Crazy Sexy Cancer
It's pretty irreverant, so skip it if you find that offensive.
"I said who put all those things in your head
Published May 14th, 2007 in Crazy sexy cancer.
Susan Mitchell, writing in Salon on the oft-smirked-at phenomenon of chemo-brain, describes it nicely. Memory holes, addled wits, the quite frequent inability to name common objects [ ] : Book. Envelope. Cup.
And when I say she describes it nicely, I mean she is nice about it. She betrays little sense of outrage or crapulence when she admits that her oncologist has difficulty getting too worked up about my forgetfulness. She is even nice when running down the checklist of all the other conditions wrought by chemo et al: neuropathy, stubborn weight gain, hot flashes, excruciating joint pain, the fact that her reconstructed globular unit is no substitute for an actual boob.
In fact, she says a couple of times how grateful she is. She says its hard to complain because after all, she notes, shes not dead. She was lucky to have had the great surgeon who stitched together probably using fat from a foot-long incision in her abdomen the macabre lump of feminine acquiescence on her chest. It is only after explaining how lucky and grateful and understanding she is of her oncologists insouciance that she gets a little cranky. She says she wishes for her old self back.
The point of her piece, of course, is not to cut loose about her bloody fucking awful post-chemo condition. She means to suggest the need for a new field of medicine that would treat the symptoms of the treatment.*
The point of my piece, however, is to complain. Complaining is not virtuous, I realize. In fact, thanks to the corporate breast cancer mascot the plucky, pinkified Breast Cancer Survivor ⢠whos popularized the insane idea that women embrace the disease as an opportunity for personal growth there is nothing in this world so unpleasant as a breast cancer sufferer who
⢠isnt grateful
⢠doesnt feel lucky
⢠wont suffer nobly in silence
⢠thinks all those pious pink volunterrorists are deluded
⢠believes that the pseudo-concerned Racers-for-the-Cure luxuriate at her expense in a false sense of meaningless philanthropy
* is hopping mad over the expectation that she pretend she still has tits
* is even hopping-madder over the expectation that she shut the fuck up
Im even hopping madder that I find myself capitulating. So howre you doing? people ask me, and I almost always answer that Im doing great. Because it would seem so ungracious to answer any other way. I mean, since after all Im not dead and wouldnt it be greedy and ungrateful of me to expect more than that?
Well, Im puttin the kibosh on that bogus shit right now.
This is what its like to survive breast cancer treatment: you feel, every goddam day, like something that oozed from a rotting log after an acid rain. I mean, every goddam day you experience everything on this list:
⢠markedly decreased mental acuity that your friends laugh off because they dont understand its not just garden-variety where-did-I-put-my-keys, but is in fact a substantial and debilitating hit in the old IQ (in fact, its really dementia, but you cant bring yourself to call it that because a) youre only 48, and b) you cant remember the goddam word anyway)
⢠crippling joint pain
⢠either diarrhea or constipation but never neither and you never know which
⢠dizziness
⢠depression
⢠episodic weeping
⢠insomnia
⢠hourly hot flashes
⢠the aura of utter despair that precedes, and is substantially more discomfiting than, the hourly hot flashes
⢠a sense of general debility
⢠extreme fatigue
⢠pain and peeling skin on the radiation site
⢠a flappy, post-hysterectomy bladder
⢠anxiety that the next scan will reveal a recurrence
⢠numbness and pain from the center of your chest to your elbow
⢠the constant sensation, from your dual 7″ scars, that youre wearing a bra two sizes too small
⢠a crushing sense of futility
⢠fear of imminent death
Nothings gonna fix all that shit. And lets face it; socially, its just a big pile of stay-away-you-repulse-me. Even I find it repulsive. If I were you, I wouldnt be touching this blog post with a ten-foot pole.
I suspect thats why Susan Mitchell feels obliged to so agreeably acknowledge her indebtedness to the wonders of medical science. Its impolite to have cancer. Its even more impoliter, when, a year or so after your last treatment and youre still not dead, someone asks you so how are you feeling, and you go, Well, Chet, my post-cancer-treatment life is actually a waking nightmare.
A waking nightmare may be somewhat preferable to death, but only just. Its definitely not a fucking cure, and Im done pretending to be grateful for it.
UPDATE: Heres a list of 10 remarks that are guaranteed to insult the cancer patient. [Thanks, Carol.]
