Here is Nathan and Noah in the waiting room.
So the appointment went well - and wasn't EXACTLY what I had expected.
So Noah went first. Dr. G was rather impressed with him and his progress. He says that Noah's muscle issues are due to his MT16 because his brain wasn't formed right in utero - it formed different - and because of that his brain isn't communicating with his muscles correctly. So this is something that he's going to have to deal with for the rest of his life. He also said that Noah will have to be dependent on someone for the rest of his life - which I hope that isn't true, but it's something that we've been planning on anyway. Noah is still small for his age. He was 91 lbs and 59 inches. Looking at the chart online - I think he's around 15% on the chart for his age for weight. And about 11% for height.
Using this Children's Growth Chart Percentiles Calculator - this is what it told me.
At 13 years and 5 months:
your child is 91 pounds, and that is
at the 20th percentile for weight.
at the 20th percentile for weight.
your child is 59 inches, and that is
at the 11st percentile for height
Back to the muscle issue, he says he's doing really well with what he's got and was rather surprised with how much strength he can put out there. He was impressed with the homeschooling and the progress he's made in the last couple years. Even though he is still unbelievably behind, we are making progress. Slow and Steady.at the 11st percentile for height
The other thing we had to discuss was Noah's "dirty neck syndrome" .... he has this perpetual dirty neck and no matter how much I scrub, I can't get it off - I keep nagging him about it. Turns out it's a syndrome that can point to pre-diabetes. It's common in obese kids (people) and those who are pre-diabetic or diabetic. We checked Noah's sugar today and it was 163 - all he had to drink was one can of 7up and he had a tiny piece of cheese. That was it. He didn't really eat until after we got home. So we're going to check it again in the morning and see what his fasting is. (Edit: It was 88 for a fasting. Which is great!!)
Nathan ........ oh Nathan. So one of the first things he said was "I'm not sure about the Russell Silver Syndrome diagnosis." ::: smacks my head ::: Really? REALLY? This again. Nathan was diagnosed with RSS in April 2010, it was a clinical diagnosis which most RSS diagnoses are. I think only about 10% (give or take) are actually genetically confirmed. Basically - Nathan was diagnosed RSS because he fit the criteria. But he's never been fully absolutely A-Typical RSS. So a lot of doctors have made comments about how he doesn't have RSS and they are going to figure out the mystery of Nathan. Which annoys the piss out of me. But I guess when it's coming from the Genetic's Doc - who previously agreed with the RSS diagnosis - then I can't be mad.
He says he has some of the facial things, and other physical "symptoms" ... but he doesn't fit well in the RSS box. That his brain issues are a major concern pointing away from RSS, and all of his speech issues. So ... he's thinking it's got to be something else. It's definitely genetic, but he can't put his finger on anything in particular. He's doing a carbohydrate deficient transferrin for congenital disorder of glycosylation. He's also banking DNA and going for a pre-authorization for a Chromosome SNP array analysis. Which is the newest and greatest in chromosome testing. He kept calling the tests Nathan had in 2010 as "old fashioned" lol. I'm like, geez, it wasn't that long ago. But Dr. G seems pretty confident that it's not RSS now. So I'm really confused.
Nathan was 42 lbs 44 inches. He's not even on the charts for his age. Roger and Dr. G were saying that he's about 50% tile for weight and height for a 5 1/2 year old. Oye.
Using this Children's Growth Chart Percentiles Calculator - this is what it told me.
At 8 years and 3 months:
your child is 42 pounds, and that is
at less than the 3rd percentile for weight.
at less than the 3rd percentile for weight.
your child is 44 inches, and that is
at less than the 3rd percentile for height.
He kept calling me a great mother and that I was doing an amazing job with them. Makes me feel good.at less than the 3rd percentile for height.
So here is Noah's Neck.
I guess it's called ACANTHOSIS NIGRICANS ....
I did a home PEE Dip on him tonight too. He's spilling a TON of blood at the moment. (He has kidney issues) ... his Kidney Doc told me that it's not so much the blood - it's more the protein we have to keep an eye on.
His pH was off, Glucose and Ketones and White Blood cells (Leukocytes) were all good ... Protein was Neg to Trace ... and his blood in the urine was off the charts. LOL. I'm going to have him repeat it tomorrow too. See how it is.
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