Saturday, December 10, 2005

He's up to 7lbs 3.8ozs. He's a hoss, eating like crazy, and gaining like crazy. I read through his chart last night, his lowest weight was 6lbs 10ozs when he was 3 days old - so he's gained over 1/2 pound in 5 days, and didn't even eat for one of those days!

He's now up to 60ccs every 3 hours - that's 2 ounces for those of you that aren't Erin or Ang, who work with CCs on a daily basis lol. He's totally off his supplemental IV. His rash is clearing up, which is amazing, because they tend not to heal well because of the oxygen shortage - but then, his O2 sats are at normal levels right now. Last night his alarm went off because it was too high, how's that for weird? I mean, why is there an alarm for oxygen levels of 98%? Yeah I know, it's for babies that are actually on oxygen...

He's awake more and more, and seriously alert when he's awake. He loves Scott's voice and will watch him when he walks around or moves around when he's talking. Scott whispers secrets in his ear... I have no idea what he tells him, but it's adorable to watch Nova react to it. I think he might be promising him a steak or a cheeseburger or something.

He hates diaper changes, blood pressure checks, and having his temperature taken. He liked his nurse tonight, but really doesn't care much for the male nurse when he gets him. He kept scratching his face so I cut his nails tonight. This is my 7th kid, why does that still make me nervous? I kept having visions of cutting the tips of his finger off. He may be the biggest baby in the NICU, but those are still tiny tiny little fingernails.

Anyway, it's 1am and I wanted to do a quick update before I go pass out for a couple of hours. Night all, more pics tomorrow. . .

posted by Erin @ 4:13 PM   0 comments

This page is powered by Blogger. Isn't yours?

Donovan "Nova" LeClair

Monroe, North Carolina
Nova was our second child to be born with congenital heart defects. We lost our daughter at 12 days after open heart surgery in 2001. Nova was born 12/2/05, with Pulmonary Atresia with VSD. He lived 6 weeks after surgery, and passed away on April 6th, 2006. This blog is his story, and the on-going story of how our family is dealing with the loss of our beautiful boy.
View Erin Monahan's Complete Profile

Click Here to Donate

Our Links:

"Poetic Acceptance"
our website for grieving parents

Press Box and Publicity

This Site Has HEART

My site was nominated for Best Charity Blog!

Heart Kids
Forever Young Mommy Steps

Heart Links

Page best when viewed at 1024 x 768

Adult Dating
Visit NCBlogs
Listed on BlogShares