Most of you probably have heard something about Nate being tested for MCAD. For those of you that know and have been praying, i can't THANK YOU ENOUGH. Your prayers have been heard and we have had peace in the midst of this uneasy time for us. For those of you that haven't heard, I'll give you an overview of the past couple days.
On Wednesday my mom and I took Nathan in for a regular newborn checkup with his pediatrician that is routinely done a few days after they leave the hospital. His checkup went great. He left the hospital on Sunday weighing 7 pounds 1 ounce and was back up to 7lbs. 8oz. at the doctors office. The doctor said everything checked out well and we couldn't have asked for a better report. When we got home there were two messages from a doctor at a large hospital in Rochester, NY where all the newborns blood work is sent. (In the hospital, every newborn is given a heelstick to draw blood taken for a series of tests that may be detected by the bloodwork, but not physically seen yet.)
So, the second message from the doctor definitley got my attention because she gave me her cell phone number and asked that I contact her ASAP. She told me that his bloodwork came back with a level of 2.7 for MCAD and that we had to take him to Rochester's genetic specialists the next day. She told me that MCAD was a genetic disorder that could make Nate very sick if not treated and if he wasn't eating well. She knew that the appointment could wait until the next day because she had called the pediatrician who told her how well he looked and that he was eating well.
Thursday, Josh and I drove 2 hours to Rochester's Children's hospital where baby Nate was re-evaluated. The doctor was pleased with how well he looked (gaining weight, good muscle tone, alert, and eating well). She explained more about the disorder and what we do to treat/manage his care. More blood work was taken to make a definitive diagnonsis of MCADD that we will know the results of in two to three weeks. However, with his first result of 2.7, they said they would be surprised if he didn't have it. They have never seen a result over 1 where the child didn't have the disorder. It was a long couple of days for Josh and I and the rest of the family. We were completely shocked due to Nathan looking so healthy to us and even to the pediatrician. This disorder is newly found and we are thankful he was tested for it and diagnosed early. We are still praying the God will heal him and his results will come back clean. However, if He doesn't, we know He will get us through this and give us the strength to take care of Nate to the best of our ability.
I will give you all some information that the doctor gave me on MCADD. It is a disorder where fat in the body cannot be broken down and used for energy. It affects someone when they are fasting, sick, or cannot eat and drink as usual. Children have more problems with this disorder since they need more energy and calories and are less likely to eat and drink when sick. Untreated MCADD can lead to severe effects. It is passed on genetically from those that have the disorder or carry the altered gene. It only affects about 1 in 15,000 people in the US.
For us, this means we have to keep a close eye on little Nathan. I have to set my alarm at night and make sure he doesn't go longer than 4 hours without eating. We now have papers that we have to keep with us in case he needs to go to the hospital. The papers show the doctors and nurses how to treat a child with this disorder properly to ensure they will not get too sick and suffer worse side effects. We know when to take him in from the doctors guidelines and just will keep praying that God will give us wisdom in these situations.
I am so thankful Nate eats well and is looking healthy. His slight jaundice that he had is almost completely gone and he has been more alert the past couple of days. He is extremely laid-back and mellow and smiles ALL the time even though I know its not on purpose :). He is such a delight to our family and we are so thankful God blessed us with him.
We will keep you updated when we know more in a few weeks. If he has this disorder, he will be followed up with regularly by these specialists and will more than likely be on an enzyme supplement by 3 to 6 months of age that will help him out somewhat.
We know God can heal him if its His will. And we know God will get us through this disorder if that is what is in store for Nate. Please keep us in your prayers as we wait on results. Please aslo pray that Nathan stays healthy so we don't run into complications from this. The doctor encouraged us by saying children with this disorder do well and grow up healthy as long as they are treated and monitored.
We know we serve a mighty God!
Thanks again for your prayers.
We love you!
Love,
Josh and Sarah
Here is a picture of Nate "sunbathing" when he was slightly jaundice.
Abby and Will just love him so much. Will loves to hold him and Abby constantly kisses his head leaving her drool marks.