UPDATE on Cody......March 2, 2010

Our Duke appointment was a long one and full of changes for Cody. His doctor wants to add more to his treatment, so we had to have blood work before we left and meet with his nurse to go over what he would be doing for the next two months.
He will remain on the Temodar but at a lower dose, and now instead of 5 days every 28 days, he will be taking the Temodar for 7 days on and 7 days off for the next two months. Then on the 7 days off he will be giving an IV of Avastin and right behind that he will be given CPT-11 which is another chemo.
The Avastin is suppose to keep the tumor from making new blood vessels which feed the tumor and make it grow.
The CPT-11 interteres with the growth of cancer cells.

Cody

s MRI last Thursday, actually showed that the tumor on the right was shrinking a little, but the tumors around his brain stem had a little more growth, and that is why we have to start the new treatment. The doctor said that could explain why his balance is off and why he is vomiting so much.

We don't know what the new round of treatments will cause for Cody, but hopefully, it will outsmart the tumors and starve them away. It will probably be Wed or Thursday before we start his chemo back up, we have to wait to see if his blood work will allow him to take the new. He will have to have blood work every two weeks when he starts the new treatments.

Please keep praying for strength for Cody to tolerate his new treatments and that the cancer cells will start to die and leave his brain. He has been through so much and I know that the next phase will not be easy either. But he never complains and seems to be happy and smiling everyday like nothing is wrong.

I will update again when I can.

P.S. We just missed Richard Petty yesterday at Duke, he had his wife at the same doctor, apparently she has brain cancer also. But the one's who came in after us saw him leaving and got pictures of him. Never know who you will see at Duke

ONE-DAY-AT-A-TIME, The Hallcox Family