Archives for category: trauma and PTSD

Last week, I found myself on the receiving end of a big, fat, loud “Pshaw.”

I guess Pshaw is what you call it, that’s what it sounded like at least. An exasperated sigh plus eye roll; an unspoken, “Oh brother, give me a break.”

Before I explain what prompted it, I must tell you this. I swear that I have very few frequent flyer miles on my Cancer Card, not even enough for free pink shoelaces or anything. While I will admit I have pulled the card out of my wallet on an infrequent occasion, perhaps in an effort to secure backstage passes to Taylor Swift or to explain away some bad behavior on the part of me or one of my sprouts, there is no big outstanding balance run up on it. In fact, I have a great credit rating with the cancer martyr gods because most often, I hide it behind the other cards in the wallet; you know, the divorce card, the single parent card and my AARP card. I assure you that even when the situation practically begs  and announces in flashing neon that I will likely secure something bigger and better for me or my kids simply by swiping the cancer card, I don’t. I promise, there are a lot of people I meet every day (who obviously never read this blog) who have no idea I had cancer. And mostly, I like to keep it that way, but that’s another blog altogether.

So that’s why the Pshaw really chapped my ass. I am so not an “I had cancer” whiner. I don’t feel entitled to special treatment because I had cancer, I mean I literally cringe when people look at me like it was some courageous feat to go through chemo. In sum; I don’t own pink.

So, in this rare instance I was explaining to a couple of people why it is that every day counts to me, and why every single day I have with my kids is so very important to me. I explained how after cancer, you never know when that tap will again come on your shoulder…so days, heck even minutes matter. A lot. And when they are taken from you, you kind of panic. Like the best gift ever is being stolen.

And I was met with a double Pshaw. Capped off with an out loud, “You just need to get over that.”

Yeah.

Actually, chapped doesn’t even begin to describe it.

Frankly, it spurned this woman in a “How dare you?” kind of way. How dare you, with your secure f***ing life that has never been threatened, with your life that has been lived bouncing in the sunny endless parameters outside of the shadow of the grim reaper….how dare you minimize my feelings? How dare you, with your dismissive Pshaw imply that I’m being a cancer drama queen for saying that days count more to me now and I don’t want to just give them away? How can you possibly understand that you just don’t “get over” cancer, ever?

Ugh. Okay, so maybe the response in my head was a wee bit dramatic and I didn’t act on it except for in this blog, since I knew I’d find a posse here. But my point is that the sentiment that the Pshaw was cast upon, that being the value of days to cancergirl, was realspeak for me. A dismissive sound was so not deserved. No, I don’t expect to be treated differently because I had cancer, but I sure don’t expect to be ridiculed or minimized for how I see things since those days like it’s some kind of woe is me, histrionic drama.

And I sure don’t expect to be told how I should feel from someone who doesn’t know how it does feel to have a team of docs be candid for a year that they are not so sure what will happen.

Boy, tail feathers are hard to get back down. Mine especially.

~~~~

“I wish had I spent more time working, or leaving the kids in daycare!” “Boy, I sure am glad I saved my money and didn’t take that Disney trip with the kiddos!” said no cancer survivor ever.

You know why? Because we remember how one day, just between school carpool (where we kvetched about our day’s chores) and dinner, we slipped into a routine mammogram appointment and in that sliver of midafternoon space found out how darn lucky we were to be able to cook dinner that night for our kids. We remember that moment when we found out how many of our chores were actually privileges. We remember how quickly we went from well to sick; how in a matter of days we got our first dose of chemo along with an even bigger dose of an uncertain future. We remember the warp speed of ”What’s that?” as our hands glided with soap in the shower, to “Game over.” And our hair was still dripping wet.

We live differently because we now know breast cancer’s dirty little secret; that the trick is not getting rid of it the first time, but keeping it away. And we now have to live in that liminal space.

I don’t feel, as the Pshaw (I felt) implied, that life after cancer means, “OH MY GOD I HAVE TO STUFF EVERY MINUTE FULL OF MEMORIES!” It’s not a frantic kind of thing. It’s just simple logic; after a near miss with an exit ramp, the days traveling on the road of life now get the appreciation they deserve. We look out the window more, taking more pictures instead of sleeping or asking/complaining how much longer we have to go. So while I don’t condemn other non-cancer peeps for undervaluing the gifts of their days, I don’t want them poo-pooing my perhaps mildly over-valuation of mine.

After treatment, I struggled with how to live in that in-between time, that time between the last chemo and the somewhat mythical, promised land of the five-year mark. I’d be a big fat liar if I didn’t say that a lot of that thinking had to do with how to use that time wisely with my kids; giving them enough of me to sustain their lifetimes. While I didn’t want an “Every Day is Disneyland” life, artificially jacked up in a Wonkaland splendor, I also didn’t want to put anything off.  No more, “Some day we will go see Rock City!” for me. We went. I wanted to live, not large, but at least a smidge larger; a hybrid life of bucket list crossed with a second chance.

I pestered my trusted financial advisor (Pop) about how much I should siphon off savings to do some special (previously known as frivolous) things with my kids like Disney and beach trips after cancer. I peppered him (and myself) with the question, ”How much less is it okay for me to work? Can I work just part-time for a few years so I can be there after school, and during the summers?” I would beg the speculation of whoever would uncomfortably listen, “How much of my IRA can I dip into, if there is a chance I may never need it?”

How much was too much, how much was not enough?  It seems I wanted permission to live a little larger and wider, and assurance about how large I could go; always hedging against the bet that I could in two years or perhaps four, find myself instantly again too sick to live at all. I wanted to use it up, but how do you use it up if you don’t know how long you need it to last?

I was looking for the sweet spot. Wanting to hit the sweet spot on the ball of living and doing and spending and being.

How do you hedge living and dying? I knew too, that just outside the sweet spot, is the place where performance and results would diminish. Too much or too little, and I would likely miss the sweet in between.  The sweet that felt like normal life.

Finding the sweet spot of life with my kids was and still is also fraught with worries for this lil’ psychologist mom. How do I appreciate and suck up the value of my days, without suffocating the endless freedom of theirs? How do I do the impossible and not make a big deal out of shopping for a prom dress, just because I am thinking I may not be there to shop for the wedding dress? How do I make an event that is a BIG TEARY EYED DEAL to have lived to see on my part, normal on theirs? How do I pack their backpacks full (in a way that doesn’t laden them down now) so they have it to subsist on if they find themselves motherless at 17?

Hindsight always offering me balance I now, in a calmer state suspect that the Pshaw was infused with the implication, “You can’t live your life that way.”  But I do. I suspect a whole hecka lot of us cancergirls do, especially the mama’s out there. And you know what? I wont apologize for it and I won’t “get over it.” I don’t want to get over it to be honest. It would be like going from Technicolor back to black and white. From living in the sweetness, to living in the bland.

The sweet spot was bigger just after chemo and it has narrowed as the years go on;  perhaps as I began to gauge that my pennies may indeed need to last longer, or perhaps as I gauge with deep satisfaction, that I have filled another kind of bank. But then just like that, after twelve years a friend has a recurrence. And it starts it up, the calculation of the exact inverse proportion is again at work; as the possibility that my life seems shorter, the sweet spot of living gets a little larger. It’s not a constant. And I wonder again, just how to live in this space.

