Seventeen Years

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My sister, mom and me at the Outer Banks sometime in the ’80s.

I hate April Fool’s Day.

I’ve never really been into pranks or trickery, and there’s something about this day that gives mischief more of a mean-spirited edge. And social media has made it even worse. Every year there are the fake engagement and pregnancy announcements, fake moving announcements, fake whatever announcements. It’s annoying and not really funny at all.

Of course, my hatred of this day is about more than just an intolerance of childish tomfoolery. My mom died in a car accident on April 1, 2000.

There’s something especially cruel about getting the dreaded call from the hospital that there’s been an accident on April Fool’s Day. For a split second I thought, “is this some kind of horrible joke?”

This year, the anniversary fell on a Saturday, just like the day it actually happened. My sister Wendy texted me in the wee hours of Saturday morning, likely awake with her thoughts, to tell me that having the anniversary fall on a Saturday again makes it harder for her. I nodded as I read her words, feeling the exact same way.

Just as it was on that horrible day in 2000, April 1 this year was absolutely gorgeous. One of those warm, not-a-cloud-in-the-sky days that make you revel in spring. As I sat in my backyard looking up at that sea of light blue, I couldn’t help thinking back to that day so many years ago.

It’s kind of amazing that I can remember most of the details of that day as clearly as if they’d happened just last week. I remember the slight nip in the air, what I was wearing (a pastel striped t-shirt from Old Navy and jeans), what I was doing when the phone rang (lying on my dorm bed, waiting for my parents to arrive for a visit). I remember bargaining with God as I careened down I-40 to the hospital in Chapel Hill. I remember realizing my mom was gone when the hospital staff ushered me into a small, private waiting room outfitted with an overabundance of tissue boxes and Bibles. I remember being taken back to see my father, unconscious on a gurney, disrobed and covered with a sheet up to his chest–preparation for surgery. I remember the stunned voices as I called family and friends to tell them the awful news.

In the years since her death, I’ve tried to mark her anniversary in a positive way. Some years I’ve volunteered or participated in a charity walk, others I just try to do fun things to keep the mood light and my mind off the sadness.

This year, I spent the day with Rodney and Alex. We ate pancakes for breakfast, snuggled in bed watching cartoons, went to swim class, went to our neighborhood Easter egg hunt and played in the yard. Nothing particularly remarkable, but without a doubt a good day.

I think this is what my mom would want–her loved ones moving on, living their lives. She’d want to be remembered–and she was–but I don’t think she’d want me or my sister to dwell. I told Wendy this when I returned her text. I asked what she had planned–a trip to Virginia with her boyfriend to see an art exhibition–and told her my plans for the day. And then I told her I loved her.

I know somewhere out there in the ether, my mom was glad.

 

 

A Letter to My Fear

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This morning I had my first appointment with a counselor at the cancer center. Our session was mostly paperwork and getting-to-know-you questions, but toward the end, she asked me what tools I’m currently using to cope with my emotions in the wake of my diagnosis and treatment.

I told her about this blog and other writing I do, and before I left, she encouraged me to use some writing exercises to help work through all the feelings I’m experiencing now. One of her suggestions was to write a letter to my fear and/or my cancer. It sounds kind of hokey, but I’m going to give it a shot, starting with fear. Here goes.

Fear,

I won’t use the salutation “dear,” as you are no more dear to me than a smear of shit on the bottom of my shoe. You are no friend of mine. You are the enemy. You live to undermine me. To torture me. To keep me cowering in the dark, unable to make a move without worry or anxiety.

You’ve always been around. Even before cancer, you’d rear your ugly head before big presentations, on airplanes and even on days that should have been nothing but happy, like my wedding or the day my son was born.

But now, you’re especially vicious. You’re around every corner, it seems. No longer content to just lurk in the shadows, you parade around in the bright light of day, emboldened and relentless. You don’t care if I’m at work, at home, in the middle of something important or joyous. Like the unwelcome guest that you are, you horn in on good moments, popping up in places you don’t belong. You rob me of sleep, of solitude, of peace.

