Not the results I'd hoped for.

After days (that seemed like weeks) of waiting, the results of my bone marrow biopsy and the final genetic testing results (next gen sequencing) of my leukemia both came in on Tuesday afternoon.

The first hope, that the bone marrow would be hypoplastic ("empty") and that the blasts would be under 5%, was not met. I have between 15-20% blasts still in my marrow. I had started with 40%.

This was not completely unexpected, as some of the genetic information came out over the last few days. If what was suspected was true, the 7+3 chemo was not a good match for my particular leukemia. While this is frustrating, I was in a bad enough condition upon admission that *something* had to be done, and so it wasn't a terrible idea to start with the 7+3. (Apparently some cancer hospitals do hold off on any treatment until they get the results from the genetic testing.)

Leukemia is not staged like other cancers. Instead, one of the ways it's grouped is by the favorability of the outcome. Best is "favorable;" worst is "unfavorable" or "adverse;" and in between is intermediate. These are the best guesses as to whether the leukemia will respond to chemo and go into remission. And remission must be obtained before a bone marrow transplant is attempted. (If you leave leukemic bone marrow and put new bone marrow in, they'll compete and the leukemic bone marrow will eventually win.)

My leukemia, unfortunately, has a lot of unfavorable things going for it.
1. Being treatment-associated AML (t-AML) automatically makes it less favorable
2. Having greater than three chromosomal mutations is unfavorable; my leukemia has fourteen(!)
3. One particular gene deletion is highly unfavorable--p53 (involved in signaling for such important things as cell cycle arrest, apoptosis/cell death, and DNA repair). And I have only one copy of p53.

But we have a plan to move forward, and it takes into account the p53 aspect.

There are two chemotherapies that are recently out of Stage 2 Clinical Trial (I think... maybe only one, or the combo?), as tested on elderly patients. If you're into that kind of thing, I think this is the paper my doctor referred to. Although I did not achieve complete remission with the first chemo regimen, this is not a second attempt (ie: failure of first attempt) but a re-induction--or a second first attempt.

I will receive a 7 day infusion of Vidaza (azacitidine), separated by 21 "rest" days and will get that 2-3 times. I will also take a daily oral chemo called Venclexta (venetoclax). The hope is that this regimen will put me into remission. The best part in my mind right now is that they are both done as outpatient treatments.

(For those who are fascinated with the genetic components, Vidaza is a hypermethylating agent--which would turn on the defective p53 and Venetoclax blocks the BCL2 protein, which would allow apoptosis.)

Before I can go home, and before I am considered recovered enough from the first round of chemo, I need to get my neutrophils up to 0.5.  They're currently too low to measure, although my total white blood cell count is slowly increasing, and neutrophils are a subset of white blood cells, so I'm hoping that they, too, will soon start to inch up.

Time to switch that positive energy into making my neutrophils rebound so I can get home and so I can start on the new chemo.

It's a plan and I always do much better with a plan.

And I need to get home to this:

The plan, clarified

Monday I finally got to meet the new chair of the St. Luke's Hematological Oncology group: Dr. Medlin. I have heard so much good about him from all the staff. And he's great. Down-to-earth, answers questions at the level I've asked (he asked my background to clarify), positive, confident.

We spent time talking about the plan for my treatment, which didn't change from what others had told me, but which was clarified somewhat.

We started with induction chemo to get my body to go into remission. We will know if that was achieved (or at least the first step toward achieving it) when we get the results from Friday's bone marrow biopsy. So yes, the bone marrow biopsy will be done on Friday. Results will take a "few days." There are two goals:

1. The bone marrow is essentially empty. We want less than 5% of cells within the bone marrow, which indicates that the chemo cleaned it all out.
2. Of the cells left in the bone marrow, less than 5% of them are blasts (cancerous cells).

If both of these things are achieved, then stage one was effective and as soon as I can maintain counts and fluids and everything enough that I need only be seen on an outpatient basis, I can go home for a few weeks.

