CODY UPDATE.......April 27th, 2010

This was our 5th trip to Duke, we traveled on Sunday, Cody was more alert this trip, and stayed awake more than he had the previous trips. He did vomit when we stopped to get something to eat, (that is why we use the drive-thru), but he did ok on the trip back.

He had lost 8 lbs. since our March 1 visit, we will be trying 4 new anti-nausea medications along with the one we already are using, to try to get him to keep his food down. One of the medications will help his stomach to empty out, because of the tumor around his brain stem, it is just not sending the right signals to his stomach . Then one will help increase his appetite, he is always ready to eat, but after a few bites he just can't keep it down. We will be giving him a couple of Boost or Insure (high protein) mixed with ice cream everyday.

We will continue on the same chemotherapy , doctor says that it is too early in treatment to see any shrinkage yet, the tumors are stable, and it will take a while to shrink. Cody has had a couple of good weeks, talking and staying awake more during the day. I hope to see more improvement over the next few weeks. We will take his 4th IV chemo on Thursday, and new pills to take on that day too, and for the 2 days after treatment. Hopefully, all those pills will stop his nausea.

His hair has thinned some, but it has not came out, with his cap on you really don't notice it. This is the least of our worries anyway, we just want him feeling better and able to eat and enjoy it like he used to. He has not had his favorite, biscuits and gravy and eggs in a couple of months, he will be trying that this week.

I will update in a few days and let you know if all those new pills are working.
Taking it ONE-DAY-AT-A-TIME, The Hallcox Family