You drive me to Google symptoms over and over again. Pelvic pain. Back pain. Neck pain. Every little twinge sends me into a frenzy. The old me would chalk it up to sleeping wrong, exercising too hard or eating too much rich food. I’d pop an Advil or antacid and keep on moving. But with you on my shoulder, such nonchalance is impossible. Nothing is brushed off. There’s no such thing as just a little ache. Everything must be over-analyzed, scrutinized, fretted over. Every little feeling could be the beginning of impending doom when you take over my brain.

And here’s the thing–I don’t know how to shake you. I know my good buddy time will help me, but he takes his…well…time to do that. So what am I to do until then? Just put up with you? Allow you to control me? Allow you to make my life hell?

And if we’re being truthful here, even time won’t banish you from my life completely. You’ll always be there in some way, lurking around along the edges, just waiting for the opportunity to strike. You can smell my vulnerability like blood in the water–you know all my soft spots and when I’m at my weakest. No predator has ever stalked his prey with more deft cunning than you.

My only course of action is to face you. To call you out. To tell you to fuck off. To allow the rational side of my brain to tamp down the irrational, obsessive side more often. I know this will not be easy. This is going to be a bloody, brutal fight between you and me. But I’m ready. I’ve fought scarier, more dangerous opponents than you. Ask them how that went. I have reinforcements, and my team is stronger than yours. Let’s do this.

Until next time,

Jennifer

I Gotchu

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Me and my baby

One of the most exciting stages of parenthood is when your child learns to speak. There’s something almost magical about a baby going from this drooly, crying blob to a little person able to express himself verbally. It’s a long process, but one with lots of fun stops along the way.

In the past year or so, my son’s vocabulary has exploded. He’s almost two-and-a-half, and since uttering his first word (“mama,” for the record), he has become more of a chatterbox with each passing day. Much of what he had to say before was merely baby babble. And he still engages in his fair share of gibberish, but more and more, his words are actual words, and they’re assembled in phrases and sentences. It’s pretty amazing to witness.

Much of his current vocabulary revolves around cartoon characters (Mickey Mouse and the Paw Patrol are big topics of conversation in our house), his favorite foods (hot dogs, grilled cheese, apple juice) and there are a couple words he’s uttered that I’m mortified he knows (we blame dad’s potty mouth for those gems). But for me, there are two phrases he uses often that just about melt me to the floor.

“I pick you,” is the toddler version of “I’d like to be picked up.” He almost always holds his hands up to me as he says it, and there is nothing sweeter as a mama than to have your baby stand before you with his arms raised, essentially saying he chooses you. Does he necessarily mean it in a literal sense? No. But in a way he does because my arms are the ones he wants wrapped around him.

Which leads me to my current favorite toddler phrase–“I gotchu, Mama.” This is usually uttered late at night, little arms wrapped around my neck, head resting on my shoulder, or in the morning when he wakes up in the bed next to me and clutches tightly for a groggy hug.

If I could bottle the feeling it gives me, I’d be a millionaire. It’s the salve that cures the trivial woes of the day. It’s the balm that heals any hurt feelings. It’s what dries my tears of fear, worry and anxiety when the darkness comes. Hearing those sweet words whispered in my ear as my child clutches me lovingly makes everything better.

Having cancer has changed me as a parent. Yes, I still have my bad days/moments and get frustrated by crankiness, tantrums and misbehavior. But I tend to pause and savor the good moments a bit more nowadays. I know how important these moments are–even the littlest ones–and I’m so thankful to be here for each and every one of them.

 

On Shoes Dropping

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Last fall when I was really sick after my first dose of Taxol, my dear friend Carla sent me an incredible book to help wile away the hours of headaches, fever and worry.

The book was “In the Body of the World,” a memoir by Eve Ensler, the writer and activist best known for creating “The Vagina Monologues.” It details her fight with uterine cancer, while giving a healthy dose of perspective in the form of harrowing tales of the horrifically abused women she advocates for in the Congo.