If either of these things are not achieved, then stage one was not effective and we need to do another, different round of induction chemo. This is the stage that makes my heart race. This would prevent me from being home for Christmas, and it would certainly be a "harder" chemo on my body, plus just an addition chemo in general. But Dr. Medlin did a great job of explaining why this is an important step and why, if this happens, it is not the worst possible thing. Previously, treatment involved this 7+3 chemo, then the rounds that follow (I'll get into that shortly), but they were not able to determine if the chemo was actually effective. So you'd go through the whole process and not even have received remission, which meant that it was not going to be effective. Adding this step, and the sensitivity that is now achievable, means that more people are in true remission and have better outcomes. I like better outcomes.

Next step, once that first round of remission is achieved, is to do four rounds of maintenance/consolidation. Dr. Medlin explained that, even when there may be no evidence of cancer cells, there are still likely as many as 10^12 cells in the body (the "undetectable level"). Much like how many breast or other solid tumor cancer patients may have surgery with clean margins and clean nodes, but still have chemo after, that is the purpose of the chemo.

And then we move on to the bone marrow transplant.  There are only three options for an allogenic donor:

1. A full-match sibling, matching on 6 of 6 Human Leucocyte Antigens (HLAs)
2. An unrelated perfect donor, matching on 10 of 10 HLAs
3. A haplo-identical donor, like a child, matching on 5 of 10 HLAs

The reason you can use a half match with only 5 of 10 is that you'd only use a related haplo donor, and there are many other factors that aren't tested/matched on, but are also important and helpful in minimizing the likelihood and severity of graft vs. host disease (GVHD). These factors tend to clump together in familial lines, so while the third option is riskier, it can be done.

I'm trying not to think about the fact that finding a donor is an "if" and not necessarily a "when." There are certainly many people who do not find a donor by any of those three means. But I'm also hoping that karma, and all my wonderful loved ones who have recently signed up to "Be The Match" have someone or else on the other side of the world with just as many amazing loved ones signing up for them and somehow we'll all end up matched. 

As far as preparation for a bone marrow transplant, it is another chemo regimen of 5-7 days. Full body radiation is not usually used in AML (more often in ALL), so probably not necessary. And then the transplant itself is relatively simple--just like a blood transfusion. The hardest/worst part is waiting to see if it takes and how bad the GVHD is. I have decided not to look too far into that at this point.

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Other than that, I'm just keeping on here in Nadir-land. Still having the lovely GI issues. My new antibiotic (meropenen, since I developed that rash in response to the cephapine) seems to give me a headache. At least, both times I've received it, I've developed a headache at the base of my skull within a few minutes of the IV beginning. Last night I slept through most of it, but this morning it is still with me. Even a visit from massage therapy and some essential oils only slightly tamed it. 

With the new blood thresholds, I needed both blood and platelets last night, which made for a long night with all the vitals checks that they do before, during and after receiving blood product. This morning my counts were sufficient enough that I didn't need any product (WBC: 0.3; HGB: 8.3; PLT: 71K). Next draw is at 10:00 am and I'm crossing fingers that I'm holding onto things well enough to not need more. I don't know how long I'll be at these higher thresholds. Hopefully my own cells will start coming back soon and that will both decrease the need for the transfusions and prepare me for possible release from the hospital.

Whether it's the interruptions last night, or day 12 post-chemo (3 of 5 Nadir), I'm thinking I might actually need a morning nap today. I'm pretty happy that it's another beautifully sunny day. I hear it's cold outside, but I wouldn't know that from my room. :)

Lower counts and little issues

When I blogged about Nadir last, I mistakenly stated/remembered that it was days 7-10 after starting chemo. So I was pretty happy that I did pretty well this weekend, just needing a little more rest, and was looking forward to Monday (Day 10) being over the worst and moving on. And then my nurse said something like, "just remember that days 10-14 can be very intense and some people lose their appetite and really do need to take those naps that you are trying to avoid, and it can be a rough couple of days." And then I remembered that Nadir is 10-14, and not 7-10.  I wasn't just getting out of it, it was just getting INTO it.

My counts continue to remain low:
WBCs holding steady at 0.3 the last few tests
HGB bouncing around 6.4, 7.7, 6.7, 7.3
Platelets also bouncing 14K, 33K, 20K, 43K

I received both blood and platelets yesterday even through my platelet level was above the cut-off. I'll get more of both today, too. (More on that later.)

