This about says it all regarding Zometa infusions.
This about says it all regarding Zometa infusions.
Sorry, as usual, for not updating more. The holidays were terrible and caused so much stress (family stuff) that it felt like all I could do just to survive, much less dwell on everything else. I think I mentioned it in the last entry, perhaps not, but my mental health effectively waxes and wanes with whether I can keep the emotional walls up and not really think about the horror of this diagnosis. When other things damage the wall, it all comes flooding back.Nothing much is new, other than a better yet sadder understanding of those around me. I wrote a letter to a parent that I never sent to clarify my thoughts, and realized it would suffice as an entry here for now. Life is OK, or as OK as it can get when you just step around the elephant in the living room and try not to acknowledge it’s existence. Anyways, a portion of that letter …
I have a rare and terminal form of cancer. That isn’t grand-standing, “pulling the cancer card” or being melodramatic, it’s fact. While treatable and thankfully caught early, unless something changes at some point we will not be able to keep these numbers down and this disease is going to start attacking my organs, assuming the damage it is doing on an ongoing basis to my immune system doesn’t do me in first. As you may know, what generally kills you with cancer isn’t so much the disease itself but what it allows to be done to your system. I got to experience that firsthand when I was in the hospital for four days with pneumonia recently (one of the primary killers of people with cancer). In fact I think, of all of the time in the last few years of staring at hospital ceilings while trying to maintain my composure, that it really occurred to me that this is probably how it’s going to be at the end.
Every time I get a runny nose I have to think about that. I can’t really go to children events safely, although I try to for my daughter’s sake and my own, mentally. I feel like I sit on the sidelines too much as it is with her due to this nightmare. I actually risked my life just to go on that Disney Cruise for God’s sake – probably the worst idea, from a health stand-point, I’ve had to make. But I had to balance whether it was more important to take a risk and make at least some memories with my daughter versus not knowing if I’ll even be around a year from now. I’m not sure if you know what that kind of a decision is like, but I hope you never have to make it.
As best as I can describe it, when I was diagnosed the world went from spinning on its axis at 600 mph to 0. But just for me. I watched as everyone else got to continue their lives like nothing was wrong. Except mine had just ended. I suppose that’s what it’s like in prison, too. Staring out the window at a world that has stopped for just you while everyone else gets to go on living like nothing happened. With most things, as I’ll touch on in a moment, I’ve just given up and accepted my new role. Some stuff, mostly related to Ariana, I still refuse to even if I should.
The sad thing is, my decline towards the end could start in earnest tomorrow. Or the next day. Next week, next month … whenever. No warning, just the starting signs of the end. That’s the other “fun” thing about myeloma and cancers in general, and why the local oncologist wanted a deeper response than the Mayo Clinic. As long as this is in my system I am in imminent danger.
Granted, you and I don’t stress about a lot (pretty sure I inherited that from you) but that’s one that keeps me up at night. Every night. And it probably always will. People talk about living with cancer a lot that have it and in the literature about it – what people who don’t have it rarely understand, however, is that it’s a mental and emotional battle, and honestly, most of us just give up. I’ve already met people who are dead now from this and other forms of cancer. Did you know that? I’ve met folks who have given up and just refused to deal with chemotherapy anymore. I keep going for my family, but I’m pretty sure if it wasn’t for Ariana I’d be in that boat. What I’ve learned in part by doing so, however, is after a while you become so numb from dealing with the horror that you just don’t have it in you to do so anymore, and you get a bit colder, a bit more aloof, a bit quieter. It doesn’t ever go away, trust me.
I vaguely remember you making a comment, I think to Amy one night when we were all together, about how when I was diagnosed was the only time you’ve ever seen my scared. That fear has never gone away. Not for a week, a day, a minute. In some ways it’s hardened me, although it’s made me so aloof in doing so that I have issues communicating with anyone I’m close to anymore. Imagine what that kind of fear is like, if you even can, that fear you saw a glimpse of. Imagine living with it as a constant companion. Look me in the eye sometime, I bet you see it.
