
Today was dose seven of my nine doses of chemo. I feel more like a
borg than a human at this point, with the bald head, the metallic/silicone port winding its way through my vena cava. . . the toxins polluting my body. If you don't know what a borg is, see the photo. With a little luck, maybe I'll at least have a rack like Jeri Ryan when this is all over.
Speaking of great racks, HAPPY BIRTHDAY TO MY SISTER SARAH! :) Sorry, I blame the drugs for that entirely inappropriate comment. She was 6 years old when I graduated high school on this very day 19 years ago.... so that makes her.... 25. The genetic counselor said my biological sister should start getting screened for BC 10 years before my age at diagnosis (36), so Sarah you have one year to get your act together and start screening.
I'll give you a summary of my day, then there is some important stuff at the end if you are interested in my pathology, treatment, prognosis, etc. I'm too tired and foggy to edit this to make more sense.
Taxol was the same story today. They doped me up with Benadryll beforehand....but at least this time I knew what was going to happen. Fortunately I didn't have the crazy twitchy legs this time.... but I knew I was going to fall asleep and I didn't resist it this time. I didn't have any visitors this week, so it was just as well. I would have been snoozing before anybody got there. I told myself to "just give in" to the sleep that was forcing itself on me. I had a moment where I didn't want to, as Nathan and I are reading
A Wrinkle in Time, and we just read the part where the children had to resist giving in to IT, which tries to take over their minds if they would just relax.... But I turned on a meditation CD on my ipod and took a snooze.
While I was sleeping, Todd ran over to my work and picked up a pile of goodies. Kristen made our dinner tonight, pasta and chicken with sun dried tomatoes and pine nuts... mmmmm, Ashley sent chocolate chip cookies WITHOUT nuts (at my request), Marty sent homemade tamales (the last batch was fabulous), Jan W. sent caramel rolls (yummy), and Tom sent me a couple of items that had belonged to his wife, Sharon, who survived metastatic breast cancer for 18 years. It's so nice to know the people at work are thinking of me. Thank you all so much. I haven't been to work since my hair fell out.
Anyway, they had to wake me up to send me home. Todd had been feeding me pretzels while I was sleeping, and I woke up with a mouth of half chewed pretzels. It was funny. Celeste, one of my favorite chemo nurses, told me in the fog that this was her last week and she is moving back to Nebraska, so I was sorry I wasn't more coherent to say goodbye to her. I slept in the van all the way home, then slept at home until about 5. Many thanks to Linda Markus for babysitting Anika today.
Some news, if you've made it this far down. We are a little confused about some of my pathology, now that we are going back over the reports. We had been the "good patients" and asked for copies of all the pathology reports, but then we failed to READ them in all the flurry of activities that went on between January and now. Plus they are hard to understand, even for a lawyer and a medical technologist. I need my own personal pathologist to do translations. Also, there was one report that we never knew existed, so I never asked for a copy. So, a few things are not as I thought.
You may recall I had THREE surgeries trying to GET all the cancer. In the first surgery they found a 1.8 cm tumor and those baby cancer cells called DCIS. In the second surgery they found MORE DCIS, thus deciding that the breast probably could not be saved. My surgeon agreed to do a third surgery (when she put in my port) to try to get "clean margins" around the tumor site.... "the old college try," we called it....to save the breast. More DCIS was found in the third surgery, so we know the breast has to go. I'll probably have that surgery in July if all goes according to plan.
Anyway, in reading the pathology reports and talking to my doctors, it turns out there was a
second tumor that was found in the second surgery. It was much smaller at 0.4 cm. My surgeon says she told us this, but neither Todd nor I remember hearing it. However, we were so devastated by the news that there was more DCIS, that we both know we may not have heard this information. I have to say, if I had known about a second small tumor, I probably would have given the breast up back in February. But everything happens for a reason...... this has given me time to come to terms with this loss, and to get clear on my reconstruction options. However, the cancer factory that is my chest has got to GO. I'm ready.
Furthermore, just today we learned that additional pathology was run on the tissue removed from the third surgery, and the pathology came back different from the results on the original tumor. As I explained in an earlier post, treatment is determined in part by whether the cancer is receptive to estrogen. My original tumor came back as Estrogen
negative. The DCIS removed in the third surgery came back as Estrogen
positive. None of this would have changed the treatment I already have received, but it does mean that 5 years of Tamoxifen (an oral breast cancer drug) is now a done deal. I was on the fence about that before. This is an important bit of information, and I'm a bit annoyed that it was not passed on to me, but this is an example of why we must be pro-active patients and review our own charts periodically.
I think the Estrogen receptor news is somewhat "good" news, relatively speaking, because it means there are more drugs they can throw at me to kill the cancer. Women who are entirely negative for hormone receptors grow frustrated once chemotherapy is over, as usually there is just NOTHING else for oncologists to do. Some view this as a blessing, that they just return to life and forget about cancer. Others become paranoid and wonder when the cancer will show up somewhere else in their body....
OH, and one more thing. Thursday I am having an ultrasound of my liver at 9am. My liver counts have been going gradually up and up since chemo started. The Oncologist said this is MORE THAN LIKELY DRUG RELATED and that they will straighten out when chemo is over. However, out of an abundance of caution, they will do a scan to make sure there is nothing there of concern. Remember, I had a CAT scan just a couple of months ago and I was clean, so it's unlikely that I have a liver full of tumors at this point, since the chemo is supposed to be killing any wayward cancer cells.
Todd says 'hi' to everybody. :)