~~~~

“You can’t take it with you,” they say about money. I don’t know if the same can be said about intangibles like memories and good times; I mean I don’t know if I will sit on a bench in heaven and take them out one by one from the backpack that I packed in this life and toted through the pearly gates with me. I hope I will. I do know this, it will be fuller as a result of cancer. And I also know this; what I can’t take with me, I can leave behind. I can leave so much more behind by using life up here, living in the sweet spot of every single day with my kids and family and friends and dog, however long it is.

I can get up each day and figure out how to squeeze every last drop out of that orange. Because the last drop is indeed, just as sweet as the first.

It all comes down to the old quote, “You better get busy living or get busy dying.” The only thing I know for sure is when we are busy living, the sweet is sweeter. Perhaps that is the answer; the sweet spot is crystal clear when we get busy living, but we miss the ball entirely when we get busy dying.

“listen–are you breathing just a little, and calling it a life?”

mary oliver

 

I treat children for sexual abuse.

It is not so much a task of erasing memories, but of diffusing them; decreasing the impact and diminishing the power of the symptoms of trauma. Helping kids sort and put fragments into drawers and compartments and teaching them how to manage how the trauma; the triggers and hypervigilance are now a part of their life.

I often compare it to having to carry a bowling ball with you for the rest of your life. If you were to say, carry it in your right hand forever your back would likely develop scoliosis. Your shoulder, wrist and elbow joints would deteriorate and hurt and your balance would forever be compromised. Your body would have to adjust to live around the trauma. People would frequently walk up to you and say “Hey, what’s with that bowling ball?” because based on your crippled appearance everyone could see that it had taken over your life.  And every time you looked down, there it would be, right in front of you, dangling and pulling at you…a reminder. The worst part would be that only half of you, one arm, one hand would be free to touch and feel the world.

But if you were to get an ergonomic backpack and center the ball in the pack, your legs and back and body would be in balance and you would develop healthy muscles to carry it. As the days went by, the ball would seem lighter and lighter till you hardly noticed its heft any longer. No one could see it or really know it even existed unless they asked what was in the pack and you chose to tell them. Best of all, both arms would be free to embrace all the world has to offer.

The trauma, well it would have to take a backseat to your life.

That is the sweet spot I hunt for, that nesting of the ball in the pack. A purveyor of backpacks I am.

But it works. Yeah, we struggle sometimes to get it in there, and you will always have those few who insist they want to carry it out in front and sometimes hit others in the head with it for various reasons. But most folks, most want to find that place to put it and move on with their lives.

But the thing about trauma is that it is a developmental, organic process; it is ever changing as we move through the rest of our lives. We can’t just zip it away and never take it out again. At various points we must in fact stop and take it back out, re-examine it, see how it fits in our pack now and maybe make adjustments to the pack. Often, this happens when we are having trouble fitting through a new doorway; it seems our pack keeps getting us stuck or is preventing our passage. That is when we have to take the ball out and rearrange things.

When I see kids, I always tell the parents that their child will likely need therapy over the course of his or her life. This is not to be mistaken with “a lifetime of therapy.” Simply put, it means something different cognitively, to have a history of sexual abuse when you are 5, than when you are 12, than when you are starting to date, get married, or have kids of your own. The triggers change right along with life stage and distance from the event. As the train moves, we see new scenery, simple as that. Therefore our posture must change as one incorporates the trauma emotionally into each stage and we  must rearrange the pack. 

Small doses of the therapy at stop-points long the way are the ticket to a healthy life, a life where the cancer lives around you, not you around it. Despite a parent pleading me to take my big eraser out of the drawer and make their child forget, bowling balls can’t be erased. But many, many things can be done to manage how they create havoc in your life and to make them less heavy. The first step is seeing what triggers it and managing that; the tricky part is that the triggers change and have many levels to them.

You gals know where I am going with this, so I will go ahead and preach to the cancer choir. The trauma (and PTSD symptoms) of breast cancer are something we will carry with us for the rest of our hopefully very, very long lives. When we are first handed our special edition awareness version of the pink bowling ball, we bitch about how damn heavy it is and protest that there must be a mistake, surely this big ugly cumbersome thing this doesn’t belong to us. We are dying (not literally of course) to finish treatment and put it down. And then, there is that moment when we realize this sucker is with us for life and that scares the crap out of us as we wonder how in the heck we will manage this huge thing from here on in.

Better learn how to understand it and manage it punkin, the rest of your long, long life will be a whole lot happier. And a whole lot less about cancer.

~~~~~

A few weeks ago, someone asked me about my triggers with PTSD and breast cancer. As my response meandered, I had the Aha! moment where I realized that the triggers that were the THE TRIGGERS were no longer THE TRIGGERS. New ones had come out of hiding of late and had taken their place. After five years, I think I suddenly had time to consider the other things I hadn’t noticed that were elements of the trauma. The deeper layers and textures, more elusive to recognize at first, that contributed equally to what scared me, what haunted me, again and again.

See, I used to get freaked out by the obvious; hospitals and thigh cancer and hearing about women who didn’t make it. Sure these things still bother me (but not as much any more) yet suddenly a secondary layer of triggers emerged; events from the shadows of that time.

One of the million elements of the original trigger stepped forward and said, “Notice me.”

~~~~~

A while back, I was torturing myself by watching the most Chock Full of Triggers for a Cancer Patient Movie of All Time, 50/50; a true horror movie for residents of Cancerland. As I watched, the panic internally mounted as the normal garden variety triggers poked their sharp sticks at me; the hair loss and buzz of the razor on your bald head, the chemo barcaloungers, and the days you arrived at treatment and your chemo buddy was quietly gone. But all of the sudden a scene popped up, startling me and shoving me into the abyss….the moment when the main character goes to chemo alone and afterward was standing outside alone, waiting for his ride that never showed.

I had many dark days after that movie; sorting the new muck out.

See, if I had watched this movie five years ago, this little snippet, this scene would have gone unnoticed but now, further along in my development/emotional life after cancer….it got me. This little part of cancer now had the time and space needed to demand the attention it deserved. This, was a new development.

