Sorry we haven't updated -- it's been crazy! We FINALLY closed on our house the week after Thanksgiving, Joey turned 11, and we had to do two science fair projects that took all weekend.
Mike and Joey took off to So Cal to visit PoPo, and also to have a little "Joey" time. When we were in CA this summer it was pretty much a vacation for Johnny, whatever he wanted to do (plus, he didn't feel well due to chemo before we left). We PROMISED Joey a LEGOLAND trip last time but didn't get the chance, so Mike took him this weekend.
Sophie went to pre-school today and luckily I had our friend Carolyn pick her up, because Johnny and I spent all day at the clinic --
but I'm not bitter.
His counts are amazing! Up for the past two visits -- his ANC is 3,140! No, there's not a
decimal in front of the three either -- that is the actual number. Crazy, I know. But he's been feeling well, sleeping well, and eating well. Since the T-day break, Johnny has been on an egg kick, lots and lots of eggs, 24/7. Cartons of 'em. So much so that when Anne was here over the break she got tired of making them for him (I was tired of it long before her...), and she showed him how to make them himself. This was so exciting for me, now if she could only show Mike how to do things himself... So Mike and I thought that because of his new craving for eggs, they might be the reason for his counts going so high. One day Johnny ate one dozen eggs (sans the yolks).
I asked Dr. Muscal if that was the reason his counts were so good for so long, and she said most likely
not. I couldn't believe it. I thought for sure it had something to do with it. But I guess not. If it did, they would tell all the kids to eat eggs to get their counts up. I still kinda think it has
something to do with it, because his diet has been so bad (sodas/chips) that when it finally got some real food, it kicked into high gear.
On the way to the clinic this morning, Johnny barfed. I thought it was because I had the heat on and he was wearing his jacket, but after he had three trips to the bathroom while we were at the clinic today, I think he might have a little bug. Regardless, his counts are still incredible and I'll leave it at that.
I also asked about the hair loss. Even though it has stopped, it is quite thin -- you wouldn't know by looking at it because it's so curly, but if you touch it, it's pretty darn thin. It's because of his oral meds, more specifically the methotrexate. Each time it is increased (he's at 75% dosage right now), it will cause more hair to fall out. Hopefully not all the way. At school some kids in his class found out how easily his hair was falling out and wouldn't leave him alone. I wasn't sure if he was making up the story or exaggerating, or even showed the kids how easily it was coming out, so I waited to mention it to his teachers. Now he can wear a hat in class, and the kids have stopped touching his hair.
And last but not least, you know how in your pediatrician's office they always have "updates" or warnings or helpful hints about kids and toys? Or like when Johnny tweaked his arm last January and the orthopedic doctor said that "he loved skateboards and trampolines", because they put his kids through college? Well trampolines are now off of our list of "fun" things to do:

For obvious reasons.
Other noteworthy info:
Joey and Johnny's school is taking them ice skating next week (I'm going to help out too), and the Gulf Coast Regional Blood Center asked Johnny to be in another commercial for 2007, taping is on Monday. Deluxe is doing another run of Johnny's board ready for distribution in Jan '07, if you want to check out the website go to dlxsf.com or Adio.com for some clips of the skate jam.
Next clinic visit is 12/27 just for labs, and 1/5/07 for vincristine and LP (lumbar puncture/spinal tap).
I will try and update before then, but just in case:
MERRY CHRISTMAS, hug your loved ones and be thankful for what you have.