Day Minus Four

Hello, I’m day minus four, and your name is?

Yesterday, during rounds, as I spoke to the physician and the rest of the team visiting my room, I informed them that today I am getting the Rabbit ATG infusion. “Oh yes,” he rapidly answered. “You are at day minus five.”

I’m not sure why I felt the need to inform my own physician’s team what drug was in the IV infusing through my port, like they didn’t know, but when he asked me how I was doing, that’s how I answered. I said I was fine. Just sitting in this bed, receiving this lovely chemo drug that has something to do with a rabbit.

Day minus five. Those few words told me they knew me well. They knew what would happen to me on each day during my stay at this University of Alabama hospital in Birmingham. This is all building up to my Day zero. That’s the big day. That’s my new birthday. Welcome to stem cell talk.

My new birthday means they have given me enough chemo and radiation in the previous (minus) days to take out my own stem cells, and a whole bunch of my bone marrow that, on one day of my life, started multiplying with more bad cells than good ones.

When my body has nothing left to fight off any infection, the hospital team will introduce a whole new team of fighter stem cells that came from a total stranger. Some dear person has donated their stem cells for me! On my Day Zero, that person, who I am not allowed to know for at least 2 years, and only if they agree to tell me after that time, will learn who benefited from their stem cell donation.

After my birthday, in the stem cell world, I will have a new name every day. I will be known as “day +(plus) 1”, then “day + 2” and so on until about “day + 17”. If all is going well by then, and there is no rejection, they will begin talking about discharge.

So today, I sit in this hospital bed listening to the clicks of my infusion pumps and meeting the many people who come in to visit for a variety of reasons, and I look out the window at my view of Birmingham. These are the “boring days before transplant”, the staff says. The preparation days. These are the last days I will see my own hair.

At day + 5, which is a Monday, I will begin losing my hair, so by Friday, day + 9, I should be bald and will get to wear some of the lovely hats my dear friends made for me. What a different day that will be.

But for now, my charting notes between you and I are up to date, so I sign off humbly and gratefully.

Day minus 4.

6 responses to “Day Minus Four”

  1. Lynn N Jim Park Avatar
    Lynn N Jim Park

    hello dear friend,

    you have been on my heart and mind daily.
    glad to read you are “fine”.
    I can’t imagine the sitting and waiting with anticipation of your new birthday and the unknown.
    while I don’t know about total hair loss, the possible idea of it returning with curls sounds lovely. 😀So give yourself a big hug from us and one for Brian too when he gets over his crud stuff. Praying for your recovery. Love you ! ❤️

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  2. cowboycleara749c2382f Avatar
    cowboycleara749c2382f

    Love you sweet friend. Praying for you and your recovery. I love reading your posts. You are beautiful inside and out, with hair or without. Hugs to you and Brian. Blessings to you and Brian and your donor. Take care. I look forward to your next post.

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  3. I am in awe of your writing talent using beautiful words to describe an experience that no one would consider beautiful. Your faith in the face of this difficult journey is a testament to all. Know that I love you and that you are in my thoughts constantly. Bless your hair bless your scalp and bless the hair follicles that will do their job in the future.

    Faith, hope and love to you my friend.

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  4. wonderlandshiny7d8bccb2a7 Avatar
    wonderlandshiny7d8bccb2a7

    Love your words and your spirit!! YOU’RE gonna make those cute hats look GORGEOUS🥰

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  5. Janice Burrough Avatar
    Janice Burrough

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