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My wonderful, generous friend, Team Phoenix sister, and leukemia survivor Vanessa came to visit yesterday. Vanessa immediately reached out to me when she heard of my diagnosis and has provided such a "been there" perspective since the start. Talking with her yesterday in person was wonderful. She also works for an organization called Tricia's Troops, which provides all sorts of amazing support to all kinds of cancer patients all over Southeastern Wisconsin. Vanessa brought me a lovely chemo support bag, and the group helps with things like housework or child care or transportation. If you're a cancer patient (or love one), check them out. And if you're looking for a place to donate, also check them out.

And after a not-terribly-long visit with Vanessa, I absolutely crashed and slept all afternoon. Guess this exhaustion thing is no joke. I had a few hours of awake time, visited with Greg and Ash, and was asleep again before 9:00 pm. Wow.


Unfortunately, what's been overlaying all of this for the last two days is a troubling side effect of, I assume, the chemo. I was showing some signs of a possible GI tract bleed, which resulted in lots of (not) fun observations and measurements. While I haven't been nauseous (knock wood), my stomach has been ouchie (for lack of a technical term), and I've developed heartburn, and some intestinal cramping. Just enough for my comment of, "I'm in no pain," to no longer hold 100%. So it's caused some changes in protocol. They bumped up my blood count tests from 24 hours to 12 hours (and now 6 hours). They immediately gave me more platelets, regardless of my count, and they changed the cutoff from 10K to 25K (it has since risen to 50K). I also got whole blood and the HGB cut-off is raised from 7.0 to 8.0. From what I can tell (supported by research that my amazing PH researcher friend Susan has done), this GI stuff is very common with these chemo meds (the bleeding less so, but we're working on that). And I'm on two antibiotics, which always impact my stomach. The most frustrating thing is that when the stomach cramping hits, it hits. So I've been afraid to walk as much and be far from my room, and going down to the Healing Garden seems way too far. These both make me sad. I'm hoping that the bleeding stops soon so I won't be burning through the platelets so quickly.

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Finishing this blog with stuff about today.

Day 11 was pretty similar to day 10. I had a pretty productive morning with several cool visits, and then a complete crash shortly after noon. After a nice snooze in the sun, and a visit from massage therapy, and a shower and a walk around the floor and in the healing garden (without an IV!), I'm back in my room, hooked up to fluids, awaiting the latest CBC counts to see if I need more platelets, and I also just found out that they think the rash on my stomach is in response to one of the IV antibiotics that I'm on (Cefapine). So I'll be switching from that one tonight. Unfortunately, instead of a half hour run time, the new one will be an hour and a half, but only once a day. I hate to be running out of antibiotics I can use, as I'll be on a lot of antibiotics for a long time.

And I had a little more energy today than yesterday. I'm not back to walking as much (and haven't been on the exercise bike), but I was able to add the squats back into my walk this afternoon. I was thrilled to see another patient working hard on strength exercises at one of the windows as I made my circuit.

I did get to meet the (new) Chair of the department yesterday and had a long talk with him about my plan. I'll try to write that up tomorrow. Until then, keep visualizing my bone marrow being completely destroyed and cheer with me when I feel crappy, because that's probably a sign that it's working. :) 2/5 days of Nadir in. I can do this!

Now entering Nadir

I've written about nadir before--essentially the low point in blood counts after chemo is given. But nadir after leukemia chemo is even more intense than it was during breast cancer treatment.

If things proceed as expected, the max chemo is in my body on day 7 of treatment. That was yesterday. Here's a picture of me being disconnected from seven straight days of chemo.

For days 10-14, the maximum killing power of the chemo takes hold and the blood cell counts (and all the other fast-growing cells in my body) are at their lowest. I'm told to expect to need lots of transfusions, lots and lots of rest, and to feel generally really crappy. After a few days, if all goes well, my healthy cells will start their recovery and I'll gradually feel better. What that means, is that I would like visitors, but it is entirely possible that I may change my mind mid-way through the day. Please don't be offended if I either cancel a visit or cut it very short.

