Sometimes You Just Have To Be A Mom

ultrasound

It’s so funny, when you are pregnant (and have only had good pregnancies), the opportunity to have an ultrasound is so exciting. But one bad experience, and seeing a machine like this loses all its fun. Excitement is replaced with anxiety. The ultrasound machine is also a staple for breast imaging, but since there’s no hope of getting an early glimpse of a precious, tiny baby, it’s no fun. When your best hope is to see a cyst or a glob of fat, it’s easy to loathe the sight of this machine.

Last week, a very tiny nodule that I’d been trying to ignore for a week or so finally reached a critical level for me. They say you should wait for any symptom to continue for two weeks before reporting it, so I’d been trying to put it out of my mind to see if it would resolve. But after two weeks, the nodule (I refuse to call it a lump because it’s so tiny, and somehow it helps me emotionally not to have to say I have another lump in my breast) was still there, though still as tiny as a piece of orzo.  In the mean time, I’d managed to find another nodule, maybe the size of a half grain of rice, just adjacent to it.

I hated to call my surgeon, knowing that it’s probably nothing. I hate to be an annoying patient. Yet, I know that being observant and quick to act worked to my advantage before, so I can’t quite accept my own half hearted assurance that it’s probably nothing. I called and they couldn’t see me until mid-July. This made me realize how my original cancer diagnosis really was an answer to an unprayed prayer. I called about that lump and was able to be seen the next morning.  Now, as an established patient with a history of cancer, calling about a lump on the same side as the original cancer, I had to wait six weeks for an appointment. I took that appointment, but knew that I’d be seeing my plastic surgeon later that morning.  He felt what I had, and assured me that it was likely an artifact of healing after surgery, but that I should have my surgical oncologist check it out. When I mentioned that I had an appointment in July, he said he’d send her an email.  I was rescheduled that afternoon and had an appointment in two days.  (Love my doctors!)

It wasn’t a great appointment time for me, I had to miss the first grade play and would be late to the bus stop. But I needed to take it, and I need to do all the mom duties, too.  So I saw the dress rehearsal of the play and got a friend to cover for me at the bus stop. My surgeon applauded my self-examination skills (I think she was shocked that I’d found such tiny bumps, it took her a little bit of effort to find them!) and was able to find them quickly with the ultrasound. They looked like little fat globs on ultrasound, so my options were “watch and wait” or biopsy. At this point in my life, with my history and personality, I can tell you that “watch and wait” will almost never be an acceptable solution to me. So we headed over to the procedure room and prepped for a biopsy.

I thought of the last time I lay on that table. And then I forced myself not to think of the last time.  She was able to aspirate the area, and thankfully that meant I wouldn’t need to have a core biopsy.  She assured me that it was nothing.  She would “eat her hat” if pathology revealed anything abnormal.  I have this crazy response to physiological stress– my teeth chatter.  It’s worse if I’m cold, but it doesn’t happen because I’m cold.  I remember it happening after at least one of my kids was born, and it’s happened after most procedures I’ve had during the whole cancer thing. Once again, I put my shirt back on and fought to keep my teeth from chattering audibly as I left the office.  And because I’m a mom, I hopped in the car and headed to the bus stop, hoping the chattering would stop before I arrived.  I left the air conditioning off and the windows rolled up, and the warmth of a car in June helped calm my chattering teeth just in time. I parked (illegally), hugged the kids, and sat to chat with the crew.  I could worry about that pathology later. But right then, I just needed to be a mom.

(Just got back from the bus stop, where I heard from the doctor’s office– the cyst she aspirated was benign.  So I guess she won’t have to eat her hat after all.)

Pre-Op Checklist and a Physician Mandated Trip to Nordstrom

pre op tubesThis week I needed to head back to the hospital for another round of pre-op questions and tests.  I decided to combine the stop at the pharmacy (to drop off the heavy antibiotics and narcotics scripts for post-surgery) and the trip to the hospital with my morning run.  The whole trip would only be 3-4 miles, but I failed to realize that the first mile and a half was almost completely uphill.  I think I’ve been spending too much time on the nice flat parts of the trail– I’ve forgotten what a workout those hills can be!

