WELL I CERTAINLY HOPE SO.
I keep being told it will be worse before there’s a chance of it getting better… I’ve had quite a bit of proof of the first portion of this statement, now I will have to practice my patience and good faith for the second.
MIBG, NOT my favorite treatment.
So far we have not gotten along so well you could say… I’ve been meaning to update everyone since my last appointment and share what I know so far. Except I really haven’t been well, and I had a pretty big dose of reality lately.
As much as I like to share when things are on a positive note … Well, the reality is, living with this disease is often dark and all consuming – although I AM bright and try to find the good in everything despite this constant torment, there are times when I must be candid and speak through my pain and suffering. I’ve actually been telling myself, “I’ll wait until I feel better to update, I’ll wait until I have something good to share” until I realized… That isn’t how MY life works, I wish I had the luxury of blocking out all of the bad and fast forward until I had something good to hear, or skip over all of the parts where I suffer and wait until I feel better…
I also know that nobody else expects that of me, so here I am, sharing the in between with you, I may even throw in an f bomb if you’re lucky. That’s how angry my pheos are, yes I’m blaming any profanity on the tumors, they’re really being assholes. MIBG has got them all kinds of angry… Let me just tell you. Ok, where do I start?
So it’s been 22 days since I had MIBG radioactive iodine injected into my blood stream, 22 days of radioactive pheo cancer hell, 22 days of worsening symptoms, and every day is a new adventure. Rather than get better, I get worse. See how fun that is? I thought the idea was that you get better as the days went on, most people do, NOPE. My symptoms get stronger, more aggressive each day, it’s super awesome. I like the spontaneity and danger of it all I guess, who wants to wake up and be normal for a day? How boring. (I would also like to be excused from any and all sarcasm, I’m going to blame the excess of Catecholamines (adrenaline) being made by my angry tumors, thereby making me very sarcastic… I think too much epinephrine and norepinephrine makes people very sarcastic) Science. YES! Science.
We went to my last appointment with some expectations and no expectations: I’ll explain.
Some expectations meaning… We thought we were going in to do a day of tests, and meet with my pheo Doctor, and have an idea of how the treatment was working so far. Since I was doing another MIBG scan, 2 week blood work, we were under the impression that we would be seeing how the treatment was taking.
What I meant about having no expectations? Well, I didn’t want to get my hopes up, so when nuclear medicine told me I would be having a MIBG scan 2 weeks after my treatment to see how I was doing, I didn’t want to get too excited about results, so I remained neutral, and said to myself “I’m going to go in with no expectations, that way I can’t be disappointed”
It was the first time I had left the house since treatment, it was an incredibly hard day. We drove out normal 3 hours to the hospital. The scan was long, painful, with the way I feel it’s so hard to do just about anything…Being scanned for 2 hours is not ideal, Laying with my arms above my head for 52 of those minutes isn’t at the top of my list. Then I gave blood, and then I waited to see my doctor to discuss the results of my blood, and maybe the scan.
We then saw my doctor, and at this point we realized there was a misunderstanding, the scan wasn’t being done to see how the treatment was working. It was actually being done to take advantage of how much MIBG radiation was in my body, and the MIBG scan was being done at this time to find any MORE cancer that’s potentially in my body that otherwise would not be picked up normally in regular circumstances with trace amounts of MIBG. NOT what I was expecting…. Good thing I had no expectations LOL. We went from thinking we would hear how the treatment was working, to hearing they were looking for MORE cancer.. So, not in any rush for those results. Moving on!
So once we got that misunderstanding out of the way, we then of course asked when it would be that we would find out if the treatment was working or not, since it was clearly not now. It turns out it won’t be for a while, it’s a long process, a few months. We will revisit this in a couple months, maybe at that point we will start having an idea if the treatment is lessening the output of adrenaline the tumors are having.
The main priority over the next few months is just constant monitoring of all of the other complications that could potentially happen from the treatment itself, and making sure my bone marrow doesn’t deplete, I don’t get any infections, my tumors don’t kill me from all the adrenaline they are producing, and we control all of the worsening symptoms and side effects being caused. Easy peasy.
