5 years later

Surviving The Storm Quotes. QuotesGram (With images) | Storm ...I was diagnosed with cancer four years and 10 months ago, but I knew long before the official diagnosis that something was very wrong. My gut told me, and it was right.

It’s been a little over five years since my gut told me that knot in my left breast was NOT something good.

It was right.

The storm is not over for me. It will never be over, but a week ago today, I saw Dr. O for my six-month checkup and was no evidence of disease…five years after my gut told me to get my ass to Dr. B for the knot in my left breast. It’s funny because last Tuesday, five years ago, is the day I first called Dr. B for an appointment. I was driving on the highway, and I’d made a deal with myself. I would call Dr. B’s office, and if the receptionist answered, I’d make the first available appointment.

There was no answer.

I hung up and smugly thought that meant all was ok.

It was not ok. I knew better than that.

Five years ago, so much about my life changed, and honestly, I didn’t think I’d live to be able to say, “five years later.” But, here I am. Five years later.

I waited until today to post because I had my yearly scan last Tuesday, and for Dr. O, no news is good news. It’s been a week. I would have heard from her office by now, so I’m cautiously believing no news is good news.

On Friday of last week, I went to the Sammons Center for my 6-month infusion of Zometa. Dr. O started me on it three years ago based on results of a clinical trial. Last Friday was meant to be my last, but now there’s more data from that clinical trial. While results are mixed on extended usage of Zometa beyond three years post initial therapy, Dr. O has decided I will stay on Zometa for another five years for a total of eight years of therapy. I agreed because she is Dr. O, and I’m just a 42-year-old woman trying to stay alive to see her kids grow up and to grow old with my husband.

It’s been a hell of a year, this 2020. My dad died in March 2020 on my husband and my uncle’s birthday. His death wasn’t a surprise, but it hurt. My mom has been in terrible health since February 2020, and just when it looks like she’s on the mend, her health goes to hell in a handbasket again. It’s been hard, but there are reminders everywhere that things work out the way they’re meant to do so.

Five years ago, today I attended the funeral for the pastor of my church. I’d left the annual AVID Dallas conference to attend the funeral. For a few days leading up to the funeral, it had been on my heart that where I was really meant to be was back in the classroom. See, two years prior, I had taken an instructional coaching job. I liked it. I know I did good work, but in my heart, I am a teacher. I was struggling with the thought of going back to the classroom. But, as I sat at the funeral, listened to the words, talked to people I’d grown up with, some I had not seen in twenty years, I knew. I went home that day and told my husband I was going to try and find a teaching job. It was nearly July. I didn’t expect to find one, but I was wrong. I found one, my dream job, actually. I was thrilled…so, so happy.

Three weeks after I took that job, I received a preliminary diagnosis of breast cancer. My world turned upside down. My husband had just started a new job. I had just started a new job. My son was seven and going into first grade. My daughter was nine and going into fourth grade. I remember sitting in my car by myself screaming I didn’t want to be a statistic. I didn’t want to be a number. I didn’t want to have cancer. I didn’t want to die. It wasn’t fair. Why me?

Five years later, my husband has a job he loves. I have a job I love. My son is twelve and going into sixth grade. My daughter is fourteen and going into an early college program where she will be both a freshman in high school and a freshman in college. I still don’t want to be a statistic. I still don’t want to be a number. I still don’t want to have cancer. I still don’t want to die. It is never fair, and I still don’t know why it happened to me.

I have good days and some really awful days where the fear of reoccurrence overwhelms me. It’s still not easier. But, I’m here and incredibly grateful for advancements in medicine and amazing doctors and compassionate people.

As awful as 2020 has been, I’m here to see it.

Five years ago, I didn’t think that would happen.


life, Uncategorized


Wear sunscreen folks. I didn’t as a kid or teenager. Because I didn’t, every year or so, my dermatologist finds something new to cut off and biopsy. This is my third basal cell carcinoma in 10 years. I’ve had several precancerous or hmmm-that-looks-funky-let’s-cut or burn or freeze-that-off over the last 15 years.