While I related to her words and experiences on so many levels, one point she made really resonated with me above all others. Ensler talks about her cancer diagnosis and dealing with the feelings of “why me?” She explains that having survived sexual abuse at the hands of her father, as well as abusive relationships with other men, she sort of felt like she’d been through her really bad thing. And now, even though she’d already been through hell, she was being put through it again.

Yes! I know it’s unrealistic, but after my mom died, I sort of felt like I’d paid my heartache dues. Sure, I knew there were plenty of bad things that could and would happen to me, but I felt like maybe I’d earned a pass to not have to experience anything really catastrophic for a while.

As Ensler and I both learned, unfortunately, life doesn’t work that way. Bad things happen to good people. Bad things happen to people who’ve already been through more than their fair share of bad things. Bad things happen on top of other bad things. Bad things don’t have a rhyme or reason. There’s no real pattern. And that’s what makes them so damn scary.

As I walk this path of survivorship, it’s hard for me to keep the fear at bay knowing this truth. There are no free passes. This shit could come back. It could come back today, next week, next year. There’s no guarantee.

I made a therapy appointment today. As I wrestle with all these feelings, I know this is the right move for me. Thankfully, the cancer center has counselors on staff to help people like me make sense of all this and try to move on with our lives. I’m excited to take the first step.

 

Survivor’s Guilt

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This morning I had my survivorship appointment at the cancer center. This is a next step in my cancer journey–addressing what I need physically and mentally after treatment.

One of the things that I’ve come to realize is most overlooked/not talked about when it comes to cancer is what happens to a person after they complete treatment. When you’re in the throes of the battle, as strange as it sounds, things are almost easier in a way. You have a focus, you have a plan, and you’re really sort of forced to take things one day at a time–handling that day’s treatment, side effects, etc. There’s a routine of appointments, blood draws, check in, check out.

But then everything sort of stops. Appointments taper from weekly to monthly to every couple of months. Your arm stops feeling like a pin cushion (that I don’t mind so much). Your hair grows back (that I definitely don’t mind). Suddenly the routine changes, and you’re supposed to go back to your normal schedule.

Except, nothing feels normal anymore. Even as I go to work, take care of my son, carry on with my regular activities, things are no longer the same. There’s a new sense of fear, anxiety and even guilt.

I’m feeling the latter more acutely this week. On Sunday, Nina Riggs died of metastatic breast cancer. She was only 39. I’ve been following Nina’s story since last fall when her incredible essay about living with terminal cancer ran in The New York Times‘ Modern Love column. Nina’s story resonated with me in so many ways–as a breast cancer patient, as a mother of a young boy, as a wife, as a woman who lost her mother too soon. We had a lot of things in common–we even lived in the same city and had some mutual friends of friends. I wrote about Nina’s essay in this blog, and she was even kind enough to comment and send good wishes my way.

I’ve cried so much this past week for Nina and her family, her two boys in particular. Though I didn’t really know her, I got to know her through her writing and I could empathize with many of the things she experienced during her fight with cancer. I know how hard it was for her as a mom to know she’d have to leave those boys. My heart aches for her in that regard, and for them as  children who lost their mother too soon.

Even more bittersweet is the fact that Nina has a memoir called The Bright Hour coming out in June, chronicling her experience living with metastatic breast cancer. She wasn’t able to live to see its official release. But I hope it will allow more people to not only get to know her great talent, but also shine a light on a type of cancer that is generally kept in the shadows. Nobody wants to talk about metastatic breast cancer because it’s usually not a happy story to tell. But the fact is there are thousands of women and men who face and live with this diagnosis every year. And their stories are important, and I’m glad at least one of them is going to be told in such a public way.

