Posting for Saturday, 12/4/04
Decent night's sleep.
Weather update: It is gorgeous outside. Clear skies and the sun is shining. A storm is heading our way, though. "Moving fast," is how the Weather Channel described it. Possible thunderstorms.
Ran into Peter on the elevator ride down to the Health Expo. The two of us checked out the vendor booths and stopped by the Cf Foundation table. Meanwhile, Julie and the kids stayed back at the hotel. Earlier today we went to se the new Pixar film, THE INCREDIBLES. I liked the movie a lot. However, it was a little too intense for Jake and Sophie at times ("This 'credibles too scary." to quote my son). Still they sat through it with that sort of "I'm too scared to look, but too scared to look away" fascination. I must say, I felt the rating was a little skewed because it is an animated film. I felt there was just as much violence and peril as a movie like SPIDER MAN 2, and that got a PG-13 rating.
After the movie we headed to the food court of the Fashion Island Mall for lunch. Jake had his usual, french fries. It's really getting to be comical what this kid will eat. Comical, yet disconcerting. We constantly worry that he’s not getting enough in his diet.
The kids and I then rode the merry-go-round. It was interesting to see how Sophie has become more reserved when we ride the merry-go--round. Jake is a pistol, screaming "Hi Mommy" every time we went round and round. Sophie, on the other hand, just smiled and stayed quiet. I remember a time when was just as loud as her brother.
Dinner with the CF group was fun. Robert and his wife, Euri, met us at an Italian restaurant. Rebecca gave all of us runners some nice gifts for raising money and running the marathon. Julie Widman (Julie's friend) and her daughter, Lucy, had met us earlier at the hotel and were also with us for dinner. You may recall that Julie's son, Cooper, has CF. Julie W. and Julie met through the Foundation. They see each other every couple of months but talk regularly on the phone. I understand why they are friends. To be able to talk to someone about the disease and what we're going through (someone other than your spouse) is so crucial. And to have someone who KNOWS what you're going through makes it that much easier. Yes, Julie and I talk about everything, but sometimes you need another person's ear. And sometimes you really need someone else’s ear that is experiencing everything you are.
We arrived late due to crummy traffic on the 405. He hit a nasty rainstorm. Hopefully that's all of the wet weather coming our way and tomorrow will be a quiet, cool day.
The two Julie's left early and took the kids back to the hotel. This allowed the team time to compare notes and talk a little about the race tomorrow. I haven't seen Wes in a while. I really think he’s a remarkable person. He exudes confidence, that's for sure. He was a little nervous about the marathon, though, and ran 8 miles this morning (!). I'm not sure that was such a good idea, but I think he needed a good long run to help him prepare mentally.
I returned to the hotel to find everyone playing Monopoly and having a much better time in the hotel room where they weren't confined to a table. Sophie really likes Lucy, a precocious little girl. While they played, I put my running gear together (my "armor" as Robert called it) and set my alarm for 5:00 am.
We're meeting in the hotel lobby at 5:45. No big deal. What a difference a year makes. In Hawaii, I was so nervous about missing the race and how well I would perform. Tonight, I'm more concerned about whether or not I should shower in the morning.