Wish Come True + Fever = Postponed Wish

2/24/2012: 4:40 PM

Davis' counts today weren't spectacular by any means. His red blood cells were 8.1 and platelets had dropped to 37. Since his numbers were trending down, the staff decided to transfuse both platelets and red blood cells. He was pre-medicated for his platelets before it was discovered that there were no exact platelet matches to be found in the Children's blood bank. Since Davis had such a severe allergic reaction to platelets, he may only receive his direct blood type. He received his chemo, his red blood cells, and we will head back down to Children's on Monday for his platelet transfusion.

We received his new roadmap (course of action) for the first phase of the Maintenance phase. Each phase will last approximately 58 days, and Davis will have about 11 phases. The first 58-day phase will consist of a couple of spinals and a bunch of oral chemo and steroids. I am asking - no, begging - for prayer now because I know how much Davis hates taking medicine. You would think that eight months of taking medication daily, he would be used to it. He still fights us nearly every day. The bright side is that we are inching our way to the end of cancer treatment, and we will be making fewer trips to St. Louis.

Other than for his transfusion on Monday, Davis' next visit to Children's (Lord willing) will be on March 9th. We are going to enjoy the break.

We ask that you pray for Davis' health and well-being while we are vacationing.

***************************
2/24/2012: 10:30 PM

Ms. Keck and Ms. Green, our local Make-A-Wish representatives, dropped in with some fantastic bon voyage gifts for Davis (and Annakate). Boy, it was like Christmas! We also received our plans, which included some amazing activities (snorkeling, Pearl Harbor, etc). Some time ago, Davis wished to see Pearl Harbor (He has read a few books on it). His wish was granted and our trip to Hawaii was planned. Yay!! I haven't really mentioned it much because there are a lot of "what ifs" that surround the trip. Plus, if Davis isn't well, it would have to be cancelled, so I decided to mention it when it looked like it was a for sure thing. And now it is! I will be sure to take lots of pictures to share.

Ms. Keck and Ms. Green at our little Make-A-Wish celebration.
Thank you, Make-A-Wish!!

****************************
2/27/2012: 10:26 AM

Late yesterday afternoon, Davis spiked a fever. We headed to the SBLHC ER to check it out, which is the routine. When we got there, Davis no longer had a fever. Great. That always happens. I am sure the doctors think I am crazy. It wasn't too long into our wait that Davis became flushed, so I asked the nurse to take his temperature again. Yep. 102.8. I'm not crazy. When Davis' bloodwork came back, I knew we were headed to Children's. His ANC (absolute neutrophil count (basically the immune system)) was 12 (healthy kids run between 2000-3000 or higher), platelets 11, and white blood cells were less than .4 (healthy kids range between 5 and 10).

Hanging out in the SBLHC ER

Even though he was pre-medicated with Benadryl, Davis still had an allergic
reaction to the antibiotic Vancomycin. It's called Red Man's Syndrome, and it's very common.

We had to wait on Stl Children's ICU ambulance transport because Davis was neutropenic. We were finally to Children's and settled into a room at 1:40 AM, and lights out came at 3:20 AM. It had taken eight hours of waiting and transport, which makes for a long evening.

transport team

Davis has been resting peacefully (a gift from the Benadryl given to him every six hours or so) since the ER visit. He hasn't eaten anything since yesterday afternoon. The docs are flushing him with fluids so dehydration is not a concern. He is being given powerful antibiotics via port every 6-8 hours. C-Diff is a concern, but the importance of the antibiotics trumps the potential C-Diff issue. As of now, Davis does not have fever, and there is not a known cause. Davis has virtually no other symptoms, so now it is a wait-and-see game. The doctors are starting to do their rounds, so I am sure I will know more later. All I know as of know is that his counts are still trending downwards. His white blood cells are now 0.1, platelets 3, neutrophils 0, ANC 0.

My guess is that we will be here for at least a couple . Typically the policy is that Davis has to be fever free for 48 hours and have an ANC trending upwards close to 500. We have the fever free part. Half way there.