Getting back to Ariana and this, I have had to enter into therapy and take fairly high-dose anti-depressants simply to get through the day mostly because of her and how the cancer is going to affect her, not me. I have had to learn that if I focus any longer term than the current day I actually begin to emotionally break down – the thought of orphaning my daughter, which is one of the most traumatic things a child can experience, starts flooding into my head. Every song on the radio seems to be about loss, every comment on a podcast I’m listening to applies, every thought that enters my head … it’s so upsetting to me that it actually physically shuts me down. There are nights it hits me out of the blue when I have the strength and energy left to put her to bed and read to her. She’s at the age where she’s started asking questions about why I am always going to doctors and why we were in Arizona, and I don’t even know what to tell her. Sorry, honey, daddy’s dying? She cries when she can’t find her blanket, how will her three-year-old mind work with that?
Most nights that I put her to bed I then go to my room and cry for a few minutes. Even Amy doesn’t know that one, she just thinks it’s when I go to the bathroom. Or she does and just respects me enough not to ask about it and risk upsetting me when I imagine she notices how glassy and red my eyes are.
You may or may not know this, but most children effectively wipe their minds of memories around age 5. Did you know that the top goal in my life is to make it past that age, simply so she remembers who her father is? Have any idea what it’s like waking up every day and that’s your entire purpose in life? To make sure you live long enough that your daughter remembers you? I talk to other parents and they are already worried about things like high school, the internet, the opposite sex, drugs and alcohol, accidents, driving. They say this shit to me and I can’t even relate. I just want to live long enough to spend more time with her. That’s it, the rest of life can just go away. It’s all I want.
If you want to know what that’s like for a few minutes, write her a letter from her dead father. Try to figure out what you’d say so you can get that minuscule an amount of peace that your 3 year old will someday know what her father was kind of like. I have a stack of those in a safe deposit box for her, did you know that? The tickets from our trip to Tiny Town are in one, and the stubs from our day at Disney World. Pictures, and lil’ trinkets and things. Pages of letters with who my favorite bands and their songs were, stories from when I was a child, life lessons, but mostly just how much I loved her. Because chances are there will be nobody to really tell her any of that, at least in the way I wanted to share it.
So like I said, someday I am going to wake up to find that the myeloma has begun my end. Again, that’s just fact. I live with that every single day. It’s why I have to take Xanax most nights simply to sleep and stay asleep, because I’ve found if I don’t that when I wake regularly at 3 am to the thought of “I have cancer” because the drugs I take to battle it make me sweat like someone poured a bucket of water on me in my sleep, I have a prayer of getting back to bed and at least getting a little rest.
I also live with the fact that, from everything I read, the end via myeloma is extremely painful and unpleasant. The funny thing is, of all the horror involved with this that’s the part that worries me the least. I guess I just haven’t thought about it enough, but I’m sure at some point that will start grating on me too.
Now about those treatments, I take chemotherapy drugs, as you know, 21 out of every 28 days, and several ancillary drugs to keep me relatively safe while doing so. Even at the lower doses I now take, the steroid keeps me from sleeping well (and I think causes that sweating issue) and causes irritability issues that force me to restrain myself constantly when dealing with everyone from Ariana to random strangers. The Revlimid is even worse. I am tired from the minute I wake up until the minute I go to sleep. I have found that unless I drink a good 32 ounces of coffee a day (which is why I now bring a French Press to work every day as you’ve seen, since that’s over $20 a day at Starbucks otherwise) I cannot make it until 5 pm. As it is, even with the caffeine by the time I get home I am rarely able to do more than sit on the couch even though I only have an hour or so with Ariana a day before we have dinner and she goes to bed. I try to come up with games for us to play where I can lay down, and a lot of nights I’m so tired that even though my favorite part of the day is getting her ready for bed and reading to her and telling her stories like I sort of remember you doing for me, I just don’t have the energy.
