Cancer Effing Sucks

My echo cardiogram was as clear as every other test has been.  That was a relief, but still left a huge question mark over my head about how we were going to treat the swelling.  I finally met with my oncologist today.  My blood pressure was 150/100 *sigh* but the swelling is mostly gone.

She feels that the swelling and other side effects were direct results of the Tamoxifen.  The problem is that there is no other drug that is effective in pre-menopausal women.  Post-menopausal women have several to choose from.  This demands that we find out where I am in that respect.

Guys, stop reading now.  You're welcome.

I haven't had a period since June of '12, when I started chemo.  That's to be expected.  Starting Tamoxifen was expected to yield the same result, so no shocks there.  The problem is that it prevents us from counting on the obvious symptoms to know my menopausal status.  So they drew blood.  Mom?  This is where you remind me how old you were when you went through it.

For now, I am still off Tamoxifen.  I don't like that, since I want every weapon available to me in this fight, but I'll deal with it for three more weeks.  At that point, I'll go back to see the oncologist and see what my blood work revealed.  If I'm pre-menopausal, they'll likely give me an injection (or injections? I don't remember what she said) to stop my ovaries from working, throwing me into menopause.  Then I can start one of the many drugs aimed at that.

More waiting.  More unsettled worrying.  More and more proof that cancer effing sucks.  I suggest you avoid it.

1826 Pills

I had a follow-up with my oncologist today.  I was glad to have an appointment with a doctor, as weird as that sounds.  I feel like I spent all summer fighting cancer.  As soon as radiation was done, I started doing...nothing.  I feel like I've just stopped fighting it, and that makes me very uneasy.  I told her that, and she said that it is a very common feeling, and that I had to trust that we've done it.  Easier said than done.

I asked if she would please do a blood draw to make sure my whites had gotten back to normal levels.  I'm pretty sure they are, since I've had two colds and gotten rid of them both within three days, but I want to be sure.  She was very nice about it and told me that they would be happy to.  That means that I got to see Marie!  She's my favorite chemo nurse!  It was awesome to see her while feeling good, instead of in a chemo-induced stupor.  I'll get the results of the blood tests tomorrow.  ::fingers crossed::

I was also given the prescription for Tamoxifen.  Because my cancer was the type that feeds on estrogen, this is a medication that decreases the estrogen in my body.  I will take one pill per day for 5 years.  1825 pills.  Wait.  There is a leap-year in there.  1826 pills.  I hope that the side effects are minimal.

There is a chance, if I was perimenopausal, that this drug will push me into menopause.  Because of the "chemopause," (fake menopause brought on by chemotherapy,) I won't know for a while if this is the case.  Oh goodie.  More unknowns.  I do know that I'm sick of hot flashes and the most common side effect of Tamoxifen is hot flashes.  *sigh*

She was happy with my progress, and I am to go back and see her in three months.  After that, I'll likely see her every six months for the next five years.  I wish someone would do blood work or a scan and say, "Yes! You are cancer free!" but that isn't going to happen.  I just have to trust that it's gone.  I have to trust the doctors.  I have to trust the medication.  I have to trust the treatments.  I have to trust God.

I'm working on it.