Chemo Round 5

Holy moly what a difference a new chemo drug makes!

This round was the first of the “second leg” of my cancer treatment tour, if you remember. The first “leg” was an A/C drug (don’t ask me to spell them right now). There were four dense dose treatments (in other words: super potent, crippling doses). The reason for this new drug (and up to 12 rounds of it) is because while the A/C treatment is super powerful, we want to make sure all the cancer cells get blasted.

You can think of cancer treatment as a sort of war on cancer. Each treatment type is a different branch of my cancer-fighting military. Surgery was the first surge. It wiped out what we hope to be all of the enemy. We wanted to be sure, so we sent in the second branch: A/C treatment. While chances are, those drugs got anything remaining, research shows that coupled with my new drug, Taxol, the eradication of cancer cells is even more successful. So Taxol is the newest branch of the cancer-fighting military we are sending in. The last will be radiation.

I got my back to school hair cut the day before treatment (it’s not actually growing, but it was looking patchy. It’s even shorter now)

The difference in side effects is almost inexplicable. A/C treatment made me feel like I was dying about 24 hours after treatment. It felt like I would never feel better again.

Before infusing the Taxol, they loaded me up with antihistamine and Benadryl (because pretty much everyone is allergic to Taxol–it’s an irritant. I got quite loopy from that, naturally. Then they pumped in the drugs. I had zero reactions, so I may be able to go lighter on the Benadryl next time.

The side effects are still hair loss (see that picture above), and sometimes nausea (I didn’t have any), low blood counts (because it’s attacking fast-growing blood cells), and mouth sores (none of those yet either). It can also affect my nails and give me joint and muscle pain. The only irreversible side effect is peripheral neuropathy, which means loss of feeling in my fingers and toes. That one they monitor super closely because they can adjust the med or skip one altogether to reduce that happening if I start to notice tingling. That is really my biggest fear.

Anyway, I got home Wednesday and took a nap while the rest of my crew headed up north to spend a long weekend with my parents at a cottage they rent with us each year. When I woke up, I felt great! So different then A/C treatment! I was refreshed and actually worked on school stuff Wednesday evening!

Thursday I woke up and packed myself up and headed to the cottage!

Grandpa and Grandma play some cards with the boys.

Saturday I even went to the beach! This is the first (and probably only) time I have been able to sit on the beach all summer due to my treatment. Chemo makes my skin SUPER sensitive to the sun. Cortney bought two SPF 50 beach umbrellas, I had my SPF 50 hat, plus I slathered in SPF 50 (twice because I reapplied) for the two hours we were at the beach, and I still walked away with a little coloring.

But it was worth it!

The kids could have stayed here all day! (Also isn’t my mom the cutest?)

She would not go near the water without her daddy.

She has mastered the art of relaxing on the beach…just like her mom!

See? Proof I made it to the beach this year!

Even though we couldn’t hit the beach for the entire time we were there, the cottage happens to be on a small, inland lake and the boys had almost as much fun swimming at the end of the dock.

Charlie and his popsicle “floaty” tricks

Eddie and his clowning!

I would say I spent most of the time in the shade near the cottage with my book or watching everyone play, but it made me feel like a real person doing real summer things to be able to even go. With the A/C treatment this weekend would have been impossible right after a round of chemo. I would have been comatose all weekend.

Yes, I still got tired quickly and sat down a lot, but I was there to watch my goofy kids have all the fun and live their best lives.

I don’t even know. These two were nut jobs the entire weekend.

And of course, to round out the weekend, my dad took us all out for huge ice cream cones for lunch on Saturday. Because is it really vacation if you don’t have ice cream for at least one meal?

I am so so so SO thankful for this new drug. I hate that I have to go through any of it, but since I do, feeling more like myself is the way to go.

I will be getting Taxol infusions weekly on Wednesdays until October 24 (we are hoping to get in 12 rounds total).  Please pray that my body keeps handling the meds well (my doctor told me that after all the A/C treatments, my blood counts were so good, you couldn’t even tell I had been on chemo! Keep doing that, body!)

This is my final week of summer before I go back to school (Eddie and Charlie still have three more weeks until their district goes back), so please pray for my anxiety and for my students as they get ready to have an English teacher who is out ever Wednesday and dealing with, well, cancer treatments.

5/16 done

Related Posts Plugin for WordPress, Blogger...