I love my calendar girl

We finally have a plan. Chemotherapy starts this Friday, and we’ve got our social calendar mapped out through New Years Eve. If all goes well, that’s the end date for chemo.

When you are first affected by breast cancer, or any cancer for that matter, first and formost on your mind is “Get this thing out of me!” and “When do I start treatment?” What you soon discover is all of what I call the “busy work” to get ready for treatment. Body scans – check. Dental checkup and cleaning (apparently, chemo and teeth don’t get along) – check. Surgical follow-ups – check. All that’s left this week is flu shots for the family (and for anyone else who wants to be around Shannon) and getting her IV port installed. And all that busy work means that we are closer to the end game, which is kicking some serious cancer ass.

Chemo will be every two weeks for 8 weeks, 4 of the first drug and 4 for the second. From what we hear, Shannon is getting the ACT treatment, or Adriamycin, Cytoxan, and Taxol, which we understand is the “gold standard” for this type of breast cancer. I am also shaving my head with her, which is nothing new. Sometime after the new year, she will start the first of 36 radiation treatments. Then, hormone treatments and ongoing monitoring to make sure this cancer doesn’t try anything cute.

Scheduling life to get Shannon to her appointments and Carter to and from day care and his doctor’s appointments is making for some fun times. I travel for work, and thankfully they are extremely understanding about me needing time off. As we move into the next few weeks, I’ll need to take less and less time off for appointments, and get to focus more on taking care of the family. Our support group of family and friends is tremendous. I already have a whole line of babysitters lined up to take care of my precious ones when I have to be out of town. It’s a blessing in disguise that this is happening over the winter, when travel for me is lessened. Other than the hair loss thing. This is North Dakota, after all.

We do have one big trip that’s been in the works for months before the diagnosis. Las Vegas for my high school reunion in 3 weeks, pending doctor approval. You see, when I was young and foolish, I fell in with a bad crowd, and briefly dabbled in witchcraft. I then hitched a ride West and got stuck in Vegas for a time as part of a traveling magic show. I was responsible for cleaning up the mess when the saw-the-wowman-in-half trick went horribly wrong. My tutors, Penn and Teller, taught me everything I know.

Either that, or I graduated from a Department of Defense Dependent Schools high school in Misawa, Japan, and we all decided Vegas was closer and cheaper than flying halfway around the world. I’ll let you, dear reader, decide which is more plausible. (Go Eagles!) We even may get to see Carter’s godfather, who will be in Vegas around the same time as us. Carter, though, will be staying in Bismarck with Grandma and Grandpa. Apparently, it’s 21 Years, not Months. Go figure.

Posted in Shannon's Journey Tagged with: ,
3 comments on “I love my calendar girl
  1. Michael Barbere says:

    This is fist time I have jumped to your blog site from Twitter. I wasn’t expecting something so moving. I am not prepared for the confrontation of health issues with my family but of course it is an inevitability. Your strength and attitude is inspirational.

    I was reading The Art of War tonight. I thought this might be relevant quote for your upcoming battle:

    “In all fighting, the direct method may be used for joining battle,
    but indirect methods will be needed in order to secure victory.”

    The use of the chemo for joining the battle is of course the direct method, but all the preparations you are making will undoubtedly be every bit as valuable to your partner.

    –Nodaki

  2. Chris says:

    Thank you for the support. I started this primarly as a form of therapy, never knowing how it would be received. The offline response I’ve received so far has been positive.

  3. Brenda says:

    What a great way to keep everyone updated – I love it!! Chris you have always had a way with words. Thanks for taking such good care of Shannie – she is very special! Love to Shannie, Chris and Carter

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