As I wrapped up my appointment this morning, the NP I met with gave me a hug and congratulated me on reaching this point. I know I should be feeling celebratory–and I do in a way–but it’s hard to totally let my guard down and enjoy this moment. It’s a process, and I have a lot of work to go, and I plan on seeking some help to get there. In the meantime, I’m just focusing on feeling grateful. I know how fortunate I am to be where I am, and that’s enough to get me through today.

 

Ultra-Sad

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Last month I started taking Tamoxifen, an estrogen blocker often prescribed to women with breast cancers that are estrogen receptors, like mine. This medication helps block the hormone from feeding cancer cells, and works to reduce recurrence.

As one would expect, though, any medication that tinkers with hormones can have some wonky side effects. I’d heard some horror stories–side effects so bad that the patients had to discontinue or find an alternative medication–but my side effects have been pretty minimal, thus far.

That said, I started noticing some mild pelvic pain a couple weeks ago. Nothing major, just a little pain/pressure, mostly when I was walking or active.

Old me would have just ignored it and moved on. New, paranoid cancer patient me lets very little go unchecked. Though inconsistent, the pain persisted for more than a week, so I called my OB-GYN’s office to let them know (per the instructions on my Tamoxifen patient leaflet).

Yesterday, I went in to have everything checked out.

Going to my OB-GYN office is kind of a sad experience for me nowadays. The place is teeming with women at various stages of pregnancy–the newly-pregnant, with their nervous significant others in tow; the second-trimester gals, all cute belly and glowy faces; and the almost-done ladies, bellies about to pop with that third-trimester look of being completely over feeling like a beached whale.

I’m done having children. I’d made that decision long before my cancer diagnosis. But I still can’t help feeling a pang of jealousy when I see these women. I loved being pregnant, and there are days that I would love to be pregnant again, but that’s not in the cards for me.

This visit only intensified those feelings. After my exam, my doctor sent me to the ultrasound room for a quick look-see just to be certain everything was kosher.

The last time I was in this part of the office, I was one of those pregnant women, excited to get a look at my unborn child. I absolutely loved getting ultrasounds. It was so cool to see my little guy moving around inside me. That blurry black-and-white screen was full of promise and excitement.

Not so much this time. As the tech went to work, I watched the screen nervously, this time hoping my womb and surrounding area were empty. She made a few measurements, and when I asked questions, she gave me some vague answers–standard protocol for ultrasounds. But sensing my terror, she reassured me when she was done that it looked good.

My OB seconded that opinion when we met in her office shortly thereafter, going so far as to say that my uterus and ovaries were “textbook perfect.” Too bad these model parts are where no one can see them!

I left the office with a sense of relief tinged with sadness. Though my decision to be one-and-done was already made, a part of me still mourns the end of this chapter of my life. And I’m angry about the no-turning-back finality that my cancer adds to that ending.

 

Smoke and Mirrors

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Searching “vintage magic” to find this image was super-fun. 

In the past month or so, I’ve gotten a lot of compliments. Some of them are on my hair (the chemo curls are coming on with a vengeance) or how healthy I look. But most of them go something like this:

“You are just so strong. There’s no way I could have managed all this.”

“You are holding up so well; I would be  a mess if this had happened to me.”

You get the picture. But the truth is not very inspiring.

Inside, I’m a complete mess. Truly. I just do a good job of hiding it.

This same thing happened 17 years ago when my mom died. I was so composed (at least publicly) throughout the months following her death that I actually had two friends take me aside to tell me they were worried I was in shock and on the verge of a breakdown or something. Little did they know I’d cried a river of tears almost every day, just behind closed doors.

My people are a stoic bunch. I’ve seen/heard my dad cry exactly four times (three after my mom’s death, the other after his beloved dog died). I don’t think I ever witnessed my grandmother shed a tear, despite burying her husband and two children, as well as several grandchildren. Tough as nails. But it’s not that we don’t feel these emotions–we just rarely express them publicly. (I’m sure this is a conversation to have with a therapist one day.)

The truth is, I still cry often. In the car. At night after everyone’s asleep. Holding my baby in my arms in the dark as he dozes off. Even sometimes after doctor’s appointments.

