I am a Congenital Diaphragmatic Hernia (CDH) baby. My diaphragm developed with a hole in it and my organs were misplaced in my chest cavity. The organs pushed on my lungs, causing one lung to be very small. I was born on October 9, 2007 at Johns Hopkins. Now it is three years later: I am saying a bunch of words, I still receive foods through a g-tube and am on oxygen while I sleep. I can't walk yet, but believe I can out scoot anyone! Here is the story of my amazing and patient recovery.
Wednesday, May 25, 2011
Endocrinology Update
Wyatt's awesome GI doctor noticed a pattern in Wyatt: he is not growing like average three year olds. His growth curve pattern is on a decline from 25%, 5% to 3%. A healthy three year old should be growing and the curve should stay steady or go upward. This is not the case with Wyatt. We recently took Wyatt to see an Endocrinologist who did some extensive blood work and an x-ray of his hand. We got the results, which indicated we needed more testing:(( Wyatt's blood shows high amounts of Alkaline Phosphatase- http://www.nlm.nih.gov/medlineplus/ency/article/003470.htm and his hand x-ray showed an abnormal growth plate. What does this mean?? Who knows? It could indicate malnutrition, which the doctor phased out because his other blood work was fine and we control his nutrients through a feeding tube, which is monitored by a doctor. It could be trauma to major organs (which could be his case), and many other conditions. So we need to get more blood work and an x-rays of his hand and kneee. Wyatt also did not begin to walk until age three, his walk is not a normal walk, and he still has hypotonia (low muscle tone). The doctor said most endocrine issues are treatable, so we will take each step at a time and deal with whatever is given to us. It just goes to show that CDH is never ending and I think it's Wyatt's mission to make my head full of gray hair!!!
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