Yesterday's counts definitely supported nadir, as have today's:
WBC:  0.2, 0.3 (since the chemo is done, these will slowly start to climb up, but will likely stay pretty low through the next few days before the climb up)
Hemoglobin: 7.4, 7.1
Platelets: 11K, 6K

No blood products needed yesterday, but today I'll get platelets again.

And to kick of the celebration of finishing this first round of chemo, I had the most wonderful morning! Milwaukee does the coolest biking event, called the Santa Rampage. At this event, literally thousands of people dress up as Santa (or elves, etc.) and ride their bikes from Wauwatosa to the lakefront. It's been happening for 15 years, and I'd wanted to ride last year, but caught a cold and it was rainy. I'd determined there was nothing that would stop me from riding in it THIS year. I bought my Santa suit on clearance last year and planned to ride my fat tire bike with all my biking friends. So I was pretty disappointed to not be able to ride in it this year, either.

However, my dear, dear friends, surprised me and found a way for me to participate--they brought the ride to me. :)  Barb did the actual ride, and then came to the hospital while Meredith came straight to the hospital and helped me get ready for it. We decorated the exercise bike, Barb wore her Santa stuff, Meredith wore her Christmas sloth outfit, and I had a silly hat. It was amazing (and we made the staff laugh a lot, too).

And then we went back to my room and Meredith cleaned it and decorated it with tinsel and the lights that my friend Chris had brought me.

And because I was so exhausted that I could barely keep my eyes open, Meredith, who is the most awesome K4 teacher ever, read Barb and I a bedtime story. And then I fell fast, fast asleep.

Greg came and watched me sleep, and then I was able to be leave the floor and walk with him to the healing garden--which is amazing. For Milwaukee people, it's like a mini-Domes with giant indoor plants and trees. I will be spending more time there.

And then I was unhooked completely from the IV, took a nice, long shower, and was able to walk without the IV pole for the first time in over a week. I wanted to run, it felt so good.

I was treated to the most spectacular sunset (which my photos cannot do justice to, but up on the 12th floor, you really get to see it from all angles).

And I had a long, barely-interrupted night of sleep.

Already today there are little annoyances: I feel like I'm getting a cold or something, with a scratchy throat, itchy ears and post-nasal drip; one of my two picc lines appears to be clogged and so they're trying to unclog it, but it hasn't yet responded completely and if not both are working, then I can't get two things (like platelets and IV antibiotics) at the same time. Food still tastes yucky, and I'm just missing my home. But I feel so surrounded by love--both from those who are physically with me, and by all the messages, texts, facebook comments, and just general good feelings. I don't have fear or anxiety--I'm able to just focus on healing. And that is an amazing gift. Thank you all.

Nearing the end of the first big step

Today's a big day. This morning they hung the final bag of my 7+3 chemo regimen. Unfortunately, each bag is a little more than 24 hours, so I won't be done till sometime tomorrow afternoon, but there is an end in sight!

Counts still dropping:
Total WBC 0.2
HGB 6.9 (after blood)
Platelets 19K

So moving the right direction, and I need more blood today.
I got a triple infusion machine to be able to do chemo, antibiotics and blood all at the same time! :)

The plan now is to let the chemo do its thing. It will hang out in my body and for the next week work at destroying my current diseased bone marrow. In a week, they will check the bone marrow and if there's zero blasts in it, we'll consider that a success and I'll be able to let my normal blood cells repopulate my marrow and blood, and take a break till we give it another hit in a month. That, to me, is totally doable.

Unfortunately today as I thought about what *should* happen and what I *hope* will happen, I went to the other side, which is "it might not work this first time." The good news is that there is a way to determine if it was not effective and there is a treatment protocol to do something if it did not. And that's going to improve the ultimate goal of achieving minimal residual disease. Here's a great handout on MRD in blood cancers, although I'm not sure why it doesn't include AML specifically. I *think* using MRD for AML is still evolving, so maybe that's why it's only in PubMed and not on the general L&LS or ACS pages.

