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April 26, 2022—Driving home from the West Cancer Center, I changed the car’s Sirius Satellite to Lithium, which is a channel dedicated to grunge and other alternative music from the 1990s. I had a pretty good morning, even for being at a cancer center. The CT scan showed no significant changes in my tumors and my lab work showed that my body continued to tolerate the immunotherapy treatment.
The song that popped up on Lithium was Praise You by Fatboy Slim—a short, upbeat tune with very few lyrics. If you’ve never seen the award-winning video, it’s essentially a low-grade recording of a flash mob performing in front of a crowded movie theater in Los Angeles.
We’ve come a long, long way together
Through the hard times and the good
I have to celebrate you,…
I have to praise you like I should
As I listened to those short and sweet lyrics, however, I was struck by their meaning related to my relationship to those of you who have followed and continue to follow my melanoma journey.
To praise means to express warm approval or admiration of someone or something. So, I want to express my warmest approval and admiration to everyone. Your love, support, kindness, and caring have meant the world to me (and to Vicki and our family). I simply can’t put words around how fortunate I have been—and will continue to be—because of all of you.
I have to praise you
I have to praise you
I have to praise you
I have to praise you like I should
In other words, Thank you.
Melanoma Treatment
Decent CT results aside, I will continue on immunotherapy (Keytruda) at least until October of this year. The protocol is for a treatment period of two years—I began Keytruda on October 1, 2020. Treatment options for late-stage melanoma are changing almost daily, so once we reach October, we’ll have to see where the journey next takes us.
Emily’s Car Accident
I’ve been reluctant to post much about Emily’s car accident, which happened at the end of October 2021. Part of that is out of respect for Emily’s privacy and part of it is that we continue to deal with the aftermath of that terrible day, which remains—for us—an almost surreal experience.
The bottom-line is that Emily has mostly fully recovered from her injuries, and she finished physical therapy earlier this month.
Thanks to those of you who continue to ask about Emily and who have offered support and encouragement. She greatly appreciates it.
Travelin’ Man
Vicki and I are back to traveling on a regular basis—although we did a bit of traveling during both 2020 and 2021. We love exploring new places, visiting old haunts, and discovering great places to eat and drink. Thanks to everyone who comments and “Likes” my travel posts on Facebook. As Bob Seger once sang:
Out to the road, out ‘neath the stars,
Feelin’ the breeze, passin’ the cars
Those are the memories that make me a wealthy soul
That said, I am working towards writing more and more travel pieces for StoryBoard Memphis and other local and regional publications. Travel is a tough market to break into, but writing about travel is something I enjoy doing. Wish me luck.
And That’s a Wrap
This will likely be the last blog post directly related to my melanoma journey. Other writing priorities, along with my advocacy work, have taken a greater amount of my time. Also, the amount of internet traffic to my new webpage has dipped significantly in the last several months. Frankly, it’s easier/simpler to post a brief health update to Facebook, which also doesn’t require as much reading or screen time for you.
As I mentioned above, more of my writing will center on travel and travel-related subjects. You will soon see updates to my Facebook writer’s page from the Travel section of my website.
Thanks, once again, for your love and support.
And as always…thanks for stopping by to listen.
June 11, 2021— For centuries, the number thirteen (13) has been considered unlucky, which developed an irrational fear of the number and anything associated with it. Some historians trace the stigma of “13” back to Judas Iscariot—think Last Supper—the biblical betrayer of Christ. Others note the fear may be attributed to October 13, 1307 when the Knights Templar were rounded up and imprisoned—or worse.
That date fell on a Friday, leading to the Friday the 13th superstition, along with a series of really terrible horror movies in the 1980s and 90s.
On Thursday, June 10th, the date of my 13th infusion, we received some good news—some really good news: my tumors have shrunk anywhere from 10% (in my lungs) to 20% in and around my right adrenal gland.
Vicki and I were ecstatic. Now, after almost nine (9) months of treatment, Keytruda (my immunotherapy medicine) was beginning to turn-the-tide in the battle against my metastatic melanoma.
In addition, my oncologist told us that my lab work looked fantastic. The results, in his words, were like a “normal person’s.” I assumed he meant someone not undergoing cancer treatment.
While this is great news, we still have a long way to go. Thursday’s CT scan was the first one I’ve had since February (which showed no change), so, for now, we’ll continue immunotherapy treatments and monitor my blood work.
Even with all that good news, it was a bittersweet morning. My oncologist announced that he’d taken a new position—heading up a cancer center in Reno, Nevada—and would soon leave the West Cancer Center. While we’re sad to see him go, we know we’ll be in good hands with a new oncologist.
In a weird coincidental twist, on Wednesday (June 9th), the West Center posted my melanoma journey story to their Facebook feed and on their website.
I received several FB comments of encouragement and support from strangers who are either West Center patients or their loved ones. As I wrote in a recent essay (see below), my goal with continuing to share my story is to provide hope and/or inspiration for others fighting cancer.
With Good Fortune Comes Greater Responsibility
So, after Thursday’s good news, my good fortune continues. I write that not with glee or contentment. I write it (repeatedly) to remind myself that there is so much more work to be done. So many goals I want to accomplish. So many people I want to help—directly and indirectly.