Every month I have a 30 minute phone call with both my pharmacist and Celgene themselves to get my next prescription. I get to talk to a stranger about how yes, I know if I have unprotected sex I’ll give birth to a child with birth defects (Thalidomide babies, since Revlimid is a Thalidomide/Lenalidomide extracted drug). Yes I know if my daughter manages to get a spec of Revlimid in her mouth it could kill her or permanently disable her. Etc. etc. It’s a fun phone call. Oh, the chemo also causes a side effect (exacerbated, apparently, by the stem cell transplant) affectionately called chemo brain. I used to be considered sharp, had a great vocabulary, etc. Now I stay silent a lot more because words that used to come easily to me are just gone. Memories are blanked, and I just stare emptily at people who bring up things we’ve done together that I for the life of me can’t even picture much less remember. My internal calendar is totally warped to the point I have to put reminders in my phone just to remember basic stupid things. It’s embarrassing at best and thoroughly depressing at worst. I always thought my brain was about all I had going for me in life, and now that’s crumbling apart.
Once a month, I have to go all the way downtown to get an IV of Zometa (Zolendronic Acid, I believe) because one of the fun side effects of myeloma is the damage it does to bones. The nurses regularly have to poke me multiple times and comment how beat up my veins are, and at some point (or perhaps when they change my chemotherapy to an infusion-based instead of oral regimen) I’ll have to have a port put in. I think mom had one of those for a while with her heart troubles. Imagine spending the rest of your life with a plastic hole in your chest, though, just to stay alive a few more days. Anyways, the Zometa infusion is fine. That is, until about 24 hours later when the pain and flu-like symptoms start, and then the next 48-72 hours are a nightmare. I don’t think its’ pain on the level you’re dealing with with the sciatica (sp?), as nerve pain is about as bad as it gets. But there’s no escaping it. Your actual bones hurt, and for some reason so do most of your muscles, which tighten up so bad it’s difficult to walk or even stand up.
Did I forget the best part about that infusion? Zometa apparently has a 5% chance of causing osteonecrosis of the jaw in people who take it. You and I both have a pretty solid background in statistics – how many treatments do I need to take before I’m at such a high risk it’s almost a certainty? Do the math. Don’t share it with me, I already know. Imagine that dental appointment though, when your dentist tells you that your jaw has begun irreversibly rotting and they’ll have to start a lifetime of cutting away chunks of it. And people wonder why horror films don’t really bother me anymore.
One more fun and recent addition is they noticed when I was in the hospital for pneumonia late last year that I don’t get enough oxygen at night anymore. After completing a sleep study with Parker Adventist Hospital and going over the results with a doctor, I am now going to have to start sleeping with a CPAP device. That’s a machine with a facemask on it to keep me from dying in my sleep, apparently. The hits just keep coming, as they say.
I won’t even get into the less polite side-effects like the constant stomach problems, etc. But believe me the list continues. There is one last fun one, which is not only is my system effectively incapable of losing weight, I gain it at the drop of a hat due to the steroid and the anti-depressant. I was in the best shape of my life when I was first diagnosed, if you recall. Now I have to hang my head and shop in the XXL racks and deal with the embarrassment of family pictures and tight clothes.
So what’s my life like now? Most weekends I spend sleeping late and napping. That’s the only quality time I’m able to get with my daughter but I rarely have the strength and energy to do that. I spend most of that time, when I’m awake, trying to pretend to be normal and thankful she doesn’t notice yet, and trying to cope with the fact that at some point she won’t want to (or be able to, because I’m gone) spend time with me anymore and I’ll have permanently lost that due to this disease as well. In other words even the time I have now I can’t spend the way I want. I can’t take her the aquarium because I can’t be in shoulder-to-shoulder crowds of people due to my immune system, nor do I have the energy to deal with it anymore most days. We eat at slightly odd hours to avoid crowds in restaurants. Hell I’m afraid to kiss my daughter half the time because like most kids her age she always has some sort of respiratory thing going on. I have to wash my hands like someone who has OCD and carry a bottle of hand-sanitizer everywhere I go. I don’t even drive my family around most of the time – I’m so tired I’m afraid I’ll get us in an accident.
I say this so you understand that the word “fatigue” rarely sends the message of what it actually is like to live it. Fatigue always sounds a little tiring, not like something that is actively ruining any enjoyment you have in life.
