So I came home last Monday from the transplant process, the hospital stay wasn’t quite four weeks long. I think I went in on November 11th and left on December 5th.
So far things have been going about as well as can be expected, I’m still having some issues but that’s normal. The transplant process itself went fine, and the next 100 days will be careful watching for symptoms of graft vs. host disease, so I’ll have a couple appointments a week for a while, if things keep going well it’ll drop down to once a week.
I’m sort of quarantined a little bit, they want me to avoid crowds and school aged kids, but I can have visitors, they recommended keeping it to no more than 2-3 at a time.
My sense of taste is probably the worst symptom at the moment, it makes it pretty hard to eat. Oddly I can still smell food pretty well, but most of it tastes kind of bad. Sweet things are decent, but salt is very absent.
That’s about it for now. Just a lot of waiting and taking my time with things.
So I was released on Wednesday, the 19th, and have been home the last two days. My ANC was 320 Wednesday morning, which was really discouraging, since it had been 400 the day before and they had told me if it remained at 400 I could go home. So I spent a few hours thinking I’d be stuck there at least a few more days. But then later in the day they told me that they don’t think anything weird is happening, my numbers are just kind of bouncing around a bit, which is fairly typical, and since I’ve been through all this repeatedly they trust me to look for signs of infection and seek medical help if I have any complications. And since I was just waiting around to recover, I might as well do that in the comfort of my own home. So I got to go home! They wanted to give me a blood transfusion before leaving, cause my hemoglobin was like 7 something, and outside the hospital they want it to be at least 8, so they did a transfusion and then another blood count and it was really good news, my ANC had gone up to 370, my hemoglobin was 9 I think(?) and my platelets had ticked up a little bit from the morning as well.
They did a bone marrow biopsy on Monday, but it was kind of too early, there were blast cells, which could potentially be leukemia cells, but they may also just be normal healthy cells that haven’t matured yet. So they’ll want to perform another biopsy sometime soon, this week probably, and if that looks good I should be all ready to start the transplant process at MGH. On Monday I’ll go in for a more routine checkup to make sure the numbers are looking good, and then my hope is, if all that checks out, we can go into the transplant process as soon as is possible. I’m nervous about it, but I’m more nervous that any waiting is giving the leukemia cells more time to regrow.
Someone contacted me about reworking the octopus to be smaller. I’ve wanted to redesign a lot of things about it for a long time, so I might actually try to do that finally. It has me digging through old project files trying to decide how to go about it. I had also begun a cuttlefish model not long ago, so I might just start with that instead. I think I should learn about rigging the model up this time, so I can more easily rearrange the legs in the future.
So my ANC has started to bounce back the last few days, 0 to 40 to 30 to 80 to 90 and then 160 today, and so I’ll probably be going home sometime in the next few days, maybe Wednesday Thursday or Friday (not likely tomorrow).
I had an infection last week, my temperature briefly spiked to
I thought about titling this post “biopsy negative!” but decided that could be misinterpreted, and “biopsy positive” could definitely send the wrong message, so I went with the primitive sounding “biopsy good”.
So this morning the doctors came in to tell me they didn’t find any signs of the leukemia in my bone marrow, so I’m back in remission. Now it’s a matter of waiting likely another 11-21 days (could be shorter, or longer), for my immune system to regrow enough to fight off infection on it’s own. Then, assuming I’m in good health (which seems likely right now, I walked three miles last night without difficulty), then I’ll head to Boston to begin the transplant process. I guess there’s a chance I could get a fever, as I did in the past, before my immune system is mature again, in which case that would delay things a bit, but once I’m strong and healthy we’ll try the transplant.
I’m nervous about the transplant process, there’s a lot of uncertainty, but in my favor are my age and health, and this is the best shot at curing me, or at least prolonging my life for a good while, so I’m also anxious to begin — the sooner it starts the sooner I’ll be able to work on recovering and finding out if it worked or not. And also the less likely the leukemia cells will regrow into a problem again.
I guess I could mention too, I’m at the stage where the later chemotherapy effects are starting to happen, my hair is just beginning to fall out, and my sense of taste seems to be changing again, though it’s hard to explain exactly how. In both cases they seem like relatively harmless effects, I’ve been lucky that my digestive tract has remained pretty healthy, and my mouth too. Sores in the mouth are a common symptom and so far I haven’t really had that, though a couple days ago my platelets were very low and I apparently accidentally bit my cheek while eating a cookie, and a blood blister formed right away. But I got a platelet transfusion the next morning and I’m not much of a bleeding risk again for now, and the blood blister is going away quickly.
