Monday, February 16, 2009
How'd It Go?
Wednesday, February 11, 2009
Some Tough Moments
Before we went downstairs for Joshua's procedure, Dr. Zeiber came back to talk to us about Joshua's home meds. Currently, Joshua is at 100% of his chemo pills (based on weight/height). Because his counts were up, she informed us that we would need to up his dosage to 120%. The fact that Joshua's counts are up is good news. We rejoice in that. At the same time, we get nervous when Joshua's dosage gets very high because it can very easily cause a crash to his immune system. Along with the increase in chemo, she also needed to increase his steroids. YUCK! As we have shared many times before, the steroids cause so many strange side effects. Thus, an increase in steroids means an increase in side effects.
The spinal tap went well and the nurses had his cherry coke Icee waiting for him when he finished. After a very long morning, at around 2 o'clock we made it to one of Joshua's favorites, Jason's Deli. He broke his fast in fine style to the point that the manager came over and asked if he wanted a refill on his fruit. I guess he noticed how quickly he downed the strawberries. It was a pleasant end to a long day.
Please pray through the news about Joshua's increase in dosage. Pray that he can continue to show his courage and strength in this fight. Pray also for Michael, Andi, and me. Pray that we will be patient and encouraging toward Joshua and each other. Thank you again for your faithfulness.
Wednesdays Are For Chemo
At least they are in our house. Usually I reserve the weekends for a "Weekends Are For Kids" post, but I thought since today is a big appointment day I might give you a glimpse into Joshua's treatment cycle in case you're interested.
Just to refresh your memory, Joshua (then 2 years old) was diagnosed with ALL (Acute Lymphocytic Leukemia).
Eventually, we settled into this basic routine:
- Joshua takes chemo pills every day.
- Every Wednesday, he takes 7.
- Every 4 weeks he has intravenous chemo sent directly into his blood stream through a port in his chest.
- Every 12 weeks, in addition to the above, he has a spinal tap to put the chemo into his spinal column.
Today is week 12, so we've got it all happening this morning. This is the 844 day Joshua has taken a chemo pill. It's his 30th time to have the medicine go into his chest. It's his 10th spinal tap. And he keeps on smiling.
For this, I am thankful and so very proud of my boy. In just a few minutes, he'll jump out of bed excited to go to the hospital. He'll bravely take his medicine with the promise of an ICEE when he comes out of his anisthesia. And he'll try hard for the next 6 days to feel good.
We continue to feel blessed for Joshua's progress, so thankful that God has sustained us and him thusfar, and continue to take one step at a time in fear and trembling. Thanks for going there with us.
Sunday, February 08, 2009
Tuesday, February 03, 2009
Marathon Training

I did it. On Saturday, I ran 14 miles. I decided I wouldn't make my training official until I had run more than a half marathon to get ready. So now I am in. I am training again with Team in Training. They continue to be such a supportive organization and have made Joshua a Honored Teammate this year. We are thankful for what the Leukemia and Lymphoma Society does and we wanted to make sure that if hundreds of people were running in Joshua's honor, one of us was running as well. I'll keep you posted on the progress. In the meantime, check out the websites highlighted above and feel free to give to support the cause.
Monday, February 02, 2009
Surprise Attack
Thursday, January 29, 2009
New Knives? What Was I Thinking?
Wednesday, January 28, 2009
25 Random Things About Me
Yes, I fell into the trap of answering this tag on Facebook so I thought I would share it here also. It actually turned out to be quite fun.
Saturday, January 17, 2009
Andi's Talking
Wednesday, January 14, 2009
Back From Clinic and Happy News
Clinic
Monday, January 12, 2009
Surprisingly Great

When I got a call from my friend, Valerie, that she wanted me to join her at a Bryan Adams concert at the Ryman. I immediately said, "Yes." Valerie was quite surprised that I was so eager to join her. Apparently, I was the 4th person she had called and the others had all laughed at her request. To be honest, my excitement was a combination of wanting to go to a concert at the Ryman (my first after living here for almost 5 years) and wanting to go to concert that I would know at least half of the songs. Even though I was only 7 when Bryan Adams hit the world by storm with the Summer of '69, my 2 older sisters heavily influenced my choice of music growing up.

Thursday, January 01, 2009
Make a Wish Trip
SHHHHH....Friday, December 26, 2008
A Merry Christmas
Wednesday, December 24, 2008
The Yearly Question
This is the first Christmas we will spend without our daddy at home. Our family has always been very close with lots of traditions that have maintained throughout our childhood and carried over to our adulthood. One tradition, that my dad started about the time me and my sisters were all able to think for ourselves (pretty young since we are all girls. haha), was the yearly questions. Dad was always good at asking questions at the dinner table or before bed, but the yearly questions were a bit tougher to answer. They always required thought and somehow a piece of yourself...questions about your future, your greatest victory, a time when you chose to forgive, a time when you should have, about making friends, or learning lessons. All questions that could transform your thought processes.
Every year I would spend time before Christmas Eve trying to figure out what the question was going to be that year. But inevitably, he would go a completely different direction than I was prepared to go. When 7pm on December 24th came around, after the nachos had been eaten and the Christmas story had been carefully read from Luke 2, the question was asked of each of us. We gave our answers, usually through teary eyes, and followed that time with sweet times of prayer for one another based on our answers. So, this year, dad will not be able to ask the questions, but I will sit beside him and share about the wonderful ways that he shaped our lives with the questions he did get to ask.
Monday, December 22, 2008
Sunday, December 21, 2008
Settled
We have visited him everyday and each day he shows signs of progress. Today, in fact, he was walking without assistance while eating ice cream from a bowl. This may seems small, but he was not walking or eating on his own 3 days ago...a major victory. It was also good to see dad smiling and making jokes with the nurses. More than anything, today was a chance to see dad being very well cared for.
I am so very thankful for my family through this process. The decisions were made quickly, without anyone's will being exerted above someone else's and with everyone's feelings being addressed and thought of. Everyone contributed to the process and no one took over. As difficult as this process was and continues to be, I could not have asked for a more supportive and loving family to do it with.
Monday, December 15, 2008
Tough Choices
Thursday, December 11, 2008
Happy Birthday Mom


