Tag Archives: subcutaneous mastectomy

After the sky falls…

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Sooo, after returning to work early-ish following the exchange from skin expanders to implants, I’ve had quite the eventful run of complications. That means I’m sitting here at home again, recovering. Not really feeling inspired to write, but bored to death with feeling bad.

I felt so nearly normal so soon after the implants were placed that I thought I was home free. But one night, I noticed the left breast seemed to be sitting a lot lower than the right. No discomfort, but weird. I got an appointment with the plastic surgeon for the next day, and in the meantime amused myself by writing about Henny Penny and the sky falling, absolutely never suspecting there was a real problem.

OK, so the sky did fall.

While driving myself to Dr. N’s office, the left implant’s pocket started filling with blood & didn’t stop. I could tell something was happening because I felt like I couldn’t breathe on that side. In the rearview mirror I could see a really big bulge over the top of my shirt, near my clavicle. Thank heavens for this fancy hands-free car phone stuff–it let me call home and leave a message for my husband: “Keep your cell phone on–I may need you!”

It’s a blur, but I did get to the office. Dr. N inserted a drain to relieve the pressure and hopefully save the reconstruction on that side. A friend who wasn’t supposed to be at work that day (but heeded the little bird who told her to show up) was available to drive me to the hospital faster than if we’d waited for an ambulance.

After the requisite 8 minutes of chaos, the ER figured out who I was and what to do with me. I was just grateful my friend was willing to stay & hold my hand while I writhed and cursed in and out of consciousness. I cannot adequately describe how it feels when over a liter of blood tries to burst through your skin, so I’ll leave it at that.

I remember thinking they’re just going to let me lay here and die and I’ll never see Brian again. But he’d been called, and soon after the thought, he was there with me, scared to death, too.

All was resolved with a timely return to surgery. Dr. N was suitably impressed by how much blood I’d lost (about 1.5 liters), and happy to have seen the cause of it–one of the little blood vessels that forms during reconstruction was torn & could be seen merrily pumping away. So, that got fixed, a new implant was placed, and I went home the next day with–yes–yet another drain. Not to mention tearful, weak, and pitiful from sudden blood loss.

So relieved to have a husband willing to help with the care and feeding of a PICC line.

So relieved to have a husband willing to help with the care and feeding of a PICC line.

A week goes by uneventfully, tho’ I’m secretly terrified of a repeat. It happened once– who’s to say getting in the shower and washing my hair (as I’d done the morning of my appointment), won’t spring another leak? I’m Catholic. It’s gotta be my fault, right?

So it’s back to Dr. N’s for inspection and to have the drain removed. All seems well until about 5 hours later, when I start feeling achy and warm. That progresses to joints screaming and hot. My temp goes from 101 to 104 within about an hour, and Brian’s making frantic calls to the on-call doc, then Dr. N, then I’m in the car and being carried back to the hospital where I stay for the next few days getting IV antibiotics.

Thank heavens for modern medicine & modern antibiotics. Infection after trauma–surgical or not–is the kind of stuff that killed people when we didn’t have what we’ve got today.

I’m home now getting the antibiotics here, as there’s no oral equivalent of what they need to give me to be sure there won’t be a recurrence. I’ve got what’s called a PICC line–an intravenous catheter that starts in my upper arm and dumps into one of the really big veins near the heart.

So far, each day is a bit better, and I’ve woven for myself an explanatory fiction that makes me less afraid I’ll have another bleed. I can think of the infection as old-fashioned sclerotherapy (therapy that scars) inside that pocket, sealing off any potential little bleeders that might lurk there.

And there’s Dr. N’s assurance that “this never happens.”

Except in one case he had where a woman’s stove electrocuted her.

And me 😉

Henny Penny’s Got Nothing on Me

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I guess it’s a friend who’s “girls” give us eggs every year that brings to mind a little red hen running in circles, kicking up puffs of dust, as I look at my own girls today. The sky hasn’t fallen, but my left boob certainly has.

Maybe you can kinda see the lowerage of the left breast. The ace wrap between them is certainly evident. This "process" is NOT fun.

Maybe you can kinda see the lowerage of the left breast. The ace wrap between them is certainly evident. This “process” is NOT fun.