Hawaii has been postponed. Dr. Schapiro, Davis' doctor, felt horrible and offered to go in his place while her colleagues took care of him here. (Everyone here has such a great sense of humor. Davis won the award for lowest platelets on the floor this morning.) She said it would be a sacrifice, but she likes us that much. Nah, she's terrific. Lauren, our wonderful Make-A-Wish coordinator, was completely understanding, and we will fulfill Davis' wish when he is well enough to go. He's disappointed, but spiking fevers are out of his control, and I am thankful that it happened now and not in Hawaii.

A picture of Davis right now.

We have a nice room with a great view of the park.

Please pray for Davis. He has a lot of anxiety and does not do well with hospital stays. Please pray specifically that this is not a port infection. Port infections are serious and his port would be removed. We thank you for your wonderful concern and support. I love that we never feel alone.

God bless you.

Keep you posted.

R.I.P. Carmen

2/24/2012:  3:20 PM

Yesterday, Carmen, Annakate's bearded beta, passed away.  He has been pretty bloated for awhile, and yesterday morning, it was showing all the signs signs of dropsy, a fatal fish disease. I am not a fish expert and I know of no veterinarians who care for fish, so I did what every mom with a computer does, I googled it. And sure enough, there was the information I needed. Sadly, the fish was dead a couple of hours later.

Luckily, Annakate is not sentimental about her fish. We had a short and sweet ceremonial flushing today. I know it sounds crazy, but I think flushing a fish is like some sort of rite of passage in childhood. Anyway, that was that. I think I will miss looking at that little fish every day.

I get such a kick out of Annakate most days. Today, I asked her to refill the Dixie cup holder in her bathroom.  Boy, did she.

Kyle took Davis to chemo today. I had to stay home because I had the flu this week, and didn't want to risk putting any immuno-comprised children at risk. I will gather all of the details from him and update later. Davis' ANC (neutraphil count/immune system) was only 12 when it was checked today (healthy kids run btwn 2000 and 3000). Yikes!  But Davis feels well and is in good spirits, and that is most important.

We will keep you posted.

Thought I would share a couple of photos from this week  . . . .

My backyard early Tuesday morning. I absolutely love my backyard.

Annakate made good use of her day off on Monday. Not much
to shoot at with her little BB gun.

Time Marches On

2/22/2012: 7:20 PM

Compared to Davis' allergic reaction episode on Friday, the weekend was pretty uneventful. We managed to visit my mom and stepdad in Champaign. They watched Davis for us while we ran a couple of shopping errands.

Davis had blood work on Monday that revealed another drop in counts. His red blood cells had dropped to 8.9 (They transfuse at 8). His platelets hadn't budged, despite the partial transfusion, and were at 11 (The docs like them to be over 75). The biggest hits were to his white blood cells. His white count was 0, which meant is ANC (immune system) was 0. Davis' nurse Kathy assured me that while this isn't ideal, it is expected. His bone marrow is worn out from the chemo, and even though Davis isn't getting massive amounts of chemo as of late, the effects of chemo are cumulative, and his body can't fight back anymore. The good in this is that his body is responding to the chemo. By weakening the bone marrow, it will have a chance to essentially start over and create and build healthy non-cancerous blood cells.  The bad in this is that Davis has no immune system. He won't be able to fight off any kind of infection on his own, and we are still trudging through the cold and flu season. Also, the white blood cells (where Davis' cancer is) can not be transfused. His bone marrow has to produce them on its own. So, we are careful and prayerful now.

We headed down to St. Louis at 5:30 AM Tuesday morning for Davis to receive another platelet transfusion. Davis was premedicated with Benadryl and Hydrocortisone via his port before his transfusion. His pulse, blood pressure, oxygen, and temperature were monitored every fifteen minutes during the transfusion. The premedication worked and Davis was fine - a little tired - but fine. Kyle's Uncle Randy was vacationing in St. Louis and spent the morning with us. Davis filled Uncle Randy's head full of Nintendo DS knowledge, and Uncle Randy listened attentively for what seemed like forever.

