Saturday, February 21, 2009
Posted by Cendy at 5:06 PM 1 comments
Labels: Thumb sucking
Wednesday, February 18, 2009
Kuyler was so mad by the time they got the test done. He was so hungry because he had not eaten since 8:ooam and the test was a 1:oopm. When the test was done, Kuyler came out with white stuff on his face where apparently he did not like the barium liquid that he had to drink. The technician said that his swallowing was fine, so that is good news. I am so glad to hear that. The next step is the brochoscopy next week. I will keep you posted. Thanks for dropping by.
His,
Cendy
Posted by Cendy at 6:40 PM 0 comments
Thursday, February 12, 2009
Kuyler
Well, we took Kuyler to see Dr. Ledbetter, the children’s pulmonologist at TC Thompson's Children’s Hospital on Monday and the visit went well. The doctor said that Kuyler does have some kind of an obstructed airway and that we need to have a bronchoscopy and a swallowing test done.
The swallowing test is scheduled for next week, February 18th at 1:00 and it is kind of an x-ray where they take pictures of him drinking to see if he is aspirating into his lungs when he is nursing. This would not be a good thing to be happening, so we have to get this checked out.
The bronchoscopy is more invasive since Kuyler has to be sedated and spend the night in the hospital. The procedure will take a little scope with a tiny camera into his nose, lungs, throat, and anywhere else to get a better view of what is going on with his breathing. In addition, the doctor is going to take cultures to see if there is any kink of infection going on. The date for this procedure it February 26th at 6:15am. Little Kuyler cannot have anything to eat after 2:15am and that is going to be hard since he eats round the clock it seems. I will really have to get him full before he lays down for bed that night or I am going to have a ravenous little man on my hands!
Well, I will go for now. Please keep us in your prayers that all goes well and Kuyler will just have to grow out of this.
His,
Cendy
Posted by Cendy at 10:10 AM 1 comments
Tuesday, February 10, 2009

Posted by Cendy at 12:15 PM 1 comments
Labels: Shopping
Wednesday, February 04, 2009

Please pray with me for the Preston Bowden family. I took this information from the prayer request I received this week from Christy Dasher. It is as follows:
I received this request earlier today- this is a friend of mine from college- please pray
cyd
Guys,
Can we please get a prayer request out for Preston Bowden and his family. This is the same Preston that attended Peerless Road while he was at Tomlinson College in the late 80's and early 90's and fixed half of our vehicles when they were down. His son Brett was diagnosed with Philadelphia Positive Acute Lymphoblastic Leukemia (PH+ ALL). August 26th Brett went through a Bone Marrow Transplant. January 29, 2009 we found out that Brett relapsed.
His wife Lorie shared this on Caring Bridge:
"Seth spent last night with Mamaw and Papaw. Baylee went back to school today. Preston is taking some time off from work. We spent a lot of time on the phone today. Took Brett to Petco so that he could buy some things for his puppy, Max. He's been saving money for quite some time and most of it is gone after shopping at Petco and Gamestop. We ate lunch at Fire Mountain. Papa and Bobo picked up Brett and Baylee around 4:00. They spent some time playing with Hunter and ate supper at CiCi's Pizza. Preston and I worked on organizing our paperwork to get taxes done this week.
We switched Brett's lab work from Thursday to tomorrow, so we had to set down and talk with Brett this evening. We needed his input on what choice to make regarding his treatment. Preston held him in his lap snuggled under his Duke blanket. Brett couldn't remember all 3 choices, so Preston spelled them out in detail. Choice A is to start over with chemo, to try to get him back into remission and work towards another bone marrow transplant. This would mean a lot of pain and sickness with harsh chemo. Brett said he didn't want to hurt and go through all that again. Choice B involves low doses of chemo to keep the leukemia from raging, prolonging his life a few months. Choice C is to make him as comfortable as possible without chemo.
Brett broke down and cried saying, "If I could choose not to hurt, I'd rather go tonight." By the end of the conversation, Brett, along with Preston and me agreed on Choice C.
We are filling our schedule for the next week or two with lots of fun family time. We'll keep going until Brett is too tired to go. We don't know how soon that time will come, but we've put it in God's hands.
Here is a link to their CaringBridge page if anyone wants to leave them a message of encouragement:
http://www.caringbridge.org/visit/theclownfish
Please keep this family in your prayers!
Gene Dasher Jr
Dear Lord, please cradle the Bowden family in your arms and give them strength to get through each day.
His,
Cendy
Posted by Cendy at 11:55 AM 0 comments
Labels: Bowden