Official diagnosis
Posted: February 1, 2011 Filed under: breast cancer | Tags: breast cancer, cancer battle, cancer diagnosis, DIEP, hospital, new boobs, plastic surgery, post-mastectomy, surgery 4 CommentsWhile looking through my paperwork from Dr Spiegel and mapping out the next month of pre-op stuff I have to do, I found something that made me laugh out loud.
I hope you find it funny, too.
If you don’t, there’s something really wrong with you.
This is the orders for the EKG and labwork I have to get done before my reconstruction. 
The handwriting is kinda hard to read, and the picture is pretty fuzzy, but if you look closely you’ll see that for Diagnosis, it says “absence of breasts.”
Other than laughing hysterically, I don’t know how to respond to that.
Mommy calling cards
Posted: January 29, 2011 Filed under: breast cancer, kids | Tags: baseball, breast cancer, cancer diagnosis, Desperate Housewives, Little League, mommy calling cards, post-mastectomy, preschool, suburbs, SUVs 12 CommentsI’ll admit it right here, live on the web, in front of however many people are reading my blog today: I’m not 100% into the whole suburban mommy thing. Thankfully, my kids are old enough now to (A) be in school all day Monday through Friday, (B) no longer need constant supervision, and (C) no longer follow me into the bathroom. Don’t get me wrong, I love and adore my kids, and I think parenthood is a noble and under-appreciated profession, but child-rearing isn’t my whole life, and I like to have some time away from my kids every day.
My favorite thing in the world is to be home alone. I know, I really should set my sights higher.
I crave peace & quiet. I get overstimulated like a small child when there’s too much noise, too many voices, or too many electronic devices running at the same time. I have been known to go to my room for a self-imposed time-out during times of chaos. Which is pretty much every day at my house. I’d like to blame it on the stress in my life from the whole cancer thing, but the truth is, I’d be that way if the words “malignant tumor” weren’t part of my life.
Like many suburbs of big cities, ours is a bubble. Everyone around here is affluent, successful, talented, well-educated and better-than-average looking with kids who are nothing if not gifted and talented. A gas-guzzling SUV is de riguer. A minivan works, too, but sedans, not so much. Nobody cleans their own house (except for me, because I’ve never been comfortable having “the maid” in my house when she and I both know perfectly well that there’s no reason I can’t mop my own floor), and everyone is overscheduled and overworked with overprocessed hair (myself included; I seriously have no idea what my real haircolor is but I know that it gets darker all the time).
Since I’ve never seen an episode of Desperate Housewives, I can’t say that my little bubble is similar to or different from from Wysteria Lane, but some of the stuff I see around here makes me think, you couldn’t write a more outlandish script if you tried.
Like the mother of the first-grader who’s in the principal’s office multiple times a week (the kid, not the mother) for bad behavior who asked the teacher to please call her (the mother) next time the kid was about to be sent to the principal, so she (the mother) could come pick the kid up from school. Apparently the mother “feels bad” for her child because his life is so rough, and it’s not his fault he has such bad behavior, he just doesn’t like to go to bed at night so he stays up until he passes out in front of the TV at 1 a.m. Every night.
True story.
Or the principal who nixed plans to have a fundraiser to benefit the family of a child with cancer–a child who had been attending that school until too sick to come anymore–because it might hurt the feelings of kids who don’t have cancer.
Another true story.
Now, don’t assume that all this goes on at my kids’ schools, because I know people in other neighborhoods whose kids attend other schools. And I wouldn’t rat out my own kids’ schools (unless it was a really, really good story). Suffice to say that these are examples meant to convey a sense of an overall picture.
I did camp out — literally, as in spend the night in the parking lot — to ensure that my kids got a spot in preschool, but not because it was the preschool to attend, but because it was the only one with an opening, and I really, really wanted to hand my toddler off to someone qualified for a few hours a week. And yes, I did willingly buy a plane ticket and fly in from North Carolina to camp out at that very preschool (and waited in the cold rain) before we moved back, to make sure Macy had a spot at the same preschool Payton had attended before we moved away.