Going through cancer solo had really traumatized me in ways I never knew until now. Yet at the time, I brushed it off to tend to the more pressing issues of dying and wigs and scared kids. Now, I suddenly began to realize that much of my current dread of rechecks and blood draws and mammograms and it coming back had more to do with the going to it alone part poking at and awakening a tender, unresolved place than with cancer. See, I’ve gotten relatively used to the “cancer” part, but am just now realizing how horrifying it was to not have a hand to hold during the cancer part and really to help me hold the ball, even now. Now, seeing others with supportive spouses and teams of people surrounding them when they are diagnosed triggers something deep and sad in me, and it is not pleasant.

~~~~~

Cancer has deep roots.

Cheesy yes, but allow me the metaphor of comparing trauma life to a flower growing. At first there is this tiny seed; neat and tidy, encapsulated and manageable. You feel very sure of its heft and potential as it appears. But you plant it and it begins to grow; green, fresh, tiny leaves emerge and you deal with those. At times it may start to wither but then a flood comes, maybe a little fertilizer (and we all know what that is) triggering a sudden growth spurt and new things appear quickly. Some parts get pruned away, some wither and find a natural death and some stay and grow strong. Then the flower blooms and suddenly, there is so much more to incorporate sensually; smells and colors and nuances you never knew were there when that tiny seed sat nestled in your palm. Lastly, it drops it’s seeds and it starts again.

The evolution of our emotional lives after cancer can be seen as a good and normal and cyclical thing if we accept it. PTSD can be managed. It doesn’t necessarily get bigger, it just changes and we must be open to that reality. As we progress along the developmental trajectory of cancer, we are not static. We only become static when we take the ball out and our fingers get stuck in it; the metaphorical equivalent of arrested development.

Emotional triggers will grow and die, grow and die. Cancer blooms and re-blooms through our triggers. We simply must take each new thing and find a place for it in our pack. Then we must heft it up, take a swig of water and a deep breath, and get on our way our way to the rest of our lives; arms outstretched and ready to embrace life, clearing that next doorway with room to spare.

 

It’s not the load that breaks you down, it’s the way you carry it.
— Lena Horne

Halloween is a coming and it’s time for ghosts and goblins and all the spooky stuff that makes you quiver and quake! (I mean of course beyond the onslaught of bone chilling pink neon of October reminding you that A) you had cancer and B) there is still not a cure, but I digress.) I’m a pumpkin carving, costume making girl myself; a girl not too keen on hard-core horror shenaniganry. But it is Halloween and I realize some people enjoy that edgy fear that is brought on by terror and fear so, if you are NOT one of those thrill seeking people, this blog is not for you. And for you adrenaline junkies out there who crave a little foray into dark crevices of a psychological thriller, I won’t disappoint.

Follow me to a place where anxiety whips you around the craggy corners and “What Ifs” taunt you as they dangle from the trees like sinister Spanish moss come alive, waiting to grab you with its gnarly fingers. Let’s go to a place where cesspools of bubbling yuck abound, spewing slime on you as they percolate endlessly. In this little House O’ Horror, you’ll find that the unexpectedness of the path is the worse part, cause one second you are on the Pleasantville train all safe and buckled in, and the next you are hanging out of the window as it careens over a cliff and you holding on by your fingertips. Ghosts from the past whisper warnings of death, wrapping around you like a filmy, wet covering of doom you can’t wipe away and skeletons jangle their bones in a rhythm that is hauntingly familiar. You run, but you cannot hide.

You my dear, have entered the haunted hallows of my neurotic little mind. You timidly tread on a path worn by years of the anxious wanderings of the crazy woman in the attic and her vigilant pacing back and forth as she scans the horizon for what is to come. Madness drives her repeatedly back and forth back and forth as she screams her banshee laughter and cackles, “It’s coming!”

Spoiler alert.

It occurs to me that I am a little neurotic. I know right? Big freaking surprise to those of you who have had the honor of standing next to me during what I personally perceived to be a high alert situation. Shocking to those who have felt the anxiety shed off of me like a constant molt of yuck and who  have heard me endlessly repeat things, as if  that could contain the worms in the can. Truth is, I come from a long line of anxious people, my momma and daddy were both Nervous Nellies; and I seem to have gotten a double whammy of the worrywart gene on my catastrophic death spiraling helix. Add to that mix a healthy dose of cancer trauma, and yep, you’ve got yourself quite a psychological horror story.

Quick psychology lesson. DSM-IV will tell you that the trait known as Anxiety shows up in a host of outfits; Obsessive Compulsive Disorder, Panic Attacks and Phobias are some. Post Traumatic Stress Disorder (PTSD) and Social Anxiety are also members of the family and Anxiety, not being chintzy can also give people a combo platter of several types. Me, I have always been a garden variety catchall Generalized Anxiety kinda girl, little bit of this and a little bit of dat; nothing special about me. 

In an oversimplified version, Anxiety is controlled by a little almond-shaped thing in our brain called the amygdala.(ah mig dah lah)Powerful little nut that amygdala is; a little panic button per se. When a normal person sees something that feels worrisome  like say a snake, that little almond is in charge of sounding the warning (or “Uh-Oh” response as Reid Wilson-anxiety guru calls it.) The “Uh-Oh” is the signal that sets off the adrenal glands, makes us fire cortisol, and engages all the other chemical responses to act; responses which are generally helpful in a normal threat situation. Note the word “normal.” 

When someone like me has anxiety, a whole, whole lotta nebulous stuff has the ability to set off that “Uh-Oh” response, things that likely the average bear never even notices as she goes about her day. Experiencing a trauma, like say CANCER introduces yet a multitude of new, invisible to the naked eye of a normal non traumatized person items to set off the panicked feelings. When these triggers, the things that poke at the amygdala and shout “DO SOMETHING!” are related to past trauma, we professionals call the response hypervigilence and PTSD. I think its fair to say that most of us who have worn the pink dress have a wee bit of PTSD after almost dying and all. And its fair to say that a lot of the cancer related triggers seem to make absolutely no sense to us or our family and friends, until of course, you backtrack to the fall of the first dominoes in the series. Phobias are a little different in that they really don’t have an identifiable precursor, but triggers generally have trauma as the culprit.

Admittedly I had this cute, overworked lil almond of an amygdala long before cancer; but now I seemingly have a whole bag o’ nuts. Cancer and all the wonderful experiences that go with it, simply makes us scared of things that the normal chick probably never even notices, like illness, wearing hats or say the smell of band aids, sharpies or skin burning. Sometimes, we are scratching our now hair covered heads going, “What the hell? Why am I wigging out at a baseball hat?”

So add trauma to an already anxious girl, and my amygdala came out of cancer in “Uh-Oh” overdrive with a hair-trigger to boot. To manage it, I have decidedly taken an offensive stance to heading the “Uh-Ohs” off at the pass. Scanning the horizon as good PTSD patients do, I remain ever watchful on the widow’s walk of my mind. Then when I spot something on the horizon (whether real or conjured in my banshee imagination) I rapidly assess the “What If’s” to proactively diffuse it. I generate a plan a,b,c and d if  “What If” happens. This serves, in my crazy little mind at least to stem the tide of adrenalin when it does occur by providing it with premade, neat little controlled channels in which to flow like levees in a hurricane.

Cancer made me start considering thinks I never thought before; new and improved“What if’s” materialized because in part, the notion was reinforced that small things can indeed rapidly become BIG things. Cancer also blindsided me, and made me feel I missed something, its cackle of BwaaHaHa! resonates to this day, echoing the notion that had I been on a more watchful guard, it wouldn’t have gotten to me. 

Cancer made me crazier. Cause I now spend likely an unhealthy amount of my life in, “What If?” It is hard for me to imagine that a lump on my thigh could possibly be cellulite and not cancer. 

I like to think, being the positive spinmeister that I am, that I spend so much time in “What If” to innoculate my brain with controlled little doses of adrenalin, so when real things occur they are not as overwhelming. (Sounds good in theory doesn’t it?) My dad always says that worry is money spent on a debt not yet owed, and boy debt scares me; I have gone bankrupt emotionally at times with worry. Ironically in the face of this habit, I will swear to you I am an optimist, because where some might see a pessimistic doomsday Eeyore I see a good Boy Scout. Albeit a good Boy Scout who annoys the hell out of others with endless preparedness drills. 

Blindsides, of which I have had many over the years, make my free-floating anxiety worse and have put my amygdala on a constant state of heightened alert. When I get blindsided, I’m useless for days; I get paralyzed by the flood of adrenalin, like a deer in the headlights, I can’t move and think.  See, I can handle a “What do we do now?” as long as “now” is played out in my head long before the event actually takes place. But when I am in blindsided like I was with cancer, I spend my time grieving in my angst and anger over my failure to see it coming. In the end, I am left not trusting myself, not knowing what is solid and true, feeling like the worst Boy Scout on the face of the earth. Blindsides have made me suspicious that the status is never ever really quo, and amplified my global need to take the pulse of everything, over and over cause certainly I missed something; some sign of sickness in the relationship or my body.

I am a shoot my ducks down as soon as they pop up girl, but now I have taken it one further, aiming my gun at the place I suspect they will pop up and sometimes even shooting  rounds at the empty space. I am a pre griever, a pre worrier, a preparer for the worst. I exhaust my friends, my dad, my kids and Grandmother Willow. And me. Sigh. I blame cancer.

Cancer did a lot of bad things to me, it took a chunk of my body, it made me have to get poisoned on a regular basis, it burned my skin, it financially devastated me and it stole a few years of my life by making me too sick to do anything. But one of the worst things it did to me was reinforce the notion that a limp in the dog could mean he will die tomorrow, that someone not calling me means they ending their relationship, that a fever could mean meningitis, and that I could die from a dog bite. It made me afraid of normal life events, like checkups and even getting a cold and made me live in “What if?” A friend admonished me the other day when I talked yet again, about Scout dying. “Jesus Lauren,” he said with the beleaguered exhaustion well-known to my friends, “You have had that dog in pine box at least five times in the last three years.” And he’s right, and I have had me there too.

Cancer made me a bit of a drama queen I guess.

Cancer leftovers suck.  They are cold and even yuckier when reheated. And the trouble is you never know when your mind, like the frugal,well-meaning grandma is gonna pull the foil off an old unidentifiable clump covered with mold and say, “Oh yes, this will be yummy reheated.” Your mind smells it and says, “Uh-Oh.”  Hell, your mind just hears the crinkle of the foil, or the refrigerator door open and you are off to the adrenalin races.

And you know what? Cancer stocks our fridges to the gills with that shit.

I talk a lot in this blog about the PTSD that comes with cancer. The smells and feelings and visual things our minds and muscles secretly recorded unbeknownst to us, and meticulously covered with foil and stuck in the freezer drawer. Vapory, ghostly wisps that covertly reheat later to poke and prod at our sweet lil’ amygdala, sometimes without us knowing it until it boils over. Double, double toil and trouble for sure. Yeah, I am a drama queen alright, but damn it, I earned it.

~ Meandering~

David Sedaris does this hilarious piece about a purchasing a genuine human skeleton as a gift for his artist partner, Hugh. He suspected Hugh would take the skeleton his art studio but Hugh instead decided he wanted to keep it in the house, hanging it in their bedroom. David writes that every time he sees it, he hears it whispering to him, “You will die.” In fact, he can hear it whispering from the other rooms in the house, pestering him as he works….”You will die.”

~Meandering~

A few weeks ago I was talking to a friend on the phone. He had a head cold and as we talked, I could feel my amygdala kicking in and I got all squirmy. I got kinda freaky in that weird way that your body feels fear, but you don’t know why. I wanted to hang up quickly and I did.

It has started to occur to me that I get a little too hinky about getting sick, about being around people who are sick or by being exposed to things that I think will make me sick. While the germaphobe thing was likely always there for me, it was dialed up a thousand notches by cancer. Illness, and all the  smells and feels of it are all too familiar and I spend a lot of time and energy avoiding it. The potential of catching something, of getting sick is the first domino; it tips all the rest of the triggers and let me tell you, it’s Guinness Book qualifying long line of them after cancer.

Getting sick scares me now because my mind travels down that well-worn Path O’ Terror to the place where small things can morph in a millisecond into big things. It is hard for me to believe now that strep throat won’t kill me by attacking my heart. I tend to pay way too much attention to small things that are wrong, a tiny red bite that may be a harbinger for lyme disease or even the interplay of my stress levels causing cancer.  Because I realize how what I wrongly assessed as a small thing in the past, was in fact a big thing and it blindsided me.

So now it’s all BIG. Cancer makes it hard for small things to stay small ever again, working like a trick mirror on the haunted trail, distorting…distorting and magnifying. “Uh-oh” comes with the slightest sniffle, with the smallest pea of a nodule in your thigh and with the slightest murmur from a lymph node.

When you are trutzing around with a grand total of about fifteen white blood cells circulating through your system, you suddenly realize a small thing like a cold can take you out. A fever can put you in the hospital, where you are susceptible to even more illness, and funny as the notion sounds, being sick delays chemo treatments, and that too can kill you. And when you get sick now those fears, silently recorded, get played.

Cold’s whisper, “You will die, I will kill you.” And your amygdala does not forget that lesson. Sneezes by the guy behind you line at the grocery store scare the shit out of you, even after five years.

I have had this little heart flutter thing of late. While I got checked and was told it was normal, but it still has a stranglehold on me when it happens. It feels like when Herceptin almost killed me, like the day 38 treatments in, when my heart almost stopped. One minute I said to the chemo nurse, “Hey Marci, listen to this,” and the next minute there was panic in the chemo lounge as my line was pulled and I was whisked to cardiac care.

Flutters rattle the skeleton and he whispers, “You could die from this.”

By week 32 of chemo you feel like you have had the flu for well, 32 weeks. Feeling sick, fatigued and vomity, swallowing oodles of pills and feeling dizzy all becomes a constant. When you look in the mirror, a sickly ghostly being looks back at you whispering, “You could die from this.” And suddenly, all the things associated with being sick, become cattle prods to the amygdala.

Now, just feeling sick scares the hell out of me. It rips the foil off the old stuff from the back of the fridge and makes me taste it again as it shoves it down my throat. The few times I have had colds or illness since cancer I am miserable, not a whiny sniffling way but in that edgy free-floating fear as you walk through a haunted house kinda way. Like a pink-eyed zombie, any illness has the ability to grab me and takes me back to the visceral depths of the places I hoped never to visit again by mimicking what I felt all those months. The muscle memory kicks in, the hard wiring fires, the tape recorder hits play and you hear, “You will die.” And even if in your mind you know better, stopping adrenalin is like stopping a train; no can do.

Scan the horizon I do, for coughing ducks.