On June 4th, StoryBoard Memphis published my latest personal essay, Happy Birthday, Spiderman. While the initial focus of the essay was about my birthday and the joy I feel celebrating another trip around the sun with my family and friends, it was also much more about the burden I carry—like many other cancer survivors—to never forget those who were less fortunate. Here’s a quote:
Sharing my journey story is both cathartic and purposeful. Those of us who are still in this fight remember all those who were less fortunate. Our grief and frustration are channeled into meaningful causes and activities. Ultimately, we want to change current behaviors, raise awareness, and stem the tide of suffering and pain.
I use my good fortune to help others whom, like me, have been saddled with this dreadful diagnosis. An advocate for skin cancer prevention and melanoma research, I volunteer with non-profit organizations by fundraising, lending my voice through personal testimonials and op-ed columns, mentoring other late-stage melanoma patients, engaging congressional staffers on the merits of upcoming appropriation bills (to fund more research), and, finally, by analyzing research proposals as a patient member of scientific review panels.
In my own words? With good fortune comes greater responsibility.
When you get the opportunity, go back and the read my story—either on Facebook or on StoryBoard Memphis. Thanks.
And, as always, thanks for listening.
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March 13, 2021— It’s been a week…man, it’s been a week. As many of you know, I love blues music, and this week has been one continuous blues song—full of highs and lows, and just about everything in-between. The theme of this post is dedicated to that legendary Mississippi Delta bluesman who made Chicago blues an international sensation: Muddy Waters.
Like Muddy’s iconic song, Rollin’ Stone, this week had me back, back down the road I’m goin’. In other words, every time I moved forward, I seemed to move even farther back.
Monday I received my first Pfizer vaccine dose. I posted on Facebook that the process was fairly quick and well-organized. In fact, Muddy was there to accompany me (see bottom photo). I’m glad to be closer to being fully-vaccinated and, hopefully, safer from the coronavirus.
This week I started a new writing gig for StoryBoard Memphis. I now have a recurring column, currently titled Time Capsules. I’ll focus on personal essays, stories, and observations/commentary. My first column (Time Capsule) was published on Thursday, March 11th.
I’ve written several pieces for StoryBoard, and I’m excited about the opportunity to continue developing and improving my craft. In addition to the new column, I have two short stories that will be published (hopefully sooner than later) in a local mystery writers anthology.
Deja vu all over again—Warning: Yucky picture!
It was a little more than a year ago (see Don’t Believe the Gripe) that I had my ninth melanoma removed. Yes, nine melanomas! The 9th melanoma (in situ) was on my upper right ankle.
It’s not only been a heck of week, it’s been a hell of a year!
Thanks, as always, for listening.
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After confirmation that melanoma had spread to my right adrenal gland, we were faced with a couple of options: remain on Gleevec and receive radiation therapy or try something new – immunotherapy (described below).
Waiting on treatment. |
Initially, we opted to try radiation therapy. The idea was to target the adrenal gland, which would be – we assumed – less invasive that starting an entirely new regimen. After meeting with the radiation oncologists and consulting with some other folks, we decided against that route. There were too many outcome variables and too many negatives (potential damage to surrounding tissue and organs).
We just couldn’t get comfortable with that option.
Up until we left on our Blue Ridge vacation (see Facebook), we continued to struggle with our first option. Several online consultations, emails with others in the melanoma community, and, simply, time to reflect brought us to a new decision: no radiation therapy, stop the current oral chemotherapy, and start immunotherapy once we returned from vacation.
I feel good about the decision. Vicki feels better about the decision to go with immunotherapy. And our oncologist assures us that if immunotherapy doesn’t work, we can always go another route.
According to the American Cancer Society, immunotherapy medicines stimulate a person’s own immune system to recognize and destroy cancer cells more effectively. Several types of immunotherapy can be used to treat melanoma.
Immunotherapy medicines are given intravenously, so that’s another turn in my treatment. Today, I started Keytruda (pembrolizumab), which will help my body fight the melanoma without destroying any existing, healthy (normal) cells.
A new turn in my journey. |
Another positive aspect of our decision is that Keytruda will also fight the tiny melanoma tumors in my lungs. There’s no guarantee that they will be completely gone, but our hope is that they continue to stay small, or even shrink a little more.
Thanks, once again, for your thoughts and support. We truly appreciate it. As my treatment journey continues, there will likely be more frequent updates.
Everyone should have a view like this. |
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August 28, 2020 – Earlier today, Facebook alerted me to a memory from 2017. I’d almost forgotten about the post until today’s notice. What I haven’t forgotten, unfortunately, was the crappy comment that came from a former high school classmate.
Note: Yes, on Facebook yesterday, I mentioned the fluke that this 2017 memory popped up right after Hurricane Laura came ashore in Louisiana.
After Hurricane Harvey hit Houston, Texas. |
extended family, I posted our thoughts on my Facebook feed.
I received the typical Facebook feedback (see below) – Likes, Loves, and a couple of shares.
One person, however, had to rain on my goodwill. I realize it’s a minor thing – especially with everything going on right now in our world – yet, three years later, the comment angers me.
Never did hear back. |
One of the definitions of “thinking” is that of thoughtful reflection. In fact, another definition states that “thinking” (as a verb) is to employ one’s mind rationally and objectively in evaluating or dealing with a given situation. So, I’ll continue “thinking” about those of you in Texas and Florida who are dealing with the aftermath of hurricanes and floods.
I will also continue to hope that everyone’s situation improves and that they do not face long-term problems. I will use my words on MY Facebook feed. You are free to use your words on yours.
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