You want to know what it’s like waiting for a biopsy result after having had breast cancer? It’s horrendous even though I knew the biopsy had less than a 1% chance to be anything but basal cell. When the nurse came on the phone to give me the results, my PTSD roared to life. I froze. I shivered. My heart raced. My stomach fluttered. Tears rolled. Before she even gave me the results, I told her I couldn’t take hearing cancer again because in my head, I’d begun to believe she was going to tell me they were wrong and it was atypical melanoma, not basal cell. As my onco-psychologist calls it, my catastrophic thinking came into play. I couldn’t stop talking. She, bless her, interrupted me to say it was basal cell and nothing more. I laughed in gratitude. Basal cell sucks but doesn’t spread or metastasize. It’s the least of the skin cancer family.

It took me ten minutes to stop shaking and to get my heart rate under control. All of this took place in a public area, too. I was alone in a crowd.

I wear sunscreen (countersun by beautycounter if you’re curious…no, I’m not a rep). I wear long sleeved rashguards when I swim. I wear a hat. I don’t care about looking cute. I care about protecting my skin. The kids use zinc based sunscreen on their faces and ears and scalps and drench themselves in Kiss My Face or Banana Boat’s new, less chemicals sunscreen. I make S wear a rash guard over her cute swimsuits. She hates it, but she wears it because she’s seen my scars. I make AJ wear a rash guard, but unlike his sister, he loves swim shirts.

I used a tanning bed exactly twice as a teenager. I never wore sunscreen as a kid, and I lived in pools during the summer. In the 80s and 90s, no one told me what sunburns could do to me later. I always thought skin cancer was an old person’s disease. I always thought breast cancer was an old lady’s disease. I was 25 when my dermatologist began watching, freezing, burning, and cutting my skin. I was 37 when a radiologist told me I had breast cancer.

Wear sunscreen folks. Check your skin monthly. Have a dermatologist check it yearly. Protect your skin. Do self exams. Get your yearly physicals. Know your body.

I’ve lived three years after a breast cancer diagnosis not because I felt a lump -I DID feel a lump, but I ignored it because I was 37- but because I knew it was wrong for my left nipple to invert when I raised my left arm. I knew that was wrong and together with the lump I felt, I knew I needed to be checked.

I’ve dealt with skin cancer crap for nearly fifteen years now because I knew I shouldn’t have weird, shiny looking places on my skin. I was pregnant with S when the first basal cell carcinoma was burned off my left shoulder. I was pregnant with AJ when the second basal cell carcinoma was cut off my left bicep. I’ve had other areas cut and frozen off -two on my left shin, three on my face, one on my left arm, one on my back- and I have five, yes five, spots my dermatologist and I watch closely for changes -one on my scalp and four on my back. If those change, at all, they’re gone. They’re suspicious and if they change, none of them will be basal cell carcinomas or squamous cell carcinomas -they’ll be melanomas. Thankfully, in the fifteen years we’ve watched the ones on my back and in the ten years we’ve watched the one on my scalp, none have changed.

Wear sunscreen. Wear rashguards. Check your skin. Do self exams. Know your body. My scars are ugly, but they’ve saved my life…so far.

Pressure bandage covering a 3 inch area of stitched together skin where a basal cell carcinoma was removed yesterday.
breast cancer, life, Uncategorized

Lines and Shapes

From morefamousquotes.com No infringement intended

It’s National Tattoo Day. I’m not sure why that’s a thing. Once upon a time, I swore I’d never have a tattoo. To confess, I used to side eye tattoos. Then, I got cancer, understood the fragility and brevity of life, lived with pity stares, developed a new attitude, and decided to live for myself. Now,I have 5 tattoos, much to my mother’s chagrin (sorry, mom, I love you, but I’m still getting more tattoos).

