A few people have mentioned that they were unable to find the order forms for Team Davis t-shirts. I assume that the information was buried in a post somewhere.
If you are interested in ordering a shirt, you may do so by clicking on the link below, printing the form, and mailing it and payment to Mandy Hanner, c/o Oakland High School, P.O. Box 378, Oakland, IL 61943.
Team Davis T-Shirt Order Forms
Just a reminder that the orders are due on Monday, October 31.
Also, for those who do order shirts, feel free to email, mail, or facebook (can that be used as a verb?) me a picture of you in your Team Davis t-shirt. I am going to make a photo album/memory book for Davis from his supporters and prayer warriors. Please specify if you do not wish for your picture to be posted on the blog; many pictures end up here.
email: abcoffey77@gmail.com
address: 9208 N Co Rd 2270E, Ashmore, IL 61912
Thursday, October 27, 2011
The Week Keeps Getting Better
10/27/2011: 11:33 AM
The week started out a bit rough but continues to improve.
On Monday, he devoted himself to school work, Wii playing (I told him that it was his PE time), and sitting around and complaining in true 10-year-old fashion.
What else is going on? Hmm. Annakate received a trophy in the mail for being a good sister to Davis. She is enrolled in this organization called SuperSibs. The organization sends her something to make her feel special about every month. This is such a great program. I hate to admit it, but I don't find myself doting on Annakate like I used to. Instead of doing her hair in the morning, I am getting Davis dressed or giving him his medication. Instead of reading her bedtime stories, I am helping him with his homework. While Kyle and I do make an effort to devote individualized attention and time to her, the program helps us by surprising her with encouragement. Plus, she feels so important.
We love living in the country. We have fantastic neighbors (In the country, everyone within a five-mile radius in any direction is your neighbor.) who look out for one another, and the space allows the kids to run and explore. I love the opportunities that country living and nature provide to my children. The wildlife alone creates our own hands-on encyclopedia. Over the course of a week (depending on the season), it is not uncommon to see hawks, owls, vultures, quail, deer, raccoons, stray cats, skunks, opossums, snakes, and coyotes in our yard. Yesterday was no exception. My normal morning routine includes opening my kitchen blinds allowing the natural light to flood in to warn everyone -mostly me- that morning is indeed here. I think I gasped before a smile broke across my face when I saw our neighbor's horse grazing by the trampoline. What a delightful surprise to the morning! No worries. I called my neighbors and the horse was home safely in its fence in no time. I sure hope the horse manages to make it over again sometime. I think my neighbors sure hope it doesn't.
Davis has developed mouth sores (very common). He has been pretty fortunate to not have too many until now. I believe that it is the methotrexate that he receives in his port that is causing them, because that was the only new chemo added. Methotrexate causes mouth sores. He has been faithfully using Biotene for months, but it simply isn't enough. He has started using a rubber-finger style tooth cleaner for infants, because even the softest of toothbrushes still cause his mouth to bleed. The doctors will check out the mouth situation on Monday. I hate it that he has mouth sores. I don't want anything to hurt him or impede his ability or desire to eat, but I can't help but think that if this is the worst of it, he is still very blessed.
We continue to pray every day for our son. We still pray against side effects, for Davis' emotional well-being, for the health of the kids in which he comes in contact, for healing and CURE. I can't help but feel that there are many life lessons to be learned from this experience, and I thank God for the blessings - the silver lining in all of this - that we have received and continue to discover. We still pray for courage, strength, and endurance, because sometimes they appear to be in short supply. We know that we still have such a long road ahead. We are so moved by your thoughts and prayers. I can only imagine how families are crushed under the weight of carrying this burden - this battle - alone. We are overwhelmed and grateful for the support we have. Not one day goes by that we don't feel both amazed and unworthy of your relentless thoughts and prayers.
We will keep you posted.
The week started out a bit rough but continues to improve.
Davis was very nauseous and tired on Sunday evening and decided to regress to some behavior we thought was behind us. He refused to take his last dose of medication. After hours of pleading and arguing, Davis was so worked up, he was out of control. Near midnight, Davis had a panic attack and couldn't breath. The thought of Davis suffocating terrified me, and I called 9-1-1 while Kyle worked on settling him down by encouraging deep, slow breaths. Thankfully, Davis was able to calm down before an ambulance was dispatched. Davis finally relaxed enough to fall asleep in the recliner in the living room. He never did take that last dose of medication. Luckily, it was a side effects medication and not chemo medication. The house quieted down and all were asleep by 1:00 AM. Poor Annakate! There was no way she could sleep through all of that chaos, though she didn't complain. She has such a tender heart. She worries as much for Davis as we do.
