Wide Open Spaces

Writers need their words. We can’t be architects of a story without them. But once in a great while, numbers can speak too. They can paint a picture in a new way, offering the chance to break through to the reader in ways that words cannot. Sometimes numbers just pop.

I decided after looking at some recent news through this very lens that I would present a facet of a story, familiar here to readers, through numbers instead.

I’ll start with the number 5. My doctor told me last week that I have hit the 5-year milestone since my cancer diagnosis. In the cancer universe, this means that I have reached a marker where the risk of recurrence is significantly reduced. It also means that I only need to see both my medical oncologist and the surgeon’s nurse practitioner once a year now. It’s kind of a big step.

And after 5? The rest of the numbers are below. You may immediately wonder, “how did she calculate them?” It was actually easy, given that I am one to save my calendars well past their expiration date. (Yes, I still use paper calendars!) In no particular order, the numbers describe much of how I spent my time over the last 5 years.



Hearing stage 3 endometrial cancer.

2 surgeries–a hysterectomy and implanting a port-a-cath into a vein for easy infusions of any kind.

9 months before I completed treatment.

21 appointments with my medical oncologist. (blood/chemo)

18 appointments with the nurse practitioner for exams

29 blood draws

6 rounds of chemotherapy with 2 different drugs given on the same day in 2 sets of 3–one set in the winter and the other in the summer.

2 allergic reactions to Paclitaxel (a chemo drug.)

12 appointments with radiology oncologists.

1 mapping scan to determine the trajectories of the multiple radiation beams.

2 tiny tattoo dots added prior to radiation treatment (so the technicians knew exactly where to position me on the table).

25 days of external radiation.

4 days of brachytherapy (internal radiation) treatment (using nuclear medicine.)

11 pounds lost in 3 weeks from side effects of radiation.

Finding 1 wig and 4 headscarves.

2 endometrial biopsies.

1 cystoscopy.

1 chest x-ray.

2 stat kidney flushes (2 saline bags) and 2 appointments with a nephrologist after my kidneys started to fail.

6 oncology nurses in the infusion suite. They all helped during my 5–6-hour days there.

8 CT scans.

880 days living with a port under my skin near my left clavicle.

15 port flushes (this is a “cleansing” using heparin. It is necessary to prevent the port from clogging up. I returned to the suite every 5 weeks to flush it well after treatment was over. We needed to be a “go” if anything suspicious was found.)

1 port removal procedure.

6 months before my hair started to grow back. Twice.

And 1 loud, fist-pumping “hallelujah!” blaring inside my head as I walked back to the car last week.


Am I crazy to relive it this way? Not really. First, I remember most of it, anyway. Plus, I am proud of the strength I needed to use, and find, for some of it. I’ve absorbed it and it’s just a piece of my identity now.

And what felt like a ton of numbers, I can see now that the sum equals one. And that’s because it is one journey; one journey amongst one million. 10 million. Even more.

So, all of us celebrate that 60-month marker. We appreciate that the number 5 is based on science and its studies of recurrence. But for many of us, we are equally celebrating the gift of time.

And that is what I figured out after doing this collective math. These numbers broke it down for me, showing me how much a journey like this robs us of time, SO much time, for both the patient and the caregivers who love us. But that was the path.

I’ve gone from weekly to monthly to every 3 months and so on, but it is still a shock to see only two oncology appointments in 2025. There are no scheduled scans. There won’t be any chance of a pop-up x-ray or procedure referral after a scheduled appointment “just to be sure.” That has definitely happened.

The result is that I’m looking at wide open spaces on my calendar. I feel like I can gallop through the squares and days on that calendar untethered. And man, does that feel good.

Photo by Bich Tran on Pexels.com

34 responses to “Wide Open Spaces”

  1. Elizabeth Osborn Avatar
    Elizabeth Osborn

    Congrats

    Liked by 1 person

  2. Oh my goodness! There’s so much joy in this beautiful post, Melanie. I feel your philosopher’s heart coming through. Cheers to your good health! 🥰❤️🥰

    Liked by 1 person

    1. It has been a long haul from point A to Z (or let’s say Y) and the relief and JOY are palpable. It’s a strange world to come out of for anyone facing serious health complications. We have to put those realizations and emotions somewhere, hopefully, useful. Thank you so much for the good cheer, Vicki, and I will toast to that! 🥰🤗xx

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      1. I love how you captured the journey – your gratitude comes shining through. So glad to know you, Melanie! 🥰

        Liked by 1 person

      2. Thank you, and I feel the exact same way about you and all your positive energy, insights, humor and generosity, Vicki. I’m looking forward to a new post tomorrow. 😍

        Liked by 1 person

      3. Your latest podcast episode is a gem! I hope you’ll be pleased. Big hugs! 🥰🥰🥰

        Liked by 1 person

  3. Oh, cool! I know I will. Thank you, thank you. ❤️

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  4. What a milestone! Congratulations Mrs Banks! And I’m so pleased numbers fit into your blog so nicely.

    Liked by 1 person

    1. Hahaha, a loving reference to numbers can only come from you, Mr. Banks! I love that, and thank you. ❤️

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  5. Very interesting, Melanie! Congratulations on 5 years in remission. 😍😍 I’ve been in remission for 15 years. My chemo was to use five drugs for inpatient treatment. Now I’m interested to find out what my numbers look like.