My own personal life? I don’t have one anymore. One of the weird things about cancer that a lot of people with it notice is that when you are diagnosed, you stop being who you were. I am no longer who I was two years ago … I’m now a cancer patient, and that’s all I’ll ever be. Maybe that’s like being an alcoholic or drug abuser? All I know is I don’t see the world the same anymore. Honestly, if it wasn’t for Ariana I wouldn’t even be here now – most of the reason I started therapy was that I was suicidal when I found out about all of this and things began progressing. I don’t want to be this, period. It’s not fun, I don’t enjoy life anymore at all outside of my daughter, I have trouble dealing with the anxiety (to put it mildly), I have trouble with the lack of support I feel from most of those around me, and what little quality time I can muster with my daughter is always tainted with the fact that at some point this is going to destroy her just as much as if daddy took the shotgun down to the basement bathroom.
Try living with that thought for a day.
I have no more real goals. I can’t dive anymore, safely, even in a swimming pool. I doubt I ever will again, and after a year and a half living this wretched existence I have trouble even remembering what it’s like. I can’t teach it, which not only did I love but I took a lot of pride in. By now I would have been a full-blown scuba instructor, and would have been tapped by the shop to actually be a trip leader to exotic destinations. That’s all gone now. Hell I don’t even like leaving the house anymore because I don’t want to be that far from a bathroom. My bucket list of going to Thailand, Indonesia, Egypt, etc? It’s like it never even existed anymore, like it was some former life. The thought terrifies me now.
My friends? What few I had are mostly gone. The scuba shop folks have all drifted away except for two that I have lunch with maybe once a month. Amy and I are very good friends with a couple we met on a dive trip that we have dinner with once a month when I don’t have to cancel because of my health. I see R. for lunch once a month or so, and my buddy L. at Wells Fargo that I met in my assistant instructor class. That’s about it – most of our friends that we see are Amy’s friends, who have honestly been a hell of a lot more supportive than my own. Occasionally I get a text or something from someone, but for the most part they’ve all passed me by. That’s pretty common too with cancer, and although it’s hard not to I don’t hold it against them. It’s tough to deal with and you definitely find out who your friends are. L. and that couple friend visited us in Arizona, did you know that? L. twice actually. The rest? A few emails prompted by an email Amy asked the owner of our dive shop to send to all the employees and silence ever since. My phone rings so little anymore I rarely leave the ringer on.
My life? I struggle to get up, go to work every day, yawn my way through the afternoon most days and come home after 5. I try to bury all the energy deficiency problems enough to have fun with my daughter and stay awake through dinner, do her bath and get her ready for bed and read her a book. I try to talk to my wife most nights, or help with the dishes, but by then I’m usually so tired it’s just easier to go into my home office and kick back in my chair. I say goodnight to Amy and then stay up another hour or so, because it’s the only real guilt-free time I get during the day (i.e., my resting is not taking away from time with Amy or Ariana) and then after taking all of my pills go to bed and do it the next day. I have nothing to look forward to in a real sense anymore – I just “do,” basically for those around me. The bills have to be paid. I have a mortgage. Ariana needs clothes. Etc.
Been a few weeks, but certainly some busy ones.
After the first month of Revlimid I had my monthly appointment with the local oncologist. Although we didn’t know it at the time (took blood tests at that appointment), the Revlimid seemed to be working. My igG went from 3,996 on April 28 to 2,628 on July 18. My igA and igM are moving in the right direction as well, and my Kappa and Lambda light chain (free) numbers did too. This has continued through August’s tests, although not as significant a drop in the igG.
BTW I couldn’t explain those numbers if I tried, save to say they are the 5-6 markers that the doctors track my disease with.
So good news? It’s impossible for me to be optimistic. Not that I don’t feel it, I just won’t admit it. Nothing has really gone right with this disease for me in the last year, and every time I’ve even attempted to summon some hope life has beaten me so far fucking down I’m just not even going to bother. It is what it is, I hope it continues, and at some point I hope I can reduce the Revlimid dosage.