I wouldn’t say it’s quite an inch lower than the right, or that the world’s going to end, but I could be convinced.

In medical parlance, the lowerage is maybe a centimeter and a half. Or two. Almost an inch.

The spouse, who has eyed the “new” boobs waay more frequently than the old ones, actually agrees. And my dear friend Peggy who has walked me through the whole process, kindly says “well, maybe the one IS a bit bigger than the other.”

I don’t think it’s bigger, it’s just lower. So (feeling like the world’s worst patient yet again), I call the doc’s office. There’s not a nurse around, but one of the other lovely ladies says, “We want them to relax into their pockets. Does it feel like that’s what’s happening?”

Relax into their pockets? Gloriosky! Whoda thought? And why wasn’t this mentioned before? And why isn’t the right one doing the same thing? Or is it only a matter of time?

The next thing she says is, “Let’s have you come in (like TOMORROW) to make sure nothing odd is going on.” Nothing odd? This is odd in my book. The sky falling is odd too, but I doubt that’s what’s happening. The next thing she says is, “We don’t want the other side to be retracting and pulling up.” OK, the sky IS falling.

“Pulling up” is exactly what the right side feels like it’s doing. The one’s going down (and feels kinda nice), the other’s pulling up, and doesn’t.

So I’ve got specially constructed evening wear (see pic). It consists of a bra I’ve worn for weeks now, a roll of ace wrap in the middle that keeps the implants from cutting into the muscles attached to my sternum, and a pain patch on my skin that maybe works, maybe doesn’t.

This all because of a questionable condition called thoracic outlet syndrome on the right side. Which means the muscles there are overdeveloped, the nerves are compressed, and everything hurts. On that side only. Unless a miracle happens and the implant “falls into its pocket”. Like tomorrow.

I don’t care if my extremely patient doctor thinks I’m a nut when the miracle happens and he sees two perfectly level boobs at my appointment. Just my luck. He’s probably got that little bubble level app on his iPhone to check things out. Or something from his garage. Like the stud finder mentioned in a previous post.

I’ll let y’all know what happens. Henny Penny, too. Maybe she can stop her frantic circling and I can get some rest.

I’m gonna live, so why am I crying…again?

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So I’ve had this marvelous breast reconstruction thanks to a very skilled plastic surgeon (which means despite bruising and surgical tape and drain holes, I’m fine with what I see in the mirror), I don’t have to do chemo or radiation, I’m walking around alive, and yet here I sit in the bathtub, in the grips of yet another crying jag.

Either I’m one ungrateful sod or it’s something else.

A good friend, who also happens to be a psychiatric nurse practitioner with lots of experience in wimmen’s stuff, tells me it’s something else. A panic attack, actually.

How embarrassing.

Which means we’re not just talking about one panic attack. I’ve been having them every time I turn around. Friends have assured me all this crying is normal. I’ve had my breasts cut out, for Pete’s sake. Which sounded right at the beginning of it all–back when illness and survival and a decent reconstruction were still uppermost in my mind.

Well, I’ve admittedly won the lottery as far as all the the above is concerned, but here I sit in my lavender bubble bath, crying my eyes out. Again. For hours. Yes, really, hours. Thank heavens I have a sensible husband who isn’t prone to panic. He just holds me and understands there’s nothing he can fix. At least not this minute.

Given to us by a dear friend and worth reading daily.

Given to us by a dear friend and worth reading daily.

The latest crying jag happened when I got convinced we’d all be homeless because of a $3,500 vet bill–payable right now, before we left the surgeon’s office or it was just a matter of hours before our doggie would be permanently disabled.

On top of a bazillion dollars not covered by own medical insurance. On top of me being off work long enough to run my disability down to zero and put an end to FMLA “protection.” Not to mention the taxes that would be due if we took money out of retirement.

And did I mention the IRS audit? The one that’s turned into two audits? Yeah, I think I mentioned the first one in a previous post.

I’m usually pretty good at ignoring unpleasantness. Even where the IRS is concerned. A trait that drove my mother crazy. She was into unpleasantness in a big way. So another thing fueling the crying jag was my certainty I was morphing into Mom.

Apparently not. My nurse practitioner friend said I needed an antidepressant. Like now. Been there, done that, but never for this particular symptom. And never had it work as quickly as it did it this time. Thanks to whatever powers that be, I haven’t had another crying jag (panic attack?) since.

