On December 12th I was in Manhattan at Memorial Sloan Kettering
Cancer Center for my annual CT scan and blood work. The scan came back
negative so today I remain CANCER-FREE. Seven years with no detectable sign of cancer which means two years officially in remission. Amen!
--
After
my scan and blood work, I had some time to kill so the results could be determined. I went to a great coffee shop called Ground Central and had a
delicious cup then went for lunch in Grand Central Station of all
places. I had a craving for a little something from the Lower Level
Dining Concourse and it was quicker to go to Grand Central than to trek
across town to the next closest location. Once I was well fed, I started my walk back
to the clinic. As I began to near the block on which the clinic is located, I
started to wonder what the scan results would be. I imagined how I
would respond if the scan came back positive. I ran through the
conversation I’d be having with my doc about where in my body the mets
were discovered. Immediately I thought of the boys and the significant
possibility of my death and no longer being in their lives. Tears began
to well up in my eyes. It hurt. I wasn’t arguing with the idea of death.
Ok. Actually, I was. I’m not up for it right now. It means so much to
have living parents in our lives and I if I had any say, I’d say I want
that for the boys. My father passed when I was thirty-three, fifteen years
ago, and I still wish we’d had more time together as adults. Yes, I am blessed to have had the time we had, and I wish we had more. And I want the boys to have the same.
So
as I imagined the conversation with my doc about how the cancer
treatment would go. I also wondered how difficult the treatment might be
and how much I’d be able to work. Those thoughts were there for both
diagnoses. How much will I be able to work? Will I be able to be a part
of the boys lives or will I be too sick from treatment to have what it
takes? And I imagined the many hours of tears blended with the many
hours of gratitude for nearly forty-nine years of living.
Then I saw my
doc and she told me my scan and blood work were clear.
I
texted my family, and some friends who knew I was seeing my doc, to say
I’m in the clear. Daniela responded and shared her joy with me and asked
how I felt. I didn’t have to look far as I began to cry, so happy to
have more time to live.
I’m
one of those folks who keeps death close to my heart or perhaps at the
forefront of my mind. Or both...? It’s one of the ways I remind myself
tomorrow is promised to no one. My body somehow endured the surgeries
and treatments that went with two pretty substantial cancer diagnoses.
How am I still here? I have no idea. Lucky I guess. I keep these thoughts close. They serve me well.
As
a child, the saying “Live like today is your last” used to mean getting
crazy. Doing everything I’d never done before and always wanted to do.
Today it means making sure people know I love them. As I walked out the
clinic and rounded the corner where I was walking and crying just hours
before, I saw a group of happy folks soliciting people. They were
smiling and working hard to engage passersby, so I looked one in the eye
and I said, “What do ya got?” She spoke to me about children dying all
around the world from hunger, diarrhea, and other issues that are easily
resolved here in the USA. She pushed hard for a $33/mo commitment.
Then her co-worker chimed in. I told them I would love to and simply
can’t afford it. She pushed again. I acknowledged her for her relentless
stand for these children, told her I love her and went on my way. The
awareness of death always seems to keep love present in my mind.
On my way home on the bus, my mind was foggy and my mouth tasted odd from the prednisone and Benadryl I take
to hold off further bad reactions to the contrast used to enhance the CT
imaging. My body hurt from the effects of the contrast. My body hurt from my lack of sleep I got the previous night from the prednisone as well as the anticipation of the scan. (I'm going to find out if there are any less intrusive alternatives to prednisone).
And I imagine my body hurt from my mind’s wondering if I was going to be
signing up for more surgery and whichever therapies would be
recommended. It’s how it goes. I took the day that followed slow and easy. No work, just rest. Plus I visited a wonderful little aquarium store after my appointment and picked up three really great little
creatures called Kuhli Loaches to add to our little aquarium community
at home. It was quite an exhausting day and it was a good day.
Hallelujah, my friend!! Life IS good! I love your honesty in telling your story. You don’t hold back! Hoping we will meet again some day. So glad to know that your son will continue to get the best of you. ♥️ Keep inspiring, Bert! ��
ReplyDeleteThank you Lorian! I'm sure we'll see one another again!
Deletebookmarked!!, I love your blog!
ReplyDeleteBert, I'm so happy for you!!!! You have been on my mind lately, so I am excited to get your update, and to know that you continue to do well. Happy New Year!!!
ReplyDeleteThank you Maria! Happy New Year to you as well!
DeleteYoour style is unique compared to other people I have read stuff from.
ReplyDeleteI appreciate you for posting when you've got thee opportunity,
Guess I willl just book mark this site.
What's up, yeah this article is in fact good and I haave learned lot of things from it oon the topic
ReplyDeleteof blogging. thanks.
Hi Bert - I've been thinking of all my cancer survivor friends the last few weeks. How are you doing? And how is your immune system? Are you worried at all about COVID19? I am fine; taking precautions, but also know my immune system is in good shape.
ReplyDeleteHi Maria. I don't know why Blogger won't let me reply to comments from my Blogger account - it's making me reply from Google Cancer Survivorship Coach account. It's very strange... Regardless, this is Bert! Thank you for reaching out to me. My immune system has never been the same since the ~14 months of chemotherapy I've received through my diagnoses. I seem to catch colds and flues quite regularly in cold and flu season. And that said, the colds and flues I've had haven't become bronchial issues. Should I contract the virus, I imagine I'll navigate like most folks. I hope. Thanks for reaching out. Take care!
ReplyDelete