I had a six-month skeletal survey as well this month and the results were good — no new lytic lesions and no progression on the one I have on my hip. I was kind of worried about that because I’ve had some weird bone pains in the last few months and I was just waiting to find out my bones looked like Swiss cheese now, but no worries yet.
On to the less fun stuff — so after month 1 on the Revlimid, my CBC test showed that my white blood cell count was extremely low. As a result the doctor wanted to put me on Neulasta, which helps with that. As one shot is around $3,000 they had to get approval from my insurance company. In the meantime I started up the Zometa infusions again (bone strength), which has always had some gnarly side effects. The first dose is usually the worst, though, so when I got the flu-like symptoms the next day (a Saturday) I didn’t think much of it.
Then the cough started, and my temperature went to 102. So I started up the Levaquin, per the doctor’s standing orders when I get a high fever. For the next few days I felt like I was making progress and then that next Wednesday I fell off a cliff. Zero energy, cough so bad it was bringing tears to my eyes. We were afraid I might have pneumonia so off the hospital I went for eight hours of tests. I actually was happy to be there, outside of the inconvenience to my family — they put me on oxygen and Dilaudid and it was the best I felt in a week. Anyways, turns out I had a viral bronchitis, which took a few weeks to get rid of.
I’ve noticed that the Revlimid’s effects are cumulative, much like the Velcade was. Towards the end of my last cycle I was really feeling the fatigue, badly, and what’s more the off week (I do 21 days on, 7 off) I felt noticeably better. Kind of scared about this cycle. I’m also scared that the rate of motion in my numbers on the next test is going to decrease like it did between month’s 1 and 2. Because, really, what I needed was more stress in my life.
Mentally and emotionally this has been a bad month outside of my week off. The time in the hospital and the sick days before it was difficult — feeling so helpless and bearing the full brunt of what it means to have a compromised immune system really drives home how sick you are when you have something like this. Spent a lot of time on my back thinking about life, and death too. One sick day before the hospital day (or perhaps after, my memory is going) I watched about 10 episodes of Chopped that I had DVR’ed. I swear in every other one a contestant chef had a parent die early, usually with devastating impact.
I’m haunted, repeatedly, by visions of my daughter asking my wife “where’s daddy?” It never goes away.
Yeah I know it’s been a while. Been a long month and not a particularly fun one.
I noticed right away that the Revlimid/Dex wasn’t as easy on my system, if a chemotherapy drug can be, as the Velcade/Cytoxin/Dex regimen was. The fatigue hit me pretty hard, and the first week or so as my body adjusted to a new poison I had night sweats, headaches … nothing too too severe, but not really pleasant either.
The new regimen is 21 days on (1 pill a day) and 7 off. Right towards the end of the first three weeks I got a stomach bug that knocked me on my ass for 3 days — zero energy, not a fun ride. The next week, my week off Revlimid, I went in for my monthly checkup with the local oncologist and to start up the Zomeda infusions again (monthly bone-strengthener, nasty side effects). At that meeting my CBC returned a super low white blood cell count, so they began the process of getting Neulasta, an expensive WBC production drug, approved through my insurance company.
The first time I had Zometa I ended up in the hospital a year ago. Sure enough, my temperature shot up as the bone pain started over the weekend so I started the antibiotic I’m supposed to take as per instructions from my oncologist. Flu-like syptoms start, temperature won’t go down and I feel flushed and miserable. It seemed like things were improving towards mid-week, and then WHAM. Fell off a cliff last Wednesday and ended up in the hospital. Temperature was back up, cough was uncontrollable and so painful I thought I had pneumonia again, etc. After 8 hours there and several tests they decided it was a viral bronchitis (which my daughter and wife then got), and by Friday things were stabilized, at least somewhat. I still have a mild cough.
Got the Neulasta shot on Monday. Feel flushed and uncomfortable, although none of the pain in my hips yet like I got when I took Neupogen before my stem cell harvest in February. Headaches and weird jaw aches, though. All in all not enjoying things, AT ALL.