What upsets me now is the realization that my mom, famous for the aforementioned unpleasantness, never had access to (and would never have accepted), the kind of help available today. It’s unfortunate the term “mental illness” was ever coined. Perhaps just unfortunate it’s used so freely for the kind of help many of us need when life becomes suffering.

Certainly some entities need to be thought of as true illness of the mind. If only so their sufferers can access state aid, have livable housing, and their medical needs met.

But should those of us fortunate enough to recover normal life with therapy and medication be thrown into a pot so discriminatory as to create fear about getting some help? I think not. To do so is irresponsible. And sad.

So I am sad for my poor mother. I think she could have been helped just as I have been. And I am sad for the women I see in clinic who are afraid to accept drugs or therapy when emotions get so awfully out of control.

I can be sad, but even so am feeling daily more able to enjoy the miracle that is life. Come to that, I’m downright happy about having a chest my husband’s not afraid to look at. And I’m not planning more crying jags any time soon, thank you very much.

At least not until the IRS checks in again.

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Things that go soft in the night…

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I can’t stop looking at them. Or touching them. I’d best not go out in public right now for fear of getting arrested for indecent something or other. I can’t believe the difference between my new “real” breasts and the tissue expanders. They’re absolutely beautiful. Even with the bruising. And the surgical tape. And the drains. Thank you, thank you, thank you, Dr. N.

One of his lovely nurses told me they don’t want the implants moving around much just yet, so I have to use this gawdawful mastectomy bra for a couple of weeks. It looks like a girdle. From the 1940s. For breasts.

"Mastectomy Foundation Garment," or:  The Bra From Hell

“Mastectomy Foundation Garment,” or: The Bra From Hell

Well, I negotiated that down to an ace wrap. Much better. Until I noticed it was flattening things out. Back to the mastectomy bra, this time with some spouse assisted modifications–ribbons that tie in the front to keep the velcro from hell closed and off my hypersensitive skin.

And at night? I can sleep on my sides. Well, not just yet. The instructions say a 30° rise should be maintained for awhile, so I’ve got a bed wedge. But I’ve rolled to my sides a few times to test things out. Instead of looking down to see two tangerines poking out from the front of me (separated by a good two inches), I’ve got breasts squishy enough to meet in the middle.

Touch them (which just about everybody in my all-female office has done), and they’re soft. They feel real. They’re actual breasts (or quite the facsimile thereof). Halleluja!.

At least that’s how I feel right now. Hope it lasts.

I’ll letcha know.

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9/11. Glass half full?

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So I went to the doctor to pick out new breasts. At least I hope they’ll be breasts. Or like breasts. Breast-like will do in a pinch. The things my chest has been hosting are definitely not. And I’ve found some other blogs where women are talking frankly about their breast building “process” (note how I avoid the word “journey”). Damn, they’re brave. I’m just worried. Really, really worried. Some journeys take a lifetime.

Surgery is on 9/11. Anybody got a glass-half-full line for that one?

Ok, beat you to it. I still don’t have to do chemo. This is a very good thing.

So from the get-go I knew saline implants were out of the question. I’ve examined enough women who had those placed during the 90’s moratorium on silicone to know you CAN hear them slosh. And thank G-d silicone is supposed to be lighter, as these saline tissue expanders are heavier than I could have imagined. I’ve lost weight just lugging them around. I even chickened out and had them reduced.

What a world. They’ve got “gummy bear” implants now. Feel like candy, look like pears, but are textured like expanders and scare the heck out of me because they’ve got to be bigger than those are to prevent flippage. You know, that embarrassing condition when your breast turns upside down at dinner. Maybe while serving the spaghetti.

So, I’m gonna go with the old tried & true, half-round, slick model. These are meant to slip and slide and smoosh. Kinda like breasts. As a friend said, “my mind breathes a sigh of relief at the soft ones settling into the space that’s already there. Like real breasts after menopause.”

There is sense in that. It resonates. I can do resonate. I just can’t do journey. At least not the whole thing. At least not right now.

I’m wounded and can’t get my bra off.