But I was never really one of those mothers. I looked like the other suburban mommies, I did indeed quit my job and surrender my paycheck to raise my kids, I do drive a gas-guzzling SUV, and I pay a ridiculous amount of money for organic milk to avoid those pesky hormones & antibiotics that my generation consumed.
My kids just aren’t my whole world. They are a big part of it, and if there was a pie chart depicting the parts of my life, the part labeled “kids” would be the biggest. By far. But there would also be a part of the pie for tennis, book club, cooking club, and friends; in other words, I have other interests outside of my progeny.
So imagine how hard I laughed when one of the pop-up ads on my web browser was hawking “Mommy calling cards.”
Have you seen these?
If you have a set, you might want to stop reading now, because I’m fixin’ to rip on them pretty hard.
It’s not bad enough that this poor woman, and apparently lots of other women, identifies herself as Lillian’s mom and Matthew’s wife, but the card itself screams MOMMOMMOMMOMMOMMOMMOM all down the side. That MOMMOMMOMMOM screaming is the reason I need to hand my kids over to someone else and take time-outs, and now the mommy calling card is not only endorsing but promoting it?
How about this one? Really cute design, I will admit; I really like the smiling fish and the cool blue color, but my first thought was, since when did we get to the point of having to hand someone a card and beg them to be our friend?
Am I making too much of this? Because it seems pretty ridiculous to me.
A quick Internet search turns up all kinds of options for mommy calling cards. Tons of cute designs and fun colors. And I am a sucker for good stationery. I adore heavy cardstock, genuinely appreciate embossed invitations, and have no problem spending good money on paper goods.
But these seem crazy to me. Really crazy. 

This one not only identifies the breeder as Elizabeth & Gabriella’s mom but also has a convenient place to mark the dance card, as it were, and force the recipient to commit to a playdate right here! right now!
You can even have photo cards, to be sure the person you hand it to knows exactly what your kid looks like. Or in case you’re worried that your Olivia or Mackenna will be confused with the other one in her playgroup.
While I do admit that Lindsey Walters is a cute little girl who likely comes from a very nice family, I can’t for the life of me imagine myself seriously handing someone a card hawking my kid.
If Payton were to make make it to the Major League and had a baseball card, I would for sure hand those out to any and all interested parties, but that’s a long time in the future and a big uncertainty. Which is another thing that disqualifies me for Suburban Mommy of the Year; my pesky realistic impression of my kids’ abilities. Some of the baseball parents we’ve met at the fields seem a lot more confident than me that their kid will be the one that hits the big time. Even though the odds are a little sobering: as in about 1 in 200 players. So 0.45 percent of all boys playing high school ball. Not very many. Payton’s Little League has something like 800 kids total, from t-ball to majors. So 4 boys in the entire FCLL, but half the parents up there think there kid is the best thing since Ted Williams. Payton genuinely believes he’ll make it, despite the odds (and more importantly, despite his tendency to depend on his innate ability rather than work hard at honing his craft). And I encourage him wholeheartedly to go for it, pursue that dream and aim high. There’s nothing that would please me more than if it happened for him. But I also tell him to study hard and have a back-up plan, just in case it doesn’t work out.
Because some kind of cosmic force is indeed in effect right now, shortly after the Mommy calling card pop-up ad appeared, I came across a website that offers snarky versions, for the not-so-perfect moms. 
Like me.
Ok, I admit, this one is a little harsh, even for me.
Hush now, I know some of y’all think I’m the queen of harsh, that I invented snarkiness and that I live to mouth off.
That’s not entirely true.
This one is a little kinder. A little gentler. Yet gets the idea across.
I admit, I like the bumper stickers that say “My kid could beat up your honor roll student” or however they word it. I wouldn’t put one on my own vehicle, but I snicker every time I see one. Bad mommy.
Here’s the modern suburban mom’s version of Sophie’s Choice, conveniently laid out on a snarky card. Hee hee.
And I make no promises about little risk of mycobacterium.
