Posts Tagged ‘LCCC’

Stepping Back to Move Forward

I try my hardest to look forward. I encourage others to do the same when exiting the gates of Cancerland and transitioning into life after. Don’t look back. Push forward. Look ahead. Yes, it’s true. Vital to let go of the past in order to embrace what lies ahead. But sometimes healing requires us to step back in order to equip us to move forward.

I always told myself that one day I would visit the hospital in Denver where I received all of my treatment and surgeries. I thought fondly of the moment I would visit my doctors. I imagined that we would rejoice and celebrate at the hard work we all put in for me to be able to sit here today and be cancer free. Hugs and tears flowing as we would reflect over the difficult road that led us to this very moment. The numerous surgeries and chemotherapies. The middle of the night calls of desperation to my oncologist. Each needle poke in my chest to access my port. Every encouraging word and prayer that pushed me over the finish line. I dreamt of the day I would walk back into my doctor’s office with long, flowing hair and without trace of disease.

As time continued to go on, I thought less of the wonder of walking back through the doors of the hospital and more about the dread and anxiety it would cause if I were to do so. Thinking about the sterile smell of the infusion center would trigger instant nausea. I cried fearful tears as irrational thoughts flooded my mind. Would stepping back into the place I fought cancer cause my cancer to recur? Irrational, I know, yet it felt so real and valid and true. Why would I subject myself to the very place that housed my darkest and most painful memories? My life has moved forward, there’s no need to step back there. We live in Austin now, and though we’d be back to Denver to visit family and friends, there was no reason to go out of our way to get to that hospital.

I recited to myself what I’ve encouraged others to do… Keep your eyes forward. The past is the past, let it go. Yet no matter how determined I was to walk the talk, everything in me was pulling me back. I was tethered to that hospital. Tethered to the nurses, technicians, and doctors that saved me. Not only did my medical team save my life, but they invested years into it. Never once giving up. Always willing to try again upon each recurrence. They had become family, and the reason I found myself longing to go back was to reunite with my DNA. They had become a part of who I am, and denying it would be rejecting my very self. I had to see them. The longer I avoided this, the longer my complete healing would be suspended — trapped in some version of recovery purgatory.

We flew to Denver last month to celebrate my brother and new sister-in-law’s wedding. We extended our trip for the entire week and made plans to visit family and friends. We even made sure to leave a couple days open to ensure that we weren’t booked solid. In the back of my mind, I knew this was it. The time had come when I would walk through the hospital doors for the first time in nearly two years. I called my doctor’s office and let them know that I would be in town and would love to swing by and say hello. The receptionist gave me a day and time that was most optimal for my doctor and nurse. Once I hung up the phone, I was flooded with anxiety. Technically, I didn’t schedule an actual appointment, so if I decided to miss, it wouldn’t be that big of a deal. I noticed myself already backing out. I wasn’t so sure I could do it.

The day arrived and I could barely contain my racing thoughts and unbridled emotions. My husband was calm and quiet, providing stability and reassurance. As we drove down the familiar roads that led us to the hospital, I was becoming increasingly nervous. How would I feel when we arrived? Could I actually do this? Was I ready? The closer we got, the more of a wreck I became. Past memories washed over me and, without success, I tried to sort through them. Before I could fully wrap my mind around what we were doing, the hospital was in view. There was no turning around now.

I was instantly transported to the past. I saw myself bald and weak, barely alive, making my way to chemotherapy. I reached up to touch my head, in order to remind myself that I did in fact have hair, was cancer-free and beyond treatment. My body was physically urging itself to stop. White knuckled, sweat forming, I became antsy. “I don’t think I can do this,” I whispered. “It’ll be alright,” my husband encouraged in response. We drove through the parking garage to the roof, where only one parking spot remained. As Matt unbuckled his seatbelt, I stopped him from opening the door. I needed to sit in the moment. I needed to breathe. I needed to overcome the crippling fear and anxiety that glued me to my seat. I cried.

Soon, I gave the okay, and we walked toward the wing of the hospital where I had been over one hundred times previously. All so familiar, the smells and sights ushered floods of memories. Under my breath I tried to convince myself, “I can do this,” and while shocked I also repeated, “I can’t believe I’m doing this.” In a few minutes, we were standing in front of the entrance to my doctor’s office. Before pulling the handle on the door and entering my home away from home, I took a moment to center myself — remembering how important this was for my complete recovery — and without thought, we were standing in the middle of the waiting area, a beaming smile plastered to my face.

It all happened so fast. A smile reciprocated from the receptionist who I had spent hours with on the phone over the course of five years, scheduling appointments, leaving messages for my doctor, and paying bills. Everything had changed, yet nothing had. We hugged, and my eyes quickly shifted as my nurse walked in to grab a patient. Without shame, I interrupted and hugged her. No words needed to be shared just yet, smiles would do. She jubilantly told me that she would let my doctor know that I was here. Matt and I picked the two seats in the waiting room that we sat in countless times prior. I breathed it all in, and pouring over me came a loud, crashing, undeniable wave of gratitude.

My doctor peeked around the corner, smiled, and motioned that we follow her. I practically ran and found myself in a tight embrace with my dear friend, my oncologist. Neither of us let go. No words needed to be said. We cried into each other’s shoulders, and laughed at the precious miracle that was and still is. I’m alive. I’m alive. I’m alive. We pulled apart and looked at one another, taking it all in. We caught up on the goings on in each of our lives. With joy abundant, we reflected over the past five and a half years. Seeing the woman who fought for me, cried with me, and encouraged me countless times through my battle against this disease was more beautiful and fulfilling than I ever dreamed it would be.

Had I not stepped back, I could have never moved forward.