At any rate, I obviously would love a complete response this first time through, which might actually allow me to go home for Xmas. So if you would like something to do over the next week, I invite you join me in visualizing the chemo trashing the shit out of my bone marrow. You can do it however you want. Here's an image of blood entering bone marrow, and the chemo is in my blood, so that can work:

You can imagine the chemo clearing everything that shouldn't be there in the blood throughout the body, including the bone marrow, and flushing it out of my body/kidneys (maybe a teenaged boy visual...)

Or you can make up a cartoon or imagery that helps you imagine what's happening.

Lots of people use pac-man visuals for chemo, gobbling up cancerous cells

You can imagine a warrior or a boxer or any number of violent cultural references.

Or you can use what I used to get through breast cancer chemo: Buffy the Vampire Slayer staking. I especially like this one because it's not just Buffy, but all those who love her fighting off the bad stuff. Also, when she stakes, the vampires go up into dust, which is just an awesome visual, I think.

If you think of another one, or had your own chemo visual during treatment, let me know!

Here's to completion of the first phase. Thank you all for following along.

Meds and tests and giving in to medicine

I thought I'd start by putting my numbers from my blood counts over the last few days here. Although I wrote about what the tests measure and indicate, I didn't give all the numbers I had. 

Copying from my last post to get the general range of numbers, I'll put in my numbers after. I have labs run every morning (between 3:30 and 6:00 am).

Total white blood cell count
Normal is 4.2-11.0
5.0, 5.1, 6.9, 4.1, 6.3, 5.4, 2.5, 1.1, 0.4

Hemoglobin
Normal is 12-15.5
They will do a whole blood transfusion if it drops below 7.0
8.6, 8.2, 9.5, 8.0, 7.4, 7.6, 7.8, 6.5

Platelets
Normal is 140K-450K, but mine have never been that high
They will do a platelet transfusion if it drops below 10K
23K, 21K, 38K, 22K, 20K, 18K, 15K, 10K, 5K

Absolute neutrophils
Normal is 1.8-7.7
They call it neutropenic if I drop below 1.5, and exercise additional precautions, including putting me on a prophylactic antibiotic; apparently once you're declared neutropenic, they stop running this and the blast percentage because the total WBC count is so low that it's really hard to get fractions.
1.1, 0.8, 1.7, 1.8, 4.3, 4.2, 1.6, 0.4...

Blast percentage
Normal is 1-5% in bone marrow, but none in blood; this goes along with the neutropenic marker and is no longer run after you go neutropenic.
42%, 28%, 10%, 2%, 14%, 12%

What this means is that today I will get a blood transfusion and also platelets. I am indebted to all who are able to donate, as it truly will save my life. I'm also a little bit scared as the consent form lists things that could potentially happen if you receive blood from another person. Still, I don't exactly have another option, so we'll do it!

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Last night was a rough night. As my blood cells dropped, I started to develop a fever. I also was ridiculously exhausted--to the point of not being able to keep my eyes open. It was kind of scary to be that out of it, but also strangely nice to not be able to do anything other than just sleep. My temp started to creep up into the 100's and I was warned that if it hit 101.5 they'd have to do all sorts of thing, including preventative antibiotics and a bunch of tests to make sure it wasn't an infection causing the fever. I have always been the kind of person who spiked fevers easily (My mom used to say, "you get a fever from a paper cut."). So part of me knew that this was likely my body reacting to all the crap being thrown at it. But it's still scary when they're doing all sorts of things, "just in case." And then my temp hit 101.8.

I spent over 12 hours drifting in and out of consciousness (sleepy-consciousness) while my vitals were taken over and over, I was given meds, and more blood was drawn and more other things sampled, and I got an X-ray in my hospital room...

At this point the urinalysis and the X-ray were both negative for anything, but it can take days for the blood cultures to come back. The longer w/o results, the better in that case, meaning nothing is growing. Again, I'm hoping it's just my body and the way it reacts to any trauma and not another thing to have to deal with.