Davis was hooked up to monitors, so Uncle Randy was the book holder.
Davis has to read twenty minutes a day and keep a reading log for
his literature class.

Davis is finishing his treatment on Tuesday with his nurse
Kathy in the foreground.

We were able to make it back to Charleston in enough time for Davis to go to school for the last hour of the day. Davis is so awesome. It amazes me that he can get up at 5:30 in the morning, be pumped full of medication and platelets, travel over five hours in the car, and still show up for math class. 

Thankfully, I am rarely sick. Well, not so fortunate now. I was up most of the night with flu symptoms: body aches, headache, upset stomach, sore throat, etc. Kyle made a doctor's appointment for me. Yep, it appears I have a viral infection. I am quarantined to my bedroom, but I don't feel well, so I don't mind. Kyle is absolutely amazing. He is completely holding the fort down and caring for the babies. I feel pretty guilty snuggled in bed and barking orders to him to change out the laundry while he is cleaning up the kitchen and getting Davis' nightly medicine ready, but I am thankful he is willing and able to take charge.

Davis will have bloodwork done on Thursday, and Friday will be Davis' last chemo treatment on his Delayed Intensification road map. Yay! He will receive any platelets and/or red blood cell transfusions and chemo. He will then get a week or two off to build counts.   

We still love and appreciate your positive thoughts and prayers. Davis struggles with change and having very little control over his life, and we are facing, however positive it may seem, another change. Plus, his counts are terribly low. We are praying that they start trending up quickly. We still pray for those things we have prayed for since the very beginning: no long-term or short-term side effects, no organ damage, no port infections, no relapses, and no secondary cancers. I have also started praying that Davis sees the good in this and that God gives him discernible wisdom to apply this experience as a chapter in a long and meaningful life.  I pray that he remembers the bad so that he has empathy for others.

Annakate has been taking karate for three weeks and LOVES it!

Here she is practicing her form.  She has it all planned out.
She tells me she'll have her black belt in 2 1/2 years. She's too funny.

We will keep you posted.

Allergic Reaction

2/18/2012: 12:02 PM

It has been an eventful last couple of days.

Tuesday evening, Annakate was complaining of ear pain. We headed to the doctor's office on Wednesday (third one in three months), and an exam and throat culture later, we were told that Annakate had strep throat. I was surprised because she didn't have the classic systems that we were used to seeing: sore throat, fever, etc. Needless to say, Annakate was stuck at home for a couple of days until the antibiotic kicked in, and Davis was shipped off to Grandma and Grandpa Coffey's for the night. We have found that it is easier to send him away when Annakate is sick with something contagious. That gives her the freedom to leave her bedroom and me the time to clean and sterilize.

Annakate at the doctor's office. This sweet, little girl
doesn't look sick, does she?

Davis and I headed over to Sarah Bush to get his counts on Thursday. The Ara-C chemo that he was on the week prior really kicks the snot out of his blood counts. His white count had dropped to 0.4 (healthy kids are between 5 and 10) making his ANC (immune system count) 208 (healthy kids are above 1500), which means he is at a critical risk for infection (neutropenic) if he were to pick up a bacteria or virus. The ANC can fluctuate rather quickly. On Monday, his ANC was over 1600, and by Thursday, it was down to 208. Hopefully, it is on the climb again. We also found out that his platelets had dropped to 11 (healthy kids run between 150-450), so he was scheduled to have a platelet transfusion on Friday.

The plan in the clinic on Friday was to give Davis his platelet transfusion, his Vincristine (IV push chemo), his Peg shots, and them come home. Two hours max. Other than the Peg shot leg pain, it was supposed to be a pretty easy, routine chemo day.

You know, if it wasn't for the generosity of donors taking their time and undergoing the uncomfortableness of donating blood, my son (and so many other children fighting blood cancers and other types of cancer) would die. I know that sounds so blunt and drastic, but it is true. I think about how cliche the slogan "Donate blood. It saves lives." has become, but I have seen first hand how the anonymous blood donations of strangers has kept my son living. I know that I will continue to donate as long as I am physically able, and I will do it for Davis and the other children in similar situations who depend on it to survive.