Chris, the Creative Visual Artist for the Norris Cotton Cancer center, (where I’ve been treated all this time — which just reminded me, someone asked for my address and I forgot who…), asked me to share some of my photography for an artshow later in October, so I need to write up an artists’ statement and get a couple pictures printed, and framed, to be hung. That’ll be fun. And after I post this I’m going to go back to fiddling around with some programming ideas, see if I can get back into the programmer mindset.
Thanks for reading!
So I’ve been back in the hospital for two weeks now, I finished the last dose of chemotherapy a week before last Friday, and have been waiting for my numbers to drop and rebound. Right now my ANC (immune system cells) are practically zero, white blood cell count is at 0.1; hemoglobin and platelets have dropped and I’ve had some transfusions, a couple red blood transfusions and a platelet transfusion.
I’ve been walking a lot, usually a two or three miles a day, often without supervision, which is nice, because I haven’t had issues passing out in months, and have been feeling pretty good.
Because today was day 14 since beginning the “re-induction”, they did another bone marrow biopsy. When I came in this time my doctor told me how the first time they did a bone marrow biopsy back in February, my marrow was 100% leukemia cells, and after that first induction it was down to 5%, and after the first re-induction it was clean, which is considered remission. This time the bone marrow was 5% leukemia cells, and we used a different pair of chemotherapy drugs, because it is assumed that the leukemia cells which survived the previous drugs are most likely ones that have adaptations that protect them from the previous drugs. So I’m not worrying much about whether this one worked or not, though I didn’t really ask the doctor about odds specficially, so I guess I’m a little uncertain in that sense.
Assuming the biopsy they did today is clear, and I’m again in remission, the plan will be for me to wait here until my ANC recovers, and then probably head straight to Boston to begin the transplant process. If I’m weak they might send me home to regain strength first, but I think I’m pretty well in that respect, probably mostly due to the daily walking. I feel quite well, though I think my hair is beginning to fall out again, which is expected, and my taste may be getting weird, which may be an indication of my tastebuds dying off, which is also expected, and also tended to happen with each of the consolidation chemotherapies.
Meanwhile my app broke when Apple updated their operating system to iOS 10 recently, so I scrambled to update it, and today it got approved and updated in the App Store, which is a relief. It also served as a refresher course in programming, which is good because I have some ideas I want to explore, to get more comfortable with what I’m doing. So I’m excited about that.
Other than that I’ve got a lot of waiting and time to kill. I’ll update again when I know something about the results of the biopsy!
So I was re-admitted to the hospital on Monday for another round of induction chemotherapy, it consisted of two new (to me) drugs, each administered once a day for five days, so last night was my last dose of each. Now I’ll be hanging around for the next three weeks, waiting for my counts to drop down and then rebound, after which I’ll head to Boston for the transplant process.
So far it’s been pretty easy going, I’ve been walking a lot, which is both good for my health, and allows me to avoid painful shots in the stomach that they give to most patients to help avoid clots from forming in the calves. Today they disconnected me entirely so I can walk around without pushing the pole of fluids with me, which is nice too. It could be a little rough over the next two weeks, I’ll probably need some transfusions as my blood and platelets die off temporarily, though it shouldn’t really be anything I haven’t already seen in the past.
I have a lot to work on, and plenty of distractions. I should make more of an effort to try out some things, and I also have to delete photos to make room on my computer and my phone. That’s all for now!
So somewhat bad news, they called me back yesterday because the cytogenetic analysis of my bone marrow indicates the leukemia is still there, so Monday I’ll be readmitted at Dartmouth Hitchcock for another round of induction chemotherpy — it’ll be a lot like the first two rounds I went through, but not the exact same since whenever something survives one treatment they try to come at it from a different angle. I don’t know the details exactly but my guess is it’ll be about a week, and after that they’ll try to go right into the transplant process, so I’ll be moved down to Mass General.
It’s scary, which I’m sure is natural. Though I feel somewhat prepared, since the original cytogenetic analysis indicated it was likely to come back anyway, and also because I figure the next step was to knock out my immune system entirely to prepare it for the donated immune cells, so it seems like another round of induction fits in well with the planned process anyway. That’s just speculation though, I’ll ask the doctor Monday and get a better idea of what I’m facing, and try to keep this up to date.
Another few weeks have passed, mostly without anything significant happening, except they asked me to go in for another blood count like a week ago and my white blood cell count had dropped pretty dramatically, down below 500, meaning I was neutropenic again. I found it concerning and so did the doctors, so they did another bone marrow biopsy on Wednesday, and on Friday told me they weren’t seeing signs of the leukemia (which was sort of the only possibility I really thought about it; seemed likely it had grown back and was crowding out healthy cells again). It’s weird reading back through all that, it seems like it was going much slower. If it had been the leukemia returning, I would have done another round of induction chemotherapy and then they would have moved me into the transplant process right afterwards.