I began getting inked after my one year cancerversary. I chose a phoenix on my ankle for my first tattoo, not because of my Harry Potter obsession, but because phoenix rise from the ashes, and let’s face it, cancer is a fire. Residing on my right wrist is my second tattoo, a healing symbol with a compass embedded into it as a reminder that healing takes time and when it’s hard, look north. My third and fourth tattoos are 3D areola tattoos done by Marie Sena, an incredibly kind, compassionate, and talented tattoo artist, one of the markedly few tattoos artists in the US who specializes in these kind of unique tattoos. My fifth tattoo, also done by Marie Sena, is a sternum piece, an homage to Adam and our kids -a bouquet of flowers, a rose for Aidan, an aster for Samantha, and a daffodil for Adam -their birth month flowers. In September, Marie will do my sixth tattoo to celebrate what gets me through the dark times in my life besides family -my love of reading and Harry Potter. It’s a custom piece of books and owls, of Felix Felicis and Hogwarts.

I’ve been asked that age-old question, “What about when you get old…don’t you think you’ll regret them?”

No. I don’t. It’s one of the ways I cope with cancer, and let’s face it, if I live to be “old,” I want to have these reminders of what life threw at me.

breast cancer, family, life, teaching, Uncategorized

Dumpster Fire

Dumpster Fire Bitmoji

Picture courtesy of Bitmoji. No infringement intended.

Merriam-Webster added dumpster fire to the dictionary in 2018. “An utterly calamitous or mismanaged situation or occurrence : disaster” is the definition.

My personal life was a dumpster fire for the 2017-2018 school year.

My father’s deteriorating health and the stress it put on my mother was unspeakably hard. My father is completely bedridden at this point. My mom is a teacher as well. Throughout the year, she woke between 4:00-4:30 am to tend to my dad, got to her school between 6:00 and 6:15 am so she had an hour to herself to prepare for her day before students arrived at 7:15. She worked until nearly 4:00 pm most days. At home, she tended my dad, assisted with his physical therapy, and did everything he needed until she fell asleep only to start all over again. While she worked, my sister tended my dad. She cooked and cleaned. She answered his questions and summons. She dealt with medical issues. The two of them are on 24/7. It is stressful and hard. I can’t make it easier for them except to take them out to eat or shop when I can. My mom and my sister are the real MVPs.

My marriage nearly came apart at the seams. I won’t talk about specifics, but let me say this and emphasize how much I mean this, no one is more surprised than me that my marriage survived this school year. The problems and challenges A and I faced this year were honestly harder than the challenges we faced during the 2015-2016 school year when I spent that entire school year in treatment for breast cancer. There were more times than I care to remember where the phrase “Get it together or you have to go,” was spoken. Things between us were worse than anyone, including our family (until now…SURPRISE!), truly knew. I’m not sure anyone except one of my best friends knew things were bad, and even she didn’t really know how bad until I told her two weeks ago. On that end, things are better. A and I have been together since I was 17. It’ll be 23 years this November. We decided we were worth fighting for, that our marriage did not survive cancer to succumb now, that S and AJ needed to us to be us. It’s not been easy to repair the damage done, but we are. We’re trying. It’s hard. But, we’re tough, and we love each other. Stress is a hell of a thing, though, on a marriage.

I struggled with a depressive episode that took me to rock bottom, to a darkness I didn’t know existed. So many friends have been so surprised by my admission that throughout winter and spring I fought depression. I guess it was easy to hide from them because, to be honest, my social life was nonexistent throughout the winter and spring. Truly, I didn’t do anything with anyone except go over to a friend’s house once to see her and her new baby. No one invited me to do anything with them, and I didn’t invite anyone to do anything. If anyone had invited me, I would’ve declined. I would’ve found a reason not to go out with my friends. I didn’t want anyone to know how depressed I was or how close my marriage was to the edge or to discuss the state of my dad’s health. I stayed to myself, and people let me. I let me.

I had a cancer reoccurence scare in the midst of all of this. My lower back hurt for weeks. It was unrelenting. Thankfully, MRIs showed a deteriorating disc and arthritis. Still, that scare added stress and added something else for me to hide, to keep to myself, because the last thing I wanted was questions and pity. I told no one, not even family. Only A. I didn’t want them to worry. My mom and sister had enough on their hands. So, I stayed silent.