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| Wii = PE at home |
Monday. The night before had been erased from his memory and the new day brought with it a better frame of mind and a good start. We were headed to Charleston when I checked in with his school. Sadly, there were several students who were out sick from his class or exhibiting signs of sickness in his class (little coughs, headaches, scratchy throats). Davis had to stay home. Davis might feel great, but since his immune system is suppressed, he is at greater risk for catching a virus or infection. Since he is unable to fight off infection by himself, he has to be hospitalized so the doctors and medication can fight the infection/virus for him. So there are times when he is perfectly well and capable of going to school, but the health of others prevents that. It's inevitable; kids get sick. Davis, however, didn't handle Monday well. He didn't see how it was fair that he had to stay home. His "not fair" list has grown longer and longer over the past few months, and I get sad for him and for me that I can't fix some of the injustices that go along with cancer and its treatment. The only comfort that I can offer him is telling him over and over again that this is not permanent, and this will not last forever, but to a 10-year-old, I am sure that it sounds like too much of a cliche to be true.
On Monday, he devoted himself to school work, Wii playing (I told him that it was his PE time), and sitting around and complaining in true 10-year-old fashion.
On Tuesday, he went to school. The kids in the class are feeling much better and appear healthy. Davis takes a few more extra precautions to be at school (wears mask all of the time, extra hand washing, etc), but he is so happy to be back. He has been attending school all of this week. He fizzles in the afternoon. He doesn't really have the energy to sustain the activity of a full day. On Tuesday, he took a nap at school. On Wednesday, I picked him up early so he could come home and rest. That's ok. He loves school, and he loves being there.
Davis's appetite has increased some. We can relax a tad because he is eating and choosing healthy choices, but I can't truly relax until he starts putting on weight. We head to the little convenience store in our village, I and I Deli, and Davis orders a hot ham and cheese sandwich every morning. I offer to make him hot ham and cheese sandwiches, but Davis seems to think that no one can make them as good as Tim can, so we will continue to eat Tim's hot ham and cheese sandwiches as long as Davis craves them. His appetite seems to be the best on the morning and decreases as the day moves along.
What else is going on? Hmm. Annakate received a trophy in the mail for being a good sister to Davis. She is enrolled in this organization called SuperSibs. The organization sends her something to make her feel special about every month. This is such a great program. I hate to admit it, but I don't find myself doting on Annakate like I used to. Instead of doing her hair in the morning, I am getting Davis dressed or giving him his medication. Instead of reading her bedtime stories, I am helping him with his homework. While Kyle and I do make an effort to devote individualized attention and time to her, the program helps us by surprising her with encouragement. Plus, she feels so important. 
We love living in the country. We have fantastic neighbors (In the country, everyone within a five-mile radius in any direction is your neighbor.) who look out for one another, and the space allows the kids to run and explore. I love the opportunities that country living and nature provide to my children. The wildlife alone creates our own hands-on encyclopedia. Over the course of a week (depending on the season), it is not uncommon to see hawks, owls, vultures, quail, deer, raccoons, stray cats, skunks, opossums, snakes, and coyotes in our yard. Yesterday was no exception. My normal morning routine includes opening my kitchen blinds allowing the natural light to flood in to warn everyone -mostly me- that morning is indeed here. I think I gasped before a smile broke across my face when I saw our neighbor's horse grazing by the trampoline. What a delightful surprise to the morning! No worries. I called my neighbors and the horse was home safely in its fence in no time. I sure hope the horse manages to make it over again sometime. I think my neighbors sure hope it doesn't. Tomorrow, Davis will get a CBC. We should know where his ANC (immune system) is then. The chemo last week should have made it drop, but we don't know how much. His ANC and his overall health will determine how much he can do this weekend. We have never really trick-or-treated in the traditional sense. We usually stop by a few houses that belong to family members. Davis doesn't eat candy, chew gum, or suck mints (We let him; he just doesn't like that type of stuff.), so he doesn't really care to trick-or-treat. I think a great deal of the weekend will be devoted to make-up school work from the two weeks that he missed. We will head down to St. Louis on Monday for chemo. He plans on wearing his Halloween costume, a doctor, to clinic.