__________________________
* I sympathize with Mitchells call for a branch of medicine focused on fixing the diseases they give you when theyre curing you, but after 2 years enmeshed in the medicorporatocracy, Im pretty sure that any therapy they could come up with to treat FLS (Feels Like Shit) would probably turn you into a bald zombie with hemorrhaging eyeballs.
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137 Responses to I said who put all those things in your head
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1 Spinning Liz
May 14th, 2007 at 12:53 pm
You know its funny, every single time I read one of your posts I think, damn her, how come she didnt get chemo brain, she still has her fucking edge. While my brain has gone as blunt and squishy as a giant sea sponge. Plus my fingers are so numb I cant type worth shit, and four days out of five I forget that I even have a stupid blog to update.
Anyway, add to your list of woes, at least for those of us with less than complete insurance coverage, the post-cancer financial disaster scenario. Ive not only lost my income, Ive lost my entire life savings, plus my house. And even though Ill never ever again be eligible for affordable private health insurance, I still dont qualify for any kind of government aid. Ive fallen through every crack in the system. Yet somehow everybody expects that I should be bouncing back to normal by now. Well, maybe Im not dead but any chance in hell of ever being normal again sure is.
As for capitulating, its only lunch time and already today Ive chirped to seven people that Im doing GREAT!"
Comments
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Yesindeedy.
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Hi BinVA, I hope you don't mind if I put this link here to the blog you mentioned, in case anyone wants to read all of the responses to the original blog post. Thanks for posting this here!
http://blog.iblamethepatriarchy.com/2007/05/14/i-said-who-put-all-those-things-in-your-head/ -
Not at all. I was hoping others wouldn't find it offensive. Usually, I'm one of those really nice kinda people, but sometimes that ornery side of me comes out ... and I kind've like it.
Brenda in VA -
Thanks Brenda so much posting this-The blog says it all----so true!
Thanks Nancy for the link.
Susie -
Oh, how very well said! Loved every word.
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Hell yeah!!
Tina -
Just what I needed today, BinVA, and Nancy, thanks for the link to the blog. I've marked it as a keeper!
Brenda -
That was awesome!! I also put her in my favorites.
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DAMN STRAIGHT!!!!!!!
i forwarded this to a choice few who needed a good old fashioned 'bitch slap' .........won't mean a friggin thing to any of them (if they even bother to read it) ....... but man did that feel good to read .......... i can almost relax and believe i'm not 'nuts' or 'melodramatic' despite how my 'loved ones' treat me post treatment .........
............ this whole "bury our heads in the sand" thing has truly made me crazy with my friends and family ....... they treat me like " you have your hair back girl ,get over it" ........ we don't want to deal with it (never did).......i read this and had an "uh ha" moment ......... screw the morons that want to avoid what we endure everyday ............ i'm no longer willing to apologize to ANYBODY for trying to LIVE WITH CANCER and cope everyday just to make them feel better!
reading this post has liberated me ............ and i'll no longer apologize for being me!
thanks to whoever posted this .......... i'm back on track with my own life, rather than worrying about everybody else and their comfort zone!
i've spent almost 2 years keeping it all to myself ........ just because i have hair again doesn't mean it's over for me!!!!!!
whew ........ thanks for the rant!!!!!! -
BinVa,
Ohhhhh what an exhale that was! Thank you sooooo much for posting this.
I think so often (because I am always reminded) how "lucky" I am to "only have" stage 1 and I "should be grateful". I don't even want to bring my whoos here where ladies are dealing with so much more.
I don't want to go back on anti depressives (detoxed now for two months). I'm still sorting it out....but something deep inside of me says to ride my own wave of who I am without "mufflers".
I even have a tattoo of Jonathan Livingston Seagull on my wrist...did that with my husband six years ago....and I love that when I paid a toll, the man knew it was Jonathan.
arghhhhh I'm going on -
Geez ... and here I was worried I might get run off from the board for copying that blog onto this site.
I realized today, while returning from yet another trip to the pharamacy, that while our loved ones are glad we're alive, they just don't get it, at least not the full impact of "IT". While not "grateful" for the experience of bc, I am grateful I found a place where somebody knows what I'm talking about!!
Brenda in VA -
Right on, Brenda! Thanks for posting this. I'll tell ya, bc has brought me from being the model survivor during treatment (plucky? you betcha!) to a bonafide bc bitch. And, once & for all...I'M NOT OVER IT!
~Marin -
Abso-frickin'-lutely!
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I just tried the link and it didn't work. Any ideas why? I'd love to read it.