Blogging is like…
Posted: January 26, 2011 Filed under: breast cancer | Tags: advertising, America's Funniest Videos, blogging, breast cancer, Broadcast News, cancer diagnosis, James Harrison, Katie Couric, kids, leopard gecko, Matthew Perry, science fair projects, Sports Center, Steelers, stupid people, tennis, Tiger Mother, viagra 1 CommentBlogging is like having children…you don’t have to be very smart to do it.
I’m making this wildly judgmental statement based on the itty bitty amount of research I’ve done since becoming a blogger.
That tag, “blogger,” still sits a little uneasily with me. I don’t feel like a blogger, and most days I’m pretty sure that what I have to say isn’t particularly important or interesting to very many people. But once I was diagnosed with breast cancer at the tender age of 40, I realized that there were some people who wanted to keep up with the latest on my situation, and that it is completely impossible to convey such news without blanketing and broadcasting. Thus, a blog was born.
It started out as rudimentary thing on Caring Bridge and grew into this. While this is certainly a step up from Caring Bridge, I still don’t consider myself a blogger. Not that I have blogger’s block (as evidenced by my rambling posts), nor do I suffer insecurity. I simply consider myself a small fish in a big pond. I recently had a little look-see on the blogging scene. Took a peek into what’s out there, and wow, there’s some bad writing, boring topics, and strange people. I’m still a small fish in a big pond, but hopefully this fish writes well about cool stuff and isn’t too strange.
The amount of stuff I don’t know about blogging is vast. It’s humbling and overwhelming but also ripe with potential. Sorta like life. And really a lot like tennis.
“Really a lot” is one of my favorite phrases. Makes me want to watch Broadcast News again (the movie, not Katie Couric).
That’s the kind of thing you can do with a blog — blab on & on about your personal favorites, or complain about things you hate the most.
Top of my list today of things I hate: science fair projects and inappropriate advertising.
Not together, necessarily. Although maybe some kid could do a science fair project on how inappropriate advertising affects people. That kid could start by watching Sports Center, as my kid does every day of his life, and see what kind of filth and scum pops up in 30-second bites around the real stories.
Just this morning, right after a nice human-interest story on James Harrison, the Pittsburgh Steeler who has been called “the most violent man in the most violent of games,” was an ad for the new Matthew Perry sitcom. The ad featured a woman complaining to Matthew Perry about losing her underwear in his apartment, or some such nonsense. It may be a great show, and maybe this is a riveting storyline, but does it really have to be on Sports Center at 8 a.m.? Can’t they just run another Viagra commercial instead?
Another inappropriate advertising incident (or IAI, for short) that comes to mind: while watching America’s Funniest Videos on ABC Family network, my kids’ retinas were burned by the commercial for the new Ashton Kucher-Natalie Portman movie about hooking up. I’m not going to pander to this media monster by adding a link; if you want more info about this utter waste of acting talent, you are on your own.
Looks like a triple scoop of wildly judgmental rants today.
Need I reiterate that this supposedly family-oriented program on a supposedly family-oriented network was rudely interrupted by a grossly inappropriate ad?
Probably not.
And yes, I did contact “ABC Family” to complain. I’m sure they are busy writing me an apology letter contained in a Hallmark card with a gift card to my favorite restaurant accompanied by a bouquet of flowers with a mylar balloon that says, “I’m sorry.”
Moving right along.
Science fair projects make the list because the 6th grade boy who lives in my house came home from school yesterday with some rude news: the science fair project he thought was optional is indeed very much required.
Cue the frantic scrambling and keep your ears peeled for the screeching to a halt of any carefully-laid plans for the evening. The timing of such everyday calamities never ceases to amaze me. Macy and I were just getting ready to clean out her leopard gecko Cinko’s tank, a project I had been putting off far too long. Just as we were gathering up cleaning supplies and girding ourselves for this task, the calamity du jour erupted on the scene.