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I asked my nurse this morning to go over all the meds I'm on, and explain them.  Here we go:

Idarubicin: chemo given daily for 3 days; done with this one
Cytarabine: chemo given around the clock for 7+ days (there's some extension of time with the IV bags and changes of lines and such, so it ends up being over 7 days; I'm still getting this one and it is due to end sometime on Saturday.
Posaconazole: oral med that is an anti-fungal
Allopurinol: oral med to decrease uric acid, which can increase with the chemo as cancer cells die, and it ultimately protects my kidneys
Ondansetrone/Zofram: anti-nausea meds given in my IV
Cephapine--IV antibiotic given when neutrophils drop
Vancomycin--second IV antibiotic added when my temp went over 101.5
Femara/Letrozole: the aromatase inhibitor that I have been on for four years already
Calcium/Vit D.: vitamins I've taken for a long time
Acyclovir: Anti-viral that will be added when the chemo is done

I was taken back 25 years when I was writing my birth plan and was ADAMANT that I would not get an IV placed because it was too invasive. I didn't want pain meds for labor or pitocin for induction. I wanted to trust my body to de exactly what it was made to do.

It's insane to think about that now. Central lines, additional IVs as needed, a med list that I can't remember and have to write down. Everything going into me and coming out of me being measured... What I wouldn't give to just have to defend my birth plan now!

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I'm gearing up for another day of hard work. I need to try to walk or otherwise exercise since I barely did anything yesterday. I'll have 1-1.5 hours of platelet transfusion, then 2.5-3 hours of blood transfusion. I'm tired, but I'm not so completely exhausted as I was yesterday. I have been told that it will get worse before it gets better, and I'm still moving forward. Two more days of chemo, and I just keep checking things off the list.


While it's been nice to see people, it really wipes me out, so please don't be offended if you ask to visit and I just can't do it. It's taken an inordinately long time to be able to type this blog post since I'm super easily distracted. I had thought I'd be able to keep up with work while I was hospitalized. While I can do tiny bits, I can't sustain thoughts or plans. So I guess resting is where it's at. (And walking. So much walking.)

A slave to the numbers

I missed posting yesterday on the one week anniversary of my diagnosis (I'm kind of big with those kind of milestones--tomorrow will be the 5 year D-day/official diagnosis of my breast cancer). Man, the holiday season seems to suck for this kind of stuff.

Anyway, I've been settling into a sort of pattern. Everyone here is wonderful, but the fact of the matter is that there is a lot of interruption that must occur in the hospital, and especially on the oncology wing. The good news is that, as I've gotten more sleep-deprived, the hospital bed is less uncomfortable and I'm actually sleeping some. The weaning of the steroids has undoubtedly helped as well (I only got those before the three doses of Idarubicin).

I have always tracked my lab counts ad nauseam and one of the nurses here told me a few days ago which numbers I really need to track, and also said that she can get the results before they appear on my medical record that I can access myself. So they keep giving me my counts. I hope I'm understanding and correctly sharing the meaning of each, but I may have to edit.
Here's what they're following:

Total white blood cell count
Normal is 4.2-11.0
If below 1, it's a greatly-increased risk of infection
We want to see this go down, as it shows that the chemo is majorly messing up the bone marrow and keeping it from making white blood cells (infection fighters) which are what caused this overgrowth in the first place

Hemoglobin
Normal is 12-15.5
They will do a whole blood transfusion if it drops below 7.0
Hemoglobin is a protein that is responsible for making red blood cells carry oxygen to the cells (as all cells need oxygen). Low hemoglobin results in anemia. This will undoubtedly go down, so there will be transfusions in my future. I've never had one, but apparently they do make you feel better when you get one.

Platelets
Normal is 140K-450K, but mine have never been that high
They will do a platelet transfusion if it drops below 10K
Platelets are responsible for clotting of the blood, and so it's important to have enough to clot if anything internal or external causes a bleed. As I get more exhausted, falling is more likely (ie: could bleed internally) and I have so many things connected to my skin that external bleeds are also more likely. I did need one platelet transfusion after my mastectomy, and I guess I handled it fine.

