Guest guest Posted December 29, 2002 Report Share Posted December 29, 2002 Hi all, I haven't posted here in about 2 -2 1/2 yrs. My son has been doing really well. I just recap his history. Corbin was born on Sept 17 1998 after a difficult pregnancy with about 10 wks of bed rest.(preterm labor) At the age of 3 days he stopped breathing and we took him to the hospital. He was diagnosed with reflux and we were told that he was severely dehydrated and had low blood sugar. He was nursing every 3 hrs and wetting his diaper, although I didn't think it was enough and planned on calling the doctor to confirm. He ended up being carnitine deficient and had elevated levels of lactate. They suspected a metabolic disorder, possible a mitochondrial disorder. At three months of age he crashed and was breathing really rapidly. 20 min of IV fluids corrected his breathing and the doctor at the hospital scratched her head and kept him over night as a procaution. His lactic acid and pyruvic acid levels were elevated. At 13 mths he had his tonsils and adeniods removed and had ear tubes put in. He was sent home the night after surgery and was readmited in critical condition the next day at noon. He was again severely dehydrated and his blood sugar was 36. He spent a week in the hospital. It took extra time to return to normal again. Since then he has been relatively healthy. He has some developmental delay. Speech and fine motor are his biggest issues. He is four years old now. On the morning of Dec. 23rd he woke up and out of no where started vomiting. The doctor said he couldn't see him until 1pm and if I felt uncomfortable I could bring him in early or go to the er. I did go to the Dr early and he sent us to the hospital. Corbin had vomited 10 x and was dehydrated and his blood sugar was 53. They kept him over night and into the next afternoon ( Christmas Eve). They did do lactate tests and finally got a urine organic acid test. I haven't gotten the results yet, but am hoping they give us the information needed to carry some sort of diagnosis or at least get closer. At our last Genetics visit just last month the Dr. said that he thought Crobin's metabolic issues were resolved, but that Corbin must be on an IV prior to any procedure that required fasting the night before. Does that sound like something someone with no metabolic issues would have to do? I'm just worried we will be drug though the whole stressfull and frightening ordeal again. Any advice on what I should do? Thank You, Barbara Mom to ,8, ADD and suspected learning disability , Max,5, Asperger's Syndrome and Corbin,4, possible mito, ADHD, oral motor and motor planning dyspraxia, fine motor and social skills delay. (possible PDD) With eyelashes any woman would die for and a smile that melts hearts. Quote Link to comment Share on other sites More sharing options...
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