Stress upon stress upon stress upon stress.

The perfect storm of calamity.

Last week, my sister told me it’s time for A and I to catch a break. She said we deserve a break. I’m not sure that’s fair. Everyone deserves a break, but I know where she’s coming from because it’s been three years of hell for us.

My mom is a believer in threes. Deaths come in threes. Good things come in threes. Bad things come in threes. She told me since we’d had three bad years with three calamitous events, it’s time to hope for the good. And, we’ve had some good since this summer began. We’ve had some really good news throughout June. My June check up with my radiation oncologist was so normal he released me from further check ups. My June check up with Dr. O, my breast cancer oncologist, was blessedly normal, and I received my second infusion of Zometa. Dr. O took me to task for gaining some weight. I deserved it, and I’m working on it. I saw her a week ago. I’ve lost two pounds already. It’s not much, but it’s a start. A starts a new job week after next. He’s excited. It’s an extraordinary opportunity for him. I’m thrilled for him. It’s the answer to prayers and pleas. That’s three…three good things. A says there’s no reason to expect for anything more than for the good to continue. Maybe he’s right. I want him to be. But, I’m a pessimist. I told him I’m waiting for the other shoe to drop. He rolled his eyes at me and told me to stop.

I posted on Twitter tonight that I’d never felt the dumpster fire bitmoji harder than I did today after reflecting on the school year and realizing how much my dumpster fire of a personal life affected my professional life. I posted that the only thing I can really do is what the bitmoji does -walk away from the dumpster fire. I can’t change what happened. I can learn from it. I can try harder. I can acknowledge how hard the last nine months of my life has been and commit to doing what I can do to ensure it doesn’t happen again. I can’t stop everything that happened -some of it is out of my hands. I can look forward to a clean slate, a new start.

That’s what I can do right now.


breast cancer, family, life, Uncategorized

The Importance of Taking Care of Me

Went to take a quick nap at 6:30 pm yesterday evening…woke up at 6:40 am this morning.
Found on Pinterest. No infringement intended.

I used to feel really guilty and really bad about doing that, falling asleep and leaving A on his own with the kids, but the truth is this: If I don’t take time for myself and recharge, I’m useless. Cancer treatment, and the medication I take every single day to hopefully keep the cancer from coming back, on top of dealing with the after effects of one of the worst depressive episodes I’ve ever had , is a lot to deal with on any given day. Some days, my body, my mind, and my heart just need to rest. Last night was one of those nights. I have no shame in admitting cancer did a number to my body, my heart -literally, since one of the medications I had to be on causes heart damage and my course of radiation also had a pretty high likelihood of causing heart damage-, my mind, and my soul.

It has been a difficult number of months for me personally. My father’s health and physical abilities continue to decline putting more and more stress on my mother and sister. I am the shoulder to cry on and ear to vent to in my group of friends, and there has been a lot of crying and venting, for them and for me. I am a fixer. I want to solve problems and fix issues. There are situations right now I cannot fix nor can I solve. It is incredibly draining and scary.

Last night, when I went to take that nap, the thought going through my head was “I am responsible for me and those two little kids playing in their rooms. I am not responsible for everything else.”

I have to tell myself that over and over because on the personal side of my life, I feel responsible for EVERYTHING going wrong right and for EVERYTHING that’s out of place. I have to believe, as Henslowe assured Fennyman in Shakespeare in Love that sometimes we can’t do anything except trust because things mysteriously turn out well. I’m putting my trust in a number of people, and that’s really hard for me. I do not, nor have I ever, trusted people easily. That’s why I have a small group of friends. That’s why I don’t open up easily to others. I know what it’s like to be stabbed in the back by friends who were secret Brutuses. I know what it’s like to have your trust betrayed. So, it’s very hard for me to trust outside my family and group of friends, and to be honest, I don’t even trust everyone in my family. I just don’t give my trust easily. I’m hoping, and I’m not someone who hopes easily either, Henslowe is right. Things will work out mysteriously well. Things will be all right because right now, they’re not. They’re so not.

