Man, am I a planner. It really does give me comfort. The unknown is quite unsettling, so I'm happy to say that I have a plan moving forward. I came to the coffee shop to get some work done, free from the distractions of my office and home, but I'll blog instead...how millennial of me.
Last post recalled my MRI results and discussion with my surgeon to have the mastectomy. After that point, it was on to figure out the whole reconstruction scenario that had overwhelmed me previously. I made some calls and anxiously waited over the holiday weekend to schedule a second appointment with the plastic surgeon I had originally met with for today (Thursday). Also, I had asked for the second opinion and had that appointment this afternoon...which I thought would work out well, because if the first one went well, I could just not go get the second opinion.
Between last week and today, I did more research (probably too much) pulling articles, reading websites, etc. And as today (and next week's surgery) got closer, I kept sort of hoping that I wouldn't have to change the surgery or anything like that. The fact that Mom and Sarah's plane tickets got booked solidified that thought.
Yesterday, Wednesday, I had my post-chemo follow-up with my medical oncologist. After discussing the Flyers disappointing
loss (so much for that Top 25 ranking) and relative merits of Garmin's
activity trackers we talked about how Bertha was doing (though obviously he doesn't call her that...). He off-hand mentioned that he thought highly of the original plastics guy and figured they'd do an expander at the time of mastectomy for reconstruction, which was somewhat reassuring to hear. He also talked about how I'll now be taking
tamoxifen daily, starting after I'm home from surgery.
Tamoxifen is an estrogen receptor antagonist, meaning it blocks the places where the hormone estrogen binds to cancer cells (or at least the cancer cells I have, since mine are highly estrogen receptor positive...). So for "high-risk" (advanced stage) PRE-menopausal women and many post-menopausal women, it's a recommended course of treatment for 5 years post chemotherapy. So, yeah, woo hoo pills. I was hopeful it wouldn't be that long, but if it can avoid a recurrence (the whole point of taking it), then sign me up.
One hassle is that the anti-depressant I'm on can't be taken with it, because it can decrease effectiveness so I'll have to change to a different one, which hopefully won't be a huge deal (PS, the right drugs really are amazing...maybe some time I'll post in depth about how long I went before being willing to try them, and the difference they've made for me, personally).
There are also fun side-effects with tamoxifen like continued night sweats/hot flashes and some other fun hormonal issues. I have to be a bit cautious about clotting (long plane flights, etc...since I often say "
sitting is the new smoking" hopefully this isn't much of a problem for me...speaking of which, I should stand up) and there is also a slightly increased risk of uterine cancer, but the benefit outweighs the risk.
After the appointment, I called Mom and basically just said:
"I'm over having cancer...."
and not "over" in the sense of "cured" but "
over" in the sense that I was sick of it. Sick of the appointments, the forms, copays, the unknown, the making of plans, etc. It's more annoying that the chemo drugs themselves! And hearing the extended Tamoxifen time (compared to what I had thought) was sort of the spoiled icing on the sugarless cake. I went back to work, was a bit out of sorts, but kept trucking away. Went home last night, called it an early night and just kind of said screw it.
This morning I woke up early because due to the appointment I was going to be late to my second class at noon and had to record some lectures so my undergrad TA could get the class started. If you're feeling really bored and want to learn about membranes, feel free to
watch/listen. I finished basically just in time to teach at nine, run around sort of crazy for a bit of final prep for her, call Mom from the car, and make my way "three towns over" as my friend Adam would say (it's really just where I used to live, 20 min away) to the plastics office just in time to sit and wait for 25 minutes in the waiting room, learning about the
Revolutionary War courtesy of the History Channel. I tried to be patient, as I knew I had been a last minute addition to the schedule.
When I was brought back, I took out my iPad, eager to take
notes. The doc came in, this time dressed in scrubs rather than the not so awesome sportcoat he had on last time. I immediately got a better feel from him, and now that I had more information, we had a good conversation about options, plans, etc. At that point, I decided to go for it with him, cancel the other appointment. So, what you've been waiting for...here's what's happening!
Wednesday, Jan 28th in AM ~10am, go in for surgery:
Breast Surgeon: mastectomy of left breast, removal of chemo port, and sentinel node biopsy with possible axillary node dissection, pending biopsy findings.
Mastectomy and port removal are pretty straight forward. The
sentinel node biopsy is the dye procedure that the trace the drainage of the breast tissue, remove nodes and test for the presence of cancer. If she gets clean nodes (pathology is run real-time), she's done, if it comes back showing cancer, or they can't determine it, they she dissects (cuts out) the lymph nodes under the armpit.
Plastic Surgeon: right breast mastopexy (breast lift) and left breast tissue expander insertion
While the primary surgeon is doing the mastectomy, he'll do a breast lift on the right/non-cancerous breast. Because the implant will sit higher and the radiation will "tighten" up the left breast tissue, a lift is needed to get the right one to match. This is the free boob job part of it. The right will still be subject to effects of gravity over time, whereas the implant won't, so given my age, a similar procedure may be needed down the road. He does this first/at the time of the first procedure because it becomes the "target" for the other side. It's also convenient because I'm already there, overnight in the hospital, etc.
After the mastectomy is done on the
left/cancerous breast, he'll insert a tissue
expander. This serves as a bit of a placeholder and will be filled with saline injections in his office over a period of a few months (probably 2x/week to try to do it "rapidly" over ~2 months). At that time, he'll switch out for an implant. After a week or so, I can start the
radiation process. After radiation, if anything else needs to be done to improve the cosmetic outcome or address any complication that arise with the radiation (which can definitely happen...a risk I'm willing to take), another procedure may be necessary. The alternative to implants, my own tissue (back/lat flap), is sort of "saved" in case it is needed later...if he were to do that first, it might get damaged by the radiation.
Based on what I've read, what the other docs have said, I am feeling good about this plan. It seems reasonable and appropriate for me, and keeps me moving forward, which I've found to be pretty important for my sanity. And, as much as I am a logical person, I usually do end up going with my gut, and this "feels" right. As many weighted pro-con lists as I've made in my life, I'll admit part of the motivation for weighting them is it allows me to add in some intuition to my quantitative evaluation.
After conversing with the plastics doc, I scheduled my "marking" appointment for Tuesday where he'll draw, take pictures, etc, and go over post-op instructions. I'm glad Mom will be there for that one. On the hurried drive back to campus to teach (thankfully was only 20 minute late) I called Mom and she was nice enough to cancel the second opinion appointment I had scheduled for the afternoon. Distractedly finished teaching, then I just had to wait for the confirmation call that the scheduling would all work out for him to be in surgery at the same time, which is does, so I'm all set!
As the exclamation point in the title implies, I'm happy to have a more complete plan, and one that I feel good about. Perhaps the excitement will turn into nervousness. I anticipate a bit of "buyer's remorse" about it all as well. But, so far, I think I've made good decisions when decisions had to be made, so am actually looking forward to this next step. Side benefit, the big conference in March I go to can actually probably happen as I won't be in radiation yet! And, I don't really have to worry about the trip to Phoenix I finally booked with MN friends for early March getting in the way (though oops, maybe I miss an expansion).
I can't forget...I got another "
welcome to cancer packet" yesterday in the mail (sidenote: that linked post was from 5 months ago yesterday...crazy what's happened since then) form the hospital where I'll have my surgery, complete with:
"pink stress relief ribbon which you can squeeze with your hand (optional)"
Another Lesson Learned: Don't ever stop laughing at the little things.