Cody Update.............August 26, 2009
Duke was a busy place today when we arrived for our appointment. News vans were all over the place, it was because this was the place that Ted Kennedy had his surgery. Cody's doctor was on the 6:00 news talking about all of the new breakthroughs for brain tumors. Dr. Henry Friedman said that Cody is not a candidate for any clinical trials because you have to be able to take care of yourself to get in one. But he is putting Cody on Temozolomide (Temodar) which he says is probably better than any clinical anyway. That is the same thing that Cody's onocolgist in Knoxville wanted to put him on last month, but wanted to get Duke's view on it. Cody's tumor has grown quite a bit from the MRI we had on July 21st and the one we had on August 21st. When we go back for our next appointment in the morning, we will find out about taking steroids to reduce the swelling in the brain. He will also have a test called "MGMT" to check how his cells will react to the Temodar. At Duke, they don't say "you have 4 months to live" they say, we will take it "ONE DAY AT A TIME". He will take the Temodar for 5 days by mouth, then 23 days off. And continue it that way, have a MRI and coming back to Duke every two months. Cody was very tired from the trip over here, but was alert for his appointment. Please pray for a safe trip home, it took us 7 hours, with three stops on the way. We ask for continued prayers as we take the next step in this nightmare called Cancer. Taking life ONE-DAY-AT-A-TIME, Gerry, Pat, Cody and Clint Hallcox