It took 3 adults, a trip to Hobby Lobby, a pack of D batteries, and lots of beer to deal with the science fair project snafu, and that shamefaced boy was up way past his bedtime, but we got ‘er done. I can say with absolute certainty that his project would make a Tiger Mother shake her head scornfully at the lazy and slovenly habits of my kid, but that’s ok. Those Tiger Mothers freak me out a bit anyway. But if you feel the need, you can read all about it here: http://www.amazon.com/Battle-Hymn-Tiger-Mother-Chua/dp/1594202842/ref=sr_1_1?ie=UTF8&qid=1296051025&sr=8-1.
On second thought, that looks kinda messy, so try this instead.
I told you I’ve been studying up on blogs.
It does help to have an in-house IT guru (thanks, Trev).
I have a lot more to say about Tiger Mothers but will save that for another day. Because today’s topic is…
Um, I’m not really sure.
It started out as one thing but morphed into something else. That happens here a lot.
Oh yes, now I remember: things I hate.
Or was it things I’m wildly judgmental about things about which I’m wildly judgmental? (hey, this blog has some pretty nifty features.)
Or was it how stupid science fair projects are and how they should be banned outright from all the public and private school systems in the world?
I have no idea.
Dear Santa,
Posted: December 22, 2010 Filed under: breast cancer, cancer fatigue, drugs, food, infection, kids | Tags: Bactrim, baseball, Biaxin, bloodwork, bone scan, BRAC, breast cancer, cancer diagnosis, Cefapime, champagne, Christmas, Christmas list, Cipro, collection agency, CT scan, dogs, ER positive, flat chest, genomic testing, good girl, health insurance, HER2 negative, home health, hospital, Houston, infection, infectious disease, injections, IV antibiotics, kids, L-Dex, lymph nodes, mastectomy, minocycline, MRI, PET scan, plastic surgery, post-mastectomy, PR positive, Santa, survivor, tamoxifen, Vancomycin, wound care, wound vac, x-ray, Zyvox 4 Comments
I’ve been a pretty good girl this year. I’ve smiled at fussy babies in checkout lines at HEB. I did my time at the grade-school class parties (not my scene, to say the least). I called the collection agency back — yes, I really did — when they left me a message saying I owed money on a past-due hospital bill that my insurance company says has been paid. I donated nearly-new clothes & home goods to charities multiple times. I helped out with the school fundraiser, even though I really, really, didn’t want to. I’ve said please and thank you and bring my own bags. I was a big girl and good sport about all the trips and baseball games I missed this past summer.
And while we’re on the topic of this past summer, dear Santa, do ya remember all the hell I went through? It all started on April 27, 2010, when I was diagnosed with breast cancer. Talk about an “aha” moment. The timeline quickly unfolded like this: the rest of April and first part of May were consumed with tests, tests, and more tests: BRAC analysis, CT scans, x-rays, PET scan, bone scans and MRI. In case that’s not enough acronyms for ya, there was also the L-Dex and then the genomic typing of ER/PR positive and HER2 negative. More injections and blood draws than my poor left arm’s veins could keep up with (literally; there’s a permanent knot in the big vein). Countless appointments with the breast surgeon (Dr Dempsey, who is on the “nice” list) and plastic surgeon (Dr S, who may be on the naughty list), and 3 different oncologists.
Meanwhile, there was research to be done and crushing decisions to be made as I prepared for surgery. The phrase “life and death” took on a whole new meaning, sweet Santa. There’s a strange juxtaposition between packing school lunches and signing field trip permission slips while also filling out my medical directive and living will. I learned pretty fast how to act normal when everything around me had been turned upside down. I think, dear Santa, I also did a pretty good job of adjusting and adapting to the new normal. I think, fat man, I’m still doing a damn fine job of that. One quick look at my profile tells you that there most definitely is a new normal around here.
Santa baby, I was a good girl after the double mastectomy and the lymph node removal that left me battle-scarred and weary. I was an especially good girl in the face of the plethora of prescription drugs I could have used & abused. I was a diligent girl when it came to choosing green drink over Diet Coke, all-natural hormone-free yogurt over Blue Bell.
