Okay, I don't even know how long it's been since I posted on this blog. I think the increasing periods of time that pass between my posts is an indication that I may close the blog down in the near future. But I'm not ready to do that yet. I've been holding off until my treatments are completely finished, and today is my penultimate Herceptin infusion. Three weeks from today will my last, and then on March 13th I'll have my chemo port removed.
I started Herceptin (Trastuzemab) on December 9, 2013. The standard course of treatment is to get Herceptin for one year, but I was not able to get Herceptin during the three weeks prior to, or post surgery last march, or during the eight weeks I was getting Adriamycin and Cyclophosphomide last spring. So, we had to add those 2-1/2 months back into the timeline.
One thing (among many) that I have come to understand through my long strange trip through Cancerland has been the significance of multiple milestones, both big and small. Well, these two coming up on March 11th and then with port removal on the 13th are big ones! But they won't be the last. I am taking an aromatase inhibitor for five years, and will have occasional check-ups with my oncologist during that time as well. I am currently considered to be in remission, and they don't call the cancer cured unless it stays away for five years. So, that will certainly be another very important milestone for me.
In the mean time, I am simply loving life. In fact, I don't know that I've ever been this happy. I'm busy at work, finished my book, enjoy seeing the kids growing and loving their lives, have started learning yoga, and am playing soccer. And those are just some of the obvious things. It doesn't include the littler and more mundane stuff--stuff that seems breathtaking when you stop to notice it. Sunlight on geese taking off from the pond, a hug from Craig, Ben and Jerry's, an awesome new chicken casserole recipe, a clear crescent moon in a hyper cold night sky, baby kale, Dolores' big brown eyes and her mini tail-tip wag, sparkly snow crystals, Glassy Babies, a stranger's smile, that cool moment when you wake up and don't know exactly which day it is, a new pair of boots, the first sip of coffee in the morning, a Facebook invite from an old friend, a really juicy clementine, the anticipation of a road trip, .... Fill in your own blanks here, and appreciate all of them.
I created this blog so that my friends and family can follow updates about my diagnosis, my experiences with treatment, and my recovery. Some of you may be put off by the title. Sorry, but this is not going to be pretty. I claim no particular strength or grace. I may reach for strength and grace on occasion, but those are standards that I will not be beholden to. I expect to cry, laugh, question, scream, analyze, whimper, shout, sob, and swear. And you're invited to join me.