And if you could see my Google search history, well, you’d know what an overly-paranoid freak show I’ve become. I consult Dr. Google on a nearly daily basis. Every little pain or twinge could be something in my mind. I read symptom lists. I read message boards and blogs, looking for people who felt the same things I do but were OK. It’s totally unhealthy, yet I can’t stop.

So, yeah, I look like I’ve got it all together. But don’t be fooled–I’m still a mess inside.

 

 

 

 

 

 

 

Fear of Flying

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I hate flying.

This is a rather unfortunate affliction,  as I’m required to fly at least half a dozen times a year for work. And even though one would think becoming a fairly frequent flyer would make me more comfortable, it really doesn’t. I loathe the rigmarole of the airport–the buggy machines at the check-in kiosks, the shoeless chaos of the TSA lines, the rush to make it to the gate on a layover. And the flight itself invokes all sorts of anxiety–I’m that freak on the plane with the white-knuckled death grip on her seat arms during any little bump of turbulence–all linked to the fact that my life is in someone else’s hands, at 30,000 feet above the ground.

But last week, a funny thing happened.

I flew to Las Vegas for work. This was my first trip since the one I made last summer to Chicago–the trip I received my cancer diagnosis during.

After six months off the road for treatment, it actually felt good to travel again. I’m not a huge Vegas fan, but my boss and coworkers decided to make this work trip fun, booking tickets to shows and making sure we had a good time after our long days at the furniture market. It has been a long time since I’ve gone out for fun in Vegas, and while I felt much older and dorkier than I did the last time (a good 10 years ago), it was still a good time.

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I saw my first Cirque du Soleil show–Zumanity. So fun!

But what was truly remarkable for me during the trip was the flight. Nothing special happened airline-wise, but rather, a change came within me. I still felt the same rush of adrenaline trying to get through the airport, but once I was on the plane, an odd sense of calm settled over me. I fastened my seat belt and rested my head against the window’s edge, taking in the scene of workers scrambling on the tarmac to load luggage and prepare the plane for takeoff. And as we taxied down the runway, instead of sweaty-palmed panic, I felt serene, watching the plane tilt skyward as we descended from the ground. The world below got smaller and smaller, and I was totally fine.

I couldn’t help thinking back to the last time I was on a plane, staring out the window with tears flooding from my eyes. I’d just received that awful news, and my mind was full of the dark fears the word “cancer”conjures. I’ve come a long way since then, and I have changed more in the last six months–both physically and emotionally–than I probably have in the last 20 years. I can unquestionably say that I am probably a thousand percent stronger than I was that day.

A colleague of mine who battled breast cancer more than a decade ago told me something very wise not long after my diagnosis–“You gain perspective.” And she couldn’t have been more right. Not only did I gain perspective as far as life goes–sweating the small stuff is not something I do anymore–I also gained a new sense of courage. I have faced one of the most terrifying things that can happen to a person. I have literally battled with something that could kill me. And I lived. I survived. If I can handle that, a little turbulence isn’t going to rattle me anymore.

Feelin’ Myself

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I don’t know what it is–maybe it’s the new year–but I’ve been in a mood this week.

And that mood has been decidedly good.

I’ve really been “feelin’ myself,” as the young folks might say. What exactly does that mean, you might ask? Well, according to the Urban Dictionary:

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Yep, that really does sum it up. I went back to work in the office yesterday, and it felt SO good to be back. I love my job, and I love my coworkers, so I really missed being in the office every day with them. And they all welcomed me back so warmly–the day was like one big warm fuzzy.

And on top of that, I missed having that nice, normal routine of getting up and leaving the house to do something every day. It just felt so nice to get back to something that feels so familiar.

