Three more days of radiation left. We had thought a while back we would be done today, but they had miscalculated the days and we are actually done Wednesday. Things went smoothly today. Jordan did great and came home and tore up the house with all kinds of energy. Tonight he has been kind of fussy and then I realized he is getting 2 big molars. Sometimes I forget about the regular baby stuff.
My heart has been heavy for the other 3 boys at radiation. Please pray for them too.
In the midst of this very difficult time, God has blessed us tremdendously with a Church, family and friends who have not worn thin in lifting us up. We are so thankful for the meals, the cards, the gifts, the help and all the encouragement we continue to get.
Fear not, for I have redeemed you; I have summoned you by name; you are mine. When you pass through the waters, I will be with you; and when you pass through the rivers they will not sweep over you. When you walk through the fire, you will not be burned; the flames will not set you ablaze Isaiah 43: 1-2
Friday, March 30, 2007
Tuesday, March 27, 2007
6 more days
Sorry I haven't posted anything in awhile. This whole radiation thing has kind of done me in. I don't think I have ever wanted anything to be over more than this. We have six more days left and I can hardly wait. All the boys are counting it down. Everyone knows each other's last day. Jackson is done on Friday and then gets to go home. Kyle is done on Tuesday and Diego and Jordan on Wednesday. There will be some major celebrating. Jordan is doing great. He is a real trooper with it all. He now holds out his leg for his blood pressure and his finger to check his oxygen. It is so sweet. There have been lots of problems with his line and some other procedural stuff though. It has been a real pain in the neck and has kept us very late the last few days. He continues to have lots of energy. Nobody can believe it because the radiation, anesthesia, medicines and chemo are all supposed to make you tired on their own. He's getting all of it and has now quit taking naps! I am so happy he has lots of energy, but all that stuff is making me tired, it would be nice if he occasionally got a little sleepy.
Friday, March 16, 2007
The Middle of the Middle
Jordan is back to himself again. What a relief! I was so happy to answer the nurse this morning when she said...any nausea or vomiting? no. Any fevers? no Any diarrhea? no Anything new? Thank goodness, no. We are at Children's now and he is getting his chemotherapy. He is happy eating his ritz peanut butter crackers ( a new staple for him) and watching Elmo. He does not like to be hooked up though because he can't move around the room and climb on things.
Last time we were here for chemo my friend Liz said, " You know what? You are at the end of the beginning of this whole thing. Pretty soon you will be at the beginning of the end, and then before you know it, it will be done." So I am happy to say, we are now at the middle of the middle of radiation and the middle of the middle of chemotherapy. At the end of next week, we will be at the end of the middle of radiation which is really the same as the beginning of the end. In six weeks that's where we'll be with chemotherapy too. I hope you can all keep track of that!
We are out of here at about 10:30 and then will be happy to be home from the hospital for a weekend. Our first weekend at home in a while.
Last time we were here for chemo my friend Liz said, " You know what? You are at the end of the beginning of this whole thing. Pretty soon you will be at the beginning of the end, and then before you know it, it will be done." So I am happy to say, we are now at the middle of the middle of radiation and the middle of the middle of chemotherapy. At the end of next week, we will be at the end of the middle of radiation which is really the same as the beginning of the end. In six weeks that's where we'll be with chemotherapy too. I hope you can all keep track of that!
We are out of here at about 10:30 and then will be happy to be home from the hospital for a weekend. Our first weekend at home in a while.
Tuesday, March 13, 2007
Home
We came home on Sunday night. Jordan is finally feeling better. He is still very lethargic and a little irritable, but so much better than a few days ago. We're continuing to trudge through the radiation appointments. Friday is one of his long chemo days so that one should go from about 8 am till 11 pm starting with radiation. One bright spot was he slept the whole night in his bed. He's never done that in his whole life. Hopefully, it was not just because he's been sick.
Friday, March 9, 2007
Admitted Again
Another short one. We have been hit hard. Jordan has rotovirus and is in the hospital again. It has been one thing after the next for the last 2 weeks. He has been having high fevers, vomiting, and bad diarrhea so he needs to be here to get hydrated. Yesterday had to be one of the hardest of my life. It started at 7:00 am going to radiation, then to Children's since he was so sick. We were up all night with him with a high fever. To top it off someone stole my clothes out of the drier here. I had to convince the nurse to give me some scrubs so I didn't have to wear hospital pajamas to the UW this morning. He did well with radiation despite feeling rotten. Today, he has slept all day. We imagine he will be here for a couple more days. Thanks to everyone that has stepped up to take the kids and help us out. Sorry if we haven't returned calls or have dropped the ball with comittments, we have just been so preoccupied.
Tuesday, March 6, 2007
Another bug
Not much time to write this week. It has been a tough one. Jordan now has some sort of GI bug and has been throwing up, a fever, and diarrhea. He still goes to radiation though. Poor little guy. He has just had one thing after the next. However, this is the first day we have not been at both hospitals in the last week. His fever seems to be getting better and he's been keeping some food down today.
Sunday, March 4, 2007
Going Home
Well they gave him the go ahead to go home today, so we are happy to be out of here. They are coming this morning to train me to give him the IV antibiotics at home and we'll have to do that for about 10 more days. We're back at the UW tomorrow for radiation. I'll be happy to get through this month. The good news is that nothing slows Jordan down. He's had 5 days of radiation, an ear infection, a cold, a blood infection and little sleep, but he is still climbing all over, socializing with the nurses, playing with the kitchen in the playroom and just generally busy, busy, busy.
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