Between the hills and the fact that it is June, I was pretty sweaty by the time I got to the hospital.  Everyone kept offering the empty chair next to them, but I was too sweaty to sit in a chair! So I hung out with my Spotify tunes and water bottle on the floor. The woman who pre-registered me for surgery has pre-registered me at least once or twice before. It’s always a little strange when someone at such a huge place recognizes me. And the woman doing the blood draw was also a familiar face.  Next time (though let’s hope there’s not a next time!) I’m going to have to remember to ask her not to use the tape that they put on after the blood draw, a band aid would be fine.  It left a much bigger mark than the needle!

I also had the requisite 30 minute nurse phone interview where I had to recount my entire medical history. I can’t imagine what that phone call must be like for someone who’s older and has lots of meds and decades of surgeries to recall.  Mostly, after I went through my surgeries list, I just said “no” a lot. I’m apparently as healthy as a horse. Except for that pesky cancer.

So surgery’s coming up next week.  I’m hopeful for an easy recovery.  I’m not supposed to run for six weeks, but I did get my surgeon to concede that I could ride a bike, so I’ll have to do that.  I don’t have to wear a compression bra, but I wasn’t in love with the compression gear he suggested if he does lipo on my tummy. This would be a good time to point out that it never hurts to ask if you have a question. While the high waist girdle with suspenders (so wretched for July!) was the best option from the company whose brochures they have in the office, a quick chat with Cami let me know that a pair of high waisted spanx from Nordstrom would provide just as much compression without the waistband issue that they’d had with the non-suspsender girdle.  And since the Spanx don’t have zippers down the side, they can go in my regular Spanx rotation. Win-win.  One more trip to Nordstrom, a few last runs, and I’ll be ready to head back to the familiar confines of outpatient surgery.

What to Wear to the Plastic Surgeon | Fat Grafting and Liposuction Edition

wntw plastic surg

Today as I was getting ready to head to the plastic surgeon’s office for my pre-op appointment, I went, yet again, through the long process of deciding what to wear.  It was hot, a perfect day to wear a dress.  Only, once you have breast cancer, every doctor wants you to undress from the waist up before you don a paper gown.  So no dress or you end up wearing nothing under that lovely paper gown.  So jeans maybe.  Only, no jeans that are too low rise, remember you’re sitting on a table sans shirt, and well, you know.   Also no jeans that are too tight at the waist. Nobody wants to show off a muffin top. But after choosing just the right jeans/short/skirt, you’re not done. If it’s a visit involving liposuction (which mine was– for the fat grafting) you need to wear the good panties.  You’ll have to be able to drop trou to show off your “donor sites.” Which means you get to show off the parts of your body that you think are the fattest. Awesome. Tummy as a donor site means just unzipping, but if you’re considering the flank (yep, that made me feel a bit like livestock) you have to shimmy down those shorts all the way to show off your outer thighs.  Which is a good time to point out that you should consider doing all your <ahem> grooming before this appointment.   Not only is this important for the part in the office with the surgeon, but also the part later where pictures are taken.  No paper gown, pants around your ankles, and someone takes pictures of you in your panties (I told you to wear the good ones!), zooming in on your breasts and your fat parts. I mean, donor sites.  So when I said you need to be comfortable with your plastic surgeon and the staff, I really wasn’t kidding.