The WBC scare drove home the fact that until further notice I’m done with scuba diving instruction and working at the Aquarium. I just don’t have the immune system for either, and if Revlimid is going to be beating on my WBC (my oncologist’s opinion) to the point where I need to suplement WBC production, then I need to be extra careful.
I spent a lot of time miserable and on my back in the last several weeks thinking about things and trying to fight off a crushing amount of depression. I have one realistic hope, and that’s that the Revlimid pounds this fucking disease down enough that I can lower some dosages and feel normal-ish, at least for a while. But this monkey on my back just gets heavier, every day seemingly. There’s no ignoring it, forgetting it. I wake up and take drugs for it, I deal with the side effects all day, I take more drugs at night, and then, depending on the level of headache or other pain, i either take something to sleep or read myself to sleep with no covers because the regimens make me sweat like a pig all night. Fun fun fun.
When I was sick in bed, my daughter was coming in daily and giving me hugs while exclaiming “poor daddy” in a way that while touching, broke my heart. She has no idea her father has a terminal condition, and this is very likely as good as things are going to be. Fuck she doesn’t even get that the cats are dead and asks where they are constantly, how the hell is she ever going to understand this?
I spent a day watching about 10 hours of DVR’ed Chopped I had stored up. In almost every episode there was at least one chef who had a parent die at an early age. Talk about not being able to escape through the magic of television.
Settling back into my life and realizing it’s not really mine, it’s a cancer patient’s and I don’t want it.
Nausea almost daily lately — not sure what the reason is but obviously not enjoying it. Popping Zofran on almost a daily basis at this point. Trying to get in to see my local oncologist for my 60-day post-transplant appointment so will see if I can go that long before dealing with it.
Having issues emotionally lately. The cat thing is part of it — I can’t think of Mischief without getting overwhelmingly sad to the point of breaking down, which seems abnormal to me. I mean yeah in most ways he was my best friend for 11 years but he was a pet. It occurred to me this past week, however, that part of this may be because I think I just get along with animals better than people. The mild discomfort and awkwardness, the emotional barriers, the shyness and slight introversion — none of that enters the equation with pets. As such I wonder if due to that I’m suffering more than most would over this? Not sure.
I want cats again but I’m afraid to bring it up with my wife for the time being.
I took Ariana on a daddy/daughter date to the aquarium this weekend, which was bittersweet. She had a blast and loved the sharks, but it drove home the demarcation between my past life and my current one. As I walked behind the scenes with her it felt like a different world, one that’s moved beyond me, and it saddened me a bit.
I’m not sure I can do justice to why in terms of explaining that with just words … your entire perspective shifts when you put on the proverbial cancer shades. I can still, if I focus hard enough, remember what life was like almost a year ago when none of this was happening and my goals outside of Ariana-related stuff consisted of becoming a scuba instructor and continuing on like usual at the aquarium. But now there’s this dark cloud obscuring it all, creating doubts and tethering the dreams I had like a ball and chain around my ankles. Whether I’ll need maintenance chemotherapy, how I’ll still be needing monthly infusions of Zometa (the bone strengthening stuff that fucks me up for a few days every time) and the potential side effects and how to work that into a schedule where I want to submerse myself in somewhat unclean water.
Pre-transplant your focus, because that’s such a big, intimidating and landmark deal, is on the transplant. Now, though? I focus on day 100 post-transplant but looming over the horizon, and now visible really for the first time, is a life with cancer as a constant companion.
It doesn’t look like a lot of fun.
I feel sometimes like I should just change the name of this blog to “Depression Spiral” or something similar. In over a decade of blogging I’ve certainly focused more on the negative than the positive since it’s cathartic for me, but there was positive there before. Now it just seems darker each week, a continuous descent into the depths of disappointment over this diagnosis and metamorphosis from what I was into CANCER PATIENT.
In other words I’m not adjusting well, in case that weren’t obvious.