The school year is coming to a close. It’s been a good year for me professionally. I was named ELAR Teacher of the Year for my campus, a shared honor as two of us were named. I branched out to take some other responsibilities. Beginning next school year, I will also work for an educational company as a consultant in addition to my teaching responsibilities. I’ve been hired by College Board to score AP exams this summer. These may seem like little things, but for me, they’re huge. I continue to grow as a teacher, as far as I’m concerned, we should never stop learning, and to that end, I’m attending two professional conferences this summer, one week long and one long weekend.

My six-month checkup is beginning to loom large on the horizon. It’s at the end of June…June 29th to be exact. Right now, I don’t feel anything about it. My heart doesn’t catch, yet, when I think about it, but the closer it gets, the more my heart will catch and cancer will fuel my dreams.

Life has not been easy over the last three years. There have been months long stretches of heavy, hard things, not just cancer. Hard life lessons. I’m caught in one of those stretches right now of hard life lessons.

I told a friend last week as I cried on her shoulder -virtually, through text messages, as I literally cried, sitting in my closet where no one could hear me- I feel like Fate, God, whatever hates me. She replied she doesn’t believe in a god, but even if she did, she didn’t believe anything hates me. She said sometimes life is hard, things are hard. Last night, the hard caught up with me. I couldn’t take anymore -no one else’s worries, no one else’s concerns, no one else’s burdens. I had to shoulder my own, and last night, my body, my heart, my soul, and my mind craved sleep. So, I slept. As the cliché says, you can’t pour from an empty cup. Yesterday, my cup was empty. I had to take care of me. Today, my cup is fuller because I took care of me last night.

Taking care of yourself is not selfish. It is self-care. You cannot take care of others if you pour yourself totally empty. You exist as a shell. I’ve done that over the last few months, poured myself completely empty. I’ve existed as a shell. I told myself no more. So, I slept. I turned off my phone. I slept.

I took care of me.


breast cancer, life, Uncategorized


I’m posting this at A’s urging. He claims it’s one of my finer pieces of writing and that it deserves to see the light of day. It’s a hard, raw piece of my life the last few months.


I stopped wearing makeup. That was the first clue, the sign everyone missed because I explained it away so easily. Some lies tip off my tongue without pause.

I wanted to sleep an extra 20-30 minutes in the morning. That was the second clue, the sign everyone missed because it was easy to believe. I’m never one to skip a chance to sleep in if I can.

I like to sleep. That was the third clue, the third sign everyone missed because teachers are perpetually exhausted. I escaped through sleep.

But, the sleep came with sad dreams, my imagination at play without the constraints I put on it during my waking hours. I refused to let what was going on for me personally affect my professional life. Once at home, though, the demons played. At night, my worst thoughts and deepest fears flew free. When morning came, I woke up, more exhausted than the night before, and I didn’t want to wake up, put on makeup, think about clothes. I wanted to pull the covers over my head, cry myself back to sleep, and hope I’d find rest and solace.

Rest and solace eluded me. They never came. Instead, sudden, intense pain in my lower back came. Unbidden. Unwanted. My scumbag brain fed my fears.

After an emotional Sunday afternoon, my husband, stressed out and nearing his breaking point, demanded I call Dr. O the next morning.

I did. I expected to be told to take a muscle relaxer and call back in two weeks if the pain had not subsided.

Instead, I got blood work, an exam, and two MRIs at a cost of over $1000 because for the first time in two years, I had yet to meet my out of pocket maximum by the end of February.

Two breathless days later, I got a call. Spinal arthritis, likely brought on by my daily AI. “Start yoga,” the nurse said. “Let’s try that before adding more medication.”

“OK,” was my reply.

Then, the nurse, gently, “Dr. O wants you to see someone for your depression and anxiety. It’s in the notes she talked to you about it and gave you a name. Have you made an appointment?”

A long pause. “No. I’m ashamed.”

“You have nothing to be ashamed of. Make the appointment.”

A long pause. “OK.”