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| My kids love Andy Anderson. Andy makes some great balloon creations. Davis asked for a circle, and Annakate asked for a square. They thought that was hilarious. |
Davis has developed mouth sores (very common). He has been pretty fortunate to not have too many until now. I believe that it is the methotrexate that he receives in his port that is causing them, because that was the only new chemo added. Methotrexate causes mouth sores. He has been faithfully using Biotene for months, but it simply isn't enough. He has started using a rubber-finger style tooth cleaner for infants, because even the softest of toothbrushes still cause his mouth to bleed. The doctors will check out the mouth situation on Monday. I hate it that he has mouth sores. I don't want anything to hurt him or impede his ability or desire to eat, but I can't help but think that if this is the worst of it, he is still very blessed.
We continue to pray every day for our son. We still pray against side effects, for Davis' emotional well-being, for the health of the kids in which he comes in contact, for healing and CURE. I can't help but feel that there are many life lessons to be learned from this experience, and I thank God for the blessings - the silver lining in all of this - that we have received and continue to discover. We still pray for courage, strength, and endurance, because sometimes they appear to be in short supply. We know that we still have such a long road ahead. We are so moved by your thoughts and prayers. I can only imagine how families are crushed under the weight of carrying this burden - this battle - alone. We are overwhelmed and grateful for the support we have. Not one day goes by that we don't feel both amazed and unworthy of your relentless thoughts and prayers.
We will keep you posted.
Sunday, October 23, 2011
Trying to Find That Routine Again
10/23/2011: 4:00 PM
Davis still continues to sleep a lot. He just can't find the energy to sustain himself for long periods of time. Provided that his class is well -- there were many sick last week -- he is planning on trying to go to school tomorrow. I am not sure if he will make it a full day; he many not have the energy to complete a whole day. School does help him keep his mind off not feeling well, and he is far more productive at school than he is at home.
I want to take a minute to thank the Oakland school and community. I was able to stop in on Friday for a visit. Some of the teachers and students made Davis a giant poster with well wishes on it. He loves it. It is hanging in his room. The Oakland community also collected nearly 200 new hats for a "Hats Off for Cancer" drive. Davis will be donating them to the Children's Hospital on their behalf.
Hoping and praying for good health and a productive week.
I apologize. I only have a few minutes, so I will try to give my best to give a detailed abbreviated version.
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| another long day of chemo |
I did not go to chemo on Friday. Davis, Kyle, and my mom set out at 5:00 AM for the long day. I stayed home and ran some errands, attended a parent/teacher conference, and spent some quality time with Annakate. To our surprise, Davis weighed 55 pounds! 55! He has lost nearly 25 pounds and weighs less than his seven-year-old sister. The doctors don't seem to be as worried as we are, so I guess that is a good thing. Davis did well without me being there. He sailed through his chemo.When it was time for the Peg shots, Kyle called me and put me on speaker phone, so that I was there to cheer and comfort Davis. Davis took the shots well. He cried, but I think anyone would. They were able to leave the hospital around 4:30, and they made it home between 7:30 and 8:00 PM. A very long day.
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| tent's looking a little crowded |
Annakate and I enjoyed our time together. I ate lunch with her at school, and when I picked her up afterwards, I let her decide what we were going to do. Shopping? Manicures? Go out to supper? Nope. She chose pie baking. We had a blast making a huge mess. She did it all, and I, of course, was her assistant. She really enjoyed making the crust and peeling the apples, and we hurried to get it finished before Davis made it home. It was to be his surprise. I giggle a bit at the irony that Annakate doesn't like apple pie and won't eat any of it. I guess the joy is in the baking. And by the way, it's delicious. I posted some cute pictures below.
The doctors have started taking metabolic panels to keep an eye on Davis's liver function. Many of the different types of chemo can cause potential problems with the liver and kidneys. The CMP test will measure the drug toxicity in his body. Kyle brought home the first report, and there are a great deal of levels that are out of whack. I plan to call the clinic tomorrow just to hear a professional reassure me that this is normal and there is no long-term liver damage going on.
This morning we went to church as a family. It was the first time in a long time. When Davis is sick or his counts are low, one of us stays home (we rotate) with him, and one of us takes Annakate. We are aware that his counts will start to drop because of the recent chemo (usually takes a few days), so we took advantage of the opportunity.
Davis still continues to sleep a lot. He just can't find the energy to sustain himself for long periods of time. Provided that his class is well -- there were many sick last week -- he is planning on trying to go to school tomorrow. I am not sure if he will make it a full day; he many not have the energy to complete a whole day. School does help him keep his mind off not feeling well, and he is far more productive at school than he is at home.
