Chemo infusion #2

I started off yesterday with a blood draw — this is a standard first step for all chemo infusions. I was happy to see that all looks stable with my white blood cells and complete blood count (CBC), no concerning drops from two weeks ago.

Next, met with a member of my oncologist’s team, a PA. Very jovial, exuberant fellow, he immediately announced his amusement with how I had filled out my pre-visit questionnaire. Its first question is: “what is your primary objective in today’s meeting?”

My answer, in large, underlined letters, was:

REDUCE STEROIDS!!!

He came in laughing an “oho, I’ve got a feisty one!” laugh, and he said “ok, we need to frame this one. This is hilarious!” I didn’t find anything funny until he explained yes, no problem, they can cut the steroids in half, given the fact I didn’t really struggle with nausea during my first cycle. I guess my very direct comment stood out as something unique. So, that was great. Reduced steroids = less crazy = more sleep.

Things then got a little exciting during the oxaliplatin infusion.

Oxaliplatin is the part where I do the icing thing; wear mitts and gloves with ice inserts, and suck on ice chips. Sarabeth was with me during this point and helped with the logistics here — it’s a lot to juggle! During the oxaliplatin, I felt the chemo fatigue and brain fog settle in. A nurse came by to check on me, and when I wasn’t really able to clearly articulate how I was doing (a problem I’ve had before), the nurse got concerned and started asking me more specific “do you feel” questions. I answered yes to chest pain, because I had felt some minor tightness around my port, and that got him concerned. He called in others (a sort of roving urgent care squad, I believe) who asked to give more details, a 1-10 scale, etc. I thought I conveyed a low number, that it was minor, but they decided to give me a Benadryl shot.

Benadryl catapulted me into a nightmare of anxiety — which I guess is not a common reaction (they told me it would make me feel drowsy). I felt dizzy, my heart was racing, and I felt like I almost couldn’t control myself from bolting out of the room. It was a terrifying sensation. When I explained this to them, they then decided to give me ativan (lorazepam), which fortunately calmed me down very quickly.

The next infusion is irinotecan, and I didn’t notice any side effects or additional trouble during that one.

The great news is that I slept well last night. I think the 1/2 reduction to my steroids definitely helped here. Also, as I was still feeling the Benadryl effects as I went to bed, I took another Ativan (they gave me a prescription) and that likely helped with sleep as well.

Today, I’ve been doing ok, all things considered. I was able to make up a smoothie this morning, had that for breakfast. Appetite has been fine. Certainly fatigue, first bite syndrome, and some odd throat sensations when I swallow, but that’s about it today. Hoping for another good night’s sleep tonight.

6 thoughts on “Chemo infusion #2

  1. “See, we’re going to put this cozy mittens on you, but fill them with ice! Oh, and here are some ice socks too!”

  2. Ice filled mittens and booties, not cool! And then all those drugs to offset other drugs. Have they said if THC might help with any of the various side effects?

    • I think there is a general understanding at cancer centers that most patients are using cannabis products to ease chemo symptoms, but they seem conflicted on how to speak about it. I certainly find gummies (1/2 CBD, 1/2 THC) to be very helpful for dealing with chemo, and I’ve been open about that with my care team. Their reactions are neutral in that area.
      This is where I lean on my online community (Colontown – an amazing resource for colorectal patients and caregivers). Plenty of detailed discussion in there about cannabis, with logistical tips, etc

  3. Pingback: Infusion #3 | foiblish

  4. Pingback: Expanding the diet | foiblish

Leave a reply to Doug Cancel reply