would wait for the neurological radiologist to be sure -- he would call me Friday. Long story short, my phone died (as in I had to get a new one, not because of a low battery) Friday afternoon. And of course he called while it was non-functioning. He left a voicemail saying that the radiologist said "there was nothing to be concerned about." I'm assuming this means she was not missing part of her cochleas. Of course he was out of the office today.
He wants to run some blood work to rule out some common syndromes. Less to have an effect on how we manage her loss, but more to give us a heads up for other potential problems. Two of the more common syndromes have renal or thyroid problems.
He also wants her to start the process of being admitted to Children's Hospital in Little Rock. Not because he thinks she needs services right now, but so that if she does need them in the future we'll already have a relationship established with the clinic.
jumping ballerinas

how could you not love them?
Monday, January 31, 2011
Wednesday, January 26, 2011
loss #2
In September we took Madie to see her audiologist, Mr. Glen, because we were concerned that she was not hearing at the level she should. He tested her in the sound booth, and she did have a 20 decibel loss in both ears. After a quick tympanogram, we found out she had fluid in both ears so we were off to Mid City and Dr. Ritch. Our sweet baby girl had double ear infections and had not once complained about the pain. We did a 10 day round of antibiotics, a 7 day steroid, and a decongestant/anti-histamine. After a month, we went back to Dr. Ritch and there was still fluid in her ears. This brought on a trip to an ENT, Dr. Watkins, who said we didn't need any more treatment, just time.
In December, we were ready for our return test to Mr. Glen. When we sat down in his office, he asked me what I thought was going on. My response: better than she was in September, but not where she was in April (her last "normal" appointment). And sometimes, it just sucks to be right. Madie had, for the first time since her original diagnosis in 2006, lost more hearing. We decided, since she only had one more day of school before Christmas break, not to adjust her hearing aids. In January, we saw Mr. Glen so he could retest her, just to make sure it wasn't a false negative and we got the same results. So he adjusted her hearing aids accordingly and she still hears at the level she did before -- she was back to her normal. We followed that appointment with one to a new ENT -- Dr. Rice.
It was a tough decision to decide to switch ENT's. Even though our previous one came very highly recommended by several people in the know, we had never felt completely comfortable with him. Not so with Dr. Rice. Finally, I feel like we're going to get some answers or at the very least we have someone willing to search for them. He was explaining that he wanted Madie to have an MRI and a CT scan but that we might be in for a fight with our insurance. His exact words were "but I feel like when you have one so young with so much at stake, you should leave no stone unturned." It was wonderful to hear that. W.O.N.D.E.R.F.U.L.
So tomorrow day one in our search. I love these twins.
In December, we were ready for our return test to Mr. Glen. When we sat down in his office, he asked me what I thought was going on. My response: better than she was in September, but not where she was in April (her last "normal" appointment). And sometimes, it just sucks to be right. Madie had, for the first time since her original diagnosis in 2006, lost more hearing. We decided, since she only had one more day of school before Christmas break, not to adjust her hearing aids. In January, we saw Mr. Glen so he could retest her, just to make sure it wasn't a false negative and we got the same results. So he adjusted her hearing aids accordingly and she still hears at the level she did before -- she was back to her normal. We followed that appointment with one to a new ENT -- Dr. Rice.
It was a tough decision to decide to switch ENT's. Even though our previous one came very highly recommended by several people in the know, we had never felt completely comfortable with him. Not so with Dr. Rice. Finally, I feel like we're going to get some answers or at the very least we have someone willing to search for them. He was explaining that he wanted Madie to have an MRI and a CT scan but that we might be in for a fight with our insurance. His exact words were "but I feel like when you have one so young with so much at stake, you should leave no stone unturned." It was wonderful to hear that. W.O.N.D.E.R.F.U.L.
So tomorrow day one in our search. I love these twins.
Sunday, January 23, 2011
no cartwheels to check for broken arms...

Saturday, January 15, 2011
two families of twins come together
I'm a twin. (I had a twin brother that was still born.)
I have a brother and sister who are twins. (Allison and Colter -- Katie really is the odd ball.)
Jay's mom is a twin. (Melinda and Melissa.)
He has twin sisters. (Patricia and Patience)
My great grandfather was a twin.
And his great grandmother was a twin.
All fraternal boy/girl twins on my side.
And identical girl twins on his side.
I love these twins.
I have a brother and sister who are twins. (Allison and Colter -- Katie really is the odd ball.)
Jay's mom is a twin. (Melinda and Melissa.)
He has twin sisters. (Patricia and Patience)
My great grandfather was a twin.
And his great grandmother was a twin.
All fraternal boy/girl twins on my side.
And identical girl twins on his side.
I love these twins.
Friday, January 14, 2011
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