The good news from my appointment today is that my surgeon said that I don’t have to wear the compression bra after the surgery. That’s huge.  His real concern is that donor site, which, let’s face it, could use some compressing anyway.  So I’ll have four to six weeks in that compression gear. The not so good news– while he said that there is “ample volume” (thanks) to use the flank as a donor site, the fat might not be quality fat.  Apparently, all fat is not created equal, and since he already did liposuction in that area, it might have compromised the quality of the fat for future use. So we chose my abdomen as a back up donor site. I’m not thrilled with that prospect because it means wearing the high waist girdle, which will be pretty hot in the summer months.  You know you’ve reached some sort of low when you’re hoping to just wear the low waist girdle for six weeks.  So fingers crossed that my flank has some good, quality fat. At least I only have to wait a couple more weeks until I know whether my fat is quality fat.  And until I can begin the countdown to the “this is really the last time I wear compression gear” day.

Kids Will Be Kids | (And a Pixie Grow-out Update)

zoo with turner

After my haircut last week, I was a chaperone on the first grade zoo field trip.  Being in charge of a big group of kids at the zoo is a nightmare. On this trip, though, they make a big deal out of getting a lot of parents to go, so I ended up in charge of Turner. And that’s it. Ironically, I realized that Turner and I haven’t gone on many adventures by ourselves, we always had Emma Clare in tow. He was so cute, holding my hand, and he was in charge of the map– choosing our next stop and directing us to our destination. (Which was probably a good thing, knowing my sense of direction!)  The arrival of three new elephants to the zoo complicated things and kept our time there short, but it was fun to have some one on one time with my boy.

unicorn with ecLest anyone worry that my hair is getting too short with all the cutting, Emma Clare would assure you that it is growing.  At the bus stop, she decided that I was ready for a more sophisticated hairstyle. She calls it my unicorn ponytail.  I haven’t had a lot of girl time with this precious one, either. But this weekend the boys are going camping, so I’m sure she’ll have some big plans for us. (I’m also nearly sure that it will involve Chick-fil-A and a pedicure!)

Social Media and Cancer

(This is an old picture. I’ll try to get something of my new haircut soon!)

Sadly, I have to admit that my phone is never too far from my hand.  It can definitely be a big distraction from real life, but it can also be a very powerful tool.  More than once, my mom has called me on a Monday morning to tell me that an acquaintance passed away over the weekend.  She was incredulous that I already knew. From Facebook. (In this case, the word Facebook must be read with an evil, raspy voice.) To be sure, there are people who share things they shouldn’t online. But I quickly found that, when used appropriately, the internet could make my life much easier when it came to my cancer.

  • Helping Hands: My friends set up a Helping Hands site that was wonderful. It let us set up a calendar where we could add tasks that I could use help with– dinners and play dates were my main needs. Other friends have also added things like rides to treatment or help running errands. Somehow, it made it easier for me to ask for help, knowing that people had the freedom to sign up to help or not– there was no pressure.  The Helping Hands site also had a place for a journal, which is where this blog began. Friends and family could check in every once in a while, or they could sign up to receive emails anytime I posted something new.  (You can subscribe to new posts on this site, too, by signing up at the box on the right.) There are other similar sites– CaringBridge has a journal but no calendar sign ups, and yes, there’s an app for that. StandWith is in its final stages of development, and will let you push specificrequests to certain groups of people (maybe rides to treatment to close friends, meal requests to acquaintances).
  • Facebook: As much as my mom hated that I found out about someone’s death on Facebook before she told me, the truth is, it was shared by someone who had the right to share. Facebook is a great way to connect with family and friends, sharing information with lots of people in a single click. It gives them a place to respond without feeling like they’re bothering anyone. I always made it a point to post a picture of myself on chemo day to let people know that I was doing ok.  It wasn’t a sad place, and I may have been plugged into a machine delivering poison to my body, but I was smiling and enjoying some kid-free time with a friend.  Now I use my Run | Lipstick | Chemo facebook page to share new blog posts and other cancer related stuff.
  • Twitter: Yep, I’m on twitter now. A twitter friend (I’d give credit, but I don’t remember who deserves it!) said it best: Facebook is for the people who love you, Twitter is for the people who understand you. I do interact with some real-life family and friends on twitter, but most of my interactions are with people with whom I share a common interest, but who I’ll probably never meet. I’ve made some great connections on twitter with others who’ve gone through breast cancer and some of the most caring care providers. Getting involved in the #bcsm (breast cancer social media) group has given me new perspectives, new friends, new things to think about. And it’s a wonderful feeling to walk into a conference venue with hundreds of people, knowing that while you haven’t met them in person (yet), you have friends in the room.
  • Instagram: Nope. Maybe some day, but I’m just not there. Plus my high school girls tell me that parents should not have Instagram. So I guess I’l steer clear for now, I’m not risking my “cool mom” status with those girls!
  • Blogging: This blog started as part of the Helping Hands site, and it was a way for me to disseminate accurate information quickly and easily. I chose to keep my Helping Hands site was private, one of the administrators had to approve anyone who wanted to be part of the community. This blog is a whole different story. I still like the idea of the control the blog gives me– there’s no reason for anyone to hear third-hand what’s going on with my health and get things entirely wrong because the story has been passed around so many times. But the more public forum of a wordpress blog, while sacrificing some privacy, helps me reach out to a much larger breast cancer community.  I hope that my story might help someone.  I hope that maybe someone will read my words and have a new perspective, a new question for her doctor, a new way to help her friend.  But it wouldn’t be honest to say that writing this blog is entirely altruistic. Writing helps me.  The people I’ve met, hearing their stories, sharing their successes, it all helps me.

