Mom just got the clearance to go home tonight! We are so excited and thankful! I started doing my dance again! He has "turned our mourning into dancing!" I will update more later tonight.
Thursday, July 29, 2010
An update and a special request
Dear friends and family,
Sorry I didn't get a post on the blog last night. We didn't get home until very late and I only had enough energy to eat a quick bite and fall into bed. Mom stayed here at the hospital without us last night because she felt well enough to be alone. During the night, she didn't seem to get much sleep because she became very nauseous and the nurses were in a lot trying to help her with this. Mom's nausea is better today.
The doctors told her yesterday that there was a possibility that she could maybe go home today. I sang a song and did a dance as soon as the doctor left the room... but I probably should have waited for today to do that. Mom continues to be doing very well today, but they are beginning to give her a couple of new things in her IV. The surgeon is supposed to be here soon and should be able to give us some more information about Mom's current progress and the possibility of her going home sometime soon. He was very encouraging yesterday, so we are hoping he will be that way again today.
While our family has been here at Santa rosa, we have met and become friends with a lot of different people- nurses, doctors, transporters to x-ray, other patients' families,etc. We have all really enjoyed meeting these people and learning their stories. We have learned a lot about suffering and how many people go through things much, much more difficult that a bowel obstruction. While we have been loved on beyond measure during Mom's stay in the hospital, we have thought so much about how other people live through hardships without prayers or support. I just can't imagine.
We met a family like that this week. We would like to bring their names to this incredible group of prayer partners and ask you to pray for and support them in the same ways you have for us. While Kasey and I were on the elevator a few days ago, there was a little two year old riding on it with her dad. She was as cute as they come! I started talking with her and quickly fell in love with her. She told us that her name was Faith and that her little brother, "Zacky," had a "boo-boo.". Her dad said that he actually was a 7 month old who was very, very sick. We told him that we would keep him in our prayers as they got off to go to the pediatric ICU on the 7th floor. We took Faith a balloon yesterday and then met up with them again this morning in the main floor waiting room. We got to sit and talk with them for a long time and learned more about their story. They had been stationed in the Army in Germany when their son, Zechariah, was born. He has had multiple health issues, including heart disease, since he was born. The Army sent them here for their son's care and he has been in the hospital since May. The dad comes to the hospital every day with Faith and sits in the waiting areas while Zechariah's mom sits with him in ICU. We asked the dad about what their family is needing, and we hurt so badly for them when he told us that their family all lives in California and that they don't know anyone here. While I know there are probably a lot more families here like them, we felt so touched by their story. We ask you to pray for the Reese family as you pray for Mom. We want them to feel God's loving arms around them in the same way that we have felt them around us.
If you are able to pray for or somehow encourage this family, please take a moment to do this. We have been thinking about how this sweet family can be supported. The dad told me this morning, "I know God has a purpose. I just don't know it yet." I guess that is how we all feel at some point (or many points) in life. We continue to be thankful that He loves us and is in control.
Kelly (for all of us)
Posted by Kelly Litton at 1:12 PM 1 comments
Wednesday, July 28, 2010
Blessed beyond measure
What a great morning! Mom is sitting here (in a chair and not the bed!) eating little bites of a cinnamon roll. She fought hard to get what she wanted! The doctors just left the room and said she is making progress in "leaps and bounds." What a wonderful way to describe her progress! There was even a good bit of discussion this morning about when she may get to go home. We are so excited! She still has a few more tubes/iv ports/ etc. to have removed before she can get to that point, but we are so thankful that it is even on the radar.
Her pain level this morning is at a 2 on a scale of 1 to 10. I haven't heard it that low (or even close to that!) since I got here 11 days ago. 8's and 9's have been much more common. I am more thankful than I can put into words that Mom is finally feeling some relief from pain. She said she is able to be attentive to the surgical pain now, since the ng tube was removed. That had been causing Mom a great deal of pain, discomfort, and distress. She has felt such relief with it out, and is continuing to progress as the doctors had hoped. Mom drilled her doctor with questions this morning and we talked about how glad we were that she was able to drill them herself today...instead of us being the ones to drive the doctors crazy this time :)
Mom just told the doctors she is "blessed beyond measure." We definitely all feel that way. Kasey and I were discussing yesterday how we have been so encouraged this past few weeks just knowing we were in people's thoughts and prayers. It has been such a support to all of us.
