Posts Tagged ‘cancer’

Countdown to Christmas Giveaway!

If you follow me on Facebook, Instagram, and Twitter, you’d know that a couple of weeks ago I posted an inconspicuous teaser:

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Today, I’m sharing one of the exciting things that I mentioned! I will be partnering with some of my absolute favorite companies to do giveaways. Ladies and gentlemen, we’re giving you FREE stuff! All you have to do is follow the rules and play nicely.

This week, I have partnered with my wonderful friends over at Thrive Causemetics and we are doing a Countdown to Christmas giveaway. They are giving away a pair of their beautiful faux lashes with Infinity Lash Adhesives for you and a friend. Just enter and nominate your favorite Thriver!

Thrive Causmetics’ mission is to positively impact women going through cancer treatment. Karissa Bodnar, the founder of Thrive, has been personally affected by this horrendous disease and is now on a mission to make women feel more comfortable and more beautiful through the hardest moments in their lives.

Though the hair on my head is not falling out through this season of treatment, my brows and lashes sure are. I have worn faux lashes off and on for the last three years, and still had yet to find ones that I couldn’t live without. I went through brand after brand, and couldn’t find lashes that both felt and looked natural. Same goes for the adhesive – I just thought there were no good ones out there… Until I tried Thrive Causemetics.

photo-20The lashes are soft and natural. They are lightweight and not visually impairing (if you’ve worn faux lashes, you know what I’m talking about). They fit comfortably on your lash line, and blend in with any remaining lashes. The adhesive is the best I’ve ever tried. Seriously. It goes on in this incandescent blue/purple color, for you to see exactly where you are applying it, and it dries beautifully clear. This adhesive is even waterproof! Several women have worn Thrive’s products during marathons and they have stayed put. This product is the real deal.

To enter the giveaway, please follow these rules.

  1. “Like” Thrive Causemetics AND Derailing My Diagnosis on Facebook
  2. Share the posted giveaway photo with hashtags #ThriveCausemetics and #DerailingMyDiagnosis
  3. Tag a Thriver and tell us how they inspire you to thrive
  4. Once completed, comment on the giveaway photo on Derailing My Diagnosis Facebook page letting me know you entered!

Good luck!

*Contest begins on Monday, December 15, 2014, and ends Thursday, December 18, 2014. Winner will be chosen at random and will be announced on Friday, December, 19, 2014.

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

Sick and Tired of Being Sick and Tired

I have struggled since surgery, both physically and emotionally. This journey that I’m on, though abundant in blessings, is a difficult one. There are great achievements and considerable disappointments.

Ready to head into surgery. (6/14)

Ready to head into surgery. (6/2014)

Surgery last week went well. The doctor was able to remove the entirety of the left adrenal gland and the tumor with good margins. Besides commenting that my insides were “sticky” because of the amount of scar tissue from my three surgeries prior, the procedure (though an hour and a half longer than expected) was smooth. He was able to complete the procedure laparoscopically, allowing my stay in the hospital to be swift. Surgery was on Monday, and by Tuesday night I was walking out the front doors to head home. Though it was a quick stay, it wasn’t an easy one. The majority of my time in the hospital, I was in pain. At times it was excruciating, and I couldn’t help but cry out in agony.

My incisions were not the problem. In fact, though the doctor had to move my stomach, spleen, colon, and other organs out of the way, my insides weren’t even that sore. Gas was the culprit. As is standard in a procedure like mine, they inflate the abdomen with carbon dioxide gas. This allows the surgeons better visibility and to have space to move instruments around. Once surgery is complete, they deflate the abdomen and close the incisions up. Sometimes, not all of the gas is removed. In my case, gas was trapped in my diaphragm, unbeknownst to the medical team. When I woke up, I was in immense shoulder pain. Both of my shoulders felt dislocated and I was entirely confused. What was wrong with my shoulders? Why were they screaming in pain?