We definitely have to be careful about the information that we share online and on social media.  And after talking at length about nipples, it may be a hard sell to tell you that there are things that I edit, things I keep out of this blog. I don’t share everything, but I strive for honesty in my voice. I share what I would want to know, the things I’ve looked for, coming up empty. I try to remember that anyone can see my words, my images– something that I remind those high school girls about all the time. (They’re probably tired of hearing how I nixed one potential babysitter because she was holding a red solo cup in her profile pic!)  But at the same time I worry that anyone can see my posts, I am in awe of the fact that anyone can see my posts. Anyone. Anyone who just heard her doctor tell her that she has breast cancer.  Anyone who is worried how her kids will react to her hair loss from chemo. Anyone who wonders what it’s like to get a nipple tattoo or to grow out her hair post chemo.  I do try to remember to put down my phone for a while each day and just engage with the people around me.  But I’m so thankful for the tools that connect me with so many people– with friends I know in real life, with people with whom I’ve only shared stories on a screen, with anyone.

Growing out a Pixie | One Year of Regrowth

hair regrowth one year

Last May, I was just starting to really see hair on my head, it was so short, stuck straight up, and was super blonde.  It was still a while before I’d head in to Dragan to get a trim– or really a shaping.  Since then, we’ve  been faithfully trimming and shaping it, letting the top grow long while keeping the sides shorter.  Eventually, the goal is to get the top to grow in to a bit of an inverted bob.  But for now, it’s still short, and getting to the tricky stage, harder to control.

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I have been literally counting the days until tomorrow’s haircut, hoping Dragan can help me find a way to style it at this new length.  In the past few days, I’ve been through loads of hairstyles– trying to see what I can do with such short, but not quite short enough, hair.  I’ve been raiding Emma Clare’s stash of hair accessories lately, the Jane Tran barrettes are my current fave, but I’ve even given some headbands a shot.  I don’t love hair in my face, so this next stage could be tough, but between the headbands, barrettes, braids, and yes, ball caps, I hope to make it to the “tuck behind the ears” stage.

edited to add: This is how it ended up today…  Still hoping for a flash of inspiration at the haircut tomorrow!
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A Life Like Any Other | The Fault in Our Stars

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Do you watch sad movies? I don’t.  I remember in high school, one night most of my girlfriends had dates or were in a tennis tournament. Beth and I were the only two without plans, so we headed to the movies to see My Life with Michael Keaton. I don’t remember many details.  Michael Keaton’s character had some sort of terminal illness and decided to make a series of videos for his infant son, teaching all the life lessons a father should teach his son. There were some funny moments, and I still remember the video where he was teaching his son how to shave. But not unexpectedly, there were a lot of sad parts. And any time there’s a terminal illness involved, you know pretty much how the story is going to end.  I don’t know that I’d ever cried at a movie before, but Beth and I sat in the dark, trying to stifle sobs. It was seriously sad, folks. And then when it was over, we headed to Oak Hill to watch the end of the tennis tournament, only for a friend to point out that our shirts were wet, stained with our tears.

