Sunday, September 30, 2007

Very Grateful

I usually like to post a picture of Troy along with an update on how he is doing but he is taking a nap right now and I wanted to post this while I had the chance. Our family has been so lucky to have such wonderful people around us that are so willing to help at the drop of a hat. We have received so many cards, gifts for Troy and Abby, loving notes, meals, and just a genuine concern for Troy and all of us. If I wrote thank you notes to everyone I would be writing for days. I have been truly overwhelmed with how kind people have been. I know we have been so lucky to have Troy do so well with his chemo and all the love and prayers I believe has been a great help. This sounds cheesy but seriously I can’t help but be grateful for such amazing people around us. Thanks to you all.

Sunday, September 23, 2007

VACATION

Well we made it back from vacation and boy did we have a blast. We are so lucky that we had no issues or problems with Troy since he had chemo 2 days before we left. The beach was certainly the highlight for Troy. Abby and Troy could stay all day and night if we let them. Most of the time they would just run from the waves and it made me tired just watching them run. The weather was perfect and everything went just great. We know that was a small miracle to not have any problems.

Troy did have an allergic reaction to one of the chemo drugs a week before we left. He got hives all over his body the day after he had a PEG Asparaginase shot in both legs. The drug that is substituted for that is not approved yet so at this time he will not have that chemo drug anymore. This was the first snag we have run into since this started so I can’t complain. I asked the doctor what that will do are far as his progress goes. He said we don’t know what the effects are when you don’t receive the shots but we do know that when the PEG shot is given in the high doses that Troy was receiving it is very effective. Kind of a bummer but what can you do? He only has one more of those shots on his protocol so that is ok. He goes this Thursday for some more chemo and then we start the intense phase which will last 2 months. By Thanksgiving or Christmas we should be in maintenance which will be heaven. I can’t wait.