I’m also starting to embrace my growing-in hair. I’m honestly just grateful to have enough to cover my scalp, but beyond that, I’m actually starting to get into the look. And it helps that I’ve gotten lots of compliments on my hair from my very kind coworkers. While the wig I wore before more closely resembled my old hair, it never looked or felt right to me–something about it was just off. What I’m rocking now is MINE, and while it doesn’t look like what I had before, it looks right because it’s me.

Physically, I’m still recovering from surgery, but I feel so much better and have my next surgery planned, so I have a timeline for when I’m going to look more “normal.” My body is still pretty rough, but I’m coming to terms with it and looking for fabulous new clothes to cover it (any excuse to shop!).

So, if you see me walking around these days, you might notice I have a little more pep in my step. It’s because it’s 2017, and I’m feelin’ myself in the new year. I hope you are, too!

 

Moving On

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The year that launched a thousand memes, 2016, was pretty shitty for a lot of people. And thankfully, that sumbitch is over.

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This year was a time of sorrow and loss for so many people. All the celebrity deaths aside (and holy hell, were there a LOT of them!), I know so many people who lost loved ones this year. My husband’s uncle passed in February, I have two friends who lost parents, another who lost her sister, some who lost unborn children to miscarriage, one who lost her cousin/best friend (who also happened to be my high school classmate)…the list goes on and on. And those aren’t the only losses–I have friends who lost jobs, promotions, etc.

On top of all that, there’s been plenty of chaos and strife, from terror attacks, to the instability of Brexit, to the Syrian crisis, to the utter shit show that was the 2016 U.S. election.

Obviously, this was a tough year for me personally, as well. Being diagnosed with cancer, learning I have a genetic mutation that makes me predisposed to cancer, going through chemotherapy and then a bilateral mastectomy was one of the hardest things I’ve dealt with in my life. I have never felt such physical and emotional pain. I have faced the terror and sadness of my own mortality.

My family has suffered, too. My poor husband has stood by me through this whole ordeal, a steadfast rock who held my hand as I cried during my first doctor’s appointment, shaved my head when clumps of hair fell out during chemo and changed my disgusting drains after surgery. And he has done all of this without complaint. I know it’s been hard on him, and I am thankful every single day that I married such an incredible person.

And with him, I’m thankful I married into such an incredible family. His family has been there for us in so many ways, from taking care of my son when I was recovering from chemo or surgery to filling my mailbox/inbox with cards and messages of love and encouragement to just being there to provide a hug or smile when I needed it.

My own family has been amazing, too. My sisters have been a constant source of support, and my dad has been so sweet and concerned–seeing his child face this has been hard for him. And my vast extended family has wrapped me in love and support, too.

My amazing family hasn’t been the only group cheering me on through this crapfest of a year. My friends–best friends I’ve known since childhood, newer friends who’ve become an important part of my life, a group of fellow moms who’ve become a huge part of my support system, former coworkers and even folks I haven’t seen or talked to in years–have shown me so much concern and love.

And my current coworkers–two of whom were literally by my side the day I got the bad news about my diagnosis–have been so wonderful. My absences due to chemo and surgery have been hard on them, but they’ve handled it like champs and never made me feel like I was letting them down. And the company I work for has blown me away over and over again with their capacity for kindness and generosity. I thank my lucky stars every day to be part of such a fantastic organization.

This year has been SO incredibly hard. It has tested and challenged me in ways I’ve never experienced. It has broken my heart on so many occasions. But it also has taught me how much love, kindness and good there is in the world. I am so grateful for every single gesture I’ve received this year, from loved ones and strangers alike. They have made this journey a little more tolerable and they have taught me that even when things are dark, there is still light in the world.

It’s that spirit that I’m taking with me into 2017. I still have some challenges ahead of me and a couple surgeries yet to complete, but I know that this year is going to be better. I can just feel it. I’ve always seen the new year as a chance to refresh and start over, but never before has that feeling been as strong as it is this year. I am ready for 2017, and I’m going to do my best to make it a great year.

I wish you all joy and good health in 2017. It won’t be a perfect year, but I am hopeful it will be much better than what we’ve just finished.