During the first night after surgery, I woke up quite loudly. Typically, I internalize pain and am able to breathe through even the most intense discomfort. This pain, however, was on a different level, and I could not contain my screaming like a banshee cries. My husband immediately jolted awake and ran out of the room to grab nurses, doctors, residents… heck, I don’t doubt he would have grabbed the janitor. He was desperate to find someone to help me. To be quite honest, I thought I had a blood clot in my lung. These are extremely dangerous and often can be fatal if not tended to. My right ribcage and shoulder felt as though a fist was trying to push through from the inside out; As though they would explode any minute. It was pain that I had similarly experienced with my first surgery. However, this gas would not be able to naturally escape. It was up high and would not be heading towards an exit. My body had to absorb it over time. The nurses and doctors, (and quite possibly the janitor) ran in and quickly tended to my ailment. Before I knew it, more pain meds began trickling through my IV. Slowly but surely I felt by body relaxing and the pain quieting. I was able to sleep that night, and felt well enough to be discharged the next day.

Once home, I rested peacefully in my own bed. With a memory foam topper, marshmallow-like mattress pad, and divinely fluffy pillows, I didn’t want to be anywhere else. Within two days, I received a call from my doctor. After surgery, as usual, my tumor was turned over to pathology where it would be tested to determine if it was malignant or benign. My doctor called with the news. It was not the news we were desperately hoping and praying for. The tumor was malignant. Neuroendocrine cancer has recurred once again. For a fourth time to be exact… but who’s counting?

I can’t begin to describe the rush of emotions that both my husband and I experience upon receiving this type of news. Though it’s our fourth time learning that cancer has invaded my body, it never gets easier. With my husband at work, and I, alone at home with our dogs, I cried out to God. “Lord, you have to protect me. I can’t keep doing this! Please heal me here on Earth. I’m not ready to die.” Once I told Matt the news, he left work early and came home. Together, we sat on the floor of our bathroom and cried. We prayed and pleaded with God to rid my body of cancer. We prayed for strength, wisdom, and direction moving forward.

Cancer sucks. And recurrences are worse. A real-life version of the film Groundhog Day. A nightmarish merry go round with zombies and evil clowns. One that slowly comes to a halt, but before stopping to allow me to get off, quickly picks up the pace and continues wildly spinning about. I have zero control; All I can do is hang on and pray that the ride stops eventually. Recurrences are truly what nightmares are made of. Once you’ve had cancer, the fear of the disease returning hides in the darkest part of your mind. Though you may not think about it often, it lurks and appears at the first sight of vulnerability.

The truth is, I’m sick and tired of being sick and tired. I’m ready for this seemingly never-ending chapter with cancer to end. I’m ready to move forward with my life, and for Matt and I to step into the greatness that we believe God has for our future. I’m ready to step out of my role as a cancer patient. I’m ready to be a full-time survivor, with cancer a thing of the past. I’m emotionally exhausted, yet I have to continue if I want to survive. I have no choice. I must fight to gain more time here. If I don’t, my end may arrive sooner. Cancer sucks.

Regardless of how defeated Matt and I may feel, we know that God is not defeated. No matter what the news is, God still holds the entire universe in His hands, and not one speck of our lives is unknown to Him. He knew that we would receive these results. He knew that I had a fourth fight in me. He knows. He believes in me. He believes in my future. He believes that, with His help, I can overcome this. So why shouldn’t I believe the same? We place our complete trust in Him. We know that God has purpose in this recurrence, and we cling to the faith that He is stirring up a story so big, we can’t begin to fathom it.

This may sound weird to you… it sounds weird to me sometimes. It is an honor to have this story. It is an honor to be chosen to fight this battle. It’s an honor to have the platform to share of God’s goodness through the darkest pits of despair. It’s an honor to be a cancer patient, and an even greater honor to be a child of God with the knowledge that I will survive, no matter what.

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Psalm 63:1-4, 7-8 (MSG)

“God—you’re my God! I can’t get enough of you! I’ve worked up such hunger and thirst for God, traveling across dry and weary deserts. So here I am in the place of worship, eyes open, drinking in your strength and glory. In your generous love I am really living at last! My lips brim praises like fountains. I bless you every time I take a breath; My arms wave like banners of praise to you… Because you’ve always stood up for me, I’m free to run and play. I hold on to you for dear life, and you hold me steady as a post.”