Later that week, I made the appointment. I saw someone. They prescribed an anti-depressant.

It’s been a month now. The world looks different. I look different. I’m climbing out of this deep, dark, awful hole I’ve lived in for the last three months. I’m beginning to get up earlier. I give myself time to decide if I want to play with make up or use that time to drink a cup of coffee while reading a chapter of a book. Most days, I drink a cup of coffee and read a book. I got a haircut today. It’s the first haircut I’ve gotten since December. My pixie isn’t a pixie anymore. I can’t decide what I want to do -grow it out or cut it back -but today I care about my appearance. I haven’t cared about it in months.

January and February are nebulous to me. They exist in a fog. My memory of them is hazy. They are sadness, worthlessness, fear, anxiety.

So much has happened in my family over the last three months. So many bad and negative things. Those and the cancer scare triggered a depressive episode the likes of which I’d never known.

I wish I’d never known.

This ladder is tall. I’m climbing it. I’ve stumbled on a couple of rungs. But, I know what the bottom looks like, and it’s not a place I want to revisit. So, I climb.

Slowly. Carefully. Delicately.

The top may be far above me, but at least I’m no longer a stone’s throw away from the bottom anymore. I’m still delicate. I’m wary. I’m distrusting. But, I’m climbing. I’m trying. The antidepressant is working. Life is still throwing curveballs, but now, I’m trying to catch them and throw them back. I wasn’t before. I took them to the face over and over and didn’t care. There are still days where I don’t care, but those days are fewer.

I’ve walked a long, dark, and sad road the last several months. I hid it with excuses but dropped clues like a bird drops feathers, and like a bird’s feathers, few picked up my clues, and even fewer put the clues together.

As the days go by, I’m regaining myself and my personality, my come-at-me-bro personality, my I-walked-the-fire-and-came-out-a-Phoenix personality, my “She wore her scars as her best attire. A stunning dress made of hellfire” personality.

Slowly. Carefully. Delicately.


Regrets and Anger

Not mine. No infringement intended

This has been me over the last three weeks. I cry where no one can hear or see me. I wipe my tears and put myself back together. I keep going. No one hugs me or rubs my back or says meaningless platitudes because honestly, I don’t let them. As a child, I became a master of hiding my feelings. It’s not a talent I’ve lost as an adult. This week, though, I’ve cracked a lot more. The facade has broken a lot more, and it keeps happening at work during my conference period. In other words, at the worst damned time.

I have fear of missing out at work. I always have. Consequently, I work as hard as I can. I want to do better, be better. I want to learn new things, try new techniques. I expect so much of myself as a teacher, but after last week, I feel so inadequate as a teacher.

I have the wrong master’s degree. Two years ago, I earned a Master of Educational Leadership. I thought I wanted to go into administration.

I was wrong. I don’t. I belong in a classroom. I know that with every fiber of my being. I didn’t even bother to take the principal certification exam even though I made an A on the pretest my university requires of all principal test candidates. I knew by then I didn’t want to be a principal. By then, cancer had come calling and had shown me, very quickly, what I’m really meant to do.

It’s increasingly becoming the expectation that you have a master’s degree in your subject or a master’s in something with 18 hours in your subject. I need five more English classes to have 18 hours of graduate English. Five classes.

I can’t afford them right now. And, I feel an urgency to get them, to do it right now, but I can’t. We can’t afford it, and A is vehemently against me taking out any loans because we have to think about our finances.

He’s not wrong, but it’s a bitter, bitter pill I’ve been trying to swallow since Thursday night. See, Thursday I found out I’ve been accepted to an accelerated Master of English program. I can’t accept the offer. I can’t afford it.

It’s a bitter, bitter pill. I’ll apply to a few other programs that are a little cheaper, but even then…it’s doubtful.

I feel like so many opportunities are going to pass me by because I worked my tail off on the wrong master’s degree, a degree I was proud of, but now? I regret it and am so angry I made another wrong decision in my life. What a waste.

