Before
even meeting with the surgeon (Dr. Lal), we were made aware of the possible
surgical options (listed here), but in our meeting with Dr. Lal, our
tentative decisions were supported, and we were even more confident that our
plan was the best for me.
All
research shows that there's not a difference in treatment effectiveness whether
choosing lumpectomy and radiation or mastectomy (and each doctor that I talked
to said the same thing). Obviously a mastectomy is a more intense surgery
with more risky side effects. However, lumpectomy requires that clean
margins are achieved in surgery (and I know more than one person who had
multiple lumpectomies due to inability to obtain clean margins) AND you must do
6 1/2 weeks of daily radiation following a lumpectomy. Reconstruction is
often more difficult to achieve balance following lumpectomy, and especially
for a woman with small breasts (ahem...), it's a more noticeable change.
Radiation can mess up the reconstruction process, as it changes the
tissues where the implant goes. And we all have our baggage, and I know
that my mom has been most frustrated by her changes that came about due to her
radiation treatments for her cancer. So if possible, I'd like to avoid
that, thus leaning to mastectomy.
Furthermore,
in addition to being Grade 3, my cancer is Ki67 positive. The Ki67 gene
codes for the Ki67 protein, which is involved in cell proliferation. The
higher the Ki67 (measured in percent of cells actively expressing it at time of
biopsy), the more cells actively proliferating, and the more aggressive cancer.
Anything over 20% is considered positive. My tumors were 62% and
55% (although the navigator told me that some women have over 90%, so not the
most aggressive). Still, enough to freak me out. A combination of
the Ki67+, Grade 3, and early diagnosis means a higher likelihood of recurrence
(although there's some controversy surrounding the predictive value of Ki67,
and not all labs even check it). But it's a BREAST cancer and if there's
no breast, there's nowhere for it to return to.
So I
chose to do a bilateral mastectomy. And while I like to think that I'm not
the least vain person, those around me soon convinced me that I'm young (ha!)
and healthy, and active, and that doing reconstruction made sense.
Additionally, it's easier to begin the reconstruction right along with
the mastectomy (and I would much rather get this all done at once).
Currently,
surgery is scheduled for tomorrow--January 8th--at 2:00 pm. (There's a
possibility the time might be moved up, as the plastic surgeon had a morning
cancellation and would rather start earlier) It should be a 6-7 hour surgery,
and I'd be lying if I said I wasn't somewhat scared. I am not a fan of
anesthesia at all, and I have never had general anesthesia. I had hernia
repair as a teenager with a local (was awake through it and remember feeling
like they'd sliced me from stem to stern!); I gave birth to three children
without any anesthesia--including one pitocin-induction; I regularly do dental
work without anesthesia (my dentist hates that!). Finally, I've been in
the waiting room for all six of my mom's surgeries in the last seven years.
I know what the waiting is like, and none of her surgeries have lasted
that long. I feel awful thinking of Greg waiting for me for that long.
It's
going to be a long day and a lot of procedures. The "old" way
to do mastectomies was to take out as many lymph nodes as they could find
during surgery. But there were a lot of issues following removal of lymph
nodes, as you can imagine. The lymph system is very important in
immunity, and removing nodes disrupts the flow of the lymphatics, so any
possible infection or injury in that area (essentially the whole right side of
the chest, neck, arm) would be affected. The new procedure is to only
remove sentinel lymph nodes to check for cancer and if there's no cancer, no further
lymph nodes are removed. Because there are between 5 and 40 lymph nodes
that drain each breast, removing the fewest number allows the best return to
normal function. In order to determine which lymph nodes are the first to
drain the breast, a radioactive material is injected into the breast along with
a blue dye, and then the surgeon can tell which nodes are the sentinel ones.
So tomorrow I arrive two hours before they inject me with the radioactive
stuff, which happens three hours before the actual surgery starts (doing the
math, that means 9:00 am arrival time).
The
surgery itself will include the sentinel node biopsy (pathology immediately
examines the nodes and if no cancer, that's done; if cancer, they take the next
nodes and so on until they get clean ones), placement of a port-a-cath on my
left side for chemotherapy, double breast removal, and the plastic surgery.
The breast implants will go under the muscle, which lies flat against the
rib cage, and so a pocket needs to be made for them to fit. The muscle is
separated and cadaver skin is sewn to expand that area. My cells will
repopulate the cadaver skin, making it my own. A saline expander will be
inserted in this pocket and it will be gradually inflated (in the doctor's office)
as I heal to make room for the eventual permanent silicone implant (this is the
part that can get messed up due to radiation). The surgery to put in the
permanent implant is supposed to be pretty minor.
The thing
I'm most worried about after the anesthesia is the pain relief. Not
that I am worried about being in pain, but that I don't do well with pain meds.
I am horribly vomit-phobic, and even laughing gas at the dentist makes
me nauseous. My mom had issues with multiple pain meds after her surgeries
(nausea and blood pressure issues) and I am so sensitive to any
medications that I don't know what strong pain meds will do to me.
This is the other reason I'm opting to do it all at once--so I hopefully
won't need to have surgery again!
But it's
the first step in my battle, so I will do it. And I know that I have the
strength of so many people who will be with me in spirit tomorrow.
~~~
Finally,
to close with some humor, I have been replaying in my mind a running gag from
Arrested Development since the first meeting with the plastic surgeon.
But after yesterday, when he marked me up with the surgical lines and
reality really set in, I've been thinking of it even more. I really have
this bizarre desire to pull a Kitty at least once before my surgery tomorrow:
Please pull a Kitty! Please, please, please! (Just make sure Greg is Michael!)
ReplyDeletesending you all good thoughts.
ReplyDeleteI'm super sensitive to Meds. Laughing gas makes me nauseous AND I'm a vomit phobe. I was amazed someone else is like me! Codeine type pain med makes me nauseous. Loritab and percaset and oxy No problem just put me to sleep. Oxy seems addicting so I don't really like taking it. Of course YMMV
ReplyDeleteReading your blog brings back so much of my experience. I tried the lumpectomy route twice and never got clear margins. I am so supportive of your decision to do the bilateral mastectomy with tissue expander reconstruction. I, too, have vomit phobia (extreme!) and general anesthesia doesn't help. The longer the surgery, the more likely the nausea. I fought it as long as I could, but ended up losing it once. My nurse told me that it just about always happens after a mastectomy. I did feel much better afterwards.
ReplyDeleteAnother similarity is the age of our three children at the time of diagnosis. I had one in college, one in high school, and one in middle school. My daughter was my rock when I was diagnosed, while I was in the hospital, during recovery, and to this day 12 years later. That was one of the best things to come out of my cancer experience.
My darkest day was getting the diagnosis. Hopefully that will be your darkest day as well and it will only be uphill (with a few inevitable bumps) from here. Please message or call me if you have questions during recovery or while getting your tissue expanded. Or if you just need another person to listen. I'll be thinking of you and keeping you in my prayers. You'll beat this!
Thank you, Judy. It is so helpful to hear from people who have been through it--and are on the other side! The more I learn, and the more stories I hear, the better I feel.
DeleteI'll be thinking of you and sending lots of positive mojo tomorrow, Lori. Whatever your previous experience, let's all of us reading this hold onto the belief that LORI DOES GREAT WITH PAIN MEDS! You are a warrior, and you totally have this.
ReplyDeleteI like the way you think, Rachel! :)
Delete