~~~~

The good catholic girl in me would like to believe (and does) that the avoidance is not so much of death, as much as it is avoidance of the ghosts of cancer; of the tastes and smells and fear and fatigue and feelings that whisper with their haunting familiarity, “You have cancer. You will die.” I will do anything to prevent those bones from rattling. I will do anything to manage ahead of time that of which I am most fearful. An acrobatic and exhausting avoidance of the haunted place where I once lived and almost died. Avoidance of anything that makes me, my muscles and my sweet little amygdala hear, “Cancer.” Anything… to avoid fear. A fellow blogger coined the phrase, “My fear kicks my other fears ass.”  Boy ain’t that the truth?

Skeletons in my closet indeed.  Boo.

 

“You got serious thrill issues, dude”

                                                                          Crush–Finding Nemo

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I’ve been avoidant. 

Okay, maybe a little lazy with a capital Z mixed in as well. 

A little unfocused. Perhaps a little scattered and overextended.

But really.

Mostly avoidant.

Despite the urging and friendly Yoo-Hoo’s of others to come back out to play, I have dug my heels in and looked away. 

In fact, I have a confession to make. Please forgive me y’all. I’ve been avoidant of reading the other bloggesses blogs as well.

Truth is, way back yonder in December I promised I’d be back soon. And “soon” by any stretch of the definition well, “soon” has done come and gone. And I still sit here, avoidant.

At first I thought I just needed a little break. I really loved writing my lil blog every week, and kinda got to where it was a part of me. Initially, it felt good to empty out the trash can, and to spill out the rummage left behind in my head by cancer. I felt humbly, that I had figured out why I was still here. At first.

My little über analyzing brain has tried and tried to figure out what’s up with the delay of my return to the blogosphere. After a year of writing about the ick and nonsense and cancer drama, I can only describe to you more what I didn’t feel than what I did.

