Chemo #2
You healthy people don't know what you're missing! In the infusion room, they give you blankets straight from the warmer, and volunteers come around and offer to massage your hands or feet. And they have board games! Last time, Jeff brought over Risk (it was covered in dust) but I made him swap it for Yahtzee. I may have terrible luck with medical stuff but I have amazing luck with the dice. It's always a celebration when you manage to beat Jeff at anything.
So what exactly happens at chemo? First a nurse accesses my port and takes a blood sample. Then the doctor or nurse practitioner takes my vitals and reviews my symptoms, and we agree that I still have cancer. As soon as my white blood cell count has been reviewed, I stop by the in-house pharmacy and take a very expensive anti-nausea pill that Jeff spends five minutes removing from the impenetrable package. I take a seat in the infusion room, and a nurse gives me saline, steroids, and the first chemo medication. Then the last chemo medication is manually injected into my IV; it's fire engine red and turns my urine the color of cherry Kool-Aid (and supposedly my tears as well). They disconnect me and I'm sent on my merry way. The whole process takes about four hours.
Then the fun begins. Nausea. (The medications keep you from vomiting, but I did have to resort to rubbing lemon slices under my nose last time.) Bone pain from the Neulasta (I wear a needle patch on my stomach that injects me the following day to boost my white blood cell count). Fatigue. Stomach cramps. Thrush. Dehydration. Low blood pressure. I fainted while getting labs drawn last week, and suddenly I was lying on the floor with an emergency response team crowded into the phlebotomist's office. Now whenever the phlebotomist calls my name in the waiting room, she yells, "Oh no! Not you again!" My legs gave out once at home, and my mom panicked and bought me a beautiful teak shower chair that Jeff now uses as his toothbrushing bench. I also fell backwards into the bathtub two days ago, but I attribute that to clumsiness rather than the chemo. I have yet to experience mouth sores or neuropathy, but there's always next week. Chemo brain has also taken hold (similar to Mom brain), but I've been assured that it will improve in a few years if I do Sudoku regularly. And of course, hair loss. It's easy to spot the newbies.
Two down, fourteen to go!
So what exactly happens at chemo? First a nurse accesses my port and takes a blood sample. Then the doctor or nurse practitioner takes my vitals and reviews my symptoms, and we agree that I still have cancer. As soon as my white blood cell count has been reviewed, I stop by the in-house pharmacy and take a very expensive anti-nausea pill that Jeff spends five minutes removing from the impenetrable package. I take a seat in the infusion room, and a nurse gives me saline, steroids, and the first chemo medication. Then the last chemo medication is manually injected into my IV; it's fire engine red and turns my urine the color of cherry Kool-Aid (and supposedly my tears as well). They disconnect me and I'm sent on my merry way. The whole process takes about four hours.
Then the fun begins. Nausea. (The medications keep you from vomiting, but I did have to resort to rubbing lemon slices under my nose last time.) Bone pain from the Neulasta (I wear a needle patch on my stomach that injects me the following day to boost my white blood cell count). Fatigue. Stomach cramps. Thrush. Dehydration. Low blood pressure. I fainted while getting labs drawn last week, and suddenly I was lying on the floor with an emergency response team crowded into the phlebotomist's office. Now whenever the phlebotomist calls my name in the waiting room, she yells, "Oh no! Not you again!" My legs gave out once at home, and my mom panicked and bought me a beautiful teak shower chair that Jeff now uses as his toothbrushing bench. I also fell backwards into the bathtub two days ago, but I attribute that to clumsiness rather than the chemo. I have yet to experience mouth sores or neuropathy, but there's always next week. Chemo brain has also taken hold (similar to Mom brain), but I've been assured that it will improve in a few years if I do Sudoku regularly. And of course, hair loss. It's easy to spot the newbies.
Two down, fourteen to go!
That pill package is awesome! It's not actually that impenetrable, but it's just so cool to play with! I think the packaging engineer's boss was out that day, and this guy just put in every thing he'd ever dreamed a package could have. Probably because this one pill is so expensive, which is why they won't give you more than one at a time from the pharmacy. I'll try to get Jami to post a picture of it next time (it's in the trash right now; ew, cancer trash).
ReplyDeleteBy "accesses my port" she means "stabs a needle into the cyborg docking port to my heart".
Jeff, you’re kinda a nerd, cyborging and all. But me too!
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ReplyDeleteI was wondering if you would be in a room with other chemo patients, or in a room by yourself. Bob was with a group, but my friend Martha was in a little private room. I think the group setting is nicer. A little warmer and more supportive. Not that there was a lot of chatting going on.
ReplyDeleteI really admire you guys...the way you make sure that the girls understand as much as possible and are not too freaked out by the whole process. It's good to include them.
Crappy that just when you start to feel better it's time for another dose.
MLM
I like being in an open room. The young guy sleeping in the chair next to me was strangely comforting last time. And there's an older fellow who got to watch us play Yahtzee last time who always waves hello.
DeleteBalding super sadass Dad says you are a superhero badass Mommy and person. Your Mom is a superhero Grammy. She does the heavy lifting with the kids. Pop Pop is there for moral support for her.
ReplyDeleteThanks super sad-ass Dad. :)
DeleteThe needle patch... is that some sort of torture device?
ReplyDeleteBasically. It sticks a tiny catheter in your stomach and injects you with medicine 27 hours after receiving chemo. It beeps at you when it’s injecting. Then you just pull it off and throw it away. Saves you a trip to the doctor’s office.
DeleteI love that you are keeping your sense of humor fully alive! "We agreed I still have cancer." LOL! Love you!
ReplyDelete