Tomorrow I will start the IV chemo, Taxotere, along with the oral medication, Xeloda. This combination is designed to work together and gives my medical oncologist some flexibility. While I get the need to get ahead of the cancer cells that were not materially affected by my last line of treatment, the knowledge that I will once again endure IV chemo hasn’t been something to anticipate with anything close to positivity.
When I was initially diagnosed in March of 2017, we believed that I was Stage II and treatment would be something that would occupy some time that summer and would be quickly left behind, not unlike my mother’s experience. We believed it was a season to be endured and then put away. And so that’s the way I approached IV chemo the first time. I would grit my teeth, deal with the hair loss and other awful side effucks and then never look back.
Oh how perspectives have changed.
Now, I will walk into the infusion center tomorrow hoping that these first six sessions, occurring every three weeks, will be sufficient for now, expecting that I’ll be willingly signing up for as many other sessions as my medical oncologist suggests, while taking the oral medication as well and for as long as possible. This is a HUGE change from the perspective of just trying to get through a season; now this is my entire reality, staying in treatment as long as they work and praying for the treatment to work for as long as possible, even if it’s miserable.
Just as with the scans that I endure every three (3) months, walking into the infusion center tomorrow isn’t just about not knowing what to fully expect, it’s also about knowing a bit about what to expect.
Chemoxiety, I guess, just like Scanxiety.
I’ve watched so many of my dear friends start down this road, where treatments don’t work and chemo is started. It’s not that I don’t know what is coming, maybe not for a bit, but certainly sooner than I’d hoped. While every story is different, each story ends the same way, no matter how involved or engaged or stubborn or accepting the patient is during the treatment. All of us will be consumed and killed by this disease and the return to chemo is a bad sign, it is the wrong direction to go.
And so I will walk into that infusion room tomorrow. I will walk into that room and I will willingly allow them to pump poison into my veins, knowing the side effects that are coming and the toll it will take on my body and my family. I will do that tomorrow because that’s how I get more time with my family. Walking into that infusion center and taking what comes after is how I stay alive as long as possible.
Even if it sucks.
Thinking of you constantly. Thank you for sharing. Love you friend ❤️
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Love you, too!
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Will be in there with you!
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❤️😘
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Sending thoughts of love and support ❤️🤗
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Thank you!
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I want to hug you Abigail. Will be thinking of you tomorrow.
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Lord, have mercy. Wrap up your precious Abigail in your loving arms and carry her through the anxiety, the procedure, the side effects and beyond.🙏🙏🙏
Love you dear one 😘
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Sending so many many prayers for you and your family. ❤️❤️❤️
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I want to tell you so many things, but the words may come out wrong. Love to you and your family!! Just know that I am thinking of you every moment and if you have any questions that I may be able to answer, I am here!! Love to you!! ❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️
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Thoughts and prayers🙇♀️🤗
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Praying for you seems like such a cliche’ answer, but know that you aren’t going in alone! Thanks for your honesty and sharing.
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Never a cliche so long as it happens!! Appreciate any and all prayers. ❤️
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I swear I have PTSD over the chemo room at my first oncologist’s office. I pray that these two meds work for you, Abigail. I am off to a full body scan tomorrow! Scanxiety continues!
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I have PTSD just walking into the building. 🤞🏻🤞🏻 for good results from your scan!!
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Thinking and praying for you! Thank you for sharing your journey. You are helping other patients not to feel alone. Love and hugs!
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Thank you so much!!
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Hi Abigail,
Hope these two meds do their thing for a very long time and that the SEs aren’t too horrible. Rooting for you always.
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Appreciate all your support!! Can never have too many cheerleaders!!
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Hoping all goes well.
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Thank you!!
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Love and light to you, dear Abigail. May the “side effucks” be less than anticipated, while the regimen devastates “those pesky mets.”
I can’t begin to tell you how deeply moved I am that you’ve been continuing to visit my blog at this very difficult time.
💕🙏🌷
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Thank you, my friend! I know I don’t always comment but I really enjoy reading your posts. ❤️
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I admire your perspective. Whatever gets the job done to spend more time with your family is excellent motivation. My mom was a cancer survivor, but at first, she wasn’t going to fight. As a deeply religious person, her attitude was perhaps this is God’s plan for me. It took the encouragement from my dad and her four boys to say, “Screw that! We want you around.”
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It’s so hard to know how you might respond to a serious diagnosis and I think it’s so individual. God also gave us the plants and the intellect to develop the meds!!
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Thinking of you ….
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Thank you!!
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Prayers. Hoping for your better health. 💜
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Thank you!!
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I am so sorry. Holding you and your precious family close in my thoughts and prayers.
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Thank you!!
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You have an army of supporters and encouragers, right behind you.
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❤️❤️
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So sorry that you are going through this.
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Thank you, much appreciated.
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Prayed for you
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Given what you and your family face, it is hard to click “like” when I read the post. I definitely don’t “like” that you have to endure what you do. I admire and am humbled by your reflections and ongoing tenacity and grit and resilience. Thank you for sharing.
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appreciate your support!
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Thank you so much for all the support and kindness as I start chemo again!!
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Wishing all the very best for you, Abigail.
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Thank you!!
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Eu gostaria de poder fazer mais por você. Eu gostaria de poder tirar toda a dor e todo o sofrimento de dentro do seu peito e fazer você ficar saudável novamente. Eu gostaria de poder mandar o câncer para bem longe de nós. Infelizmente, isso não é possível. O que eu posso fazer é oferecer palavras de conforto nesse momento tão difícil da sua vida.
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Many thanks for your kind words. I appreciate you reading and commenting!
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