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Anyone tired of pain and angst and wimmen’s stuff can go home right now. But I can’t get off this bus and writing’s a distraction, so I’m gonna stay right here and bore y’all to death.

I’ve taken the muscle relaxers (the ones that cause 6 hour crying jags). And the lorazepam (goody, now I get to wake up feeling like the world’s going to end). I’ve got one NSAID pain patch plastered to my front, another to my back, and my husband nearly broke his thumb trying to push the muscle spasm or rib or whatever it is that hurts like hell back to where it came from.

Ain't it cute? Don't it look nice and soft and squishy? Nawp. They lie. And where's the stud-finder, dammit?

Ain’t it cute? Don’t it look nice and soft and squishy? Nawp. They lie. And where’s the stud-finder, dammit?

So I lie on the “Miracle Ball” for the requisite minutes and then do it again out of sheer desperation. Now I’m sitting against a yogic torture device called a Spoonk that’s advertised as the Western answer to acupuncture. All this because I’ve got what feel like armadillo plates riding against my ribs and the suckers are pulling my back out of joint.

And I still don’t have to do chemo. Yay! That heads up my gratitude list every day of the week. But tonight I’m doing my best imitation of British whinging, just for fun.

Actually, the anatomic explanation above isn’t quite right. I quizzed my plastic surgeon about exactly where these tissue expanders live and learned they aren’t just lying quietly on top of my ribs “under the muscle,” as I so casually assumed. During surgery the pectorals are actually butterflied lengthwise, their points of insertion left intact, and the expanders jimmied between the layers like stuffing in mock duck.

All’s quiet for awhile (or else surgical pain overrides awareness of anything else), but a couple weeks later, when they whip out the stud-finder to start filling the expanders (see previous post), the muscles stretch and spasm. And in my case have pretty much never stopped. I wake in the morning with the equivalent of tennis balls stuck under my skin. That’s if I slept at all overnight. I don’t remember having any dreams at all during these last two months. Once things quiet down I should have quite the cinema line-up for REM sleep.

So maybe the surgeon’s right and I have what he calls “reactive” pectorals (he is a pretty smart guy). You mess with them, they kick back. Like the frogs’ legs my mother once made me watch her cook. I see this fairly often during cesarean section; we’re not anywhere near the pecs, but similar slabs of muscle in the abdomen can do the same thing. It’s usually handling the peritoneal membrane underneath them that causes spasm and vomiting even with adequate anesthesia, but in some folks “just” pulling apart the abdominal muscles produces the same effect.

Trouble is, these suckers are STRONG. There is no denying a pissed off pectoral. Because of where they are, they pull on the ribs and yank those circumferential items slightly off-kilter, causing spasm in other, unforeseen areas. Which has been my problem lately.

This is more like it. The deflated inflater. More like what I just got at Petco--a dog toy with "squeakless technology." Yep, that's what this thing is.

This is more like it. The deflated inflater. More like what I just got at Petco–a dog toy with “squeakless technology.” Yep, that’s what this thing is.

My husband was horrified to find thumb-shaped bruises where he’d been pressing on my back. I assured him I’d not complain to authorities, as this was likely due to my using twice the recommended number of non-steroidal patches (along with a handful of naproxen, if truth be told). This all messes with blood clotting abilities. Whereupon he’s horrified I exceeded the recommended dosage. Whereupon I’m amazed that we’ve been married lo these 23 years and my MO still surprises him.

Now something I forgot to mention is the saving grace of having a physical therapist who really knows her wimmin’s business. Also high on the gratitude list. Every whining complaint I’ve thrown at her has been no surprise. She’s heard it all before. Thank heavens.

Thank heavens I’m not the only one who feels these plastic things getting hot against my chest wall. That the saline ports are hard, and hurt. That tissue I’m told has been denervated may be numb-ish to the touch on the outside, but has plenty of sensation pushing through from the inside.

But hey, Dr. Susan Love says says most women don’t even finish their pain meds. Must be true, right? She’s written a fat book about everything breast. If Marcus Welby, Dr. Quinn, and Hawkeye Pierce joined her for a focus group and came to the same conclusion, well, maybe I’d suspend disbelief. We’ll just not consult Dr. House.