One, I don’t think I’m asymptomatic anymore. In the last week I’ve started having regular and constant lower back/spine pain as well as a sore spot in my hip/buttocks, both the spots that lit up as being active on my PET/CT scan. I mentioned this to Dr. F. at chemotherapy last week and he said we could certainly get an MRI ordered and then “radiate” the spots, which didn’t sound fun. I deferred to after the holidays to get my mind around the concept. Either way it’s been a significant milestone in feeling lately like I’ve begun slipping from mortality somehow, that THIS IS HOW IT BEGINS. Perhaps that’s not accurate, but it’s the feeling I have, right or wrong.
Secondly I feel like the LexaPro is just not working anymore. Ever since about four weeks ago when Dr. F. casually noted that the CyBorD treatment didn’t seem very effective and I should ask Dr. M. at the MC about abandoning it I’ve felt like I was slipping emotionally. I now feel about as stable as I felt before I started LexaPro (not very) — prone to overwhelming and random fits of depression and sorrow, inability to control my emotions, etc. I need to call the docs today to see if they can up the dosage or something, but I have no idea if that’s how you do it with these kinds of drugs. Zero experience.
My daughter’s second birthday party was this weekend (she turned 2 yesterday). Combined with the overwhelming feeling that everything is finite for me lately (only X number of her birthdays left, etc.), it has been difficult to say the least. The holidays coming up will be the same, if not worse. On top of that my parents are being as toxic as they’ve ever been, which I cannot understand and feel is actively taking years off my life at this point. You’d hope, if you ever go through something like this, that the people around you could rally a bit and re-prioritize. When you get the opposite the effect is really chilling.
I’m finding it really difficult to excise this cancer part of me from the rest of my life. Sunday night we took our daughter to Sesame Street Live, her first live stage performance. As she sat on my lap in her gorgeous dress, enraptured, clapping along, saying the character names, I looked around at all of the other children and her and couldn’t stop the thoughts. How unfair this is, how wrong, how isolating.
I have distilled my entire life down to one single fear at this point. I don’t fear death itself anymore — that has been scoured away over the last several months as I’ve been forced to confront this reality and realized that while I don’t want to die, I’m not afraid to be gone for myself at least. I fear the pain that this disease pretty much guarantees me on the way there a bit. But really the only fear I have is the impact that my death, which feels imminent even if I know it’s years away, is going to have on my daughter. How unfair it is that she won’t have a daddy after a certain point, and thanks to the method may not have much of one even before I’m gone.
We play every night together, talking, singing, and I cannot get that thought out of my fucking head as her innocence and the pure happiness of being that only children possess washes over me and highlights these facts. I can’t even escape it when she’s not around — I was watching Chopped the other night, one of the only TV shows I watch, and one contestant just randomly mentioned that his life was transformed when his father died at 12 and only cooking saved him. It’s kind of hard to sit there and not have that effect you, but to hear it, knowing you are going to do that to someone? It’s too much, just too hard. I wonder, very seriously, if I’m making a mistake hanging around. It’s not like there’s hope here. I know that sounds defeatist, I know I need to be positive, but the pragmatic side of me knows this is a death sentence. This isn’t a cancer, to my knowledge, that you get to survive indefinitely like some tumor you get removed. Unless they cure it I’m always going to be under it’s shadow until it eats me alive, literally.
Is it better to stick around, torturing myself while I slowly but surely wither away and knowing that at best I’ll have a limited amount of time to share with my daughter before I yank that away and leave her with the hole a prematurely dying parent leaves in a child? Or is the courageous choice to take myself out of the picture now, before she is capable of remembering more than flickering glimpses, to give her a chance to have someone else, perhaps even better, fill that role?
I cannot describe the sheer agony of knowing that all you ever wanted in life, all that mattered to you, was to be the hero to a little girl who’s already been through too much. And knowing instead you’ll destroy her no matter which way you turn or what you do.
Live with that for a day and then tell me I’m crazy to be considering this stuff pragmatically. Then ask another cancer patient about it, because I can’t find a column or blog written by one where I don’t see the same theme repeated over and over and over again.
So I dunno. My inability to doom her right now to having a father who killed himself answers the question, as it’s my understanding from researching this (quite a bit of research) that of the two (dying when she’s young or committing suicide) the latter is far worse. I’m just not sure I can reconcile it indefinitely.
