Sunday, September 27, 2009
Saturday, September 26, 2009
Dessert
Wednesday, September 23, 2009
Round 1
Today we had 3 appointments at Primary Children's hospital. Dallan took the day off work so we enjoyed a hospital "date" with Caleb.
Our first appointment was with urology. Caleb's bladder and kidneys are structurally sound and show no signs of reflux. So we decided to put Caleb on a low daily dose of antibiotics for 6 months before using catheters at home. Hopefully this will help break the cycle of bladder infections he has been dealing with for the past few months.
Our next appointment was the dentist. Now, who really likes going to the dentist? Not Caleb! They gave his teeth a quick polish and painted some fluoride on them, and it took Caleb quite a while to forgive us! He coughed for so long afterward that he broke out in little dots all over his face!
Our last appointment was with the dysphasia clinic. Caleb's g tube looked great! We met with a dietitian and decided to add a beta protein scoop to his feedings once a day. We have been concerned that Caleb is getting extra fluffy, but decided to keep his feedings the same and monitor him closely before cutting his calories again. He is already getting so few calories, that we want to make sure it's appropriate for him.
So, Round 1 of follow ups done! Round 2 is in a couple weeks with the ENT, pulmonology, and neurology.
Our first appointment was with urology. Caleb's bladder and kidneys are structurally sound and show no signs of reflux. So we decided to put Caleb on a low daily dose of antibiotics for 6 months before using catheters at home. Hopefully this will help break the cycle of bladder infections he has been dealing with for the past few months.
Our next appointment was the dentist. Now, who really likes going to the dentist? Not Caleb! They gave his teeth a quick polish and painted some fluoride on them, and it took Caleb quite a while to forgive us! He coughed for so long afterward that he broke out in little dots all over his face!
Our last appointment was with the dysphasia clinic. Caleb's g tube looked great! We met with a dietitian and decided to add a beta protein scoop to his feedings once a day. We have been concerned that Caleb is getting extra fluffy, but decided to keep his feedings the same and monitor him closely before cutting his calories again. He is already getting so few calories, that we want to make sure it's appropriate for him.
So, Round 1 of follow ups done! Round 2 is in a couple weeks with the ENT, pulmonology, and neurology.
Sunday, September 20, 2009
Consider the Lilies
When I was expecting Caleb we knew he had significant challenges. We did not know if he would be born alive, if he would live after birth, or if we would ever get to take him home. This song brought me so much comfort during those months that he was tucked inside. After Caleb was born, a dear friend, who knew how much I loved this song, sent it to my hospital room in her CD player. I listened to it over and over during that tender hospital stay.
This same friend brought me lilies on Caleb's first birthday... (Please turn off Caleb's playlist if you'd like to hear it too)
This same friend brought me lilies on Caleb's first birthday... (Please turn off Caleb's playlist if you'd like to hear it too)
Tuesday, September 15, 2009
sweet

Last night Matthew came home from his school carnival, and he came running right into Caleb's room with a big smile on his face. He said, "I got some cotton candy! Do you think Caleb could have a taste? It would just melt right into his mouth!" He was so excited he had thought of a treat that might be okay for Caleb since he is only able to eat through his g tube. I loved that Matthew couldn't wait to share something sweet with his little brother. Caleb enjoyed his first taste of cotton candy, and he especially loved the snuggle from Matthew that came with it!
Dear Matthew,
Thanks for sharing your cotton candy with me! It tasted very sweet in my mouth! Thank you for looking out for me even when I couldn't go to the carnival with you.
I love you Matty.
Love
Caleb
Monday, September 14, 2009
KIDZ

Last Winter I met Tara from the KIDZ website while at Primary Children's hospital for Caleb's g tube surgery. I've enjoyed reading her KIDZ web site that shares stories of other parents with special challenges, gives creative ideas, and provides inspirational thoughts. I've been given the opportunity to post there from time to time, so you'll have to check it out!
A friend indeed
Sunday, September 13, 2009
The Shepherd will supply thy need
I listened to this song over and over when I was expecting Caleb, and now I listen to if often with him on my lap. It has become one of "his songs" to me. (Please turn off Caleb's play list if you'd like to hear it too)
Holding
Saturday, September 12, 2009
Friday, September 11, 2009
Labor day
Bladder
Caleb has been battling a bladder infection for several weeks now. We've been on 4 different antibiotics but he still seems to be uncomfortable.