Thank heavens the therapist knew to insist I request a reduction in the bigness of these things before I had more trouble with an already compromised right hand (that would be from the heartbreak of thoracic outlet syndrome, which is a wastebasket diagnosis and doesn’t really exist, as we all know). As soon as they let a little–a measly 2 ounces–of fluid out of the right breast my hand stopped its neurogenic tingling, my breasts regained just the eensiest bit of squishiness, and I felt like a new person. This is what I’m told will happen when the expanders are exchanged for “real” implants. We’ll stick with the smaller size, thanks very much.

But now the pecs have caught on and decided to take up the slack. Hence the new muscle spasms and this new-ish rant of mine. Bear with me and I’ll apologize (again) next I see you.

What follows is something not for the faint of heart: placement of the expander within the muscle.

I really don’t want to freak anyone out, but can’t seem to post the link without opening the graphics.

Treat your children well…

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I don’t know what I was expecting going into this Angelina Jolie-breast-preservation-mastectomy thing. Or maybe I do, if I get honest. I think I was expecting to look and feel pretty much like I did before the two, Two, TWO surgeries in one. Yeah, the Wrigley’s gum commercial dates me. I’m speaking of mastectomy followed immediately by “reconstruction.”

I’m feeling stupid because I let myself believe reconstruction meant restoration. They’re not the same. I’ve got what pass for breasts (very nicely, under clothes), but are really nothing but foobs (fake boobs, previously discussed). Kinda awful to look at without the clothes. They’re shaped by triangular-ish plastic inserts with a port for sequential infusions of saline. They could be made really, really big if I was into that sort of thing and wanted to lose the use of my right arm. More on that in another post.

And you know how they find the port to do the infusions? (Boy, what an education this has been.) With a stud-finder. Now that got my husband’s attention. He has mostly averted his eyes from the foobs, but pull out that stud-finder and he’s Johnny on the spot. It is kind of interesting. The expanders can shift, and they do, so the ports have metal in them to help with detection. Out comes the stud finder, for every infusion. First to “X” the spot, and again to check right before they stick the needle in. My doctor’s stud-finder is blue.  Hmmm.

Wall sculpture

Does she, or doesn’t she?

Weird as it is, the process works, even if the result doesn’t look quite right and the “foreign body sensation” means they’re always on my mind. Always. It’s like having something in my eye. I feel them moving against my chest wall, and I can’t keep my hands off them. I’ve had to tell my husband to poke me if he sees me holding my chest in public. The edges of the expanders wrinkle and flex just like an IV bag. Or a flattened beach ball. The ports feel exactly like the squeaker in a dog toy, only harder, and the right one hurts from the inside when I lift something and my pecs flex. You wouldn’t believe all the little things we do without thinking that require pectoral muscles. Opening a mayonnaise jar, for one.

In the mirror (and I’m always looking in the mirror), I’ve got mounds. And that’s what they’re called in surgical parlance. “Breast mounds”. Don’t know how I feel about that. I get the mental image of a bunch of men in lab coats thoughtfully considering the desirability (in one way or another) of various breast shapes and how to achieve them. I joke with the nurses that in terms of shape, my left one is Mt. Ranier and the right one, the one that gives me trouble pain-wise, is Sugarloaf. I actually like Sugarloaf better when I look down and compare the two, but they’re certainly not the breasts I’d grown to know over time. The ones the surgeon frowned at for their degree of ptosis (read sagging).

I was never taught to appreciate what I had while I had it, as I imagine many of us find, plodding through life. In the words of that gawdawful song, “you don’t know what you got ’til it’s gone.” I’ve got old photos that catch half of me sitting naked on our porch in California (because that’s what we did in California), and wonder why the hell I ever hated my little booblets. Or my not-quite-flat stomach. Or my skin that wouldn’t tan. They were fine. They were lovely. But nobody told me so because that’s not what’s done in our world.

In our world–the world of women anyhow–there’s always room for a lot of improvement. And when I was  kid, I was one of the many victims of the depression-era hangover that said children shouldn’t be encouraged. Certainly not about body-related stuff. The closest I ever got to a compliment from my mother was, “there’s nothing wrong with you–you’re not deformed.” This in response to my teenaged despair about never finding pants long enough outside the boys’ section of the store.