Davis' platelets from the Red Cross

Davis was hooked up to his platelets. Occasionally, he has to be given Benadryl because sometimes platelets make him sneeze. Weird, huh. Davis' doctor was never convinced that it was a true allergy, but his nurse believed otherwise. I know it sounds crazy to be allergic to blood and platelet products. People aren't actually allergic to the blood or platelets. They are allergic to the antibodies that are found in the blood and platelets. Since every donor is different, there are different levels of antibodies in each unit of blood or platelets. And that can be problematic for some.

Beginning of the platelet transfusion. Platelet
transfusion #5 or #6, I think.

Davis received a platelet transfusion last Friday, and all was well.  There was no sneezing, no reaction of any kind. Yesterday was different. Ten minutes or so into his platelet transfusion, Davis began to sneeze and snot. We have seen this before (although an unusual allergic reaction to platelets), so we were not alarmed. The nurse ordered him some liquid Benadryl to take. After his first dose of Benadryl, the situation changed very quickly. Davis started complaining that his back was itching. The nurse and a nurse practitioner kept examining him. His blood pressure, temperature, and oxygen was monitored. By the time his second dose of Benadryl was taken (15-20 minutes later) and the platelet transfusion was suspended, Davis' lips and eyelids were swollen, and he could no longer speak (He had lost his voice). It was decided then that the allergic reaction was severe. Although his oxygen levels were still strong, the medical staff didn't want Davis to become anaphylatic. Davis received an epi-pen injection, medicated (albuteral) oxygen, and hydrocortisone via his port in a matter of minutes. To be honest, there was very little time to feel any emotions. Plus, the medical staff was so diligent; it appeared they had everything under control the entire time. After twenty minutes had passed, Davis was his old self again. In the future, Davis will be pre-medicated with Benadryl via his port before any platelet transfusion.

onset of swelling

examination and monitoring

suspension of platelets moments before epi-pen. You wouldn't believe
that there were four grown women hovering over him from
behind a curtain in this shot.

breathing treatment

The allergic reaction definitely took a huge chunk of time out of our day. He was given his Vincristine and Peg shots a while after his reaction. We had to wait another hour after the Peg shots to see if he was going to have an allergic reaction to them. Actually, the wait was a formality. Davis was so full of antihistamine blockers, there was no way he was going to have an allergic reaction to the Peg shots. For sure, he was pre-medicated for those. To the best of our knowledge, the Peg shots he received Friday are supposed to be his very last. Yay! The doctor was pretty sure there were no Peg shots in Maintenance; however, she is more familiar with the B-cell Leukemia roadmap than she is with the T-cell Leukemia roadmap, so she may have misspoken. Hopefully not.

There was still quite a bit of inflammation and swelling at the epi-pen injection site when we were free to go. We had to keep an eye on it and make sure it went away, and with time, it did. We finally made it back to Mattoon a little after 6 PM, three hours later than expected. Davis slept all the way home - a blessing from the Benadryl.

Visiting with friends. Our friends from Florida were home for the
weekend, and Davis seriously objected when we considered skipping our evening with them.
It makes sense now. What young man wouldn't want to keep these pretty little ladies company?

Davis is feeling a tad bit crummy this morning. No, that's mildly putting it. He is a grouch. I guess he has earned a little grouchiness. Hopefully, I can convince him a nap will help his mood. Next Friday will be Davis' last chemo treatment before the Maintenance Phase begins. He will have a week or two off from chemo in between the phases in order to let his counts build. The next phase cannot be started until his ANC is 750 and his platelets are 75 (built back on their own, no transfusions). I know the road ahead is still very long and difficult, but it brings me such joy to look back and see what success we have had beating cancer the last eight months.