It would be at that point that I decided that I’d rather not cry at movies.  I’d rather watch movies that  make me happy.

So based on the very little that I know about it, I’ll probably not go see The Fault in Our Stars.  But I saw an interview with the author of the book, and I was intrigued by something he said. “We imagine sick people as being fundamentally different from us… [and yet] their lives are every bit as complex as any other…  They have all the love and hope and anger and fear…”  John Green said he wrote this book because he wanted to show that sick people still feel. More than that, they feel the same emotions that healthy people feel.  They get angry, they fall in love.  I replayed this section over and over, I wanted to preserve his words. I’ve been thinking about it ever since.

Being around someone who is sick, I mean really sick, is hard.  It’s hard to know what to say. Should I say I’m sorry? (It’s not my fault.)  Should I say it’s all going to be ok? (It might not be.) Should I offer to help, or will she be insulted and think I’m insinuating that she’s not strong enough?  Will it hurt too badly if we become better friends and then she dies? It’s so easy to get wrapped up in the questions and end up paralyzed with fear, and just do nothing. Say nothing.  I can’t say I’ve never been guilty of this. I can’t say that going through cancer cured me, either. But cancer did crystallize a few things for me.  And John Green eloquently put those thoughts into words.  I am so lucky that my friends rallied around me when I was diagnosed with cancer. Yes, they graciously offered to help me with anything I needed. But they let me be independent when I wanted to be. They’d ask how I was feeling, about my treatments. They didn’t ignore my cancer, but they let me talk as much as I needed and then they let me move on to talk about my kids, their kids, their jobs, a recent shopping exploit. Between coffee dates, lunches, shopping trips, bus stop chats, and phone calls, I was able to live a life that was “just as complex as any other.”  Sometimes someone with cancer really needs a casserole or a ride to the doctor. But usually they really just need a friend.

I love the idea of seeing a young woman who doesn’t let her illness end her life before it takes her life. I love the idea of seeing her hang out with friends, egg someone’s house and cheer with joy while doing it, of seeing her fall in love. But I don’t love the idea of seeing her life come to an end, presumably with those she loves by her side.  So while a few of John Green’s words will probably live in my mind forever, I still don’t think I’ll see his movie.

Epilogue

epilogue

I felt so poetic last week, talking about how Vinnie’s tattoos were the “The End” to my cancer story. Of course, we all know there are only really two things that come after the words “The End,” an epilogue and a sequel. Luckily, we’re not here to discuss Cancer: Part 2. But I was hoping not to have an epilogue to write. Certainly not a week later.

I have been faithfully wearing my silicone scar sheets since January, when I also had steroid injections to help flatten out my slightly bumpy scars.  Of course, before the injection, we discussed the risks, among them: bruising, skin atrophy, fat atrophy. My doctor said these were rare, and he uses the lowest dose available, which he then dilutes again, to reduce any risks.  I had some bruising and as it faded, the scars have completely flattened and smoothed out, but the skin has retained a pink hue in the area. Wearing the scar sheets except when I’m in the shower, I haven’t spent a lot of time worried about the redness because I never really see it.  But I ditched the scar sheets for my trip to Vinnie’s, and he commented (several times) how thin the skin was in that area. It wasn’t where he was going to tattoo, so it didn’t change my plans that day, but his concern gave me something new to obsess over. Just what I need.