Santa, I was a brave and good girl when the nasty infection set up shop in my still-raw chest wall. I endured the 103-degree fevers, 22 days in the hospital, multiple tissue excisions and untold poking & prodding without much complaint. I missed the comforts of home, my dogs & my kids more than words can say, but I only cried twice. And even then, it was when no one else was around to see.
We don’t even need to recount the 18 days during which I was attached to the wound vac 24-7. I would really like, dear Santa, to permanently erase that memory from my grey matter, por favor. But I would like to remind you that I was a trouper during the home health days, and all those hours that were consumed with wound care and the administration of IV antibiotics. And while I’m at it, can I get a little shout-out for not killing Dr S, even though he probably deserved it?
Oh Santa, I do crave some credit for all the antibiotics I’ve endured — and continue to endure. From the Vancomycin to Cefapim, from the Cipro to the Zyvox, from the Biaxin to the Bactrim and Minocycline. Those last two will be part of my daily routine for a few months yet, but I’m already looking forward to the day in which I don’t have them on my kitchen counter anymore.
So Santa, how about we make a deal? I’ll set out all the milk & cookies you want in exchange for one little thing. All I want for Christmas is to have it easy for awhile.
R.I.P., Elizabeth
Posted: December 8, 2010 Filed under: breast cancer, kids | Tags: breast cancer, cancer diagnosis, cancer treatments, champagne, death, Elizabeth Edwards, family, gratitude, grief, infidelity, John Edwards, loss, love, Mom, mortality, resilience, stage 4, stage IV, strength, survivor, tumor 9 CommentsI just read, yesterday morning, that Elizabeth Edwards announced that “future cancer treatment would be unproductive” and that she had only months or maybe even weeks to live. And then she died. That same day.
I’m so sad. For her. For her kids. She’s suffered a lot already (let’s not even mention her jackass husband and all the suffering he brought into her life). She wrecked up my childish yet dogged desire to believe in a limited amount of suffering in one person’s life. I wanted to believe that losing my mom would be the worst thing to ever happen to me. So far it is, but when I look at Elizabeth’s Edwards’s life, and the fact that her 16-year-old son was killed in a car crash, I am smacked in the face with the reality that there is no limit to the amount of suffering in one’s life.
Obviously, I don’t know her, but she seemed to have a lot of class, regardless of politics or religion or her jackass of a husband. She lived most of her life in relative obscurity, practicing law and raising the family she vowed to create after Wade was killed. My heart breaks for her remaining children. Cate, who is in her late twenties, will likely become the mama to Emma Claire, 12, and Jack, 10. All three of them will have to navigate the treacherous terrain that is life without their mama. No matter how old you are, you never stop wanting your mom. Former press secretary Jennifer Palmieri said about Elizabeth, “Any room she walked into, she made it a home.”
That’s a real talent.
Elizabeth faced her breast cancer publicly and bravely. She was diagnosed in November 2004 and made headlines when she urged her jackass of a husband to continue his presidential campaign despite her Stage IV cancer.
Stage IV. That’s as bad as it gets, and the fact that she wanted him to continue his dream despite the tumor in her breast and the spots on her rib, lung & hip, is the epitome of selflessness.
She was brave, and she was a fantastic example to cancer patients everywhere that life goes on. Despite diagnosis, life goes on. Despite treatment, life goes on. Despite surgery, life goes on. Despite complications, life goes on. Despite John Edwards making a fool of himself and a mockery of all that his family held dear, life goes on.
And life did go on for Elizabeth. She worked hard: raising her family, writing 2 books, advising President Obama on health care reform, and doing her best to make a difference–for her family, for countless cancer patients, and for herself. Although she was all these things: attorney, author, advisor, advocate, she said often and proudly that her job was to be a mom.
She knew her cancer wasn’t curable, but treatable. She did all the right things and tried to stay strong, despite life on the campaign trail.