What I didn’t feel anymore was the gratification of the purge; I didn’t feel the expected satisfaction of succinctly tying up so many loose ends and setting them free. At the end of it, I no longer felt the organized glee of putting them all into neatly categorized drawers and boxes and sliding the drawers shut.

No, I didn’t feel the satisfaction of the emptied attic. It left me with nothing to do with my hands. And really, what’s the point of being the crazy old woman in the attic if there is no fodder, if there are no chests to open and frantically grab and wildly throw the contents about while screaming about cancer? 

The empty space, albeit peaceful, haunted me more some days than a head chock full of trauma bits.

I mean, who was I if I wasn’t the girl with cancer? What should I do with a mind born to dissect and analyze everything to death when there was thankfully, no apparent death to analyze? 

Perhaps (I entertained but for only a moment) I am a tad histrionic after all, thriving on drama and needing crisis to feel like I was alive, forever needing something to do with my racing mind and hands. Perhaps it’s why the stillness, which I did not really resent, felt odd.

What I felt was nothing. Not good or bad, not relief or angst. Nothing. A void. An absence of something that had taken up a whole lot of space. Emptiness where the cancer was, a big empty attic previously taken up by the cancer.

And a reluctance to refill the room with those thoughts again.

Early on in my cancer diagnosis, I was sitting in Grandmother Willow’s office. This was shortly after the dirty little secret of breast cancer was whispered in my ear; that the trick is not it getting rid of it the first time, but in keeping it away. Grandmother Willow was trying to stem my rapidly racing thoughts as they made loop after loop, trying to assure me that one day this cancer would all seem an afterthought.

Because I can sometimes be a Little Miss Know It All, I often tend to call bullshit on theories that don’t match up with my picture of the world, and that day was no different. I remember thinking maybe she was the crazy old lady in the attic because I could see nothing but a life from here on in with the grim reaper as my constant traveling companion, forever bound like members of a chain gang with his endless whisper distracting me for eternity.

I distinctly remember her telling me about woman who recently came to see her who, after a whole first session of spilling her current emotional history said, “And oh yeah, and I had breast cancer ten years ago.” “Oh yeah,” like she had forgotten about it. “Oh yeah,” like it was an afterthought.

“Bullshit,” I thought.

Sitting bald and frightened on her couch, it seemed inconceivable that cancer would one day take up so little room in my life; that it would become such a non entity in my identity. That in the game board of Lauren’s life, cancer would become such a non player in my current emotions on any given future day.

Yet, this is how I have felt these last months. I have felt the absence of cancer. 

After years of thinking about nothing but cancer, I have somehow managed to get to where it is not part of the complexion of my being. One day last week, a neighbor stopped to tell me she had gotten her port out that morning. I felt this blankness when she said it, not lack of empathy, but more a situation where I was unable to summon the empathy because I had forgotten how it felt to be in her shoes. I knew she must feel relief, but I couldn’t feel the taste of it in my mouth anymore. When I started to try to remember what I had blogged about ports, I couldn’t even remember what I had written. All I could remember was how hilarious it was that Wendy had made hers into a daisy.

When I went back to read that blog, I swear to you,  it was as if someone else had written it. Sometimes this happens with my mom; I can’t remember what she looked like until I look at pictures, and then I am surprised at features in her face that I forgot.

I was detached from cancer. Detached from the chain gang.

Years ago, big surprise, I had to take Concerta for my ADD. With that drug, the thought of food and hunger vanished. I’m not saying I wasn’t hungry or my appetite was curbed, I am saying that the thought of food no longer crossed my mind. I’d be sitting there feeling faint and go, “Oh, yeah, I haven’t eaten in two days.” This little pill took away the emotion and rituals and grooves in my brain that were attached to food and eating; it eliminated the craving and the timing and desire to indulge in this so familiar and daily ritual.

This little blog did the same with cancer. I don’t indulge in cancer much these days. But, it’s not healthy to not need food, nor is healthy to avoid part of your being.

I remember reading how Lance was in an doctor’s office finding out he was just covered with cancer. It seemed insurmountable, yet a few days later after he talked to doctor after doctor about what each intended to do with each and every metastasis he proclaimed, “We had talked this thing down to size.”

Blog by blog, a bite of the proverbial elephant (or grim reaper) at a time, I too had talked the memories and trauma, the cancer down to size.

While the bell can never be un-rung, somehow, somehow….swirling my pen around in the well un-cast the dye. Like a magnet, my pen pulled the dye cast long ago from the water, bringing it from pink to very, very pale, almost indiscernible pink.

Perhaps I lived my way into (at least some of) the answers.

Perhaps I am just reluctant, not avoidant. Perhaps I am detached; not sure that I want to re-attach, or how to re-attach without it filling the room up again.

Perhaps, I have just moved seamlessly, as we do with grief, into acceptance.

Perhaps, I have indeed outlived it.

So in these last months, my life has been filled with all the stuff of teenagers. Colleges visits, college apps, obsessing about the right high school and college choices, proms and dances, driving lessons, graduation preparations for two and undergoing some good old-fashioned teenaged drama teaching me I better grow some thick skin real fast. (Suddenly, I have become a whole lot less smart and a whole lot less funny.) My pop survived another wicked pneumonia, and Scout is still the best dog ever made at the dog factory. Through all of this, I have worn some very good friends down with my new looping obsession; my anticipatory grief that life is gonna change real soon as the kids and people and dogs I love fly away. But in all this, we are busy, busy, busy here at the ranch distracted by life not death; indeed life is moving forward at warp speed.

And oh yeah, six years ago I had cancer.

 

 

I’m back.

 A little at a time, so as not to fill the attic,

but I’m back. 

xoxo

Lauren

While the Who’s down in Who-ville
Loved preparing for Christmas a lot,
The Grinch it seems, most certainly did not!
He did not like their holiday festivities,
Not one bit, he did not!

December 12 has some seriously
Bad mojo for this Who you must see,
For when I rip November from the calendar,
It plum steals my glee!

 It slides into town
with its trumpet sounding and squealing,
A nasty wasty old Grinch,
Just slinking and stealing
All of the infinite joy
of my holiday season!

I’ve puzzled and puzzled about why this is so,
(And I come to the conclusion
That I’ll never know.)
It comes, shouting and screeching,
“Twelve! Twelve! Twelve! Twelve!
Stop what you’re doing
(beseeching, beseeching)
Boo Hoo to your Who-who-ing!”

December 12 has all the tender sweetness
Of a seasick crocodile.
Yes December 12, has been you see for a while,
has been downright vile!
For us Who’s in Who-ville, 
(Right where we Whos be)
It’s been super duper awful, you see!
 
The sleigh full
of unfortunate December the twelves
(Despite the all of the efforts of Santa Claus’ elves,)
Started on a day far far away,
In 2001; on a cold winter’s day.

Now part of the problem was you will see,
Was that we Who’s down in Who-ville love our holiday glee.
We, yes we Who’s liked Christmas alot,
But that Grinch, well the Grinch
Most certainly did not!

He crept through our Who-house feeling oh-so contrite, 
As he made his way through
in the still of the night,
(Stuffing my joy in his bag
As he slithered and swagged,)
He did, he did! And then pulled it up tight!

Yes! Just seven days after I got punked,
From that nasty old rotten, spotted green skunk,
When I was given hallmark greeting betraying
His true and his hidden green leopard funk! 
‘Twas a sweet anniversary card
Promising undying love; yes I sighed,
Yet on December 12,
I awoke to find in that
The undying love
Had in fact died!
My mouth hanging open
For a minute or two,
I found a note saying,
“Pooh Pooh to the Who’s!”
Leaving crumbs too small
For my little Who-mouses,
The Grinch took my life in his sack,
And left for new spouses!