My dad was better, always ready with a “don’t you look nice” at odd times and when I got dressed up. Much of his life was spent around female models, and he did them the favor of always being professional, never making comparisons, and as I mentioned in another post, never “improving” on them in paint or bronze. He also didn’t make the mistake of being afraid to include me in his life or touch me once I reached puberty.

I’m glad I took photos of myself before surgery, because even at 53, even with “ptosis,” my breasts were still lovely. Not because they met media criteria, but because they were mine, they were intact, and I was used to them. And for most of my life they weren’t diseased.

These new things, these foobs, aren’t mine yet. I’m reminded every time I lift something that they aren’t breasts, they’re pectoral muscles. They clench. They spasm. They can be seen doing so under the skin. My skin is stuck to them. But only just. Skin without fat under it is thin. Transparent, really. Foobs are a constant reminder that man cannot improve on divine intent, evolution, or whatever it was that got us here.

But I’m going to have to develop some affection for these poor, benighted things, as they’re being asked to do what muscles were never meant to do–masquerade as fat. And I’m going to have to do all the exercises the physical therapist prescribed if I hope to get strong enough to stay up all night and catch babies.

The plastic surgeon tells me I’m not a “high needs” patient–the kind we health care providers all know and dread because they can’t be helped–yet I certainly feel like one. I’d kind of like to be one. I have no reason to keep going to his office,  but the support from the nurses there makes me miss having an appointment every week. What a catch-22. Something helps, yet availing myself of it feels wrong, or weak, or…well, just weak.

Foobs aren’t exactly trouble-free. I still have pain when I first wake up and the continental plates shift across my chest. Then there’s the end of the day when I just can’t stand myself any more. Fatigue hits like a ton of bricks when I’ve simply pushed a cart around the grocery store. My brain functions like Swiss cheese. Honestly, NOBODY would want me delivering their baby right now. But I feel like I should be better than this. I just know my friends would be stronger–they’d be done with it all and probably back at work again, ignoring the fatigue. Like midwives always do. Like women always do.

It scares the hell out of me, but I’m going to do the polar opposite of what my work ethic wants. I’m staying home until all this is over with. You’re all invited to join me.

“They’re heeere…”

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Foobs.

Fake boobs.

Rising out of nothingness…Suddenly. In Biblical fashion.

The surgeons very kindly took me seriously when I said the prospect of traditional dual mastectomy horrified me. They inflated temporary tissue expanders to about half capacity before I left the operating room. So when I explored my chest in the recovery room there were these little convexities–booblets–complete with my very own nipples, right where I’d expect to find them. Mightily encouraged (this is all hearsay, mind you–I’ve no memory of it), I am said to have gleefully exposed them to anyone who’d look–the spouse, my dear friend Peggy, and whatever nurses & techs were trying to keep me breathing instead of flashing the entire floor.

So I’ve discovered an inner extrovert. If it only emerges after anesthesia, I’m good.

I was apparently good that day, as the spouse was heard to say, “Gee–it looks like you’re nineteen again!” Bless him. We won’t talk about how he knew what I looked like at 19, except to say that it involved a communal swimming pool and some self-conscious skinny dipping. There are those who will remember the ’70s & how that used to be OK. Nowadays, if I’d been much younger, there’d have been arrests.

But, nobody gets to stay 19 forever, even a second time ’round. I left the hospital with the medical equivalent of saran wrap holding my chest together. This would stay on an additional two weeks, providing increased heat within really thin skin that needed to establish new circulation, and a way to peer at the nipples–which until the surgeon told me, I didn’t realize might dry up and blow away.

So now, three weeks out from the original surgery and with regular infusions of saline, foobs have emerged from the primordial booblets. Given my profession and the profound effect words have on women’s sense of self, I’ve always been careful to give body parts their correct names–at least with patients of a certain age  and comfort level. But special circumstances create the need for new vocabulary. An email friend who’s been through the same process tells me this stage is the “foob” stage. From the Latin, of course: fake boob.

Seems entirely appropriate to me, as these have certainly passed up my 19 year old booblet moment. Booblets are cute and unassuming. Foobs, well, foobs make their own way in the world. Anyone who accidentally runs into me won’t hurt me, but might come away with some serious bruises right about foob height. Which means we’re not talking “real” breasts yet.

