February 2, 2021

Happy Groundhog Day! Do you feel like you’ve done this day before? #covidlife Today was a repeat day for me, too. Chemo treatment #3 in the books!

Patrick got the shoes in the picture!

As I mentioned before, I decided to dress up a bit for these appointments. This time, I wanted to wear a new pair of boots, so of course, it called for my purple wig. I questioned my choice when I sat in the waiting room getting side-eyed by my elderly cohorts. I didn’t want to make anyone uncomfortable. But every nurse said they loved it and even my oncologist, when he entered the exam room, exclaimed whoa! and said he thought it was great. Not that I needed anyone’s approval, but it was nice to get the reaction I was hoping for—a smile.

I’ve had so many family and friends supporting me lately by reaching out in a variety of ways, even friends I haven’t necessarily kept in close contact with. (Thanks, social media for keeping us connected!) It hit me today I’m not always so good at doing that for others. It’s not that I don’t care, but I feel self-conscious reaching out blindly. I’ve always been more comfortable listening or watching in groups and will typically interject myself only when someone asks me to. I figure, why will they care to hear from me? I don’t know what to say/do. Social media makes it easy because we can just use an emoji on a post and call it good.

But you know what? Being the recipient now, I can clearly see it does make a difference. It’s always nice to get a message when you’re going through a difficult time. It’s ALWAYS uplifting to know people are thinking of you and wishing you well. I’m grateful every time.

I like when I can make someone smile, so why do I allow myself to hold back? I’m willing to wear a silly wig, but I can’t send a short message when someone needs it? I’m thankful today for this reminder to be better. I’m going to add it to my to-do list. Maybe like Bill Murray’s character in the movie Groundhog Day, becoming a better person will get me out of this #Covidlife we’re stuck in. Wouldn’t that be great?

January 5, 2021

You guys! I wish I felt like celebrating. I am happy to report that today is day one of my cancer cure.

I had my first chemo treatment. I’m not going to lie; I was nervous. After almost two hours of blood draws and port flushes and anti-nauseous drips that took over half an hour to administer, my nurse, Sister Rose, came back into my room in a special blue gown. She donned not one, but two layers of gloves, and then proceeded to handle the chemo drugs that had been specially made for me when I arrived. The first ones were red vials. She said she had to manually push them into my port IV because she needed to periodically check the blood draw. This stuff is what is sometimes referred to as the red devil. I told her it looked like jello shots. While she laughed, I suspect she said an extra prayer for me today. After two vials of the stuff, I got another IV bag drip of a different kind of chemo. Both have similar side effects: nausea is top of the list, hence all the extra drugs; low blood counts, so I’ll go in tomorrow for a booster shot to help produce white blood cells; fatigue (already feeling it!); cardiac damage, which is why I had a heart test prior; and hair loss (my crowning glory!). There are of course a myriad of other things, like skin rashes and mouth sores and extremity numbness/tingling, that may come along.

Me in the home stretch. I was so glad not to have to wear that mask the entire time!

But honestly, right now, I’m just thrilled to have made it through. So far so good. I entered a clinical trial for added nausea medication; maybe I got it, maybe I didn’t. Either way, things are working. I’m tired but I’m now 1 down, 15 more to go. And I’ll handle things day by day, grateful for a cure.