Quinton was taken to our local hospital in Salisbury, MD on 8/21/10. After numerous tests it was determined that Quinton needed to be taken to John Hopkins Hospital for immediate Surgery. During my pregnancy, it was discovered that Quinton had a Choledocal cyst in the area of his liver. The cyst was watched throughout my pregnancy and birth. The cyst was 1cm by 1cm and never changed so they were never concerned about the cyst. The doctor just said that Quinton would have yearly check ups to monitor the cyst. A few days prior going to the ER, Quinton started to have symptoms of Jaundis which lead us to the hospital. Once at the hospital, it was determined that the cyst was blocking the Liver ducts from properly working and draining all the fluids to the intestine. So once at John Hopkins, more tests were run to confirm that in fact that the cyst was blocking the bile duct of the liver. It was determined that surgery was the only option to correct the problem. The surgery that they performed was called Kasai. They removed the cyst and the bile duct below the gall bladder and reattached the intestine to the bile duct (new plumbing as the doctor called it). On 8/23/10 Quinton under went a 3hr surgery to correct the problem. His condition is known as biliary atresia and there is no known cause or treatment for this. It is a liver disease. As you can imagine, Michael and I were beside ourselves. The doctor stated that they have been studying this disease for approximately 30 to 40 years and they still have no idea what causes it and how to exactly treat it. They had sent liver tissue away to be examined to find out more about Quinton's liver. The doctor stated that a very small percent of people with biliary atresia after surgery have no problems but must be watched their entire life. The other 85% to 90% require a liver transplant within the first 1 to 5 years of life. Quinton is at home and is doing VERY well. The doctors are very pleased with his progress so far. Quinton will require frequent check ups and tests throughout the early stages and his entire life. This is a long, tedious process. We have to go to Hopkins every two weeks for checkups and blood work. Quinton takes 5-6 medicines every morning and 3 evey night. It was much easier to give them to him in the beginning, but now he's starting to realize what's going on and he fights me. He is a very strong little man. He truly is doing very well. They also have us putting more formula into the same amount of water for his bottles. They want his calorie intake increased cause one of the side effects of the medicines is decreased appetite. We have Quinton in an experimental study through Hopkins called the BARC study. It is to help find a cure/cause of biliary atresia. We figured that if it may help save even one other child and bring no harm to Quinton, then we would participate.
On November 21, 2010 we were transported to Hopkins. We took his temperature earlier this morning and it was 102.5. Being concerned, we took him to PRMC ER and they ran tests and confirmed that his bilirubin level was elevated. Once at Hopkins, they did an ultrasound. They told us that they "suspect" ascending cholangitis. It's basically a "bug" drained from his liver to his intestine and then went back up into his liver and caused an infection. They're only treating it as this as a precaution. They're giving him antibiotics and monitoring him. They said we should be able to go home in 7-12 days. Quinton is already showing improvement. We were at Hopkins for 4 days. They did suregery and put a PICC line in on November 24, 2010 so we could go home for Thanksgiving and give Quinton his antibiotic at home. Those two weeks went by and healed the infection. In March he started crawling and his liver levels are excellent!