I managed to keep my emotions in check for a day or so, but by the end of the second afternoon, I was somehow convinced that my skin was going to burst apart it was so thin, and then after my implant popped out and landed in the floor, I’d need a skin graft to hold it back in. (Yep, a little dramatic. Cancer has trained my brain to eschew the logical and jump right off the deep end. Stupid cancer.) Luckily I was able to get in to see my surgeon the next morning, and he confirmed that the skin was definitely thinner than he’d like, but I was in no danger of losing an implant if I wasn’t wearing a sports bra to keep it from falling out.  While I was dreading the idea of a skin graft (which I’d completely made up in my head, that probably isn’t even close to an option), I was secretly hoping there was some sort of collagen cream or something (also completely made up) that I could slather on once a day to fix everything.  My surgeon’s suggestion was somewhere in the middle.  More fat grafting. At which point my brain sort of turned off. More liposuction from one site, then injecting the fat under the thin skin near my scar. It won’t grow back any skin, but it would support the skin and make it less susceptible to trauma and leave me with a better cosmetic result. Oh, and that probably won’t take care of the redness.  So then he’ll send me to someone to laser it.

Good grief. I was done two days ago. I. Was. Done. I could not comprehend the idea of more surgery. More compression gear.  More restrictions on my activity. I’m sure it wasn’t a crazy reaction. But I told him I couldn’t make the decision that day. I wanted to be done. He agreed, there was no need to rush, we could watch it indefinitely, and make any decisions later. I knew in my heart that I’d likely agree to it, but that day, I just could not.

I gave myself some time to consider my options, and really, I needed to come to grips with the fact that I needed, no, I wanted, more surgery. Yes, I want to be done. But I want to to finish well. And so I called the office and asked to schedule the surgery sooner rather than later. I’m still waiting on the final date, but am hoping to do it within the next couple of weeks. It will be outpatient surgery, and I’ll be in compression gear (super glam spanx-y bike shorts and the wretched ugly compression bra) for probably four to six weeks. I’m hoping not, but betting it will mean more pain meds and more time on the couch than on the trails.

I remember pre-cancer, thinking how great it was that now women can have a mastectomy and reconstruction at the same time. How cute and naive of me. I knew a lot about breast cancer, but didn’t realize that even in the simplest scenario, there are two surgeries and several procedures involved. Many women who opt for a lumpectomy have multiple surgeries to make sure that they’ve gotten all the cancer, only to end up with a mastectomy, either out of medical necessity or for their own peace of mind.  I didn’t mean for this post to be a downer, but I guess this is just a glimpse of the fact, that even under the best circumstances, breast cancer isn’t easy. I’ll be fine physically, and that’s the most important. And though it will take longer, I’ll get over the fact that I have to go through another round of surgery and restrictions.  Because while I’m not thrilled to be writing an epilogue, I’m really glad I’m not writing a sequel.

A Road Trip to Little Vinnie’s | Nipple and Areola Tattooing with Vinnie Myers

vinnie-101

OK, guys, just so you know, we’re talking nipples today. No graphic images, but if it’s too much information for you, then tune back in later this week.

I’ve talked about my surgery before, but I’ve mostly talked around the details– like they were somehow too private to put in such a public forum. Yet, I’d tell anyone who asked, and it’s not like you can’t figure out the details with a little googling if you really want to know. So I’ve decided to let it all hang out, as it were.  Like most women facing breast cancer, I had several options when it came to surgery, but I definitely went the more aggressive route. I figured if I was going to survive this and live another forty or fifty years, I didn’t want the anxiety of dreading the annual mammogram. I just wanted to be done with it, once and for all.  Given my age and the aggressive nature of triple negative breast cancer, while my surgeon assured me it wasn’t necessary, she also agreed that a mastectomy wasn’t an overreaction. I chose to have a bilateral simple mastectomy. I now have scars across each breast (strategically placed to be hidden by even a pretty skimpy bikini top) and all of the breast tissue, most of the fat, and even my nipples and areolas were removed. I wasn’t the best candidate for nipple sparing surgery, and it didn’t sound like a great option to me, anyway, so I decided to go the “simple” route and get rid of it all. After my skin was stretched out to accommodate what was lost to surgery, silicone implants were placed under the muscles of my chest wall.