It seems lore is true,
The Grinch hated the NOISE! NOISE! NOISE! NOISE!
Of we wee Who’s down in Who-ville
And all of our joys!
And too the Grinch it seemed, 
(We all know a ton)
Hate hated the fun of the season!
(No one knew the reason)
No one, nope no one.

 Yep, December 12 was a mean one that year,
Starting a trend
Of instilling fear
Cuddly as a cactus,
(And we now we know from the years)
We were just getting practice!

 Twelve months later, exactly I’ll say,
I was in my kitchen with the kiddos
Forsaking the day.
Putting my good-vibe-voodoo
On December the twelve
Doing our holiday baking,
With my little Who-elves.
The Grinch sleeping late,
Why, he was just awaking!
(Perhaps sniffed the Grinch
My holiday baking?)

‘Twas a warm December 12 afternoon,
And I, well I said, like a hap-happy loon
“It’s too warm for a sled or for green grinchy snow,”
(Cause he needs snow to slide into town we all know)
A day mild and fair, I threw open the sashes
Said “Stay out you old grinch! Let in the fresh air!”

Sirens heralded the Grinch coming,
In his stolen sled chase,
“Oh My!” I thought summing,
“He will show his green face!”

 I ignored those horns thinking,
 “How could it be so?
For really you see,
His sled couldn’t possibly go!
Coming? Not he, could it be?
Oh palease; there’s no snow!”

But the Grinch crashed his stolen sled,
(with lights blue and lights red)
On foot he leapt o’er our fence
(And into my yard with police chasing, guns drawn)
That old louse!
As looked with great dread at the path that he cut,
and I screamed NO! and slammed the door shut,
That Grinch slunk up my deck steps,
I said to the wee-Who’s “Lay down!” as he crept!

Then that nasty old Grinch
Hid in our Who-ville for an hour or so,
(Not in my chimney, but on the down lo.)
Though we all ended up safe,
(both my Who-son and Who-waif.)
And although the police came and showed that old Grinch who’s boss
He succeeding in making our cookies taste like Toadstool sandwiches,
(With arsenic sauce!)

 Charming as an eel old December 12 was that year!
The hex, you are seeing, it becomes oh so clear!

 The December 12 Grinch slid into town,
Like clockwork he was,
Making not yet a sound!
He came two years aft to the day
But this time by phone the bad tidings
He chose stage for his play!
When that nasty wasty skunk of a doctor
Caused a nauseous super ‘naus
By announcing that unfortunately I had cancer
And well, there would be no Santa Claus!
Now I can’t fault the doctor
(He was just made to be Grinchy)
Horns strapped to his head,
Why, he was forced to be winchy!
Like little Max, he surely didn’t choose,
To be tethered to the gigantic, Sleigh O’Bad News! 

You nauseate me, December 12, you are a greasy black peel!
So often now, it seems quite surreal!

 Last year the December 12 Grinch,
Brought nary a pinch.
So smart and so slick,
He smiled at this little Cindy-Lou Who,
With a great Grinchy trick!
No termites in that smile did see when I spied and I spied,
(I didn’t I think to ask why Santy Claus Why?)

I awoke last year on the twelfth to see,
The dawn of my five-year cancerversary!
December 12 patted my head assuringly as I cooed like a dove,
Seeing my tree not lit on one side and promising to fix it above!
On the best date of my life
(to a theater grand)
With stars on the ceiling and cherubs with fife
And jolly old soul playing the Wurlitzer organ
 In this magical land!

My whole tree seemed lit up,
As I sat content with my milk duds and my Grinch given cup!
Watching White Christmas;
Gosh! My heart was filled up!

Later we went to the tackiest light display ever seen;
(My ultimate happy place)
Yes! This lil Cindy-Lou Who went to bed with no green, 
And a smile on her face.
Yes! Little Cindy Lou Who sighed a satisfied sigh.
(It seemed you might see, she had found the right guy!)
Candy cane in her little Cindy-Lou Who-hand,
It seemed there was finally no Grinch in the land!
Dreaming her sweet Who-dreams with nary a care,
It seemed that the Grinch had decided to spare
This me-Who
(and too)
my little Who’s Who’s!

But alas! Cindy Lou eventually awoke to the clatter,
Of learning it was just a good date on a bad date,
(And that lots be the matter!)
“Boo-Hoo! Boo-Hoo!”
Cried Cindy-Lou Who,
“The Grinch took my joy up yonder to Mount Crumpit
(Of that he was clear,)
And yes she is still waiting for the Grinch to fix up there,
And bring it back here!”

Yes the December 12 Grinch is one rotten tomato,
With ears full of vegetable gunk,
(And not sweet potatoes!)

Today on this eve of this eely December twelve
I glare at the calendar 
(Sitting by my Elf on the shelve.)
Cause surely again the Grinch getting ready to finish his goal
And I already can detect, the garlic in his soul.
He’ll slink down my chimney as I snooze, asnooze snooze.
And on the stink of his breath, carry difficult news.

A friend’s biopsy will come,
As the Grinch makes his way,
And I can tell you that over that old bum,
I’d take the seasick crocodile
Any old day! 

December 12, December 12; it remains so very true,
Especially for these three little wee-Who Whos,
You are indeed a nasty wasty skunk,
And “The three words that best describe you
Are as follows and I quote,
Stink, stank, stunk!”

 You’re a foul one December 12,
You do indeed have garlic in your soul,
And I wouldn’t touch you with even a nine… no eleven
No! A gazillionth and a half-foot pole!

You’re a rotter, December 12, you are a sinful sot!
Trying to steal my Christmases
I dislike you I do, and that a whole lot!

 But wait! Do you hear what I hear?
It’s coming near!
Do you hear the bells ringing?
Rising over the snow?
It sounds like wee Who-folk singing!
A warm blanket-like glow,
And it’s starting to grow!
A tinkling sweet sound
So sweet and so clear.
Come on everyone,
Put a hand to your ear! 

“Fahoo Forays, Dahoo Dorays
Fahoo Forays, Dahoo Dorays
Welcome Christmas, Christmas Day”

“Hurray! Hurray!
Hurray,” I say!

Because my dear Who-friends,
(I am just now Who-summing,)
That the best part of the Grinch
Is that he tries to stop Christmas from coming!
Each year around twelve twelve, we-Who’s feel his pinch!
But every year Christmas still comes in spite of the Grinch!
It is still in our grasp,
(Despite our Who- gasps)
Yes Christmas keeps a coming,
As long as we little Whos keep, 
This little Fahoo tune humming! 

Every year it turns out okay,
(No! More than okay,)
When we see that the Grinch
Cannot steal Christmas Day!
The story without fail we wee-Whos realizes,
Yes we see just as soon as our hearts grow three sizes!
The lesson itself always comes to full circle,
Not despite, but because of what happened
(I know, what a quirkle!)

Every year a sled full of blessings
Slides into Who-ville,
And we pull our wee Whos close; all warm, cozy and still.
Andwe find that the sled is packed full of assorted Who-lessons!

Listen close now you little Who-Lasses and lads,
It’s not about  iphones, itouches, or even ipads,
It’s only about the What we Who-haves,
(And most certainly NOT about what we Who-hads.)