I want to take a minute to thank the Oakland school and community. I was able to stop in on Friday for a visit. Some of the teachers and students made Davis a giant poster with well wishes on it. He loves it. It is hanging in his room. The Oakland community also collected nearly 200 new hats for a "Hats Off for Cancer" drive. Davis will be donating them to the Children's Hospital on their behalf. We continue to feel such love and support, and we are so grateful for it. We appreciate your prayers and positive thoughts, because that is what is getting us through this.
Hoping and praying for good health and a productive week.
We will keep you posted.
Thursday, October 20, 2011
Feels Like Snow Days Around Here
10/20/2011: 9:54 PM
We were released from the hospital a day earlier than scheduled. Davis's ANC was 240 and on the climb. He was given the orders to eat and rest. He was homebound while his counts were building. The goal was to get his ANC over 750 and his platelets over 75 so that he could receive the chemo that he missed last week.
The last two days have felt like snow days. We were all home together for huge chunks of time. Davis couldn't go to school because of his counts, Annakate was dismissed at 10:50 every day because of parent-teacher conferences, and Kyle was in and out on account of the rain. I love it. The kids have built tents, played Wii, completed projects, wrestled, etc. It's been fun - and loud.
One of the highlights of the last couple of days was when Davis's friends, Wade, Gage, and Drew, popped by for a quick visit. They were running around in no time. Davis was able to get the scoop on what he has missed in the last two weeks at school. I love how the boys just pick up where they left off and no matter how pale, thin, or sick Davis is; it doesn't seem to phase them.
Davis is still struggling getting his days and nights straightened out. He goes to bed at 1:00 or 2:00 AM and attempts to sleep in until 9 or 10 AM. I try to wake him up at a decent time but it is near impossible. We send him to bed at a decent time, but he manages to keep busy with a notebook (writing and journaling) and a flashlight. The English teacher loves this, but the mom wants him to sleep. He has draped blankets from his top bunk down around his bottom futon bed. Then, he placed a card table inside of the tented area and draped more blankets over the card table. It is inside the tent within tent that he sleeps. It is a struggle to check on him because of all of the blankets. I tried to lay down in it for awhile- you know, to encourage him to go to sleep, but it was simply too small. My days of sleeping under blanket-covered card tables are long over. I headed back to my bed. I am sure it is a mom thing, but I can rarely sleep when my kids are awake, so I would get up and check on him every twenty minutes or so. Finally at 2:20 AM, he was out.
Annakate is doing quite well in school. We are so proud of her. I was a bit worried because we have pushed a lot of the school/homework/reading responsibilities back on her. We struggle sometimes to keep the school routine of studying for tests and reading that we kept in past grades. It is such a relief to see that she is a very bright girl who has managed to do well despite not receiving the one-on-one attention that we have given to her and her schooling in the past.
Tomorrow, Davis will receive his chemo via his port at 8:30 AM. He will then receive chemo via spinal right before lunch. He is still placed under anesthesia for the spinal taps. Between 4 and 5 PM, he will be given the Peg shots, and he will be allowed to come home. Typically, there is 24 hour wait between the chemo injection via port and the Peg shots because the Pegs can weaken the effect of the methotrexate that is shot into the port. However, they are very confident that the time they are giving between the doses is sufficient. I pray that they are right. I am still a bit nervous. The longer the wait, the better, I think.
I am attaching the lyrics and the link with the hopes that this might bless someone else who is struggling.
Healer
Hillsong's Healer
You hold my every moment
You calm my raging seas
You walk with me through fire
and heal all my disease
I trust in You
I trust in You
I believe You're my healer
I believe You are all I need
I believe You're my portion
I believe You're more than enough for me
Jesus, You're all I need
Nothing is impossible for You
Nothing is impossible
Nothing is impossible for You
You hold my world in Your hands
For me, the last line here says it all.
Again, we thank you all for everything. We appreciate and feel your positive thoughts, love, and prayers.
We will keep you posted.
We were released from the hospital a day earlier than scheduled. Davis's ANC was 240 and on the climb. He was given the orders to eat and rest. He was homebound while his counts were building. The goal was to get his ANC over 750 and his platelets over 75 so that he could receive the chemo that he missed last week.
The last two days have felt like snow days. We were all home together for huge chunks of time. Davis couldn't go to school because of his counts, Annakate was dismissed at 10:50 every day because of parent-teacher conferences, and Kyle was in and out on account of the rain. I love it. The kids have built tents, played Wii, completed projects, wrestled, etc. It's been fun - and loud.