After making a surprise trip to the infusion center to visit my chemo nurses, I walked out of the hospital with my head held high. Healed. Death did not win. The enemy did not succeed. What was meant for harm was made beautiful. Restored. For the first time since I was diagnosed with cancer, I saw the whole picture. Not just a peek, or a glance, or a flash of its beauty, but a deep knowing that there was purpose in my pain. God’s redemption over my life overwhelmed me. He saved my life. He formed a team of doctors and nurses to come alongside me, and he knitted them into my story with deliberate intention.

It would have been easy to go the rest of my life without stepping foot into that hospital once more. Easy to avoid the pain, post traumatic stress, and anxiety. Easy to shove the feelings down deep into my soul. But it would have dishonored and dejected the journey that led me here. Sometimes we think healing involves forgetting or avoiding. That in moving forward, we shouldn’t dare look back. But there is power in addressing the place of our deepest pain. There is redemption in stepping back to reflect over how far we have come. There is honor in gratitude. There is healing in acknowledgement.

Sometimes we must step back into the depths of our grief in order to walk in confidence towards the future.

MJ and Steph

Lamentations 3:21-23 (The Message)

“I’ll never forget the trouble, the utter lostness, the taste of ashes, the poison I’ve swallowed. I remember it all — oh, how well I remember — the feeling of hitting the bottom. But there’s one other thing I remember, and remembering, I keep a grip on hope: God’s loyal love couldn’t have run out, his merciful love couldn’t have dried up. They’re created new every morning. How great your faithfulness! I’m sticking with God (I say it over and over). He’s all I’ve got left.”

Life Awakened: Five Years Later

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Life after cancer is more confusing than anyone told me it would be. Honestly, they didn’t tell me much of what to anticipate when the disease was gone and the dust settled. Possibly because most didn’t even expect me to survive the first year, let alone the second, third, fourth, and least likely the fifth.

From the moment I was diagnosed and through the subsequent years during treatment, the focus for all of us was to simply get through it. To survive. To make it out somewhat intact. Yet, there was never any conversation beyond survival. Merely congratulatory well wishes upon my last treatment and the classic line, “We hope to never see you in here again!”, as if I were a prisoner released from a lengthy stint behind bars.

No one told me what life would be like back in the “real world.” No one told me that I’d experience post-traumatic stress disorder triggered by sights, smells, experiences, relationships, and even food. I wasn’t aware that I’d feel like I didn’t belong in this seemingly regular, normal, everyday life. I never imagined being more comfortable in a hospital than in a grocery store. I didn’t think I’d be shy about regaining my independence. I had no clue what life was supposed to look like or what I was even supposed to do when I arrived at my destination, when I reached my goal, and when I survived the statistics that labeled me. I didn’t know what to expect because I wasn’t expecting this… Life.

We had conversations about notarizing wills, what items would go to who, if my husband would remarry, and that eventually, grief would settle and everyone left behind would learn to cope with my death. We clung to the hope that maybe, just maybe, this period in time would fade away into the history of my life’s story. That, as a grandmother decades from now, I’d share tales of a battle won with my grandchildren. I never thought I would die from cancer, but as oxymoronic as it may sound, I wasn’t sure if I would live through it either.

I wasn’t prepared for the difficulties that a life almost lost has brought me. It’s been a recurrent struggle, a back and forth tug of war between then and now. Cancer isn’t just a moment in time. It’s not just something that happens and eventually goes away. It doesn’t sit on a timeline nor does it have a beginning or an end. From the moment it physically rooted itself into my anatomy, it also marked my very DNA and soul. Though free of disease, I will forever be marked by it. Though I walk without cancer, I will forever carry it with me. It has changed who I am, and the biggest conflict I now face is rediscovering who that really is.

Today marks five years since I heard those life-altering, fateful words, “I’m sorry, you have cancer.” And Friday marks two years free of this disease. I always thought that time healed all wounds, and though I still believe there is some truth in that, I think that healing requires more than days gone by. If only I could go back to that very moment when life as I knew it was forever changed. If only I could look that Stephanie in the eyes and say, “There is no right way to heal. There is no correct way to grieve. There is no road map nor compass. You will learn as you go, and you must trust that God has given you the grace for each obstacle you will face. Cry when grief falls upon you. Dance when joy is overwhelming. Laugh from the very pit of your soul. And love like your heart knows no bounds. There is no destination to be reached but rather a life to be well-lived. Keep looking forward and never let what happens today steal your joy for tomorrow.”

This new year has been full of incredible abundance and freedom. It’s the beginning of regaining my life. For the first time since diagnosis, I finally feel free. Free to feel. Free to release. Free to let my guard down. Free to really live this life that I’ve been gifted. I feel like I’ve finally awoken to the life that I so longed for after cancer. I think it’s due in part to the fact that I’ve ultimately given myself permission to.

As a cancer survivor, there’s a balance between recognizing and honoring the journey itself and also accepting survival with open arms. Though survival is the one thing I vehemently fought for all of these years, it’s also the one thing I must face head on. I’m alive, now what? It’s easier to live with a victim mindset always focused on what once was and what should have been; It’s more difficult to move forward with victory on my side, accepting that though cancer has forever changed me, it will not define me.

I expected that on this day, my five year anniversary, I would be in jubilant celebration, reflecting in awe of the miraculous road I’ve walked. Without a care, concern, or any hint of grief or sadness. After all, it’s been five years. FIVE. My doctors said I probably wouldn’t even make it to ONE, so this moment in time truly is a milestone. But here I am, and though I absolutely feel elated to be free of the shackles that bound me for years, I’m still coping with the grief that lingers after trauma. And you know what? I’m okay with that.

Though no one told me what life after would feel like, I’m learning that there is no “right” way. I’m learning to embrace what was was, what is, and what will be.

Isaiah 43:18-20 (ESV)

“Remember not the former things, nor consider the things of old. Behold, I am doing a new thing; now it springs forth, do you not perceive it?”

Moving Forward Regardless

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Looking down at the file in hand, he reads aloud, “It looks like the report says that there’s an eight millimeter spot on the bottom of your right lung.”