My plastic surgeon is awesome and did a great job, but the obvious downside is that I was left with nipple-less breasts. I have to admit that I’m pretty happy with how I look when I’m dressed– I can totally rock strapless dresses, halter tops, and even a sports bra like nobody’s business!  But it’s pretty hard to think of your shape as “normal” when you step out of the shower if you’re just staring at nipple-less mounds of flesh.

I realize that any story that’s mostly about nipples hardly needs a good hook. But I’ve got one anyway. So, there’s this guy in Maryland named Vinnie, and he has a tattoo shop… (One hundred percent all true.) Plastic surgeons can do a few procedures and even some basic tattooing to replicate the idea of a nipple, but a nurse at Johns Hopkins thought that perhaps a bona fide tattoo artist would bring a little more artistry to the table. She asked Vinnie Myers if he could essentially tattoo a picture of a nipple on her reconstructed breast.  Years later, Vinnie has given up traditional tattooing and has become THE go-to guy for nipple and areola tattooing worldwide. He sees seven to ten women a day, and over three quarters of his clients fly in from across the country and around the world. (Expect to wait up to six months for an appointment!) I feel so fortunate that he’s virtually in my backyard, and I was able to score an appointment right away because I could fill the spot of a cancellation. I managed to get there, tattooed, and back before my kids got off the school bus. That’s a good day.

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So for the details:

  • Yes, it hurts. But because of the nature of a mastectomy, most of the nerve endings in that area are pretty messed up, so it’s not nearly as painful as a traditional tattoo.  It hurt some while he was doing it, but any soreness wore off quickly.  After just 24 hours, what can only be described as discomfort is barely noticeable. (If you take a friend along, she’ll likely be in more pain watching than you are!)
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  • It was quick. Including the before and after pictures and the prep and post-procedure instructions, I was in the office for an hour. The tattooing took maybe half that.vinnie-116
  • It’s in a real tattoo shop, complete with a motorcycle out front and a neon “TATTOO” light in the window. But the office where Vinnie does nipple and areola tattoos is private and reflects his love of art and travel. It is clean and feels hygienic without the sterility of a medical facility, something most breast cancer patients are so over by the time they get to this step. Vinnie is professional and friendly, and his wife is the one who takes the pictures and does all of the care instructions at the end.

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  • You have to pay out of pocket. Insurance is supposed to cover it, and they give you a form with the appropriate codes to be reimbursed. I’ll still have to submit it to my insurance company, and I expect I may have to do more follow up than with something done in a medical office, but it should be covered like all my other reconstructive procedures.
  • Eat before you go.  We made the mistake of thinking that we’d eat once we got to town and made sure that we had time. But it turns out that Finksburg is a pretty teeny town, and since we weren’t tempted to eat at the gas station/Subway, we ended up eating from one of the only other places we could find.  Also a gas station. It’s a good thing Sally and I are so much alike, not everyone will consider a lunch of cheetos, pringles, and twizzlers as acceptable. So if that doesn’t meet your standards, you might want to stop at the Chick-fil-A on the way.                 vinnie-102
  • And yes, it looks real. Even though I’ve looked at more pictures on his website than I care to admit (WAIT– don’t click that link if your kids are reading over your shoulder!), I was surprised by how real the tattoos looked in person. Unless you knew they were tattoos, you’d never even imagine that they weren’t real. And even knowing, I bet you’d still be shocked. While plastic surgeons use only a few pigments, Vinnie uses as many as necessary to give a full, three-dimensional, tromp l’oeil effect.  And since he uses standard tattoo grade pigments (different from those most plastic surgeons use), his tattoos won’t fade over time.