It’s not about the toys and pantookas and wuzzles
But indeed about giggling
At how that old Grinch puzzles,
When despite all of the havoc he tried so hard to bring,
We still have within, what makes our hearts sing. 

Every year, December 12 comes on, sure as snow,
Yet I find tidings of good,
(Despite all that I know)
That mean old Grinchy Grinch
Squeezes my hand with a hard pinch
 Yet I softly pat his green  hand,
Cause it’s well in my land!

He reminds me of the true Christmas meaning,
Not despite his antics, but because of his antics
(That’s the lesson I’m gleaning!) 

Every year, my Grinch of December twelve comes round to remind,
Both my little Who’s here in Who-ville,
(Who are both very kind)
And this little Cindy-Lou Who
(Who likes Christmas a lot)
That Christmas comes, yes it does,
No matter what!

Because Christmas, most certainly was never about,
What was taken, or what we Whos find we’re without,
Christmas remains as that old Grinch was so wise to see,
Just so long, as we have we.

When you clasp the tiny warm Who-hands,
Of the tiny Who’s that you love,
And have a little faith in your God above,
Christmas is ALWAYS merry! VERY!
(and chock full of love!) 

December 12 didn’t stop Christmas from coming;
Cause in our Who-noggins that sweet truth
Of God’s love keeps a Who-drumming!
It came! It came just the same!
And yes my Who-friends,
That truth will always remain. 

And in this crazy little Who-life of mine,
(Which by the way is so dandy and fine)
I say, “Welcome Christmas bring your cheer!”
And I stand hand in hand
With those Who-folk I hold dear.
Tiny wee Who-hands,
And wee furry Who-paws,
(And of course that most certainly
includes, You-Whos and you alls!)

 A lucky girl is this little me-Who,
(Yes indeedy, I know that it’s true!)
Cause no matter what ever be the green Grinch’s  hand,
This little Me-who can always find to clasp 
A nice warm Who-hand!

No matter where Cindy-Lou Who is being an elf ,
she thinks yes she does to her little Who-self,
(as she sits in Who-land )
“It’s a wonderful life
 In fact, it’s quite grand!”

“Fahoo!” I say,
As I prepare Who-pudding to feast. 

“Dahoo!” I say,
As I carve the roast beast.

 ~~

“And the Grinch, with his grinch-feet ice-cold in the snow,
Stood puzzling and puzzling: “How could it be so?
It came without ribbons! It came without tags!
“It came without packages, boxes or bags!”
And he puzzled three hours, `till his puzzler was sore.
Then the Grinch thought of something he hadn’t before!
“Maybe Christmas,” he thought, “doesn’t come from a store.
“Maybe Christmas…perhaps…means a little bit more!”

Welcome Christmas, bring your cheer!
Cheer to all Whos far and near!
Christmas day is in our grasp,
so long as we have hands to clasp!
Christmas day will always be,
just as long as we have we.

Welcome Christmas while we stand,
Heart to heart and hand in hand.”

~Dr. Seuss

Years ago, then President Kennedy made a speech about the space program and our need to keep advancing it. He referred to the story of some little boys running through the green, green fields of Ireland and coming upon an orchard wall that seemed perhaps too high to climb. Instead of turning back the boys took their hats and threw them over the wall, and thus, then had to climb the wall to go get their hats; the toss leaving them with no choice but to go over the wall to retrieve their caps.

I have always been a throw my hat over the wall kind of girl. Sometimes it’s because I am just dying to know what’s on the other side, sometimes it’s just for the thrill of the climb. Being an eternal sunshiny optimist, I think it’s mostly because I believe that what is on the other side of the wall is not better than what I have, but something new and different and grand to experience. Mostly though, just like those little Irish boys the toss is made to force me to do something I thought I couldn’t do, to make something happen, to experience something that would not have had I not done so. Truth be told, I get a wee bit agitated when there are no walls to climb, my fingers itch and fidget with a cap in hand, and I start to actively search out walls when that happens. 

When we are making our way through our life and come across the cancer wall, I think that most of the time our oncologists and surgeons rip the cap out of our hand and toss it over the wall for us. They lay out their neat tactical plans of how we will scale the wall and give us visions of how 85 or 95 percent of the people have made it over, and how they are living life on the other side of the wall. We want to visit this magical and unbelievable land on the other side and really don’t have much choice but to go after our cap to cover our bald heads; then too, to go after it is infinitely better than staying on this side of the orchard wall, where things appear to be dying.

But after cancer, as we continue onward through the vast field that is our life, what do we do when we come upon a wall? Do we bemoan the fact that it is unfair, because we already had to climb the big wall o’ cancer? Do we even have the strength or gumption to climb anymore? I mean honestly what’s the use if we are gonna die while trying? Do we avoid walls altogether? Do we see it as a positive or negative? An adventure or labor? 

Cancer makes us hesitate. It makes us want to hold on to what we have and clutch tightly to our caps because well, we might need it to cover our bald noggin again sometime soon. Cancer makes us afraid to plan and take on new things. Throwing our hat over a wall feels like buying green bananas. Cancer eats zest. Cancer makes us afraid. Cancer makes us tentative and bit distrusting of planning for the future. Cancer makes us think the devil we know is better than the devil we don’t. In the months just after treatment is completed it is hard to believe there are better days ahead, it feels counterintuitive to trust that the ice is thick enough to skate out on and into our future.  

After five years, I prefer to look back at that time of caution and fear as a time when I was just resting and gathering my strength. I remember it now, with my sunshine spin, as a place where yes I may have taken the cap off and considered the toss but in the end held kept it in my hands as I sunk down with my back against that wall to as they say in the south, sit a spell.

But I can tell from my perch high atop of yet another wall, five years and a million walls out from cancer that once you catch your breath and no longer need that cap to cover your head, cancer becomes a catapult sailing you high over the wall and into life after. Cancer catapults both our caps, and us. Cancer makes us want to experience everything that is behind wall number one and two and three and four. Cancer in the end, makes us adept and easy hat tossers, and skilled climbers with a penchant for finding even higher walls. Cancer makes us grateful for the toil of the climb.

To move from a place of fear, from a place of clutching our caps to our chest to a place where we are making the toss we have to believe that the days ahead are better than the days behind us. We must believe we are capable of making the climb and will live to see the other side in order for us to throw. We must be willing to give up the status quo and the safety of what we know, for perhaps the devil we don’t (which may in fact, be a devil of a good time.) We must toss our hats over with glee and sense that an adventure beholds us, not a tragedy. We must be excited about the climb. But mostly we must actively find our own walls by beginning to move through life again. That is what life is all about Charlie Brown; making the run to kick over and over, even though the ball may get pulled out at the last minute.

A tad impulsive I am yes, and admittedly I have been known many a time to toss before I totally think it through. Sometimes I have created my own walls just so I can toss. But I have found that ninety-nine percent of the time the climb is worth it and that the sweat and toil of working toward a goal remind me I am alive. If I thought about it too long, I might not make the toss; cancer has given me the luxury of not having a lot of time to think about it.

Life is in the preparing to climb. Life is in the climb. Life feels like drawing the deepest of breaths when you are on top of the wall. Almost always, I find not greener pastures but my hat, and lots more life experiences to fill it with.

There are a million things that cancer took from me but two million more I have because cancer, many found on the other sides of walls I would have never thrown my hat over had it not been for cancer, and many found while making the climb.

And heck, I’d rather die while climbing a wall than die while standing at the bottom, anxiously peering at it, clutching my hat, trying to screw up the courage to make the toss. As Mr. Buffet says, “I’d rather die while I’m living than live while I’m dead.”