Silence. Though there are four of us in the room, nothing can be heard but the crinkling of the paper on the blue examination chair as I shift my weight. Suddenly the room grows smaller.

“We’ll need to send this over to our imaging team so they can explain further. Sometimes different technicians read results differently than others,” my doctor shares, noticeably attempting to maintain positivity.

My words are trapped. I desperately cling to hope, but with each breath it’s dwindling. Thoughts racing, I can’t seem to organize a simple sentence. The news hits me so violently, my breathing becomes labored. The wind is knocked out of me and I’m struggling to make sense of the force behind this reality.

All of a sudden, the questions begin to flood my mind. Each one determined to be asked first. They claw their way to the forefront of my brain, spilling out in jumbled words as my mouth involuntarily opens. “What does that mean? Is it cancer? It’s not cancer, right? How big is eight millimeters? You said it’s on my left lung or my right lung? On the bottom? Are you sure? But all of my scans for the last 26 months have been clear. How can this be?”

With more grace than I could ever muster, he shares, “This report says it’s non-specific, so let’s try not to panic. Let’s stay positive. We’ll need a few minutes to pass this by our imaging team. They’ll be able to give us more details. Maybe the technician that wrote this report was mistaken.” The door closes as my doctor and his PA leave the room in search of answers.

It’s just my husband and I now. We look at each other in disbelief. Our eyes speak while our lips cannot. The furrow in my husband’s brow tells me that he is confused, scared, and in shock. My eyes jolt to every corner of the room, frantically seeking explanation. I look back at him in astonishment and defeat. What is happening? I’m convinced this must be a bad dream and that I’ll soon wake up to find relief. But it is not a bad dream. It’s real. And it is in fact happening. Soon, my strong, compassionate, empathetic guardian of a man encourages me as only he can. “We have to have hope that it’s nothing. The doctor says this spot could simply be an infection in your lung that your body is fighting off. He says this could happen to any of us. It could be nothing. It may not be cancer.” Oh how I love him each time he speaks hope over my fear. His words are a salve to the fresh wound of this news.

Confusion lingers between us as we wait for my doctor to return. I valiantly fight back tears as I quickly map out the what ifs. I have climbed to the top of the ladder of worst case scenarios and tell myself ultimately, if I die, it’s okay. I’m going to heaven. But Lord, please take care of my husband. I step down one rung and quietly think to myself that if it is cancer, I know how to fight it. And I’ll do whatever I have to. With each step down the ladder, I consciously choose hope above all else. My breathing slows. My fidgeting lessens. Calm is just around the corner. I’ve addressed the worst of the worst, and there’s no need to go there again. I bring myself back to the moment and take a deep breath. “Don’t worry about tomorrow, for tomorrow has it’s own worries.”

The door opens, and I’m standing now. Give it to me, Doc. I want the answer. I need to know. “Unfortunately we don’t know anything more. Our team confirms that there is a non-specific spot. It’s too small to even biopsy. I know you wanted answers. I wish I could give them to you. I’m so sorry. This isn’t how I thought this would go.” Me neither. Me neither. My mind rewound to the beginning of the day. We woke up early, before the sun. For hours, we drove to what we fully expected would be celebratory news. We tossed ideas back and forth about which restaurant we’d celebrate at after we learned the results. Yet, here we were, without those results, left with more questions than we had when we first arrived.

The rest of the appointment is a blur. I know I asked a million more questions, several of them rhetorical. I know we agreed to do a follow up PET scan in six to eight weeks to monitor this spot on my lung in order to see if it grows or becomes more visibly malignant or benign. According to my doctor, if this is an infection, it may resolve itself on its own and may not even appear on my follow-up scan. We can only hope. I know my doctor was patient as I asked what treatment would look like if the spot proved malignant. Consultations with a thoracic surgeon to see if the spot could be removed. Possible chemotherapy. “We just don’t know yet,” I remember him saying.

One of the most profound moments of the day has set the tone for these proceeding weeks as we wait for my upcoming scan, and proves the importance of proper bedside manner. As my appointment wrapped up, and the four of us turned for the door, I hugged my doctor. He whispered in my ear, and thinking of it brings me to tears just like it did in that very moment. “You are strong. You can do this.” Having a doctor who believes in and encourages you while understanding your fear and uncertainty is a game changer. Cancer is fought with a team. Strength builds with unity.

So here we are now. Two weeks out from learning that I have an unidentifiable spot on my lung, and less than four weeks away from my upcoming PET scan that will hopefully identify said spot. While it may not seem like it, there are many choices to be made when fighting this disease. Joy is a choice. Strength is a choice. Peace is a choice. Hope is a choice. Faith is a choice. When facing cancer, these choices are excruciatingly difficult at times, and they can also be fleeting. In the car on the way home, through tears, my husband and I decided that we would choose hope. We would fight back the fear and doubt, and focus instead on our faith. We would try not to waste our energy on worrying, because worrying is a quick ticket to stolen joy.

If this spot is not cancer, we move forward. If this spot is cancer, we move forward. We will move forward regardless of the outcome. We are called to be courageous in the face of death. We are called to be brave in the presence of fear. We are called to walk firmly in faith when doubt tempts us. We are called to choose joy above all else. And with each day that passes, we move forward with our choices made.

Matthew 6:34 (MSG)

“Give your entire attention to what God is doing right now, and don’t get worked up about what may or may not happen tomorrow. God will help you deal with whatever hard things come up when the time comes.”

PC: K Mitiska Photography

Cancer: A Family Affair (Part 4)

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Written by Todd, Stephanie’s youngest brother who was 21 at the time she was diagnosed.