So it was good it wasn’t the leukemia, though it still isn’t clear what is going on. The doctor said it could be a virus or other infection, and when my body overcomes it the ANC would bounce back, so they’re going to track me for a couple weeks and do another bone marrow biopsy if I don’t get better in that time. By Wednesday my ANC had dropped further, so I’m back to taking an antibotic and antifungal, and avoiding public, and crowds, and kids. In some ways it didn’t concern me much because it seems like wiping out my immune system entirely is the next step anyway, and this would sort of be a head start.
They started scheduling appointments for a transplant in Boston, but that’ll probably be pushed back some dependingo on whether I return to normal soon or not. My red blood cell count ticked up slightly, so that’s also good news. But it’s still really low, and I get light headed a lot standing up.
So I think it’ll be an uneventful Labor Day Weekend for me. But so far it’s been really nice out. And Stefan and Justine both visited which was nice.
I started playing with twisty puzzles again, a few my cousin Kirsten sent me that I did solve but tend to mess up while soving a lot of the time. Or can’t reliably solve particular problems on them. I’m actually messing something up right now where I can’t quite solve it. And normally I figure these things out on a normal Rubik’s cube, which I have somewhere still, but seemed to have misplaced. Which is mostly annoying because there aren’t really a whole lot of places to look. Seems like I should have seen it by now.
Anyway, the transplant process is still moving forward, I should know in another week or two when exactly. I’ll try to keep this a bit more up to date as things are happening, if I can.
So without even realizing it I neglected to post for almost an entire month!
The third round of consolidation went well, much like the second round — I walked a lot, I felt okay.
But a few weeks afterwards, around my immune system’s nadir, I woke up with a fever, which put me back in the hospital for eight days or so. I also passed out twice, once the morning I had the fever and once the morning before that. I knew my hemoglobin was really low and I should have gone to get a transfusion, but it didn’t seem like that big a deal at the time. Luckily all that worked out fine, but it was a miserable time in the hospital, I had fevers most of the time I was there, which made them reluctant to give me a blood transfusion, since if my temperature went up a degree during a blood transfusion they’d have to stop and write it up as a potential reaction, even though it would probably just be due to the fevers I was already having. So that first night they would pack ice under my armpits and behind my head to keep my temperature down. My hemoglobin was really low for a while, as low as 5.6, which I think is far lower than it has ever been before. (Normally in the hospital they would give me a transfusion when it was below 7.)
All ended more than a week ago. Then I got to spend a day with Allison & her family that Friday, which was really nice.
Sometime in the last month I had another appointment in Boston with the doctor and team of people who are going to do the transplant. The plan right now is to have one more appointment to go over everything in late August, and aim for the transplant process to start early in September. It’ll probably be about a month in the hospital, I’ll get another dose of chemotherapy drugs that is more intense, like the first two treatements, with the intention of destroying my immune system completely. Then they’ll take bone marrow or possibly just stem cells from the bone marrow of a donor, and give them to me much like a blood transfusion, through a vein. Then ideally the donated cells will embed themselves in my bone marrow and begin to grow as my own immune system.
One of the bigger concerns is that the donated immune system might see me as a foreign invader, and attack me, which is called graft-vs-host-disease (GvHD). So they’ll be watching my skin, lungs, and liver, for signs that the new immune system is attacking those organs. This will be a risk for the rest of my life, but I think it is immediately afterward that will most likely be the biggest risk. From what I’ve read and watched videos of people who’ve gone through this, a little bit of GvHD is actually a good thing, as it indicates the new immune system is growing and functioning, and there is even a graft-vs-tumor-effect, where the new immune system actually sees my old immune system, in particular the cancerous immature blast cells, as invaders, and actively seeks them out and kills them. If I do have problems with it, they may treat me with steroids, though I don’t actually understand the mechanism there. The doctor also mentioned that there has been some recent success with partial match donations being treated with some chemotherapy after receiving the donation, which is counterintuitive, as that is when you would expect the donated immune system to be most vulnerable, but apparently it can help with the process. (Whenever I hear “graft-vs-host-disease” I think of David Cross’s character Tobias in the show Arrest Development, and how he developed GvHD because of his hair plugs, so they threw a fundraiser for him and then everyone revolted when they found out it was just his hair plugs causing the problem.)