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I think I have read this at least fourteen friggin times just to see if what I am reading is really and truly there! And YES..it is!! Finally...someone said it all!! I don't even know what else to say except I too am going to send this off to a few "choice" people and I hope that this article stays here forever!
Thanks
Vickie -
Brenda, that is some post!
I have to admit that since I am in the middle of chemo for a second go around with cancer my nerves and emotions are kind of on the surface right now... how the author is feeling is what I call my cancer-monster. I get the same way and feel everything she expresses, but I try to keep the monster tamped down a bit because I might lose it the next time I am in chemo and the chemo-nurses tell me that NONE of my s/e's are from the chemo...
So far they have been defending it- "Oh no! Abraxane doesn't cause pain, swelling,nails peeling off!" You see, it is all one big coincidence that these things are suddenly happening to me at the same time.
I sure enjoyed reading what she wrote- helped me get some of the built up ya yas out that I have been holding in. -
That is so perfect. My LE is acting up bad and I was sitting here feeling sorry for myself. I am now laughing so hard that tears are running down my face. I would love to forward it to some of my friends, but they would probably be horrified. I just love it...thanks so much for posting.
Liz -
Wow, that was powerful and empowering. Great post!
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Thanks for posting this. As everyone else here has said, we can all relate to this ongoing saga of sh-t!! I'm so glad that at least we all understand, that does help, and you know what I learned a long time ago that I don't give a rat's ass what anybody else in my life understands or doesn't. I know what I go through everyday, and I do the best that I can, and that's all that matters.
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Thanks for sharing that Brenda! Now please fax a copy to every medical professional in the world. Just as a favor to me. Start now, it won't take that long! heeeeheee
Seriously, thanks for sharing.
Deese -
thanks brenda! im faxing a copy to my onc. for sure.. last visit i had with her, and told her about my stiff thumbs, won't move ,sore joints. bladder problem,(and no, i won't use depends) she said, no.. its not from the FAMARA, because you haven't taken it in two mo. like this poison leave you body immediately! and then kind of showed me the door in a polite way.. and said, get a PCP that you can trust, and talk to her/him about it.maybe you have fibromaliga.
boy, was i pissed off..for being so totally ignored.
and to some of the women i work with, who are dumbstruck that i didn't get a free BOOB job at time of double mast.and tell me that they would make me feel more femine!! i tell them that i didn't want a couple of things, that looked like an orange, cut in half, and stuck under my thin,scarred chest skin. no, these mimi-waterbeds, without feeling, will not return me to my old sexy self!!
and to the male ass----, who said, well, you probably won't miss them much, cause they were small anyway!! like the size of my boobs, has anything to do with breast cancer!
purging, purging.. lol tx -
Love it!
Thanks for the link. Talk about a theraputic read?!
Isn't cancer supposed to be what it isn't and all you didn't know it is?
Definately sexy...lol!
Indi -
Quote:
This is an excerpt from a post on Crazy Sexy Cancer. The author of the book wrote this on her blog.
I wanted to clarify that Twisty Faster, the author of the above blog post, isn't the author of the book, "Crazy Sexy Cancer". That is just the label Twisty gives to all of the posts she makes about her cancer journey. If you click on the "Crazy Sexy Cancer" category under the title it will bring up all of her cancer posts.
I've been reading her since before her diagnosis and I love her. She has documented her cancer journey with sobering pictures and cutting wit. Here's another very good post, but I'd skip it if you happen to love the Komen Foundation.
http://blog.iblamethepatriarchy.com/2007/01/26/good-news-bad-news-2/ -
Thanks for the clarification. I appreciate it.
Brenda -
"...and then we're going to tie a pink ribbon around it"
WTF?!
I am stuck in the dichotomy of it all. Somewhere in between getting strength from the pink symbol and getting pissed off at the little pink symbol.
I will keep reading her blogs. They are empowering. -
What a great read. I can't wait to see her documentary on 8/27/07 on TLC at 9/8c.
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Ooops...I mean 8/29/07. Hugs...
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Wow great read. I feel like carrying copies around to had out to the clueless. I don't think most could handle the reality though.
Sue -
This is great, Brenda!
~Thank you~ -
Bump-
Just a reminder to watch Kris' documentary on TLC, 7est/8pm central on Wed 8/29.
Thanks to the original poster. I have been reading all about her and may even buy the book as I enjoy reading her blog. If you want to see a trailer of the film or check out her blog go to crazysexycancer.com
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