Occasionally after receiving a bill in the mail, I set it down on the counter, tell myself I’ll take care of it in a few hours, and forget about it for weeks, sometimes even months. When the sight of the bill on the counter triggers my thinking about paying it, I’ll sometimes push the thought further back into my mind, only for it to reappear when the next bill arrives. This bad habit of mine – described in psychological lingo as avoidance coping – was the strategy I first used to cope with Stephanie’s cancer diagnosis and treatment. For months, I refused to seriously think about her battle, because doing so led to painful thoughts.

I remember well the day in January, 2012, when Stephanie called me and told me that she had just received a cancer diagnosis. Sitting in the passenger seat of my wife’s car, I thought to myself that the diagnosis couldn’t be too bad. Sure, cancer is serious, I told my wife, Amy. And a hysterectomy is also serious business. But I was sure that 25-year-olds couldn’t die from it. And so when Amy and I flew out for my sister’s surgery a week or two later, I was saddened by the invasive surgery Stephanie had to undergo, but also comforted by the thought that it would act as a magic bullet. That thought was enough for me to look down on my sister in her hospital bed post-surgery and think that, while this was a massive bump in the road in her and her husband’s life, it wasn’t a tragedy. Life for them would return to normal in a matter of months, I remember thinking.

That all changed when Stephanie’s prognosis came back shortly after her surgery. The gravity of that prognosis hit me when I realized that I would have a better statistical chance of more than quadrupling my measly college savings at a roulette table than my sister would of living another year. So what did I do with that tragic information? Stuck my head shoulder-deep into the sand. For someone who had taken that approach for years, it wasn’t too hard to do. I was in college, nearing graduation, and working hard to prepare myself for law school. And so instead of continuing to talk to her on the phone almost everyday as I had done for the previous few years, over the next few months I only called a few times. A “hey, how is chemo going,” here and there. To me, this was the best way of dealing with the situation – pretending it didn’t exist. Coping with her prognosis was like my approach to the bills in the mail I periodically receive: if I pretend they don’t exist, they don’t, at least for a while.

That approach didn’t hold up when I first saw my sister bald in person. She was in Oklahoma for my college graduation, and seeing her was like being hit with a ton of bricks. I couldn’t evade the issue any longer, and so I directly confronted her prognosis for the first time. Before walking out on stage at my college graduation ceremony to receive my diploma, I shaved my head to honor her fight with cancer. Walking across that stage and removing my cap was, and will likely continue to be, my proudest achievement.

After a recurrence of my avoidance strategy came back when I moved to Washington, DC a few months later – I refused to read her website to avoid the fear of her dying – I finally put that strategy to rest. I realized that, were Stephanie to die, I would regret not spending as much time talking with her as I possibly could. That basic thought was profound, and it influenced not only my relationship with Stephanie but with my other family members as well. I began to talk with her, my brother, and my parents much more, coming to realize the benefit of confronting her prognosis head on.

Stephanie’s fight with, and now defeat of, cancer has been defined by her courage, bravery, and wisdom much beyond her years. I am incredibly proud that she has influenced so many. Her battle, though incredibly tough over the years, has provided me with an opportunity to learn what life is all about.

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Psalm 90:12 (ESV)

“So teach us to number our days that we may get a heart of wisdom.”

Dear Stephanie: A Letter to Myself Before Cancer

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Dear Stephanie of January 2012,

You are both stronger and weaker than you could ever imagine. Life is about to show you that. Though you won’t be sure what she means, take the advice of your friend and “buckle up.” In fact, why don’t you grab the seatbelt next to you and buckle into it as well. You always liked roller coasters, right?

You are young, healthy, vibrant, and full of energy and dreams. You are working hard and thoroughly enjoy your job. You have married the love of your life and are thrilled to come home to him every day. This truly feels like the beginning of an incredible journey, and hand-in-hand you and your husband both feel ready to conquer anything. You’ve found the church you call home, and for once you finally feel like you belong to something far greater than yourself. The friendships that will develop through this church will become family. Trust and embrace them.

You feel ready. Ready for the future. Ready to start pursuing the dreams you and Matt have. Ready to do whatever it takes to achieve your goals. Ready for what God has for you. You think that means a white picket fence and two children. You think that means unending happiness with only minor bumps in the road. You think you know what God wants for you, and though you are certain of His goodness, you don’t know its depth just yet. You feel ready for a reason, but it’s not the reason you think. Stay ready.

You’re really rockin’ that hair. I know how much you love it. Go on with your blonde self — enjoy it. You are in shape and look good. Really good. You don’t believe it, but you are perfectly beautiful as you are. Stop worrying so much about it. Soon you will find that when looks fade, character will remain. Start thinking about your identity.

Your husband adores you. You think you have an understanding of his love and commitment, but you really have no clue yet. You reminisce to your first date, your wedding day, and all of the fun newlywed adventures you have experienced together. It’s been a year and a half, and you both laugh at the words of friends who have married before you: “The first year is the hardest.” You say to each other, “If the first year is the hardest, we’ll be smooth sailing for the rest of our lives because this is easy!” You were right, the first year was the easiest, but it will get harder. The man that stands by your side now will stand by your side through your darkest times. He meant every single word he vowed to you. Cherish him.

You like plans. You like goals. You like lists. You struggle with control. You want things just right. But your version of right isn’t always right. Let your pride take a step back. Though you have perfected the plans of your life story, be ready to erase. God’s plans are far greater than the little ones you have constructed. It’s okay to go with the flow. You’ll need to learn to do that soon. Be open to new things. Surrendering your life and all of the plans you blueprinted is scary, but marvelous.

You have experienced pain and loss, but you don’t fully know grief. It’s bitter and refreshing all at once. It comes swiftly and unexpectedly, but can truly heal if you let it. Though you are emotional at times, soon crying will become second nature. It doesn’t mean that you are weak. In tears, there is strength. Allow yourself to feel. Allow yourself to experience the pain and then work through it. Don’t avoid situations because they make you uncomfortable. Dive in.