God continues to keep His hand on Davis, and we continue to pray for complete healing and good health until his very last treatment and beyond. We feel so blessed.

We will keep you posted.

No More Ara-C! Yay!

2/14/2012:  12:20 PM

Happy Valentine's Day!

Warning . . . This may be a long one. I just feel like I am doing a little bit of catch up.

Kyle did an amazing job while I took to some warmer weather for a little R and R. The cruise was wonderful. Kim and I managed to get plenty of physical activity. One day, we kayaked the mangrove estuary where the Gulf and Atlantic Ocean meet. Another day, we rock climbed, repelled, zip lined, and snorkeled (what a workout!). That last time Kim and I were in Florida together was seventeen years ago, so the get-away was nice, and the homecoming was even better.

Super Bowl Party. We ate and left. We didn't watch any of the game.
I'm partial to the Titans, the Tri-County Titans, that is. :)

Rock climbing and repelling. Boy, was it hot!

Friday ended up being a very long day for Davis and Kyle. The family went down on Thursday night and stayed in a hotel because Davis had to be in clinic early. He was scheduled to receive chemo via port and chemo via spinal, but it was also determined that he needed a unit of platelets and two units of packed red blood cells. The blood transfusion added an additional four hours to the day alone. Because of the time crunch, Kathy, our clinic nurse, actually came down with Davis' Ara-C chemo and administered it in his port while he was still under anesthesia after his spinal in recovery.

I had mentioned a couple of updates ago that Annakate had developed a swollen lymph node on her neck and that we were doing a "watch and wait" with her after taking her to the pediatrician. Because of the concern, she was given an examination by Davis' pediatric oncologist. The oncologist agrees with Annakate's pediatrician that there is nothing for which to be alarmed. What a sigh of relief.

My mother and step-father drove down to St. Louis and looked after Annakate while Davis was in clinic. They spent the weekend watching the kids while we attended our church's couples marriage retreat. It wasn't ideal for us to bring our kids along on a marriage retreat, but with Kyle administering
the four-day Ara-C chemo, it was the only way to make it work. My mom and step-dad were going to take the kids home on Saturday so that Davis could be ready for his 5th grade band concert that evening, but Davis wasn't feeling up to par. We thought it best to keep the kids with us.

marriage retreat

It was a good we did.  Saturday night, the Ara-C chemo froze in the refrigerator. Refrigerator malfunction. Kyle called Davis' doctor who happened to be on call, and she had to order two new doses. (Frozen chemo = ruined chemo). The pharmaceutical company had to make it, and we arranged to pick it up at Children's around noon. We have to watch the time, because there is a window of time that the chemo has to be administered. It has to be administered around the same time everyday. Between the frozen chemo and our arrival at Children's, Davis developed a low grade fever. The doctor directed us to the ER, where a CBC would determine Davis' ANC. If his ANC was below 500, Davis would be admitted and transferred to the 9th floor. If it was above 500, Davis would be given a broad spectrum antibiotic and sent home. Five hours later, we knew his ANC was 675. Seven hours in the ER, we were finally given discharge papers.

Kyle is doing a saline flush before he discovers the chemo is
frozen.

The Ara-C causes fever; however, there is really never any good way to know if the fever is being caused by Ara-C, a viral or bacterial infection, or a line (port) infection, so the doctors always cautiously treat any fever.

Poor Annakate. Can you imagine a healthy, rambunctious eight-year-old sitting in a hospital ER for seven hours and then sitting in the car for another three?  How boring.  She makes me so proud. She did such a good job hanging out and complaining very little.

Annakate is making the best of the all-day SLCH ER trip.

Both Kyle and the ER nurse struggled putting fluids into the port. It was difficult to push the syringe. This issue, the impending snow, and Davis' low grade fever concluded with another drive to St. Louis yesterday (Monday). Our clinic nurse, Kathy, discovered that it was difficult to push the meds. She gave the needle and little wiggle. Problem solved. Apparently, the needle had lodged against the side of the Davis' port wall restricting the flow of fluids. Davis received his very last dose of Ara-C in clinic. We were informed that Ara-C is not on the maintenance roadmap. This is just one more step that makes maintenance more of a reality.