It’s a long process, I will be feeling like this for a long while. I knew that, but it’s hard to know what to expect until you’re in the situation. Surgeries are the most difficult things I’ve had to endure, but I’ve known what to expect once they’re done, this is so different, because not only is every day a surprise … I also can’t know if it’s even worth doing in the end.
It seems like every couple days we are increasing all of my medications to try and control my vitals, to keep me out of the hospital, and despite these efforts… They’re still out of control. I literally have left the house once since I have been back, the stairs are a danger zone, getting up too quickly is a danger, going to the bathroom is a danger, showering is a HUGE danger, breathing too hard is a danger.
It’s not as if I am doing anything at all to provoke these episodes, I cannot cut down my activity level any further… Existing is and breathing is all that is left lol. When you are told to stop showering, because it is a danger to your health, it is quite frustrating.
I can be sitting in bed doing nothing at all, and when these new “MIBG spikes” is what I’m calling them – happen, it feels like my heart is being dredged in cement suddenly, and it takes everything it has to beat… It hurts so much, each beat is accompanied by a very unique pain, and my head is filled with pressure, so much that my eyes feel like they’re going to pop out of my face, my chest is filled with pain, and it feels like I am having a heart attack. This lasts for a few minutes, and then I’m so very fatigued… And nauseous, I feel I could sleep forever. Except then I am plagued with insomnia later at night. I’ve had plenty of pheo attacks, I still do, except this is above and beyond those, it’s the effect of my blood pressure sky rocketing while my tumors release a dangerous amount of catecholamines from the MIBG treatment. The problem is that … my medication continues to be increased, which should lower this, except this continues to actually go higher and higher, NOT supposed to happen. So I will continue to do nothing, relax, and just endure this vicious assault MIBG has on my body, because what choice do I have? It’s scary knowing that every time this happens, thinking about the damage it has on my body, I try not to think about those parts, I try to remain naive to that, you can only do that for so long though.
I will continue to be closely monitored, AND I decided while writing this…. The good I am taking out of this so far, is … My bone marrow is good so far!!! (YAY) for strong marrow results, that’s good right? SEE, I knew I’d find a positive in there, f*ck you pheo. I also found an f bomb, HA. I will continue to go every 2 weeks to do blood, make sure I’m alive, check my cell counts, make sure my thyroid is functioning… And all of these other great and scary things. SO MANY COMPLICATED FUN PUZZLES! So….. Let’s hope I can stay out of the hospital between then, yes?! Today was A SUPER CLOSE CALL, crisis level was high in the Simard house, Doctor Serge to the rescue as usual, formally known from now on as doctor cupcakes (lol) – when in doubt… Just prescribe cupcakes. Words to live by
Hm what else…. Oh! The taste of eating batteries has calmed down a bit also, that has been a welcome change! It’s not quite as strong. Yes yes more good news! See, as I continue, I find more good. So yes even though the adrenaline, heart, blood pressure, vital elevation attack side of things are worsening …. The taste of batteries has decreased and my blood work was okay so far, SOOOOO there’s a bit of a bright side. Now we just have to make it through the next 6 months or so of this, and we are smooth sailing.
The last time I put on makeup was Christmas, a random thought I know, but it is strange not physically being able to do anything.. Especially things that were once just an everyday routine for me, now they are a “luxury” Now since I am barely allowed to shower – or closely monitored when doing so because it is my most dangerous activity, (you should see the calories my Fitbit claims I burn just by breathing) 😂 I’m gonna get really crazy and say… I really would love to be able to be normal and plan a vacation, or EVEN just go out for dinner one night, or actually just do anything at all.. At this point I’d like to just be able to walk up or down the stairs without my body imploding. I would like to be able to go a day without my body attacking itself while doing nothing. So I will say this, I’d like to be able to soon be well enough to just .. Have a day where I can feel good enough to just leave the house, change my surroundings, and feel like my normal fabulous self for even just a few hours. This is me being realistic with my expectations, I will find a way to be FAB… I always do 😉💋
Day 22, I pray this disease will become a little more manageable – because nobody should have to fight this hard.
I promise to update as my body allows, but for now…. It is tired xox
Pheo VS Fabulous