Socking It to Cancer: In Praise of Silliness

Yesterday the Book of Faces kindly reminded me that it was two years ago to the day that I kicked off (hee hee) wearing silly socks to treatments as a way to cheer myself through the process. I had been diagnosed with my first recurrence at the time and was beginning a six-week-long course of daily weekday radiation treatments, alongside which I also took a chemotherapy pill. There was plenty of opportunity for lots of silly socks!

The sock idea was serendipitous. The ultrasound that revealed the cancer took place in mid-December, and I’d just found a pair of Christmas socks that made me giggle–black and white cats wearing red scarves, their faces positioned so that they could peer over the tops of your boots, with little shaped pink ears for accents. The few pairs of silly socks in my bureau at the time were either cat- or holiday-themed (sometimes both), and though I’d never really warmed to the trend of wearing novelty socks as a visible fashion statement, the prospect of peekaboo cats made me smile at a time when smiles were in short supply. So I bought them and donned them and posted a photo (pictures or it didn’t happen) while we were waiting for test results.

Peekaboo kitties

It wasn’t until I received a package with three additional pairs of silly socks from my mom, though, that the idea of wearing silly socks to treatment really took root. She’d seen some colorful happy face and floral socks at her local drugstore and thought them cheerful, so she packed up three pairs with an encouraging note and sent them to me. The lavender in the happy face socks matched my radiation mask, so I decided I’d wear them the first day of treatment.

The lavender smileys faced my direction, too!

Then, I started thinking more about socks: how most people wear them most of the time, but they’re often covered by shoes or boots or pant legs. Present, but invisible. That got me thinking about how so many people face challenges–illness, loss, pain, grief–that are invisible to others. Wearing silly socks seemed a way not only to cheer myself up throughout treatment, but also to honor the unseen battles so many others face daily. I decided to call them #sillysocksforstrength and invited others to join me in wearing their own silly socks, in honor of all those fighting battles unseen, on #funsocksfridays.

I was–and still am–overwhelmed by how many people wore socks on Fridays, and even more so by the many gifts of socks I’ve received. I think I may well have the best curated collection of silly socks anywhere! My collection is wide-ranging. It includes lots of cat socks, both with and without messages. Next in the sock drawer are the other animal socks, bird socks, ladybug socks (my family nickname), and magical creature socks (yay for unicorns and mermaids!). Perhaps unsurprisingly (and a little embarrassingly?), I have an arts and literature category. Then there are the role model socks that feature people like RBG and Wonder Woman, cheeky message socks, bright florals and stripes, and socks for different holidays. I still wear silly socks not only to each treatment, but almost daily. The socks themselves make me smile, and the kindness and care they embody gives me strength.

I’ve also seen some of my friends gift silly socks to others they know who are having a difficult time, and it makes me happy to see the practice spread. I’ve gifted several pairs myself. In many ways the best part has been seeing other people have fun with their socks. Silliness is underrated, and I think we should all embrace being silly more often. It’s a tough world out there, and a little spot of joy on your feet is an excellent antidote.

Here’s to #sillysocksforstrength! May we wear them, may we share them, may we smile whenever we see them. Sock on, friends!

Good News, Good Medicine

We got some good news from my recent CT scan: the targeted chemotherapy drug sacituzumab govitecan hziy, otherwise known as Sasquatch, is working! The scan shows that the involved lymph nodes have shrunk significantly, 80 percent by my oncologist’s estimation. Some of them appear to be almost gone.

I have something called “stranding” and some swelling in my upper left chest and shoulder. The “stranding” is a kind of ropy tissue that they think is scar tissue from where Sasquatch killed cancer cells, radiation-induced fibrosis (RIF), or some combination of both. The same with the swelling–they think it is inflammation associated with the healing process, and/or lymphedema associated with fibrosis. As long as it doesn’t get worse, they aren’t concerned about it, especially since the adjacent lymph nodes have shrunk. It may be taking the drug a bit longer to work on some of the tumor growth in my skin, since both cancer and prior radiation have negatively impacted blood flow and the lymphatics there. Hopefully ongoing work with my lymphedema therapist will improve the stranding over time.

I believe in Sasquatch!

It is such a relief to get good news! I’m grateful every day that Sasquatch received expedited FDA approval when it did. For now, I’ll stay on the drug and continue with the same dosage schedule. My medical oncologist will get some more information about research into the efficacy of alternative dosing schedules when he (virtually) attends a medical conference on breast cancer in mid-December. After that, we’ll know more about whether and how we might change my regimen going forward.

Our silly kitties are good medicine too!

It was literally this same week last year when I had a punch-biopsy of my skin and then had to wait on the results. I was days away from a big 50th birthday celebration, and finding out the cancer was back for a third round was devastating. There won’t be a big party this year–just Steve and me at home, a small cake from my favorite local bakery, and a couple of Zoom calls with family and friends. But we’ll be celebrating this much better news, and that’s the best gift I could have hoped for!

Those of you who followed my CaringBridge blog (or are on my personal Facebook page) know that when I was diagnosed a second time, I started wearing #sillysocksforstrength to encourage myself and others who were fighting battles unseen. I still wear my silly socks, and these are the ones I chose for my appointment yesterday:

Fierce!

This third time around, I upped the game a little by adding a pair of combat boots. I still have mixed feelings about all the language of fighting and battles we use when we talk about cancer (you can read more about that here if you’re interested in my thoughts on the subject), but the various talismans of joy, silliness, and strength I’ve adopted buoy my spirits. So here’s to vintage hats, silly socks, and kick-ass boots–and good news and good medicine!