I’ve got another one or two infusions to go before the tissue expanders reach their limit. Or I reach mine (this is not a comfortable process). A couple months after that, once things have stretched and settled to the extent they will, the expanders are exchanged for implants that feel much more like “real” breasts. And with any luck, I’ll start feeling real again, too.

Surgery sucks.

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Except when it saves your life.

But it’s awful in ways having my appendix and gallbladder out 20 years ago weren’t awful. Those surgeries felt like dental procedures in comparison. Of course, there is the thing about being somewhat younger back then. And the thing about once the last stitch is taken out at the two week post-op visit the deal is done. Finito. Fini.

None of that now. I’m already at the two week mark, but listen to me whine. Talk about being blindsided. I went blithely into surgery with my previous experience, expecting more of the same. Oh, maybe I’d use my time off for actual recovery and not plan any camping trips (I mused), but I had no real thought that things would be markedly different. After all, they weren’t even opening a major body cavity. Silly me.

In the be-ribboned world of breast cancer, I’ve won the lottery in several different ways. I don’t need anyone to tell me that. I deeply appreciate having found it in time enough that I’ll likely not be another woman trying to “live” with breast cancer until she can’t any more–often for less than five years.

Because a very experienced and persistent radiologist saw something that could hardly be seen, followed it up in slap-bang fashion with a series of biopsies that proved what he thought was there, leading to an MRI that showed something suspicious in the other breast, the decision to have bilateral mastectomies was a no-brainer. Waste time fishing around on the other side just to prove the “concerning” spot was indeed concerning (and what if it gets missed–the worst of it just micrometers outside the sample, or the real bad spot is just too small to show up…yet?), no thanks.

And because of his persistence and the expertise of his colleagues–the radiologists who nailed the lesions with their fancy x-ray guided biopsies–I get to go ahead with the plan to inflate the tissue expanders that were placed under my chest muscles rather than default to chemo or radiation and let cosmetics be damned. As it turns out, both breasts had cancer, invasive sorts of different types–a veritable smorgasbord of cancers and pre-cancers–but none was in my lymph nodes, nor in the little arteries and veins that course through the breasts, nor near enough to nipple and skin that I’d need those removed as well.

So. Onward. Stiff upper lip and all that.

Waitjustaminute. Not quite yet. I’ve got drains draining and pain paining, and have hit my wall for today. In other words, I am not feeling at all like doing anybody’s happy dance. I’m hoping against hope the appointment come Monday wherein they begin expanding the expanders and (hopefully) pull out these !#%! drain tubes will relieve some of their associated discomfort.

Discomfort. Now there’s a word. The expanders are flat things that resemble the stingray that killed Steve Irwin. The edges are thick, bump into each other through the muscles over my sternum, and slice upward into my armpits. The swelling associated with all this bumping and grinding gives me a bustline like Tarzan’s and the discomfort plays hell with my attitude.

Do you a favor. I won’t even get into the drains.

Until next time. Maybe.

It’s my party and I’ll cry if I want to…

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So I spent the last two days trying to take a friend’s advice. “Quit feeling sorry for yourself and write something interesting.” He was a little more tactful than that, but I got the message.

I did try, honest. He even gave me a good jumping-off point: my original mission statement for the Situational Midwifery blog–a soapbox about things encountered as a midwife. The things that piss me off about women’s health care. About how nothing has changed much under the sun. How women and their problems are often blamed for, well, women and their problems.

I’ve got half a lifetime’s worth of subject matter, but right now that’s not not exactly what’s rising to the top. Go ahead and look forward to future harangues, but for now they’ll be about my own stuff.

Participation is optional. Nobody is required to read a blog. I haven’t been a professional writer for more than half a lifetime now, so for all I know, it’s crap. Or it’s crap to men, or it’s crap to folks who haven’t faced something similar. I’m ashamed to say I’m one of those. I got so tired of my mother’s crying jags and worries and photos of grotesque surgeries that I was nowhere near as sympathetic as I might have been. At 15 years old. So I understand that point of view, too.

So read on, or not. Part of what I’m learning these days is to stand up for myself. My friend has given me yet another opportunity to do so, even though I’m afraid he’ll take this the wrong way. If I never hear from him again my husband (who loves this guy), will be really pissed. Then I’ve got two problems.