Oh, did I mention I feel like every week my blogging gets darker and darker?
OK, just checking.
I’ve been trying to get a letter written to Ariana for a while now — I have it started and saved but it’s simply too painful right now. I realized that I was kind of blogging to her, which was getting dark, so I decided to sort of tell her the story of my life in future letters. I realize, as I have more and more time to reflect, that I will be the only one with either the information or the interest to really let her know who I was. Fuck, of the few people I know anymore who even know a little about me I think half of them have opinions of me that aren’t entirely flattering anyways. I had always hoped to relate the stories of my life, my experiences and the lessons I learned (or should have) in person. It just doesn’t feel like that’s feasible anymore.
As usual the Zometa infusion has made this weekend brutal. It feels like it’s kicking in later than usual this time — Sunday was awful, with the usual bone and muscle pains and cramps, but then Sunday night was even worse. I think because it hasn’t been cold in previous months outside that sleeping without sheets helped somewhat. Sunday night, however, it was freezing so I’d pull the sheets up and then wake up two hours later soaked like someone had poured a bucket of water on me. Change clothes, go back to bed, and two hours later repeat the same cycle. All night.
What else … oh, got a letter from my insurance company last night that, at least how I’m interpreting it, implies they will not cover me having my stem cell transplant at the MC in Arizona. I had no idea the transplant coordinator had started initiating research like that so it was a complete surprise and obviously a slap in the face. I’m hoping I’m simply reading the paperwork wrong, but I’ll need to confirm that tomorrow — it just seems like too much effort and too much risk today.
Went in Friday to start my third cycle of chemotherapy and talk to my local oncologist about my results. There are two primary numbers for my particular flavor of multiple myeloma that I’m trying to reduce to close to zero, igG(S) and igG Kappa. Don’t ask me what they mean — they’re just numbers to me representing this disease and the explanations are a bit beyond my comprehension. Anyhow, after 2 of 4 prescribed chemotherapy cycles I’ve only made a 25% dent in the igG(S) and really haven’t changed the igG Kappa. According to Dr. F., that’s not a good sign that the CyBorD chemotherapy regimen is working. He said generally you’d expect a more substantial impact up front for a variety of reasons, and that at this point it seemed likely that (a) I’d need to change regimens and (b) the chances of being ready to do the stem cell transplant by January are low.
Learning all of this was like getting slapped in the face with a bag of bricks. I just can’t seem to catch a break with any of this, and I feel like I’m being railroaded towards a fairly unpleasant demise every time I get more news. I cried in the car driving home, something I haven’t done in a long time — even through the LexaPro it’s just too much. All of the old thoughts about not being around for Ariana came rushing back, etc. I know there are other therapies and that it was wishful thinking to believe I could have any semblance of normalcy in life after being diagnosed with this, but whatever glimmers of hope I had for that just got trampled Friday.
On top of that this was a Zometa infusion week, and sure enough starting Saturday that fun began again. Nothing as bad as that first cycle but really cloying bone and muscle pain that has lasted until today. I feel like I got thrown out of a car, if that helps paint the picture. New this month was/is that I feel like I sprained something in every muscle in my shoulder blades on my back … just an odd sensation.
The plan is now to see what Dr. M. at the Mayo Clinic in Arizona thinks about everything when I get down there on the 12th. I’m thinking if we hit it off I’m going to have him take over my care as well — I’m not sure what the point of Dr. K. in Rochester is when I’ve never met him and they’re all on the same team. Minnesota is too far from me while Arizona is an easy trip at any time of the year, too hard to get to, can be inaccessible in winter and I have no connection with the doctor there. I’m sure he’s a genius like the rest of these guys, but I like feeling like the people in charge of my life care. So we’ll see.
I switched therapy to be twice a month since (at least up until this weekend) the LexaPro was having a significant impact. The timing of that, as well as the rest of all of this shit, is really making me feel like there’s some force out there taking a direct interest in fucking me over as much and as insidiously as possible. I just don’t get it.