Beyond that the other major concern is probably infection, so they want me to brush my teeth four times a day, which I’m not used to but am sort of looking forward to I think. I’ve always had a poor opinion of my teeth — it seems like I’ve had cavities virtually every dentist visit of my life, and I’ve gone pretty regularly every six months for years. But one thing I’ve had a problem with for years is my habit of brushing in the morning, which for me didn’t develop as something I do in the morning, but as something I do before I leave the house. So on the many days where I don’t leave the house (especially as someone who worked from home before quitting and working for myself, (or trying to at least)), there are a lot of times where I brush either very late in the day, or just once before bed. But I have flossed regularly for most of my life, and used a rinse for most of my adult life. A lot of that has fallen apart during these long hospital stays. I wasn’t allowed a tooth brush for much of my stays (they worry about bleeding with low platelets). So I think that’s why I’m kind of looking forward to scheduled brushing four times a day.
After that first month they’ll still keep a close eye on me, I think for at least the first 100 days. After that it’ll sort of be the next five years of checking to see if anything grows back, if nothing shows up that would imply I’ve been cured, I think, is the idea. I know with some cancers it’s never really clear whether you’ve been cured, there’s always a risk of even a lone cancerous cell you missed growing back to overwhelm things again given enough time.
I read an article a while back about research into giraffe evolution, which involved some gene sequencing to match it’s closest living relatives, and then comparing the two genomes to find out what evolutionary changes occurred to make giraffes unique, and one of the interesting discoveries were genes that helped the heart be able to pump blood all the way up the neck, I think. And then the article ended by mentioning how because elephants are bigger than most animals, it was thought their rates of cancer would be higher because they have more cells in their body each with the same potential to go haywire. But they don’t, and now it’s thought they have some genetic mechanisms to help avoid cancer, and since giraffes are also very large, they expect giraffes to have similar adaptations. I found all that interesting, I had never considered it before. It made me wonder about whales too. And recently I saw a lot of headlines about research that shows a kind of shark that lives for several centuries, one headline said it doesn’t reach sexual maturity until it is 150? But I didn’t read any of the articles about it.
I think there are muscles or clams or something that live several (~4?) centuries, and are able to reproduce well into their second or third century. I think the next few centuries of human technological advancement will see us figure out how to incorporate many of those benefits into our medicine, and likely take complete control over our health, to a degree we can’t really imagine yet, in much the same way people from a few centuries ago could hardly imagine the things we’re able to do right now. Only the changs ahead are probably much bigger, because we’re beginning to understand how we work on a fundamental level now. Though I’m skeptical of claims that we’ll improve our lifespans dramatically. I’m sure we’ll do that eventually, but in the foreseeable future it seems like the problems caused by aging will remain.
But I digress.
For now I’m just enjoying the summer weather and trying to advance the projects I find interesting. Also I need to hurry up and sell my car! And renew my drivers license! I bought a shiny copper plated colander to wear while getting my photo retaken, but I’m nervous about wearing it, I’m not really one to cause a scene typically.
Anyway, my cousins have mentioned a few times now that my comments seem to be broken, so they can’t leave messages. I need to figure that out too!
So I’m back up at Dartmouth Hitchcock for a third round of consolidation chemotherapy. It started yesterday afternoon and if all goes to plan I should be heading home Monday evening after the last dose. The last two went well so I don’t expect this to be too different, they let me walk a lot and that allows me avoid these painful shots in my stomach that they usually give daily to most patients to help prevent blood from pooling or clotting in the legs. The shot is usually painful, first with the pinch of the needle, and then with the stuff they inject, so the nurses don’t like giving them either, so it’s a win-win. Plus, walking is probably my best bet at keeping my health up for the next step, the bone marrow transplant, which is apparently going to be a much harsher and longer process than these consolidation chemotherapies (which really havent’t been too bad, the complications in the weeks following have actually been worse, the nosebleed and the fever, but even they were relatively tolerable).
I got to see Allison a few times before coming back in, which was just great, hanging out with her really helped take my mind off things some. Not that I completely forgot whats going on and what lies ahead, but it stopped occupying my attention so much, which had started to happen for a while I think.
I forgot my phone cord so my phone is about to die, but I have my laptop and cord, so email or facebook are reasonable ways to contact me, or leaving a comment here (though my cousin said she couldn’t? I haven’t been able to figure out any problem with the commenting yet).
My plan was to go back to programming some, but without being able to test it on the phone it’ll be hard to go to far. Stefan also left me with plenty of reading material, and I still have a book Jared lent me that I haven’t finished, so I guess I should spend more time with paper and less time with liquid crystal displays.
Guess that about sums it up for now!