One of the highlights of the last couple of days was when Davis's friends, Wade, Gage, and Drew, popped by for a quick visit. They were running around in no time. Davis was able to get the scoop on what he has missed in the last two weeks at school. I love how the boys just pick up where they left off and no matter how pale, thin, or sick Davis is; it doesn't seem to phase them.
Davis is still struggling getting his days and nights straightened out. He goes to bed at 1:00 or 2:00 AM and attempts to sleep in until 9 or 10 AM. I try to wake him up at a decent time but it is near impossible. We send him to bed at a decent time, but he manages to keep busy with a notebook (writing and journaling) and a flashlight. The English teacher loves this, but the mom wants him to sleep. He has draped blankets from his top bunk down around his bottom futon bed. Then, he placed a card table inside of the tented area and draped more blankets over the card table. It is inside the tent within tent that he sleeps. It is a struggle to check on him because of all of the blankets. I tried to lay down in it for awhile- you know, to encourage him to go to sleep, but it was simply too small. My days of sleeping under blanket-covered card tables are long over. I headed back to my bed. I am sure it is a mom thing, but I can rarely sleep when my kids are awake, so I would get up and check on him every twenty minutes or so. Finally at 2:20 AM, he was out.
Annakate is doing quite well in school. We are so proud of her. I was a bit worried because we have pushed a lot of the school/homework/reading responsibilities back on her. We struggle sometimes to keep the school routine of studying for tests and reading that we kept in past grades. It is such a relief to see that she is a very bright girl who has managed to do well despite not receiving the one-on-one attention that we have given to her and her schooling in the past. Davis has been craving spicy foods as of late. The docs and nurses say that this is pretty normal. Chemo changes and kills the taste buds, and people tend to crave spicy food because of the taste. Davis has eaten a lot of Thai, Mexican, and chili the last couple of days. We don't mind at all. We are thankful he is eating.
Davis went to Sarah Bush and had a CBC (blood panel) and a CMP (checks metabolism and nutrients in his blood). His blood was a bit problematic. At first, it was runny and then it was clotty. The lab tech finally was able to get enough after a few finger pricks. St. Louis called us a short while later with some awesome news. Davis's counts are making a quick comeback. His white blood cells were up from .8 to 2.8 (healthy kids range between 5 and 10). His hemoglobin was holding at 10.3. His platelets were up from 64 to 160 (healthy kids range between 150-450), and his ANC was 1148! His ANC was 240 on Tuesday and was 0 one week ago (healthy kids are greater than 1500). Even though his counts will take a hit from the chemo tomorrow, he is cleared to go to school on Monday as long as there are no sick children in his class.
Tomorrow, Davis will receive his chemo via his port at 8:30 AM. He will then receive chemo via spinal right before lunch. He is still placed under anesthesia for the spinal taps. Between 4 and 5 PM, he will be given the Peg shots, and he will be allowed to come home. Typically, there is 24 hour wait between the chemo injection via port and the Peg shots because the Pegs can weaken the effect of the methotrexate that is shot into the port. However, they are very confident that the time they are giving between the doses is sufficient. I pray that they are right. I am still a bit nervous. The longer the wait, the better, I think.
We still continue the same fervent prayers that we have prayed from the get-go. We pray that Davis is spared from short term and long term side effects. We also pray for his overall health and the health of his classmates, so that he may attend school for as long as possible (and we want his classmates to stay healthy too. It isn't fun being sick.) Most importantly, we pray for his overll well-being, healing, and CURE.
I know I have often shared the fact that I draw strength and comfort from music. A few weeks ago, we sang a worship song at church that we sing every so often. It is pretty popular; it is called, "Healer" by Hillsong. Honestly, I had forgotten about this song until we sang it the other night. I'm not sure what it was about that night, the song, the heaviness of my heart, but it was like the song was written for me. It was as though it was crafted and existed for me when I was ready to need it. Over the last few weeks, that song has been swimming around in the back of my mind. When Davis was in the hospital and the doctors couldn't get the fever to break, when he would cry in my arms because the homesickness was too much for him to bear, when I was tired and the weariness began to deplete my patience and faith, I would sing, hum, whisper this song. I guess every person who has been on this road finds their escape - their way to cope. I think God provides me the music - the songs - because he knows best how to reach me. I am grateful.
I am attaching the lyrics and the link with the hopes that this might bless someone else who is struggling.
Healer
Hillsong's Healer
You hold my every moment
You calm my raging seas
You walk with me through fire
and heal all my disease
I trust in You
I trust in You
I believe You're my healer
I believe You are all I need
I believe You're my portion
I believe You're more than enough for me
Jesus, You're all I need
Nothing is impossible for You
Nothing is impossible
Nothing is impossible for You
You hold my world in Your hands
For me, the last line here says it all.