The faith you have now will soon become the only thing you can hold onto when your dreams, desires, goals, and plans are radically changed. Your faith, though it seems large now, will have the most impact when it is the size of a mustard seed. You’ve hoped for things before, but the hope that will birth inside you will reach magnitudes you can’t even begin to fathom. God is for you. He is on your side. He goes before you. He will protect, encourage, and supply you. Wrestle with Him. Pursue Him. He has never and will never leave you. When He is quiet, be still.

You have a story. The life you live now will soon change to reveal your purpose. The woman you are now will be pruned in order for a new creation to spring forth. At times you won’t recognize the woman you see in the mirror, but she is still there… stronger than before. Though there will be days and even months of painful struggle, the reward for staying steadfast will overwhelm you. Don’t give up. Keep your eyes focused on what matters most, and everything lackluster will fade away. It’s okay to be weak and to allow God to be your strength. He will overcome.

I write to you from a familiar date. You’re a numbers girl, I trust that you’ll understand the importance. On January 25, 2012, you will be diagnosed with cancer. And three years (almost to the day) later on January 26th, 2015, you will complete your final chemotherapy treatment and will be well on your way to a new journey. Be encouraged. Those three years will have an eternal impact. They will be some of the hardest years of your life, but will develop you in ways no other experience could. Be grateful.

You are brave. You are strong. You are fierce. You are a warrior. You are a fighter. You have the tools you need. You can do this. I believe in you.

With utmost expectations and encouragement,
Stephanie of January 2015

 Proverbs 16:9 (ESV)

“The heart of man plans his way, but the Lord establishes his steps.”

 

What We Need When We Need It Most

Sometimes the simplest things in life bring the most joy. Though I’ve shared monumental moments of my journey including a phone call from Peyton Manning and being on The Ellen Show, often what brings my cup to overflowing are the little things that happen in the most perfect timing.

Yesterday, I woke up and began my day as usual. Preparing breakfast and lunch for my husband, ushering the dogs outside, and analyzing the cleanliness of our home. Do I need to vacuum today? How much laundry needs to get done? What’s on my list? Long gone are the days of planning my schedule according to how many minutes it will take me to get ready… That is, until yesterday.

For the past few months, I’ve been in awe of my hair. The specific type of chemotherapy that I receive weekly does not cause hair loss. My doctors and nurses shared that though it may thin, my hair should accompany me this season. Praise God, the hair on my head has indeed remained healthy, thick, and full of curls. And, it’s still growing. I’m amazed actually. For those who personally know me, you know my hair has always been a big deal. I’ve written frequently on the topic, HERE, HERE, and HERE, as well as several other places. I used to spend too much time on my locks each morning. My hair used to be my pride and joy. Then, just like that, cancer took it away.

Having hair while undergoing chemo is paradoxical. It causes many, including myself, to scratch our heads in confusion. When most people see me and hear that I am actively fighting cancer by ingesting chemotherapy once a week, there’s a shortage in their minds. What? How is that even possible? Hair and chemotherapy? That’s the epitome of an oxymoron, right? Wrong. It all comes down to the specific chemical mixture of the chemo drug. Not all cause hair loss, just like not all make your skin fall off. (Oh yes, if you’re new here, that happened to me also.) Each drug has different side effects, however the most common is hair loss. This time I got lucky. Though suffering extreme nausea and weakness, at least my dome will be warm this winter!

If you’ve kept up with my infrequent posts these last couple of months, you’ll notice that I’ve been down in the dumps. I’ve undergone great loss, and this fight has been particularly harder than the three before. It’s taken more effort to stay on top of my emotions and remind myself that this is not forever… One day at a time. I know I’m not alone when I say, there have been more moments than I can count when I’ve been near my rock bottom, and God has reached down to pick me up in remarkable ways. Sometimes His ways are through the right person saying the right thing at the right time. It could also be through receiving a blessing at a moment when you needed it most, or even an answered prayer that you thought was an impossible dream.

Let me share my heart for a minute. God speaks to me in many ways. He speaks to all of us in fact, we just need to listen. On Sunday night, I envisioned Jesus smiling at me. It brought me both pause and joy. Have you ever imagined Jesus smiling at you? It’s an incredible image. My mind began to wander… why? Why was He smiling at me? Now I think I know. Yesterday morning, He gave me a gift that only He knew I needed.

For some reason, I decided to get my flat-iron out. I got the hair-brained idea (no pun intended), to see how long my bangs were. My hair has been growing for 40 weeks now and determining its length is near impossible considering the tightness of each curl. I have longed for the day when my hair can be put up in a ponytail again. For fear of disappointment, I have kept my hair styling tools tucked away. Until yesterday, I didn’t think I would use them until my hair noticeably needed taming. A spark arose within me, so I pulled out the flat-iron and began to straighten my bangs. Utter shock and amazement followed.

Oh my word. I have bangs. My hair is long. Compared to being bald, I have long hair! The tears began to flow as I looked at myself in the mirror. My initial thoughts were vain and aesthetic. My hair is long enough to style! I finally look a little more like my pre-cancer self! It’s been nearly three years that my hair has been anywhere near this length! Soon, however, my thoughts transitioned into a realization. God just gave me a gift.

The reality that I’ve been fighting for my life for these last three years and have been abundantly blessed to still be here, caused the tears to flood my eyes and overflow onto my cheeks. Tears for all of the moments I looked at myself in the mirror and saw a bald, sick, weak, and dying patient. Tears for all of the times I felt like giving up. Tears for the heartache, grief, and loss that Matt and I have endured. Tears that even though I’m still in the most difficult battle I have ever faced, God is FOR me. He is on my side and He cares about the little things. He knew the gift He had up His sleeve would make my day. He knew that urging me to do the simple task of flat ironing my hair would propel me into a fit of immeasurable gratitude. He, above anyone else, knew how much having bangs would mean to me. Though seemingly little to most anyone else, these bangs represent so much more than long hair. They represent life, perseverance, and blessings. They represent the goodness of God.