Pruning What Doesn’t Belong

A fourth surgery in less than three years? No problem. In fact, I told my doctor if he needed to cut me open from my shoulders to my knees, I wouldn’t care. Just get the job done. Remove what doesn’t belong.

Last week Matt and I drove to a meeting with our newly appointed team member. A urologist, who happens to be the top adrenal surgeon in the state. He’s one of the many doctors on our team who helps navigate and combat this dreaded thing called cancer. I currently have a gynecologic oncologist, radiation oncologist, general oncologist, and now a urologist, among the slew of techs and nurses helping as well. Adding a new doctor to the team is always met with some hesitancy (on my part), as I become comfortable with those who have treated me over the last couple of years. My team of doctors and I have grown as a family. The hospital where I have received 99.9% of my treatment is a second home.

Adding a new doctor is like welcoming a new in-law to the family. Will I like him/her? Is he/she going to be able to keep pace in our conversations? Can I see myself spending hours and hours with this person? Can I place my trust in this person’s hands? As my medical team has become family, it’s quite entertaining to see what role each of them falls into. The one who is like an aunt whom you can cry and laugh with, and tell your darkest secrets to, all the while feeling great comfort. The epitome of a distant uncle who awkwardly hits it to you straight and leaves you hanging mid-air wondering what he’ll say next. The sister figure who has your best interest in heart, but doesn’t mind telling you the truth when you need to hear it. The cousins who greet you and play catch-up for the mere minutes you have to see them. Every person on our team fills a role in our medical family. Each one serves a purpose and is vital in my fight against cancer.

Though we’ve only met my new doctor once (on our four-year wedding anniversary, might I add), I can confidently say that I trust him. Matt and I both do. He is smart, professional, and compassionate and, after our meeting with him, we are ready to move forward in the next step. As I’ve mentioned HERE, I have a tumor on my left adrenal gland. The CT and PET show “activity” in the mass, however, based on its location, there is not 100% certainty that it is malignant. From what our doctor discussed with us, we know that adrenal masses happen and are often completely benign. Of course, based on my history, we have to be cautious. Caution and cancer go hand in hand.

Upon having our conversation, my doctor, husband, and I decided it’s best to proceed with surgery to remove this unlabeled mass. Usually, there is talk about doing a biopsy whenever a spot shows up on my scan, but it’s quickly ruled out. This time was no different. For a minute we passed over the idea of taking a biopsy of this tumor, but the risk of spreading the cells (cancer or not) is too great. IF it happens to be malignant, we don’t want  it to spread and wreak havoc elsewhere in my body. This is a disease you don’t want to piss off. Therefore, I’m going under the knife once again.

This will be my fourth major surgery since diagnosis. At this point, I like to consider myself a professional. I’m not concerned. In fact, I would rather be cut open to remove the entirety of the unknown intruder cells as opposed to just peeking through the door, taking a piece, and testing them. My scan is showing something that shouldn’t be there, and although it may not even be cancerous, I don’t like things where they don’t belong.

Pruning is a must in all areas of our existence. While I have undergone surgery to remove malignant masses in my body, likewise I have undergone metaphorical surgery to remove toxicity out of my life. We often hear certain things being compared to cancer. “He is a cancer in the group. He pulls everyone down with him.” Nothing about cancer has a positive connotation. It is the worst of the worst. It will destroy you from the inside out. Ridding ourselves of cancer and its metaphorical meaning is vital to live a healthy life. We prune gardens, cutting back the weeds to allow flowers to blossom, and likewise we should be pruning our lives.

Is there an area of your life that is so full of weeds, it’s taking over your world? Are the weeds drowning out who you really are? Have you ignored the weeds, hoping that they’ll go away on their own? We must cut back what doesn’t belong and rid ourselves of what shouldn’t take residence in our lives. It could be a toxic relationship, hidden addiction, or unhealthy patterns. We all have areas that need to be pruned.

Just as surgery hurts, pruning hurts as well. Removing what doesn’t belong will cause pain, and that’s often why many people avoid it. But once the weeds are removed, the blossoms can thrive. Though we are believing this mass is not cancer, it still doesn’t belong. Therefore, this coming Monday (6/16), Matt and I will venture into the hospital once more to do some pruning. The doctor believes he can perform the surgery laparoscopically. If this is the case, my recovery will be much easier. We are confident in this process, and are expecting wonderful results.