Again, we thank you all for everything. We appreciate and feel your positive thoughts, love, and prayers.
We will keep you posted.
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| Hospital Visitors: Grandpa and Grandma Fanello |
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| Hospital Visitor: Uncle Randy Coffey |
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| Hospital Visitors: Grandpa and Grandma Coffey |
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| This was my view for nearly 15 hours every day while Davis was in the hospital |
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| The long-awaited smile. Getting ready to leave the hospital. |
Tuesday, October 18, 2011
Homeward Bound . . . Maybe
10/18/2011: 10:15 AM
Davis is feeling so much better. He has conquered nearly everything on his checklist to be released from the hospital. His ANC (immune system) was in the 60s yesterday, and today it is over 200! No fever for over 48 hours now. The nurses seem extremely confident that we will be released today despite Davis not having an ANC over 500. They are under the impression that Davis can count build at home. We are still waiting to hear from the doctors. They make the call.
The biggest stress yesterday was finding a hotel in the St. Louis area for Wednesday evening. Davis has to be back at the hospital at 6:45 AM on Thursday for a spinal, so it makes sense to spend the night before. I am not begrudging the Cardinals of their success by any means, but our timing and their World Series timing collided. After some frustration, I left the task up to Kyle, and he found us a room. Thanks, honey.
Davis managed to do a bit of homework and eat some yesterday evening. He has his days and nights mixed up too. He was awake from 5:00 PM to nearly 1:00 AM. He watched a couple of movies and tinkered around during that time. Of course, he is asleep now. He is doing a better job at taking his medication too. It is still a drawn-out process.
Wait. . . Talking to the nurse . . .We are going home! Today! The doctors have moved his LP (spinal tap) to Friday because they are pretty sure his ANC won't be over the needed 750. With the chemo starting on Friday, Davis will have to be admitted again on Friday evening (or Saturday morning) to receive Day 2 of chemo - the dreaded Peg shots. Since the clinic will be closed on Saturday, he will have to receive them in-patient. Because of Davis's anxiety, the doctors have given us the option to stay in a hotel on Friday evening. Davis would come in on Saturday morning and be admitted for the day. Ahhhhhh. I can't wait to sleep in my own bed and see Annakate. I am not looking forward to the three hour trip home and the road construction, and from what I have heard, it is freezing outside. When we were admitted last week, it was nearly 80 degrees. Needless to say, I am a bit underdressed for the weather. I am still in flip-flops. Poor planning, I guess.
Nothing else going on. We will hopefully be discharged sometime this afternoon. Past practice has usually been between 3:00 and 5:00 PM.
Thanks for all of your prayers and positive thoughts. You are fantastic at rallying around us in our time of need.
We will keep you posted.
Davis is feeling so much better. He has conquered nearly everything on his checklist to be released from the hospital. His ANC (immune system) was in the 60s yesterday, and today it is over 200! No fever for over 48 hours now. The nurses seem extremely confident that we will be released today despite Davis not having an ANC over 500. They are under the impression that Davis can count build at home. We are still waiting to hear from the doctors. They make the call.
The biggest stress yesterday was finding a hotel in the St. Louis area for Wednesday evening. Davis has to be back at the hospital at 6:45 AM on Thursday for a spinal, so it makes sense to spend the night before. I am not begrudging the Cardinals of their success by any means, but our timing and their World Series timing collided. After some frustration, I left the task up to Kyle, and he found us a room. Thanks, honey.
Davis managed to do a bit of homework and eat some yesterday evening. He has his days and nights mixed up too. He was awake from 5:00 PM to nearly 1:00 AM. He watched a couple of movies and tinkered around during that time. Of course, he is asleep now. He is doing a better job at taking his medication too. It is still a drawn-out process.
Wait. . . Talking to the nurse . . .We are going home! Today! The doctors have moved his LP (spinal tap) to Friday because they are pretty sure his ANC won't be over the needed 750. With the chemo starting on Friday, Davis will have to be admitted again on Friday evening (or Saturday morning) to receive Day 2 of chemo - the dreaded Peg shots. Since the clinic will be closed on Saturday, he will have to receive them in-patient. Because of Davis's anxiety, the doctors have given us the option to stay in a hotel on Friday evening. Davis would come in on Saturday morning and be admitted for the day. Ahhhhhh. I can't wait to sleep in my own bed and see Annakate. I am not looking forward to the three hour trip home and the road construction, and from what I have heard, it is freezing outside. When we were admitted last week, it was nearly 80 degrees. Needless to say, I am a bit underdressed for the weather. I am still in flip-flops. Poor planning, I guess.