Her final statement reflects upon the kind of person she was and the sheer strength she embodied:
“You all know that I have been sustained throughout my life by three saving graces – my family, my friends, and a faith in the power of resilience and hope. These graces have carried me through difficult times and they have brought more joy to the good times than I ever could have imagined. The days of our lives, for all of us, are numbered. We know that. And, yes, there are certainly times when we aren’t able to muster as much strength and patience as we would like. It’s called being human. But I have found that in the simple act of living with hope, and in the daily effort to have a positive impact in the world, the days I do have are made all the more meaningful and precious. And for that I am grateful. It isn’t possible to put into words the love and gratitude I feel to everyone who has and continues to support and inspire me every day. To you I simply say: you know.”
In a 2007 interview she spoke realistically about her cancer, saying, “When I was first diagnosed, I was going to beat this. I was going to be the champion of cancer. And I don’t have that feeling now. The cancer will eventually kill me. It’s going to win this fight.”
Her cancer did win, but she is a champion nonetheless. Rest in peace, Elizabeth.
Portrait of a survivor
Posted: November 23, 2010 Filed under: breast cancer | Tags: bloodwork, breast cancer, cancer diagnosis, champagne, coffee, CT scan, infection, IV, lymphedema, mastectomy, pink ribbons, port flush, Race for the Cure, reconstruction, recovery, recurrence, survivor, tennis 4 CommentsWhen you think of a breast cancer survivor, what comes to mind? A granny all decked out in pink? A joyful gal in a ball cap crossing the finish line at the Race for the Cure? How about a sad sack sitting in yet another hospital waiting for yet another test? You might think that surviving the diagnosis, the surgery, the treatment(s) and any subsequent complications means you’re done, right? Wrong. You’re wrong. It doesn’t end there, and there’s no prize for getting through it.
Welcome to the next phase of survivorship: the constant vigilance required to ensure the cancer isn’t making a repeat appearance. Although I’m just getting started, I’ll quit my bitching just long enough to say I am grateful that my doctors are vigilant, that I have good insurance, and that I can get the majority of my tests done 10 minutes from home. That said, it’s still a giant suck-fest.
Today’s test is a CT scan to check 2 little spots–1 on my liver & another on one of my lungs. These little gems were uncovered during a CT scan the last time I was hospitalized, in mid-August. No one seems too worried about them because they are so small, but once you’ve had cancer, you learn the hard way that there is no sure thing. There is no guarantee. A spot is a spot, no matter how small, and a spot is never a good thing once you’ve had The Big “C.”
Hence today’s CT scan. I’ve never had an abdominal scan before, so I didn’t know that in addition to the fasting and IV contrast (where they inject dye into my veins), I also get to drink the dye. So instead of my daily cup of coffee (which, by the way is the #1 reason I get out of bed each morning), I had to gulp down two big cups of Sprite mixed with contrast dye. No ice. No vodka. That’s just mean. I don’t like Sprite on a good day, and by good day I mean one in which the Sprite is mixed with vodka. Lots and lots of vodka. The only good thing about drinking these 2 vile cups is that I could have burped loud enough to seriously impress a room full of middle-school boys. Too bad the waiting room was full of old people, who either wouldn’t hear it or would think it was rude to launch into a Buddy-the-Elf style burp.
After the Sprite-fest was the IV contrast. Ugh. I really don’t like needles, but have had enough of them in the last 6 months, whether IVs or blood draws or shots or port flushes, to kinda get used to them, but I still don’t like them. My veins on the left side have been used so much that they rebel. They act nice at first, so right after the big stick, to pierce the skin and enter the vein, it seems as if it’s going to work, but just as the nurse is threading the needle higher into the vein, that vein says, nope, no farther. The nurse typically digs around a while before giving up and moving to the other arm.
Cue the complication: because my infection was on the right side, and because I’m working hard to avoid lymphedema (swelling from surgery or trauma that can be permanent and that is seriously contraindicated with tennis), I’m supposed to avoid getting my blood pressure taken or blood drawn from my right side. But that’s my good side! That vein hasn’t been used & abused so much that it pouts and throws a tantrum like a toddler who’s way past nap time.
Sigh.