Last Ara-C!  How can you not smile?

Davis is still running a low-grade fever. We are monitoring it closely. Cultures taken Sunday and yesterday in lab have not grown any infections. His ANC on Sunday was 675, and yesterday it was 1115. Wow. The climbing ANC nearly guarantees that Davis won't need to stay in the hospital to wait out the fever. Despite on-and-off fever and a horrible headache (both side effects of Ara-C), Davis is off to school today. He was feeling a bit overwhelmed about falling behind, and he didn't want to miss the Valentine's party.

Davis will have another CBC on Thursday. His counts are being monitored closely because the combination of Ara-C and methotrexate can cause him to be neutropenic (ANC

We have this Friday and next Friday, and then we will have completed the delayed intensification phase (road map). Wahoo!  Yay!!  We will have a short break, and then Davis will start the long and steady maintenance road map  that will run 2 1/2 years. Treatments will cut back from once a week to once or twice a month. Although he will still be at risk for infection because the port is staying in, he will be able to live a more normal life (if there is such a thing anymore). 

Radio Interview

This morning, I had a chance to partake in a radio interview to promote an upcoming St. Louis area Easter egg hunt sponsored by the Gateway chapter of LLS (Leukemia and Lymphoma Society) and several other organizations. The interview was to inform people about the statistics and signs of blood cancers (Leukemia, Lymphomas, Myelomas). The panel consisted of the the deejay; Debbie Kersting, the executive director of LLS; Dr. Huang, the pediatric hematology/oncology department director; and myself sharing information about our family's journey. If you are an early riser and wish to listen to the thirty minute talk show, feel free to stream it on your computer. Here is the information I was provided.

The interview was with radio personality Kristi Carson. The program will run at the following times:
KHITS 96 on Sunday, March 4 @ 5 am
KSHE 95 on Sunday, February 26 @ 6 am
The Point 106.7 on Sunday, March 11 @ 5 am
KFTK 97.1 on Sunday, March 18 @ 5 am

All radio stations are out of the St. Louis area.

We thank you all for your love and support. We count our blessings each and every day. We continue to pray for Davis health and that soon the worst of the treatments will be behind us. We do not doubt the power of positive thought and God's healing touch. We don't have to look far or long to see how wonderful He is.

We will keep you posted.

Life at the Coffey house is in a bit of a whirlwind.  Amanda is floating in the Gulf of Mexico with her friend Kim Arthur while the children want to see her.  Thank God for skype.  We get a free trip every year with our seed company and I told her I would stay back this time with Davis and Anna.  My brother and I took one about five years ago, so it technically was her turn.  As far as Davis goes, he had a bit of a scare Sunday night with some troubles breathing.  We took a speedy trip to the ER to get him checked out.  Cody Yocum and Brother Doughty were there when we got there.  Apostolic Center people are quite awesome.  Annakate had texted a little girl from church on our speedy ride to the hospital and the news got to a few of our friends.  It turns out he is ok.  It was probably a little anxiety attack. The poor little guy has so many things going through his head.
    As you can probably tell, I do not have the writing abilty of my wife.  But I sure can brag on the Lord just like her.  We are a blessed family.  God will heal my son and God will get all the glory.  This has been a tough stretch in our lives, but God is preparing the way every step we take.  We are truly nothing without the Lord.  When you say a prayer for our son this week, please think of someone who has walked away from the Lord and pray for them.  God richly bless all of you!! 
 

Fluids on the Go

2/4/2012: 10:18 AM

Davis is rocking his own CBC so it
doesn't clot.

After school on Wednesday, I took Davis over to get counts. We are used to the routine. The process - one tube for a CBC (complete blood count) and two small tubes for a CMP (complete metabolic panel) took nearly an hour because Davis' blood clots very easily. The tech has to keep poking different fingers to get a good draw. Davis isn't bothered by the pokes and is pretty patient, so it is no big deal.