I’m going to be 40 this week. 40. At least I lived to see it, but damn, is it really all downhill from here? It feels like it, especially now. I have a mountain of debt from cancer. I have a mountain of credit debt again (see cancer debt). I have so many regrets. I’ll never be rich. I don’t want to be, but I wish things were easier. I wish they were different. I wish I were different. I wish I weren’t sad and angry, but I am.

40 years have almost passed for me. I’m angry and full of regret, so really, I guess it’s no different than any other birthday for me.

breast cancer, kids, life, Uncategorized

Surgery and Self Esteem


My self esteem took a nosedive on Friday for no other reason than I looked in a mirror as I changed clothes.

Scars everywhere on my torso. Port. Mastectomy. DIEP reconstruction. Oophorectomy. 7 scars. Seven vivid reminders of cancer.

Sometimes, it’s just too much, and Friday, the second anniversary of my mastectomy, the second anniversary of finding cancer in the sentinel nodes, the second anniversary of finding ER+ cancer in the breast tissue, the scars overwhelmed.

My life has changed so much over the last two years. Sometimes it catches up to me.

Friday was one of those days.

breast cancer, family, kids, life


My mind is consumed right now with worries and concerns that aren’t truly mine to bear, yet I feel if I don’t shoulder them in some way, no one will. Some are above my role, so to speak. Some are on my shoulders because others put them there for they don’t know how to carry them, or worse, don’t want to do so.

My mind spins.

I want to scream at the world, but the wind would just blow it back to me.

This is my safe space, my place to process, the place cancer created, but not a single worry and concern on my shoulders right now relates to cancer. I was no evidence of disease at my check up and blood work on Monday. For that news alone, I am grateful. I am humbled. I am relieved.

Yet, I am Sisyphus. The rock I push rolled back down the mountain on Friday, not from cancer. Thankfully, not from cancer. As I look at the rock, I question my ability to shove it, inch by painstaking inch, back up the mountain, for this time, is the burden truly mine to bear? My heart says yes, my gut says yes, and I’ve made it a point over the last three years to listen to my heart and gut instead of my brain. So, I square up in front of the rock, this boulder, this weight upon my shoulders. And, I take a step. The rock doesn’t budge, but I stand here with all my weight pressed into it, willing it to move up the mountain, just a bit because if I move and let go, I don’t know that anyone will move in to take my place, to hold the rock steady, to push the rock, to assume the burden.

This has been my role for as long as I can remember, shouldering burdens that are not mine to bear, taking blame for problems I did not create but feel responsibility.

It is the definition of absurdism.

breast cancer, life

Things I learned today -Today sucked edition

1. Everything is estrogen, and my cancer was strongly estrogen positive; therefore, I’m doing everything wrong if I’m trying to stop my cancer from returning.

2. I’m 39 years old and still haven’t learned to keep my damned mouth shut.

3. When I think I being helpful, I’m not. See #2.

4. Cortisol, the stress hormone, causes fat storage and if I were less stressed, I would lose weight, and I need to lose weight because fat causes estrogen, my cancer was estrogen positive. See #1.

5. I can’t sleep because I’m not listening to my body. When my body says it’s tired, I should go to bed. The fact that I do and lay there for hours means I didn’t listen well enough.

6. I’m a smart person, and I can solve all my issues by stopping negative thoughts.

7. Since I had my ovaries and tubes removed to stop estrogen production, I’ve thrown my body out of balance, but it was necessary because everything is estrogen. See #1.

8. From now on, every time I reach for a Dr. Pepper or fried food or fast food or TV dinner, I need to remember they are estrogen in disguise. See #1.

9. By choosing to mask my true feelings about my cancer diagnosis in order to protect others, I’m failing at being good to myself, which causes stress. See #4 and #1.

10. I fail at being supportive enough to others. See #1, #2, #3, #4, and #9.

If anyone wants me, I’ll be Dimmesdale’ing myself in my master closet, looking over my shoulder in defiance of God’s warning while hoping not to turn into a pillar of salt, pushing my rock up the mountain, and ignoring the sword hanging over my head.