And just like that, I can see Him smiling at me again.

Psalm 37:4 (ESV)

“Delight yourself in the Lord, and He will give you the desires of your heart.”

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Putting a Bandaid Where It Doesn’t Belong

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Life is not meant to be lived passively, but proactively. I need to remember that. We all do. Instead of allowing life to pass by and just happen to me, I need to stake my claim and walk forward refocused in my purpose.

Recently, my journey has been harder than usual. I often feel like I’m only capable of handling a certain level of difficulty. That level has been reached, and I’ve come to the end of my capabilities. Facing an impossible level, I’ve been given a choice and, unfortunately, I chose wrong.

I have been knee-deep in a murky swamp. Mud, muck, and dark waters have enveloped me. I’ve felt slithering snakes swimming past my legs, taunting me and begging for my attention. The mud between my toes has encased my feet, urging me to stay put. Instead of trudging forward, I chose to sit down. Instead of forging a way to get out of the swamp, I stopped in my tracks. I convinced myself that I was taking a break to gather my strength and to rest. But at some point, breaks end. Eventually, you must get up and keep going.

This wasn’t a break. This was me sitting down, giving up, and not wanting to deal with what I was facing. Like a child not wanting to do something, I metaphorically went limp on the ground.

These past two months have sucked me dry — physically, emotionally, and spiritually. Chemotherapy has been increasingly difficult, and good days have become few and far between. I receive the poisonous toxins once a week, therefore plenty of my days are spent on the couch, pretty useless. My nausea is often overpowering and unbearable, sitting at the base of my throat like a volcano waiting to erupt. I’m tired. There are days when I can’t imagine anything better than the comfort of our bed. Exhaustion is exhausting. Not having energy to live life on my terms is an invitation for sadness to overwhelm. Some days, the harder fight is not against cancer, but against the subsequent emotions.

Beyond the daily battle against this disease, I have faced other obstacles. Difficult hurdles and layers of grief to top off this already bumpy journey. My grandfather, whom I lovingly called, “Papa,” passed away. We were very close throughout my life, especially so in these later years as we fought the same fight alongside each other. Never would I have thought I would be fighting cancer with my Papa, but it deepened our relationship in special ways. We understood each other through each surgery, treatment, and side effect. We lifted each other up on rough days. He fought a good battle, and ultimately won the victory. Boy, do I look forward to seeing him again.

Not only did I lose my grandfather, but only a few weeks later, a close friend of mine went to be with Jesus as well. This time, it was unexpected and sudden. The type of tragedy you can never prepare for. It still doesn’t seem real. A dislodged blood clot after surgery… A mere few hours prior, I was giving her a hug, kissing her on the forehead, and wishing her well as she was to head into the operating room. We joked, laughed, and prepared for how life would look like after the procedure. I lent my words of wisdom (having gone through several surgeries before), and let her know she would be fine. The shock still comes in waves. I just can’t believe she’s gone. How I miss her so.

The combination of grief, stress, frustration, exhaustion, and sickness has weighed me down, and I simply crumbled underneath it. I sat down in the mucky swamp and, instead of resting, I merely existed. I went through the motions each day. Chemo every Wednesday. Nausea pills every six hours. Church on Sunday. Grief, like my nausea, at the surface ready to explode. Yet, I couldn’t deal with any of it.

I covered my grief and uncomfortable circumstances with bandaids. I’ve watched too much TV. I’ve eaten horribly. I’ve been snappy with my husband. I’ve introverted. And, as many of you have recognized, I stopped writing. I just couldn’t bear pouring my reflections out to the world, when my thoughts were jumbled, messy, and self-pitying. Writing is cathartic for me. It helps me process, and in turn, heals my soul. Equally as my words encourage you, they often encourage me. There are more times than I can count when I read back through an entry and know God Himself was speaking through me to me. Yet, for several weeks, I avoided it. I sat down in the swamp and went limp.

It wasn’t until I was removed from my circumstances, and was stuck in a car for thirteen hours with my husband, that I pulled the bandaids off… finally facing the wounds that were hidden underneath. We talked and I cried. Releasing what had been burdening me for weeks. And, in true character, my husband gently led me back to The Lord. I am so grateful for an encouraging husband who holds my hand, understanding and grieving with me, and guides my eyes upwards.

The problem with placing a bandaid on a wound that doesn’t need one, is it doesn’t heal. Some wounds need air for a scab to form and the healing process to take place. My wounds needed air… The refreshing air of Jesus. And instead of reaching for Him, I put a bandaid on, covering myself from healing, and went limp. The bandaids paralyzed me and put me in a passive position.

While the grief, sickness, and emotion has been painful, I have learned from it. When life gets hard and uncomfortable, our human reaction is to give up. But have you thought how your circumstances might change if you were proactive in the midst of trudging through your own swamp? We have all faced difficult seasons in our lives. Many can say that, though our circumstances may not have changed, once we became proactive, our perspectives sure did. Instead of convincing ourselves we need a break and sitting down in our muck, stand strong, be proactive, and pull the bandaid off. Allowing God to touch our wounds and heal them is a powerful act. It’s painful, but so worth it.

What swamp are you sitting in? I challenge you to pull your bandaids off, stand up, and allow God to guide you in healing.

Psalm 119:50 (ESV)

“This is my comfort in my affliction, that your promise gives me life.”

 

Raising The White Flag

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There are moments when we reach the end of our rope. When no matter how hard we try to hold the pieces in place, everything continues to slip out of our grasp. When we desperately wish for things to go according to plan, just this one time. When we are this close to throwing in the towel.

We don’t realize that in those moments, all we need to do is surrender. Place our pieces on the table, push them over to God, and raise our white flag.

Surrendering is typically the hardest obstacle we face in life. Why is that? Why do we find it so hard to let go of control? Surrendering is not giving up. Surrendering is not admitting defeat. Surrendering is the strongest act of humility and trust. Surrendering is an acknowledgement that we can no longer do it on our own. To surrender is to gain.