We received the counts Wednesday evening, and chemo was on for Friday. Davis' counts had jumped considerably from the previous week. His ANC was in the hundreds the week before making him neutropenic, and this week it was at 1224! Not the healthy 1500 and over we like to see, but a great recovery from the 213 from last week. Actually, all of his numbers trended up except his hemoglobin.

Beginning of fluids

Friday started pretty early. Kyle woke Davis up at 4:45 AM to eat a bowl of cereal. Davis couldn't have any food after 5:00 AM due to the lumbar puncture he would receive at noon. We were pulling out of the driveway at 5:20 AM. A quick trip to my in-laws to drop off Annakate and we were on our way to Children's. Poor Kyle. No company. Davis and I slept the entire way down to St. Louis. We were ushered into a room at 8:20 AM where Davis met with his doctor. He was accessed and a blood draw was sent off to determine if his hemoglobin had dropped below 8. Davis was immediately started on fluids (a saline, sugary mix). He was to receive a chemotherapy called Cytoxin. Cytoxin can do damage to the kidneys and bladder if the body isn't properly hydrated. Therefore, Davis is pumped full of fluids, his urine output it monitored and tested to see how concentrated it is, and when the urine reaches a certain dilution, the chemo (a 30 minute bag) is administered.

Midmorning, we found out that Davis' hemoglobin had dropped and he would need a transfusion. The rest of the morning was a bunch of waiting. My in-laws, Gary and Marylee, popped in, and kept us company. Davis' mood improved considerably.

At 11:00 AM, we headed to the APC (Ambulatory Procedure Center) for Davis' spinal. His appointment was at noon, but the child scheduled two ahead of him had some major complications, so Davis didn't actually go back for his procedure until 1:10 PM. The waiting added to the length of our day. We were back up on ninth floor at 2:00 PM.

Waiting on Davis to wake from anesthesia after spinal. The nurse
tried cushioning his leg with an egg crate. Davis experiences right leg
pain after a spinal. We were hoping this would help. It didn't. It
is now assumed that there is a nerve near when he is accessed for
the spinal.

A little after 2:00 PM, Davis' urine tested at the hydrated level, and Cytoxin was administered. He hates this. The chemo makes his nose sting, and there is nothing that can be done. He held his nose to a blanket and cried for thirty minutes straight. After the Cytoxin, Davis received the Ara-C (four day chemo) on a pump over ten minutes. The unit of blood Davis was to receive was then started. Blood takes forever to transfuse. When Davis was all finished and his fluid pump was hooked up, it was 5:45 PM. Davis was the first patient there in the morning and the very last to leave. We pulled in the driveway at 8:45 PM. A very long day indeed.

Blood transfusion.

Because the Cytoxin is so very potent, Davis was put on a 4-hour fluid pump for the evening. It was quite interesting. He was basically on an IV drip via his port. He was given a little travel bag for his bag of fluids and the pump.

Davis will have Ara-C (four days of chemo) this weekend and next. Kyle will administer the chemo every day and de-access his port on Monday. Davis started a new oral chemo. He will have to take it for the next two weeks. Davis hates it; he says it tastes disgusting. But since he is still not able to take pills, he is stuck drinking this bitter liquid.

If all goes well and Davis is not hospitalized for any illness over the next couple of weeks, Davis will be done with this roadmap (treatment plan) on February 24. We will then officially be in the 2 1/2 year Maintenance Phase and chemo treatments are expected to decrease to once or twice a month.

We are happy to have our very long day behind us, and we are blessed to have a son who is doing so well despite the circumstances. We thank you for your thoughts and prayers and encouragement, because it is a constant reminder that even though the journey is long, we are not braving it alone. I am pretty sure now that a family can't survive cancer and not be completely and permanently changed by the experience. The mundane is washed away and perspective is altered. I am thankful for that.

We will keep you posted.

We killed some time with the timer on my camera. What started out
as a picture of Davis and Mom turned into 45 minutes
of hysterical picture taking.