    Liked by 1 person

    1. 15 years, Miriam! Wow. That is truly a blessing. And I can say that because I remember reading your book. You had extensive, even experimental treatment (5 drugs is one indication!) and the side effects were severe, if I remember correctly. You are in such a great place now! Congratulations as well! You probably could pull some of your numbers together, maybe from old bills you kept, or actually your memory too because some of those appointments are seared in our brains forever. Thanks so much Miriam! 😍

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      1. We should celebrate our remissions together, Melanie! 😍 I wear compression stockings every day because of the lymphedema but I’m thankful for life. 😊

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      2. That would be so great, Miriam! I wish I lived closer or you lived closer. 😍 Maybe we can just do it online. 💕 Yes, lymphedema was the complication you wrote about, it was difficult for you to walk. YOU are a warrior, Miriam. :)

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      3. It would be great to celebrate online, Melanie! <3 Which month did you completed you treatment?

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      4. It ended at the end of August. What about you?

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  6. After reading (and re-reading) this post all I can say is wow! 🤯! I’d venture to say that we all know someone that’s been diagnosed and treated for cancer but this post was a true insight into what a patient goes through physically. Throughout the entire process of treatment your life your plans your future comes down to all these “numbers.” While celebrating that great #5 year remission it must also seem a little weird to get off the treatment treadmill and onto regular life. Big transition! And one I know you’re embracing! Make those big plans. Live that big life! I am beyond happy for you and your family that you can celebrate that 5 year mark!! Best number ever😍

    Liked by 1 person

    1. Yes! I thought that using numbers might show some readers what is actually involved (although like you say, everyone knows someone who has been through it) but somehow, adding up and laying out the numbers can be an eye-opener…even to me. And yes, it is a (wonderful) adjustment to not have to consider or work-around those 4 or 6 or 8 yearly appointments when I want to make plans! I feel free as a bird! Thanks so much, Pam! ❤️

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  7. Thanksgiving is the perfect time to count your blessings via numbers, the language of medicine and medical treatments.

    With others here, I share my congratulations and gratitude as you say, for the “wide open spaces on my calendar. I feel like I can gallop through the squares and days on that calendar untethered.”

    CHEERS! :-D

    Liked by 1 person

    1. Yes! I didn’t even think about “counting” blessings, Marian. I am, indeed. :) Thanks for the CHEERS and constant support. ❤️ Have a wonderful Thanksgiving!!!!

      Liked by 1 person

  8. petespringerauthor Avatar
    petespringerauthor

    Gosh! I can’t believe it’s already been five years. Your positive attitude and strength shine through each of your posts, Melanie. I’m sure it’s been a tremendous help to be surrounded by a supportive family too.

    I like the idea of writing this post in numbers, a reminder of all you’ve been through. It’s a testament to your desire to want to be cancer-free and what’s it taken to get there. Strength comes in many forms, but in my eyes it doesn’t get any more powerful than this.

    Liked by 2 people

    1. You’ve been reading my stories and updates since Day 1 of my diagnosis Pete, so you truly know about all 5 years; it surprises me too! Yes, the numbers effectively explain what a journey entails and I’m glad I put them together, if only to take it in and then give myself closure. That is super kind of you to comment on strength. I do feel that I am a strong person, that trait was forged early on, but it 1000% helped me through it (and trust me, there were moments…) Thanks so much for the support, Pete. :)

      Liked by 1 person

  9. Mine ended at the beginning of August for my radiation. I finished the chemo in June.

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    1. My two chemo “sets” were bookends for the radiation in the middle. (It’s funny how the treatment varies depending on the cancer and the circumstances.) So, I read this as we ended in the same month – August! That’s pretty amazing. We’ll have to figure out how to put it on the calendar. 😍

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  10. I had four cycles of chemo and had surgery after each two cycles, and had radiation at the end. I got three tattoos. We have to mark August on our calendar. 😍

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    1. Ok! We’ll stay in touch about when in August since we “see” each other pretty regularly through our blogs. I’m looking forward to it. 😍

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      1. That’s a good idea. I’m looking forward to it also. 🥰

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  11. Good news and so happy to hear this, Melonie💕

    Liked by 1 person

    1. Thank you Cindy!!! It’s like a virtual hug. I appreciate your well wishes. It is great to connect. ❤️🤗

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      1. You’re so very welcome and I love those. With you as well!!!❤️

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  12. Cheers to many more great years of good health Melanie. I too live by the paper calendar. I need to see things right in my face, not have to click on a digital calendar. :) <3

    Liked by 1 person

    1. Thanks so much, Debby! ❤️❤️ Yes! Between you and me, I dislike (immensely!) digital calendars. Paper is super easy (okay, basic) but I don’t mind that at all. xx :)

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  13. Math…one way to think about your experience…

    Loved the writing the hope the relief the joy!

    Can’t believe it’s been 5 years for us as well (after never loosing touch but never been this close!)

    you are tops! Love you Mel my friend!

    Liked by 1 person

    1. I like that word “relief!” It’s a huge relief. Thank you very much for your kind thoughts and I’m glad you enjoyed it. I have to be honest, I’m not positive I know who this is, but it’s super nice of you to share here. (If you want to add your name or initials, please do so, but it’s totally fine either way.) 😊

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