Nothing else going on. We will hopefully be discharged sometime this afternoon. Past practice has usually been between 3:00 and 5:00 PM.
Thanks for all of your prayers and positive thoughts. You are fantastic at rallying around us in our time of need.
We will keep you posted.
Monday, October 17, 2011
His Counts Aren't in a Hurry
10/17/2011: 11:25 AM
A lot of the same here. Yesterday, we had a few visitors, and that helped to break up the monotony. Davis still sleeps a great deal of the time.
The doctor stopped in shortly after Davis awoke to take some morning medication. As she was talking to us, he became very quiet and reserved. I think it dawned on him that he wasn't going home today, and there is a good chance that he will be here on Tuesday as well.
What the doctor had to share was promising. None of the cultures that were taken grew any bacteria or fungus. That rules out some of the most serious infection types. They have adjusted the super-antibiotic and he is now getting the proper levels. His metabolism was processing it too quickly initially. His counts are beginning to climb. His white blood cells are up to 1.3 from .8, and his ANC is up to 65 from 30 something yesterday. His monocyte counts (monocytes are the little soldiers in your blood) are up to 35. This is a indicator that an ANC jump is coming. The doctor seemed pretty sure that Davis would meet the requirements to start chemo on Thursday. That means that it is expected that his ANC will be over 750 and his platelets will be over 75. This is comforting since his chemo was postponed last week.
Davis did develop some blurred vision, dizziness, and a headache last night around midnight. The doctor on call was unsure as to why he developed these symptoms. The best guess is that the Benadryl given to pre-treat him before his super-antibiotic hadn't kicked in, and the combination of the two antibiotics running in his system at the same time was causing a bit of trouble, but that is a bit of a long shot. The important thing is that when he woke up this morning, the symptoms were gone.
From the medical point of view, the goal for Davis today is to count build and eat and drink. It breaks my heart to think that a goal for a ten-year-old is to eat and drink. Just something I never thought of before cancer. From the mom point of view, the goal for Davis is to work on some homework. His teachers are so kind and understanding; they are not requesting work at all. I just think if I can get him to do some, it may relieve some anxiety later on this week. Essentially, he is going to miss two weeks of school and maybe more. Anyone who has ever had to make up weeks of work and keep up with the new daily work knows that it can be overwhelming.
I wanted to let all of you know of a fundraiser being done on our behalf. Mandy Hanner, a friend and fellow teacher at Oakland High School, has organized a t-shirt sale. If you are interested in purchasing a shirt, you can print the attached order form, complete it, and mail it to her. The t-shirts are gray with orange writing and say "Team Davis" overlayed on an orange cancer ribbon. The reason for the orange is that it is the color for Leukemia awareness. It also happens to be one of Davis's favorite colors and one of Oakland's school colors. So, I am learning to love orange. If you need more information or have questions, please email me at abcoffey77@gmail.com, and I will be sure to help.
T-shirt order form: Team Davis Shirt Order Form
We are so fortunate that Davis is making a quick recovery. Although the last few days have been draining and scary, the doctors assure us that Davis is responding to treatment appropriately. And while the stay has been longer than we have liked, we know that it could have been weeks.
We so love all of your prayers and positive thoughts. We have the best support system imaginable. We are truly grateful. We are praying that this is the last infection Davis encounters and that his treatment resumes. We never forget to pray for the requests that have become routine: no side effects, healing, and CURE. We want nothing more than to have this illness behind us. May God bless all of you who walking this journey with us.
We will keep you posted.
A lot of the same here. Yesterday, we had a few visitors, and that helped to break up the monotony. Davis still sleeps a great deal of the time.
The doctor stopped in shortly after Davis awoke to take some morning medication. As she was talking to us, he became very quiet and reserved. I think it dawned on him that he wasn't going home today, and there is a good chance that he will be here on Tuesday as well.
What the doctor had to share was promising. None of the cultures that were taken grew any bacteria or fungus. That rules out some of the most serious infection types. They have adjusted the super-antibiotic and he is now getting the proper levels. His metabolism was processing it too quickly initially. His counts are beginning to climb. His white blood cells are up to 1.3 from .8, and his ANC is up to 65 from 30 something yesterday. His monocyte counts (monocytes are the little soldiers in your blood) are up to 35. This is a indicator that an ANC jump is coming. The doctor seemed pretty sure that Davis would meet the requirements to start chemo on Thursday. That means that it is expected that his ANC will be over 750 and his platelets will be over 75. This is comforting since his chemo was postponed last week.