Luckily, the nurse was very nice. She listened to my long, drawn-out story about my bad luck on the right side and bad veins on the left, and rolled up her sleeves to try and make it work. Work, it did, with just a little big of digging on her part. After the IV it was time to lay down on the CT machine. No big whoop. No trick there, just suck it up because it’s hard plastic instead of Tempurpedic. And then the fun part: injecting the contrast. If you’ve never experienced this, let me be the first to tell you that if you have to go through this, remember: as the dye enters your vein and travels throughout your body, you will feel a warm, wet sensation. Don’t panic and think you’ve wet your pants. Don’t worry too much about it because before you know it, the “did I wet my pants?” sensation is replaced by a crushing headache and the feeling of wanting to simultaneously vomit and pass out. It’s also ok to want to cry for yo mama. The good thing (!) about all this is, it doesn’t last very long. So before you know it, the “wet pants, gonna puke, but wait I might pass out” feeling is over, the scan is done, the nurse yanks the needle out from your vein, and you are free to go. Come back in three months, though, to do it all over again.
So the survivor vigilance is a lot of work. It’s hard enough to live with a monkey on one’s back, wondering if/when the cancer is going to recur. It’s hard enough to wonder, am I doing enough? Asking the right questions? Worrying about the right issues? Researching the right stuff? It’s hard enough to put complete trust, and thereby one’s life, in the doctors’ hands. They are human, ya know. As schooled and trained and rich in experience and purpose as they are, they’re still human. So as much as I do trust them, there’s always that little voice in the back of my head wondering, what if they’re wrong? What if they made a mistake?
Nobody said it would be easy, but I really didn’t think it would be this hard. That’s why I have this cute little pillow on my bed, to remind me that yes it’s hard, but dadgummit, I am indeed a survivor. Period. 
It certainly does…
Posted: November 17, 2010 Filed under: breast cancer, cancer fatigue | Tags: breast cancer, bumper sticker, cancer battle, cancer diagnosis, cancer sucks, champagne, existential, recovery, survivor, the Gap, the mall 2 Comments
Saw this coming out of the Gap last night and was compelled to stop in my tracks and take a picture — even though the owner of the car was standing right there looking at me like I was a wack-o. I’m pretty sure she didn’t want to get started on a conversation with me, of all people, on the myriad ways in which cancer does indeed suck. We might still be there, standing in the parking lot of First Colony Mall, me a bit winded but still mighty revved up, her wondering what on earth she possibly could have done to deserve this and desperately trying to think of an excuse to get the hay outta dodge.
But I digress. The topic today is how many ways cancer sucks. There’s the obvious: it kills people. There’s the more subtle: it may not kill ya, but it’s serious. There’s the financial: it’s expensive. There’s the practical: it’s time-consuming and draining. There’s the physical: it’s far-reaching in its ways to mess your body up (and it causes me to end a sentence with a preposition, something I am loathe to do). There’s the existential: what is the meaning of this? There’s the guilt: Why me? (or why me, and not someone else who’s really pretty bitchy?) There’s the sad: it’s just sad. There’s the depressing: it’s hard to stay cheery in the face of all this. There’s the hopelessness: you can do everything right and still get burned.
And that’s just what I came up with real quick off the top of my head, but I think I’m on to something.
One-upmanship
Posted: November 15, 2010 Filed under: breast cancer | Tags: bilateral mastectomy, breast cancer, cancer battle, cancer diagnosis, cat, cat fight, recovery, stitches, surgery, survivor 7 CommentsSo I was minding my own business at the pack & mail when a guy in the store started talking to the store owner about the stitches in his finger. He had been bitten by a cat and had 5 stitches. He wanted to show Monica, the owner, his stitches, and she was grossed out and didn’t want to look. She asked me if I was squeamish. I had one of those moments of wondering, does she want me to answer truthfully, or make nice and say something normal?
Y’all can probably guess where this is going. I said, I used to be squeamish but I’ve had to do some stuff lately that I never thought I’d be able to do.
The man asked if I wanted to see his stitches, or if I’d be grossed out. I didn’t hesitate to one-up him. I said, 5 stitches? Dude, I had a double mastectomy; 5 stitches is nothing.
I think I might have ruined his day. But, a little perspective is a beautiful thing.











