CODY UPDATE.....JUNE 20th, 2010


Cody had his MRI on Monday, and he has his clinic appointment on Monday at Duke. His MRI shows that the tumor's are still stable, not grown any, but still hasn't started to shrink any either. We will see what his team of doctor's has to say, and if they will continue on the same path or change it.

Cody has not been feeling good this week, he has been very tired and sleepy. And also, not able to talk very much, that worries us. He has completed 7 of the IV chemo treatments of CPT 11 and Avastin now, and has been on the pill chemo Temodar since last August. His bloodwork continues to be good each time we go for his treatments (which is every two weeks), he is still eating pretty good and as long as I keep the nausea meds in him he keeps it down. I guess the chemo is finally taking a tole on his body and that's why he is so tired. I had his hair buzzed off after Clint's wedding it was getting so thin that it looked bad, but now it even looks thicker, he wears a cap all the time anyway, so he doesn't mind. I had him fix Gerry a father' day card today, he drew pictures of fish on the card, and wrote happy father's day dad on it, it was hard for him to look down and use his left hand to write it, but he did a good job, we worked on it this morning and then again this evening until he got it finished. He knows that everything that he does, that he does it slow. He told me one morning while he was eating breakfast, he said: "mom, I'm sorry that I am so slow". I told him that if it took all day that would be fine too, I reminded him that at one time he had a feeding tube and I was so happy to see his food going in his mouth. Cody is so appreciativ
e of everything that I do for him, he often says "thanks mom for taking care of me", I always tell him that, I would not think of letting anyone else take care of you, he just smiles at me. Cody is such a special young man, and we love him so much, it is so hard to see him struggle with all he is going through, but we will never ever give up on the miracle of healing.

Ple
ase pray that we have a safe trip to Duke and that they will see something positive from the MRI and find the right treatment to help shrink it.

I will update when we get back...ONE-DAY-AT-A-TIME, The Hallcox Family