Davis did develop some blurred vision, dizziness, and a headache last night around midnight. The doctor on call was unsure as to why he developed these symptoms. The best guess is that the Benadryl given to pre-treat him before his super-antibiotic hadn't kicked in, and the combination of the two antibiotics running in his system at the same time was causing a bit of trouble, but that is a bit of a long shot. The important thing is that when he woke up this morning, the symptoms were gone.
From the medical point of view, the goal for Davis today is to count build and eat and drink. It breaks my heart to think that a goal for a ten-year-old is to eat and drink. Just something I never thought of before cancer. From the mom point of view, the goal for Davis is to work on some homework. His teachers are so kind and understanding; they are not requesting work at all. I just think if I can get him to do some, it may relieve some anxiety later on this week. Essentially, he is going to miss two weeks of school and maybe more. Anyone who has ever had to make up weeks of work and keep up with the new daily work knows that it can be overwhelming.
I wanted to let all of you know of a fundraiser being done on our behalf. Mandy Hanner, a friend and fellow teacher at Oakland High School, has organized a t-shirt sale. If you are interested in purchasing a shirt, you can print the attached order form, complete it, and mail it to her. The t-shirts are gray with orange writing and say "Team Davis" overlayed on an orange cancer ribbon. The reason for the orange is that it is the color for Leukemia awareness. It also happens to be one of Davis's favorite colors and one of Oakland's school colors. So, I am learning to love orange. If you need more information or have questions, please email me at abcoffey77@gmail.com, and I will be sure to help.
T-shirt order form: Team Davis Shirt Order Form
We are so fortunate that Davis is making a quick recovery. Although the last few days have been draining and scary, the doctors assure us that Davis is responding to treatment appropriately. And while the stay has been longer than we have liked, we know that it could have been weeks.
We so love all of your prayers and positive thoughts. We have the best support system imaginable. We are truly grateful. We are praying that this is the last infection Davis encounters and that his treatment resumes. We never forget to pray for the requests that have become routine: no side effects, healing, and CURE. We want nothing more than to have this illness behind us. May God bless all of you who walking this journey with us.
We will keep you posted.
Sunday, October 16, 2011
Slow Recovery
10/16/2011: 11:10 AM
Other than that, nothing else going on here. We just sit around. Davis does play on the computer some, but he won't watch TV. He just sleeps.
Thanks for all of your kind thoughts and much-needed prayers. Although we know we are never alone, it does get lonely here from time to time. Davis misses his home and his routine. But we know that we are where we need to be. We are truly blessed to have such good family and friends who care for us so deeply.
We will keep you posted.
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| Red Man Syndrome |
Davis has made some marked improvements over that last 24 hours. He has been without fever for nearly 12 hours, and his counts are beginning to trend upwards. His ANC was 12 yesterday and is 32 today. It will need to be in the triple digits before we can head home.
The antibiotic used to treat staff infections caused the allergic reaction called Red Man Syndrome. Since he needs the antibiotic, he is pretreated with a counter medication before the antibiotic is administered. The antibiotic is then given over two times the normal time span to slow the reaction down. It seems to be working for the most part. He still has some redness and itching, but it does not appear to be as severe.
 |
| Scary, huh? |
Davis did manage to eat yesterday. Actually, he ate more yesterday than he has in one entire week. We have had no luck today. He has slept a great deal of the day away. He still sleeps 15 or more hours a day. This slows down normal daily functions: eating, drinking, taking medication, walking. However, sleep still trumps those activities because it works as a coping mechanism while the body is fighting the infection.
Speaking of infection . . . we still don't have a confirmed diagnosis of what type of infection it is. All the docs seem to know is that it is responding to the high powered antibiotics, so it is probably a bacterial infection of some type. They can't identify where it is in the body either.
The doctors won't give us a timeline for being discharged. It depends on his counts. We are set for chemo on Thursday and Friday, and one doctor thought that we would be able to go home and make it back for Thursday chemo. She quickly followed with, "No promises, though." I am still optimistic.
Other than that, nothing else going on here. We just sit around. Davis does play on the computer some, but he won't watch TV. He just sleeps.
Thanks for all of your kind thoughts and much-needed prayers. Although we know we are never alone, it does get lonely here from time to time. Davis misses his home and his routine. But we know that we are where we need to be. We are truly blessed to have such good family and friends who care for us so deeply.
We will keep you posted.
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