Tuesday, December 1, 2009

Gantt, Mark, and Rob's little overnight trip.






Some of you know that Mark has been interested in Monster Trucks lately.  I helped a little by getting my truck lifted and getting off road tires.

Since I had both boys while Jennifer was spending the night in the hospital, I had the idea to take them to see Grave Digger near the coast of NC.  We were able to meet Dennis Anderson, the founder and driver of Grave Digger.  He has done more for the sport and Monster Jams than any other person.  Mark had a blast and got Dennis to sign his hat and one of his toys.

Enjoy the pictures.  Some of the photos are from Marks perspective.  It is interesting to see how big it looks from a 6 yr olds eyes!!


Couple more pics....

In order for the trucks to get in the garage, they have replace the huge 66 inch tires with much smaller ones.  Mark thinks they look kind of funny.




Monday, November 30, 2009

Home at Last

We made it home today around 6:30pm. Took us almost 2 hours with all the darkness, rain, and traffic. But what's most important is that we made it safely and we're all home together again!!

Sunday, November 29, 2009

Answers and Plans

So Brett got to meet the UNC Tarheels Basketball Team this week! When they stopped by we got some pics as well as had them sign a poster. Here's Brett with his poster.



This is our awesome new room! It is so big and it is in the corner of the 5th floor. Hardly anyone walks down the hallway so it is much quieter than the previous room (and MUCH quieter than the PICU!)

As for Brett's condition - he is feeling much better, and pretty much back to his normal smily self. I know he can't wait to be back home with his brothers. The docs pretty much decided (based on the bacteria that finally grew from the culture) that the infection DID originate from his broviac central catheter. Therefore, the central line must be removed. However, we can continue to use it to finish out the round of IV antibiotics first. Despite the trouble breathing (brought on by the infection) that landed us in intensive care, his lungs are in good shape. Tomorrow (Monday the 30th) makes 7 days of antibiotics since a negative-for-bacteria blood culture, so we are going to go 14 more days after that (IVs that we will administer at home) just to make sure his lungs are in the best possible condition for when he gets the line out, because he'll be going under anesthesia for that. Chances are he'll be getting a bronchoscopy as well, but Rob and I still have yet to make our final decision on that. The procedure to remove the line will probably happen the week before Christmas. There are no plans to replace it. The good thing is that it will be one less thing we have to worry about and take care of at home. If he were to need another line in the future, he would just get another broviac or PICC at that time. As for being discharged, we are hoping it happens tomorrow.

Some pics with the team