I didn’t survive cancer to just stand there. Neither did you.

Walls don’t come to us, we must go to them. As they say, ships in the harbour are safe, but that is not what ships are made for.

The prospect of a short life has made me to run gleefully to them, and throw my hat over the wall again, building my wings on the way down the other side.

Just not angel wings…not yet at least.

“One thing about trains: It doesn’t matter where they’re going. What matters is deciding to get on”

~The Polar Express

Pink.

Who knew such a benign and gentle hue could summon such strong emotions, and could wield such power? Read the rest of this entry »

Once, when Amelia was about three or four years old, she, Colton and I were driving along. The two of them were of course in the back seat and all of the sudden Amelia yells, “Who’s driving the car!?” In the seconds that I was trying to figure out what she meant, Colton chimed in and answered, “Mom is.  The person who has their hands on the big wheel up in front is the one who is driving the car.” Read the rest of this entry »

I am so sick of talking about breast cancer.

In fact, Grandmother Willow and I recently had a fifty minute-ish chat about it as I crawled all over my psyche looking for clues to my blues. This little Suzy Sunshine was très dissatisfied with her last months of little black rain cloud funkity funk and darn it, I told her, I needed to find the source of my gloomy river and fix it pronto. I speculated, as I have during several recent chats that the business of tiptoeing around the mine field that is cancer while writing this blog has had a little something to do with my sad state of affairs. Maybe even a big little something to do with it.

A minefield indeed; a desolate battleground from a long ago war. A place where still, even years later, I must tread carefully as mines are left that have yet to be detonated. Shards of shrapnel remain, ready to slice into my still tender skin as I wander through, and the remains of what was lost still litter the ground creating sometimes massive obstacles to my progress. A land where I occasionally find a bullet in the soil; a tiny yet lethal missile that missed its mark many years ago, which in my hand weighs heavier than I would speculate of its tiny mass, as I mentally gauge the potential it carried as it was fired in my path all those years ago.

I spend most of my days in my professional life seeing and talking about very ugly things; cesspool of human failure things. Over the last 20 or so years in working with abused wee ones, I have learned a little about the cost of caring, the cost of going over and over traumatic events and quite awful things. Compassion fatigue has often been an unwanted traveling companion in my life. It takes a toll on your psyche to care and listen, and it is the high internal price you pay for dealing with highly emotional traumatic events of others over a long period of time. 

Like with the artist formerly known as Prince, PTSD is the reaction formerly known as Battle Fatigue, (the cost of dealing with your own highly emotional traumatic events over a long period of time.) And you know what? Cancer is a long ass battle for sure, its got physical and mental staying power. The endgame (that is really the never-ending game) is that dealing with cancer and thinking about cancer and worrying about cancer is freaking exhausting. Revisiting the war zone that is and was cancer, even years later, is exhausting.

I my friends, have cancer fatigue. Cancer has done wore me out.

Because even after five years, there are still bombs that have yet to detonate and that scares me. Daily, I find a bullet in the soil and pick it up and realize how close it came to taking me down; while that act of holding the bullet in hand is in itself is frightening, more terrifying is the realization that there may still be bullets in the gun.

As I write this blog, I realize that I have been anxiously and cautiously tiptoeing along, carefully calculating each step and holding my breath even as I sleep. I’m feeling physically exhausted and mentally fatigued by the constant mindfulness to cancer, from the perpetual heaviness of the armor I attempt to don as I write, and by the tiny yet constant effort needed in the hunch up of my shoulders as I tread.

Years ago, when I got fired for having chemo brain and then opened my own practice I found, as cliché as it sounds, a gift in it (I mean besides not having to work with really dysfunctional people anymore.) I made my own schedule, and likely worked 100 more hours a week but all the sudden one day I realized that my 20 years of amassed compassion fatigue had virtually disappeared. 

Now, statistics people could find all kinds of confounds in the causal nature of this phenomenon in my life, such as I was so focused on cancer that work ick seemed small next to it, or it was because I had a break from all the yuck during treatment. But because I know me better than anyone knows me, I will tell you my theory. In owning my practice, I can schedule cases as I like. I can review quite ugly photographs when I am ready and I can say no to the task when I am not ready. I can set boundaries about when and where and how I talk about the sometimes very violent/graphic details of sexual and physical abuse. I can set the pace of cases I see, and take breaks as needed (although I find I don’t need as many breaks as I thought I would.)

The compassion fatigue evaporated as the trauma was more in my control.  Work and trauma no longer controlled me; I controlled it. I could control the ebb and flow of kids and cases, and set boundaries about not talking about child abuse in the walls of my house or on weekends or at cocktail parties for that matter (and not look like a bad/rude/chemo brain employee for doing so.)

When I first got sick, my oh so wonderful Pop and bestest friend MJ called me at least once, if not twice, if not three times a day through diagnosis and in those early weeks of the crazy firehose of test results and treatment plans. Cancer was coming at me from all angles, as you all know it does when diagnosis is fresh, and tests and results are being done, and war strategy is being made. I talked cancer, and ate cancer, and I slept cancer, and like poor Jan Brady lamented with sister Marcia, “Cancer Cancer Cancer,” was all I heard.

One day I just got to where I wanted to talk about something else, anything else, but cancer. Heck, discussing toenail fungus or dead pets would have been infinitely better than talking about cancer at that point. I had to set the limit and say, “Look, I want to take a week off of talking about cancer okay?  Let’s take a break and talk about something else, anything else for a while when you call.” And because they are good people they did just that, and it helped. A lot.

The moral of the story here is that sometimes you just have to take control and set a boundary with cancer, even after five years. Sometimes, you have to place a moratorium on cancerspeak, and that goes for you, the people around you and for that neurotic little voice in your head.

One of my girlfriends told me that right after she was diagnosed and just before chemo started, she and her 12-year-old daughter (with her onc’s blessing) took a long before cancer came a knockin’ planned trip to Greece. My girlfriend really has the coolest kid; I adore that little cutie pie for her effervescent and eccentric grooviness. Don’t you know that girl took a piece of paper and wrote “CANCER” on it, put it in a box and placed it on the mantle in the house. As they left for the airport, this cool kid was pulling the front door shut and she turned back and said to the box, “Cancer, you are too heavy to carry all over Greece. We know you will be here when we get back and we will be ready for you.”

After five years, it is sometimes still all about cancer. Some months it’s worse than others (if you get my potentially ungrateful sounding drift.) So for the rest of this week, I am declaring a moratorium on cancer. I am instead painting my toenails a delightful shade of robin’s egg blue and with my sweet daughter, I am boarding a plane to Disneyworld.

And with that I will say, “Cancer, you are too heavy to carry all over Disneyworld…even in an elephant that can fly.”

Look out! Look out!
Pink elephants on parade
Here they come!
Hippety hoppety
They’re here and there
Pink elephants everywhere

Look out! Look out!
They’re walking around the bed
On their head
Clippety cloppety
Arrayed in braid
Pink elephants on parade

What’ll I do?
What’ll I do?
What an unusual view

I can stand the sight of worms
And look at microscopic germs
But technicolor pachyderms is really too much for me

I am not the type to faint
When things are odd or things are quaint
But seeing things you know that ain’t, can certainly give you an awful fright

What a sight!
Chase ‘em away! Chase ‘em away!
I’m afraid, need your aid
Pink elephants on parade
Pink elephants…
Pink elephants…
Pink elephants…

Pink Elephants on Parade~ Disney’s Dumbo

 

 

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