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It was a good experience.  It’s amazing how a procedure that takes a half an hour can make such a big difference.  After my final surgery, I struggled with whether I thought my breasts looked normal. I’ve come to really hate that word– what is “normal” anyway? But I did struggle. Being the last surgery, it felt so final, and I worried that I wouldn’t be happy with how I looked. Over the months since then, I have grown accustomed to how I look and am fine with it.  But remarkably, with the tattoos, the reconstructed breasts that once gave me pause instantly looked like, well, real breasts. A trip to Little Vinnie’s Tattoo Shop definitely lends a sense of closure to the whole breast cancer thing, as one friend calls it.  Of course, I don’t ever expect the thought of breast cancer to be too far from my mind. But it’s as if with every stroke of his humming tattoo machine, Vinnie was writing the final words in my cancer story. They definitely look like nipples. But it felt like he was writing “The End” across my chest.

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Thanks as always to Sally Brewer for these poignant images.  These images are copyright protected and are not for sale.

Nike Women’s Half Marathon | I Am Stronger Than My Body

prerace

Friday I headed into Georgetown with my friend, Sarah, to pick up my packet for the Nike Women’s Half Marathon. Nike knows how to throw a race– and a party– so after standing in line for maybe three minutes, we still had plenty of time on the meter to wander around. Perfect for a few photo ops. They even had a huge wall and theme colored sharpies so that everyone could leave a message– why they run, encouragement for themselves and others… I decided to go simply. Suck it, cancer. I will do this.

I have to admit that cancer didn’t really take all that much from me. I made it through the treatments pretty well.  I didn’t miss any major life events.  Maybe a couple of field trips, but I can handle missing a trip downtown with 25 kindergartners.  But I did miss this race. I had been looking forward to it, and there was just no way that I could run it last year. But this year, I was determined. Cancer had taken this away, and I was taking it back. Suck it, cancer.we run dc 3

They were so efficient putting together my bag at packet pick-up, I didn’t notice until I got home that I’d gotten assigned to the wrong start corral.  I don’t quite run less than an eight minute mile, at least not for longer than a block or so. I guess Nike was a little more optimistic about my performance than I…

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It was a beautiful morning for a run. Crisp, cool, and sunny. And the course was so lovely. I’ve run parts of it before, and I’ve walked or driven most of the rest of it. But running through, with so many clapping and yelling words of encouragement, trees in bloom, was special. After mile 5, I still felt great and felt pretty confident that I would make it. Through East Potomac Park I started getting stiff and stopped to stretch a few times. After the third time or so, it became one of those situations where you start talking to yourself.  (Please tell me I’m not the only one who does this.) “You’re stronger than your legs,” I told myself as I stretched against a tree. And then it came to me. “You’re stronger than your body.” (Rats, that could have been my #5words2cancer!) I’m stronger than my legs. I’m stronger than cancer.

we run dc 1a

As I came out of the Ninth Street Tunnel and with less than a mile to go, I knew I had made it. A few times before and during the race, I was fighting back tears– not sad tears, not really happy tears, just overwhelmed. This was one of those times.  Yet the sun, the spectators, and loud music quickly overcame my tears and I finished strong. “On Top of the World” by Imagine Dragons will forever hold a special place in my heart. Perfect timing. At the top of that hill, the finish line in sight, I was on top of the world. My only goal had been to run the whole way, and after my knee started bothering me a month ago, my goal had become to merely finish. And yet, I made it. I met my original goal. I ran. I finished. I was stronger than my body.

finisher 1a

finisher 2a

Not only do they know how to organize a race at Nike, they know that most finisher’s medals end up in a drawer or hanging in a closet. But when it comes in a blue box from Tiffany? Oh, yes, then it gets worn.

finisher pendant a

I wanted that necklace. Yet I wanted to earn it, I wanted to be proud of it if I were going to wear it.  After today’s race, I will wear it, and I will be proud of how I earned it. I not only finished, but I finished well. I finished strong. I am stronger than my body.