Last week we spent 4 hours in in the hospital to see if we could find out what the problem is. He had an ultra sound on his bladder and kidneys, and they appeared to be okay. Then we had a VCUG. Doctors sedated Caleb, put a catheter in, then filled his bladder with contrast so they could watch how he empties. It quickly became apparent that Caleb is not emptying all the way, so his bladder is a breeding ground for infection. The good news is that he doesn't appear to be refluxing into his kidneys. The challenging news is that there is probably not an easy fix. We may need to start using catheters at home or consider surgery. We have an appointment with a urologist on the 23rd to see what our options are. Hopefully we can find some manageable solutions!
Last week we spent 4 hours in in the hospital to see if we could find out what the problem is. He had an ultra sound on his bladder and kidneys, and they appeared to be okay. Then we had a VCUG. Doctors sedated Caleb, put a catheter in, then filled his bladder with contrast so they could watch how he empties. It quickly became apparent that Caleb is not emptying all the way, so his bladder is a breeding ground for infection. The good news is that he doesn't appear to be refluxing into his kidneys. The challenging news is that there is probably not an easy fix. We may need to start using catheters at home or consider surgery. We have an appointment with a urologist on the 23rd to see what our options are. Hopefully we can find some manageable solutions!
Sunday, September 6, 2009
Rise and SHOUT!
Caleb's name means "having courage in the face of overwhelming odds."
So you can bet that Caleb never doubted that BYU would be victorious over Oklahoma! You see, Caleb knows a little bit about being the under-dog. He knows what it's like to face seemingly insurmountable challenges. And most of all, he knows that no matter the odds, you can come out shining!
And that my friends, is why Caleb bleeds BLUE with the rest of us!
Go Caleb and go Cougars!
So you can bet that Caleb never doubted that BYU would be victorious over Oklahoma! You see, Caleb knows a little bit about being the under-dog. He knows what it's like to face seemingly insurmountable challenges. And most of all, he knows that no matter the odds, you can come out shining!
And that my friends, is why Caleb bleeds BLUE with the rest of us!
Go Caleb and go Cougars!
RISE AND SHOUT!
Caleb's game face. He keeps his composure almost as well as Bronco!
25 words
Today in Relief Society we had the opportunity to listen to President Monson's talk "Joy in the Journey." This is one of my favorites talks. I love how he taught that we should never let a problem to be solved be more important than a person to be loved. I love how he said that we should focus less on what is missing and instead realize the abundance that surrounds us. I loved his council to make memories, to cherish those around us, and to find joy in our journey now! Today, however, I learned another truth from his inspired words.
Lately, I have been thinking about what I would want my children to hear from me if I knew my time with them was limited. If I only had a few words left, what would I want them to be? President Monson spoke of a man who was a prisoner of war for 2 years and was finally allowed to write a letter to his family. His letter was limited to 25 words or less. That story was so tender to me. I thought about what I would want my 25 words to be. There have been times when my heart has been in agony as I've watched Caleb struggle. I've worried about what I would want my last words to be if I had to say good bye.
As I continued to listen to president Monson's talk, I heard him teach us that the most important thing we can do is to create a legacy of love. It brought my heart peace. I realized I didn't need to worry so much about last words. I needed to continue creating a legacy of love now. And maybe then, if time was short,words wouldn't be so necessary because those who I cherish will already know.
Here is President Monson's talk in it's entirety. It's worth watching again and again.
Lately, I have been thinking about what I would want my children to hear from me if I knew my time with them was limited. If I only had a few words left, what would I want them to be? President Monson spoke of a man who was a prisoner of war for 2 years and was finally allowed to write a letter to his family. His letter was limited to 25 words or less. That story was so tender to me. I thought about what I would want my 25 words to be. There have been times when my heart has been in agony as I've watched Caleb struggle. I've worried about what I would want my last words to be if I had to say good bye.
As I continued to listen to president Monson's talk, I heard him teach us that the most important thing we can do is to create a legacy of love. It brought my heart peace. I realized I didn't need to worry so much about last words. I needed to continue creating a legacy of love now. And maybe then, if time was short,words wouldn't be so necessary because those who I cherish will already know.
Here is President Monson's talk in it's entirety. It's worth watching again and again.
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