Absolute neutrophils
Normal is 1.8-7.7
They call it neutropenic if I drop below 1.5, and exercise additional precautions, including putting me on a prophylactic antibiotic.
Neutrophils are the first line of defense in an infection, so something that would normally be fought off by a healthy person (ie: ear infection) can almost immediately become septic. It may be an overabundance of caution, but I've chosen, with my team's support, to require everyone to mask up now that my levels are low even if they don't have symptoms. It's just not worth the risk.

Blast percentage
Normal is 1-5% in bone marrow, but none in blood
Blasts are partially-differentiated hematopoietic stem cells that populate the white blood cell (infection-fighting) line. In leukemia, they divide uncontrolled (cancer thing) and fill up the bone marrow, preventing effective blood cells of all types to be formed. In leukemia they also spill out into the blood and can be viewed and measured that way. That's how my initial diagnosis at Dr. Shah's office was made. There should be under 5% blasts at any time, and more than 20% are sufficient to diagnose that some sort of leukemia is happening. Mine were 30% in Dr. Shah's office.

So I've been tracking my numbers and while my blasts were trending downward, yesterday they took an uptick, which completely freaked me out. Being mostly stuck in a hospital bed with only your own thoughts (and the internet) is not a great way to be reasonable. Suffice to say that my blasts had gotten down to 2% and then yesterday shot up to 14% (thus the panic) but are heading back down, being 12% today. And that's what we want because it means that the chemo is working. If you want to visualize or vibe or pray, feel free to work on dropping those blasts!

But Dr. Thompson was happy that the other blood counts are all about where they should be. He said an increase in WBC would not be good now, and they are definitely trending down. Neither my hemoglobin nor platelets were low enough for transfusions today--although it's always possible tomorrow. Slow and steady.

I had been able to sleep significantly more last night, and had a hard time waking up this morning. Then late this morning I could barely keep my eyes open. It's got to be the cell counts, and the absence of steroids. I had some people who were going to visit and I had to turn them away. My eyes were rolling back in my head I was so sleepy.

And as I was napping, I felt like I was running a fever. I have always had chills and body aches with low grade fevers since I was a kid. I wasn't sure whether to say or do anything because I was already getting antibiotic in my IV since my neutrophils had fallen so low. At routine vitals, it was found that I had a temperature over 100. It was explained that they'd watch, but if my temp got to 101.5, then the big guns/protections would be pulled in. I'd need blood cultures--from the port but also peripheral. I'd need a urinalysis. And then a chest X-ray--all to insure that the fever was from the chemo but not an infection. I was shivering and the nurses turned up the heat in the room and I put on some fuzzy socks and more blankets. I stopped shivering, but my temp eased up to 101.3. And an hour later, it was at 101.4. The nurse put in a call to the doctor to get things going. :( And then I pried myself out of bed and Greg walked me around the floor. It was tough to keep moving and I just wanted nothing more than to crawl into bed and sleep, but it worked. My temp went back down to 100.8 and just now it was 100.0. I have to remember there's a such thing as too warm!

Not much else to report. I feel like my brain is quite foggy and it's hard to hold a conversation, so if you do come visit, know that I may not make sense. I'm glad I started this blog post awhile before I crashed. I still don't know if I was correct in all that I wrote, but I hope it made a little sense.

Oh, the other big thing that happened today is that I was able to trash the Tele (EKG telemetry). Everyone has to be monitored for a little while, and I'd been doing pretty well but then I think I actually moved in a strange way and caused an irregular heartbeat (v-tach) and so I was kept on the Tele. I did create a game with it where I walk around the floor and whenever there is a display, I seek out my name and measurement and try to get it to settle down and have a normal pattern. After that, I started playing the 87 game--I'd breathe slowly and steadily to try to bring my heart rate down to 87 (because Class of 87 rules...). It broke up my walks.

but it also meant that I had six electrodes stuck to my chest and a heavy transponder to carry around with me. I was pretty happy to say goodbye to the Tele.

And I am almost 5 days into the 7 day chemo regimen. I know it'll be a little longer and it's possible it'll be a LOT longer, but I'm moving forward. Here's hoping those numbers stay/move where they are supposed to be, and I rebound at least a little bit in energy. For now, I think I'm going to take a 7:00 pm nap...