Life with cancer has taught me to raise my white flag more often.

I’ve been MIA these past few weeks, and I’d be lying if I said I wasn’t going through something. I was reaching the end of my rope. I was desperately grasping for straws. I was tired, unsure, stressed out, and frustrated. Sometimes I feel like my life is a bulbous onion. Layers and layers piled on top of one another. Each layer a new level made up of the stuff that makes your eyes water. Often too, I feel like a circus performer, trying to balance an innumerable amount of barrels on my head while walking across a tight rope.

We all have periods in our lives when we’re juggling too much already, only to have a few more balls get thrown into the mix, causing all of them to come tumbling down.

My car needed a repair. A repair that would cost us more than the value of the car itself. The only wise decision my husband and I could make was to purchase a new (used) vehicle. Our current lease was up soon, and we had been looking for a rental home for months. Each day we sat in front of the computer, scanning every place we could think of for used cars and rental homes. Nothing. Nothing in our price range. Nothing in our location. Too much mileage. Too expensive. Too much. Too little. Too far. Nothing. I felt defeated. I felt like we would never find what we needed. And amidst the stress of determining our next steps, my dear grandfather passed away. He fought a courageous battle against this disease, and ultimately won. Oh, and my weekly chemotherapy treatments… the cherry on top.

Stress, frustration, exhaustion, and grief all wrapped up into a tear-filled, multilayered onion.

I found myself in the shower one day — naked, alone, and vulnerable. I began to weep. Tears cascaded down my cheeks and spiraled down the drain alongside the water. My pent-up emotions heaved from my heart as I lamented my anguish. Soon, a song began to rise within my spirit. Bubbling up, forcing it’s way through my emotions, and cleansing them upon release.

“I surrender all. I surrender all. All to thee my loving Savior, I surrender all…”

The words flowed out and my arms raised up. In my weakness and vulnerability, I began to worship. God Himself gently placed this hymn that I had not sung for years in my spirit. He was urging me to let go. To give Him my checklist, my worries, and my grief. And in that moment, I did. Before I knew it, the burden was lifted off and I was in complete peace over what my husband and I were facing. The feeling you get when someone you love gives you a great big hug… that’s what happened. Tears of stress transformed into tears of joy and hope.

As if God was saying, “You can’t do this, but I can. Give these tasks to me. I’ll take care of you.” Within one week, we found a car and a home. Upon my surrender, He was faithful.

Have you experienced something similar? I have, many times. Yet in those dark moments, it’s easy to forget His faithfulness. It’s easy to doubt His ability. In our humanness, we believe that we are in control. We think that if we don’t do enough nothing with happen, or if we do, we’ll reap favor. Too often, we lose sight of The One who is ultimately sovereign over our lives. No amount of us “doing” can achieve what He can. We cannot achieve our impossibles. Only God can. And, in order for this to happen, we must surrender our pieces to Him.

Surrendering is scary. Full surrender is handing both your worries and fears as well as your dreams and desires completely over to Jesus. It’s entrusting Him to handle it. It’s relinquishing control over your life. Surrendering is hard, but necessary. After all, His abilities far outweigh our own. Surrendering comes down to trust. Do we trust God?

What do you need to surrender today? I challenge you to raise your white flag.

Mark 14:35-36 (ESV)

“And going a little farther, he fell on the ground and prayed that, if it were possible, the hour might pass from him. And he said, ‘Abba, Father, all things are possible for you. Remove this cup from me. Yet not what I will, but what you will.'”

Photo: Flickr/lundgrenphotography 

“Hi Stephanie, This is Peyton Manning.”

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The Sheriff. 18. PFM.

Peyton Freakin’ Manning.

The Denver Broncos quarterback is referred to by many nicknames. However, after Saturday afternoon, I’d primarily refer to him as genuine, kind, and authentic.

There have been many moments of incredible blessing in my fight against cancer. Abundant and overwhelming amounts of gifts, kind words, and support. The platform to meet with others and share my story. Innumerable opportunities for writing and motivating. Open doors I would have not experienced without this disease barging into my life. Though cancer has brought tremendous grief and loss, it’s also brought with it a wave of encouraging gifts and bright rays of hope.

Through my journey, I have been stripped raw of my previous notions about life. Cancer tends to do that — quickly sloughing off areas that don’t really matter. It cuts down to the marrow and brings an awareness of who we should be and how we should respond to those around us. What car we drive, what house we live in, and how much money we make is trivial in the grand scheme of things. Life is about relationships. Life is about compassion towards each other. Life is about finding joy no matter the circumstance. Life is about uncovering hope and sharing it with those around us.

On Saturday, Matt and I spent time with family. Catching up with his dad and grandparents, chatting about my upcoming season of treatment, and sharing laughter as usual. I’m blessed by his family, and from the moment he brought me home to meet them, they welcomed me with open arms. When I was diagnosed nearly three years ago, they wept with us. They rallied around us and have fervently prayed alongside us for my healing. His grandparents are some of the sweetest people I have ever met. His grandfather, a ninety year old World War II veteran, shared his excitement about his upcoming “honor flight” to visit the memorials in Washington DC. Matt’s grandmother told us how she loves her new iPad and enjoys playing Candy Crush and keeping up to date with her grandkids through Facebook.

Soon, we said goodbye and began the trek back home. Barely ten minutes into the drive, my phone began to ring. Immediately, “No Caller ID” appeared on the screen, and I was left wondering who was on the other end. Considering our adventures through medical bills, I tend to assume it’s someone asking for our money. I answered, “Hi, this is Stephanie,” and was shocked at the voice I heard in response.

“Hi Stephanie, this is Peyton Manning.”

