Information as of: 8/19/03

• Actual Age: 2 months and 17 days old (11 weeks 0 days)
• Gestational Age: 34 weeks and 0 days (this is how far along I am if I was still in my mommy's belly)
• Corrected Age: -1 months and 14 days (this is how old I am if I had been born on mommy's due date, Oct. 1 2003)
• Weight: 1865 grams or about 4 pounds 2 ounces
• Length: 34.5 cm
• Head Circumference: 27.5 cm
• Current Issues my doctors are working on:
  • Lungs:
    Even though they are better than they used to be, I am still on the Conventional Vent on low-moderate settings. I will probably be on the vent for awhile longer. I currently have moderate-mild chronic lung disease. This means I will might have asthma when I get older and get colds easier. See, my lungs will keep growing till I am age 3! So, while I have immature lungs right now, I will have time to recover. My lungs will never look like other people's, but they will be normal for me! Mommy knows lots of kids with asthma who didn't have all the problems I do! So, if that is the only lasting effect, that isn't too bad!
  • Belly:
    My belly got a tear in it when my bowels stopped working because I had a bad infection! But, the doctors made me better from the infection and my tear healed itself. BUT, when I healed, I got a scar that is now blocking part of my bowels. So, now I will have to have surgery-- but luckily not for a few more weeks. I will be sick for awhile after the surgery, but I am a fighter and will fight hard afterwords. There is a chance that long term I will have trouble getting all my nutrition (short bowel syndrom) and mommy and daddy will have to make me eat a lot or my growth could be stunted! But, the surgery will otherwise fix my bowels so that when I am in kindergarten, I shouldn't be any different than my friends! The doctors are talking about setting the bowel surgery for the last week in August or first week of September or so. Well, we go major news this week. I started having bowel movements! I am not supposed to be able to do that. Mommy thinks I just got tierd of waiting for the doctors to fix me and did it myself. You have to do it yourself if you want it done right! Well, I'll let everyone keep trying to guess how I did this. The doctors thought it was impossible. And I have now proved them wrong with 6 perfectly normal bowel movements in 48 hours!!!! So, now the doctors are going to reward me with a bunch of GI Studies to figure me out. There is now a chance I might not need my surgery and I could be eating my next week. BUT, I could still need some surgery. My GI study is on Friday and maybe they will figure me out by then! What does a little guy have to do to get some food around this place!
  • Brain:
    After my 7 week head ultrasound, we found out that my body is growing faster than my brain (between my 5 week ultrasound and 7 week ultrasound I got my first growth spurt)! This might be a beign phenomeon because I was so very small where my brain will eventually catch up (they say about 24 months of age). It could also be indicative of some brain injury (though if it is, we can't tell for sure or have any idea how much). Or, it could be a progressive issue where the brain will get worse. All we really know is that I am still at risk (some babies like me have completely normal ultrasounds all the way through but have severe problems anyways as they grow up and some kids who have one or more concerning ultrasounds turn out normal) and we won't know whether I will have problems until I start missing milestones (things I should do at certain times like sitting up and crawling). The 9 week ultrasound results were good news. My brain is maturing normally in the past few weeks (for example, the ridges in the brain and such are developing). They shouldn't be able to see how much my brain has matured, but I do still have some extra fluid between my brain and my skull that allows them to see it. But, they said that the ultrasound looks better than the last. So, now they think there is just an anomoly that my brain is growing at a different rate than my skull. They are hopefull it will even out evenually and that it is not much to worry about. Though we still won't really know till I do or don't hit milestones!
  • Eyes:
    My eyes are open now! They were closed (fused shut) when I was born. I might have something called ROP. Lots of preemies have it. It means that I could be blind- but that most likely I will just have to have laser surgery and wear glasses. Well, I still have Stage 1 Zone 2 ROP after my exam today. I have progressed a little and the ROP is now effecting more of my eye. But, I am still stage one. Therefore, chances are that it will go away on its own and I might have to wear glasses later. See, I want to be like my daddy! If it gets worse, I can have laser eye surgery to help it, but there is only about a 10% chance that will happen!
  • Lines
    Lines are the IVs and such that they get my blood from or feed me my Triple Mix food. I have been a stinker with my lines. I have pulled several out, one got infected (a pic line), and one IV burst my vein and burned my skin on my hand for the size of a quarter! Ouch! So, my infection from my pic line is gone now, but plastics is following my burn to make sure it doesn't scar too bad. They said it did not get the muscle, luckily, but it did eat all the way through the skin. Well, in order to continue my super sized food, I needed a better line than my ivs and such. So, yesterday they took me down to the Operating Room and gave me what is called a Central Line. This will deliver my food and such right next to my heart. They taped this down good. They told me I was not allowed to pull this one out! That would be bad! I handled it well and I am fully recovered already. When are they going to figure out I was ripping them out because I don't like them! So, they give me one to my heart??? But I need it badly!