One of the doctors was here earlier and told Mom that she has handled this horrible illness with such grace and that the whole team has been honored to be a part of her care. Mom said that this has been a very humbling experience, and that it is not such a bad thing to be humbled at some points in our life. I am continually amazed at Mom's attitude and am so thankful that I have such an incredible mentor to watch and learn from.
Kara is headed out to Madrid in the morning to finish the work she has for her Master's degree there. I am headed to back to Abilene in the next couple of days to be a mommy again. I think my little ones and I are starting to really miss each other. I will continue to give thorough updates, even as I am away from San Antonio for a little while. Kasey is going to stay here for a bit longer to help Mom get transitioned back home.
I have had several requests for Mom and Dad's address. It is: 6519 Pemwoods, San Antonio, Texas, 78240.
Thank you all again for your care and concern,
Kelly (for all of us).
(By the way... I got a new phone- well actually i had to get two new phones because the first one was broken out of the box! My new phone erased all of my contacts... grrr! This phone situation has been a quite long and frustrating process! If you are one of the people I normally talk with... Or if you have my number in your own contacts, send me a quick text and tell me who you are so I can plug your number back into my phone. Thanks!!!)
Posted by Kelly Litton at 12:49 PM 14 comments
Tuesday, July 27, 2010
Afternoon Update
We are thanking God for answered prayers this afternoon. Mom was able to get her ng tube removed this morning! She cried tears of joy and thanked the doctors and the Lord for her relief. I know many of you have been praying specifically for that today, and we thank you.
Posted by Kelly Litton at 4:20 PM 10 comments
Day 14
Mom is having a very hard morning. She was in a great deal of pain throughout the night, but they were able to somewhat manage this with medications so that she could sleep. She is in extreme pain this morning and very frustrated to still have her "ninja tube" in her nose (down to her belly). The doctors came in the morning very early talking about a possible need for a blood transfusion. This was the first time we had heard about this possibility. Our specific prayers right now are:
1) That Mom is able to get the ng tube removed today. This is causing her a great deal of pain and anxiety right now. As soon as this is removed, she will be able to eat...which should aid in healing her body.
2) That Mom's hemoglobin levels would increase and she would not need a blood transfusion.
3) That Mom's pain would decrease.
Posted by Kelly Litton at 8:00 AM 11 comments
Monday, July 26, 2010
Thankful
Today was filled with some new positives. Mom has done well following surgery yesterday and seems to be (hopefully) on the road to recovery. We fully expected her to be in a lot of pain and asleep most of the day, but we were pleasantly surprised when we were wrong. Mom talked to us a good bit of the day and seemed to be in good spirits. We worked a good bit of the day trying to figure out some of her pain medications, but as of tonight, we think that is all settled. We have been amazed at Mom's strength. She is incredibly tough. I think I have always known this, but it has been amazing to be reminded of this as she has been in the hospital these past 13 days. Mom has been poked and prodded, cut on and stuck, but she takes it all without complaining....usually with a smile on her face as she tries to ask the nurse or doctor about his or her family. Mom currently has an ng tube in her nose helping with some pressure in her belly. (She is calling this her "ninja tube".) This is really, really bothering and hurting her. We are hoping things look good enough for this to come out tomorrow. We met with the surgeon this afternoon and he was very pleased with the results of the surgery and her condition today.
Posted by Kelly Litton at 9:45 PM 5 comments
Sunday, July 25, 2010
Post-Op (#2)
Mom is back in her room following her surgery. She still hasn't come fully out of the anesthesia yet, but she has been able to talk well enough to ask about the surgery and ask my dad for a kiss. We were hoping for a definite answer and fix from the surgeons, but did not get that. We did, however, feel encouraged by the surgeons and felt like the surgery was a success. Mom's surgery took about two hours. During her surgery, we were surrounded by sweet friends who brought us food, prayed with us, and even made us laugh. We are continually thankful for the outpouring of love that has been shown to us through this ordeal.
Posted by Kelly Litton at 7:44 PM 8 comments