The steady southern drawl behind the five-time NFL MVP and Super Bowl champion was saying my name. Peyton Manning was calling me on my cell phone. Believe me, I’m still in shock. In utter amazement, I asked, “Are you for real!?” only to be answered with a polite, “Yes, it’s Peyton.” Peyton… THE Peyton. Manning. Peyton Freakin’ Manning. Oh my word. My Denver Broncos quarterback was talking to me. He went on to explain that my husband had written him a letter sharing my story and that he wanted to personally reach out to to tell me that he was praying for me and cheering me on. We spoke for a while. He asked about my upcoming treatment, sharing well wishes and telling me to continue to fight strong. He was so nice. Yet nice doesn’t fully describe him. Invested. Peyton was invested in my story, and was genuinely interested in knowing how I was doing.

The conversation came to a close, as the team was heading to San Francisco for the upcoming pre-season game against the 49ers. I thanked Mr. Manning for taking time out of his busy schedule to call me. We said goodbye and hung up. Then, I screamed. I stared at my husband wide-eyed, with the largest grin plastered on my face. I could not believe that Matt had written Peyton Manning, and more-so that Peyton Manning had read his letter and personally responded. I cried tears of happiness and disbelief and asked, “Did that really happen?” more times than I can recall.

The man that you see throwing accurately targeted passes to his receivers is more than a great football player. He is a class-act, devoted to more than just the game. Though meticulously focused on the field, he understands with great awareness the impact he has outside the lines of the gridiron. His life displays compassion, and he has always focused on using his platform as a way to bless others. This was no more apparent to me than during our conversation. This man, with arguably the highest profile job in professional sports and a full schedule both on and off the field, took a moment out of his life to reach out to me and share encouragement.

Though a small gesture to some, the lasting impact our conversation will have on my life is unforgettable. Life is about relationships and those around us. No matter his fame and presence in the National Football League, Peyton Manning gets it. He understands that life is found in bringing joy to others. For that, I am grateful.

Thank you, Peyton.

(As a side note, Peyton Manning played a phenomenal game after our conversation, going 12/14 for 102 yards, 1 touchdown, and a rating of 120.8 in just over one quarter of play in a 34-0 Broncos win. That being said, I’ll gladly assume the position of the good luck charm for the Denver Broncos this season.)

Philippians 2:4 (ESV)

“Let each of you look not only to his own interests, but also to the interests of others.”

Don’t Worry, I’m a Professional

Being a professional is a good thing, right?

I’m no longer a novice, and am far beyond proficient. I’m now an expert at chemotherapy. This upcoming season of treatment will be my fourth go around, after all. In fact, pretty soon I’ll be over the hill with above 50 chemo treatments under my belt. I’m choosing to see this as a positive. I’ve got this chemo happy hour pretty well figured out. Not much can be put past me. Nausea, hair loss, exhaustion, pain, soreness, and aching? No biggie. I’m a pro.

Truth be told, I’m not nervous for my next round of treatment. It could be that I’ve done this for nearly three years and it’s become somewhat of a new “normal” to me or that I have complete peace in my journey knowing that God is sovereign over every detail. Upon learning that I would have to endure more chemotherapy as a result of my latest recurrence, many have asked if I am scared or nervous for this next season. I’m neither. At least, not yet.

I better not be. Happy hour starts next week.

Over these last few days, I’ve had several preparatory conversations with my doctors and nurses in both Houston and Denver. We’re all on the same page, and that in itself is comforting. Our plan goes into effect soon—I will be choosing a recliner in the infusion center next week, and will be ingesting my chemo cocktails in no time.

Each season of treatment is unlike the last, therefore, I’ll be receiving a different type of chemotherapy this time around. Though a self-proclaimed expert in all things chemo, I am still unaware of how this specific prescription will affect me. As a patient, we are given the rundown of possible side effects. Everything from low white blood cells and platelets to extreme tiredness. These are things I should expect with this type of chemo. I may or may not lose my hair… We’re praying for the latter, but won’t be too distraught with the former, however, I do love my curls! Though I won’t know how I’ll react until I receive treatment, I will generally feel as I have felt on chemo these past few years. Gross, tired, and sore.

Side effects may be similar, but the actual regimen called for this time is different than my past experiences. I will be receiving chemo once a week for three weeks in a row, with one week off. I will be doing this six times. Essentially, I will only have one week a month for the next six months where I won’t be getting treatment. It sure does seem like a lot. That equals 18 more sessions, but who’s counting? Yikes.

I’m ready for it. Ready to drive to the hospital every week. Ready to flood my body with copious amounts of poisonous toxins. Ready to feel like crap on a daily basis. Ready to fight. Ready. It’s amazing what you’ll do to try and stay alive.

As always, we will need abundant prayer, support, and encouragement. Remember 10 Ways to Help Someone With Cancer? The tips I provided last year are still very applicable to this journey ahead. We will be needing meals for when I’m feeling too tired, weak, or sick…Though Matt can cook a nice grilled cheese sandwich, his expertise does not reside in the kitchen. He does, however, drive to get take-out far better than anyone I’ve seen before. Gift cards to restaurants help as well. We will need endless support and encouragement, and please keep in mind I am not the only one going through this. My husband is the rock behind the scenes; my guardian standing firmly by my side. He needs as much encouragement as I do. We will also need understanding and grace, as our schedules will firmly revolve around how I am feeling each day. With what you’ve shown us in these last few years, we know you will rally beside us just as strong this time. Thank you for that.

Chemotherapy isn’t fun. It’s not something that I would choose to do had it not been crucial to my recovery. Going through yet another season of treatment doesn’t produce butterflies and rainbows. Instead, it’s brutal and exhausting. Chemo sucks. I love it and I hate it. No matter though, I’m a professional. I’ve got the port to prove it.

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Isaiah 41:10 (ESV)

“Fear not, for I am with you; be not dismayed, for I am your God; I will strengthen you, I will help you, I will uphold you with my righteous right hand.”

Photo: Kimberly Mitiska Photography

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