Monday, January 14, 2013

Survivor??


Lately, I haven’t had much to say. This blog started as a place to keep people informed, then morphed into a place where I could moan and groan and complain “oh woe is me”. I like to think I did my best to maintain some dignity and grace as I trudged thru this muddy place I like to call “cancerland”. I like to think that my words have helped someone else; either on their own walk thru cancerland or by reminding them that the grass isn’t always greener, that everyone has a shitty story to tell and therefore we should judge less and love more.

 

Actually…what I would really like to do is say “good-bye” to this blog. I would like to end it on a positive note…With a picture of the certificate I will soon receive, the one that says NED. No evidence of disease.

 

But I am not ready to do that yet. Not yet.

 

Because I don’t know if I believe it or not. The NED part, I mean.

 

Is it unfortunate that I am “too informed”? That I have read too many horror stories of women just like me, women who battled against the big “C” with every weapon available to them, only to succumb to it later? Possibly. Probably.

 

The odds are in my favor. “Statistically” (how I loathe that word) I am a breast cancer survivor. Most likely the chemo and the rads have gotten rid of any rogue cancer cell that was lingering in my body. At least, that is what all of my oncologists tell me.

 

I have 7 more rad treatments left. That’s it. 7. And it hasn’t been as horrible as I had anticipated. As a matter of fact, my rad onc Dr. Mc says my skin looks really good, “considering”. I could get into the appearance of my skin, but I won’t. It’s a dull story and compared to how I felt after my surgery, and how I felt for the 20 weeks following my first chemo, I feel fine.

 

I would like to just get out of cancerland and go back to the real world. But I know that for the rest of my life I will be walking with one foot in cancerland. While my “active” treatments may be coming to an end, I still have a lot of cancer treatments ahead of me. The Herceptin (my miracle drug) will continue to be infused once every three weeks until July 2013, I will soon begin popping a daily pill for the next 5 years to block my overproducing estrogen from producing cancer (can I just say here, that like all the things I have been told to do to get rid of this nasty cancer, I don’t want to take this pill?) and there is still one more surgery I need to have. And then I just wait. And every day that I wake up without cancer will be a day worth celebrating.

 

But I would like to wake up and NOT have cancer be the first thing I think about. I would like to go to sleep without cancer being the last thing I think about too.

 

I knew how to live my life before cancer. I figured out how to live my life with cancer. I have no idea how to live my life as a survivor.

 

2 comments:

  1. like always, just one day at a time, as best you can ..

    ReplyDelete
  2. Thank you, Leah for writing your blog on your breast cancer experience. I am still new in my treatment. My diagnosis is invasive Micropapillary carcinoma, ER+, PR+, Her2+, positive lymph nodes. I just did my first Taxotere/Carboplatin/Herceptin treatment on July 9th. It knocked me down pretty good. I have 5more of those withHerceptin in the weeks between chemo. Then Herceptin till July, 2014. Radiation starting in November, and will start Tamoxifen some time and take for 5 years. Your blogg has helped me so much to know that what I am feeling from these treatments is to be expected. I hope and prayvyouvare doing well!! I started a blog as well. It can be found at www.ibethtriposbc.blogspot.com. Best wishes to you.

    ReplyDelete