Please be praying for myself, Matt, and our newly added team of medical staff. While I receive all of the fun parts of surgery (sedation, pain medication, and doting nurses), Matt sits in the wings for hours awaiting the results.

While we prepare for pruning, ask yourself what needs to be pruned in your life?

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John 15:2 (ESV)

“Every branch in me that does not bear fruit he takes away, and every branch that does bear fruit he prunes, that it may bear more fruit.”

 

 

Caregiving: A Perspective From Both Sides of The Coin

(As featured on Cancer Knowledge Network)

Most of you know me as the writer in our family. Little do you know, my husband is talented in written form as well. Recently, Matt and I were asked to co-write an article for a Canadian publication. We were invited to share our perspectives on caregiving and the vital role it plays in one’s journey through cancer. I was, and still am amazed at my husband’s words. They have touched my soul, just as I know they will yours…

Stephanie (Survivor):

A cancer diagnosis never affects just the person afflicted with the disease. Though the doctor found a malignant tumor growing inside of me, she might as well have told my husband that he had one growing inside of him as well.

In June of 2010, I walked down the red-carpeted aisle of an old, spacious, and magnificent cathedral to marry my best friend. From our second date, I knew he was the one I would spend the rest of my life with. We shared laughter, adventure, and innumerable conversations. He stole my heart and has protected it from the moment it entered his grasp. Within weeks of meeting each other, we fell in love and began planning our future – when we would have children, where we would live and raise our family, even the color of paint we would choose for the walls of our dream home. We had life figured out and were valiantly prepared to take on the world together, hand in hand.

One and a half years later our plans were derailed. At the age of 25, I was diagnosed with a rare and aggressive form of cancer. It was as if the canvas we had sketched our dreams on was wiped clean. The plans we had set forth were redefined and put on hold. We soon entered into the gates of Cancerland and were quickly thrust into an unknown arena. Decisions had to be made, and treatment began immediately.

Through multiple surgeries and treatments, recurrences, and cancer-free scans, my husband has stood firmly by my side in every moment. He has courageously taken the role as my caregiver, and has sacrificially offered to help with my countless needs. Not many realize that I am not the only one in this fight. My husband is firmly planted next to me on the front lines. When I rested in hospital recliners receiving treatments, Matt sat on the uncomfortable chairs beside me without complaint. When I was weak and pitifully sick, he would assure me and rub my back in comfort. When I had moments of depression and couldn’t battle fearful thoughts, he would encourage and pray for me. He shaved his head when I lost my hair so I wouldn’t feel alone. At my weakest, my husband mustered up strength and bravery to help me through. All without second guessing or complaint.

I’ve often shared that the role of a caregiver is equally as important as the patient fighting cancer. Though I was the one ingesting toxins to battle the disease within me, my husband fought just as hard behind the scenes, making sure I could withstand the fight. He has sacrificed so much just to care for me. His patience, concern, encouragement, compassion, and love have altered the way I fight cancer. I am stronger with him beside me.

He is my guardian. We fight this disease together.

Matt (Caregiver):

Have you ever seen the movie The Bodyguard?

Kevin Costner is a total badass in that movie. I watched it a lot when I was a kid. He ran around, protecting Whitney Houston from stalkers and bullets. He was a hero. I wanted to be a hero.

I can’t say I was fully prepared when my life started to parallel that story. My wife was diagnosed with a rare and aggressive form of cancer over two years ago. When we got the news, I knew that the roller coaster ride would soon commence. Life would never be what it once was, nor would it play out in the way I had intended. Instead of buying a house, a car, and having kids, we would be shuttling off to surgeries, chemotherapy treatments and radiation appointments, all the while keeping track of our mileage in hopes of writing the expense off on our taxes.

Let’s face it; in reality, I’m not fending off over-obsessed fans or valiantly diving in front of bullets (thank the Lord). My role is more concealed. Instead of being front and center, I’m like the Kevin Costner waiting in the wings, keeping an ever-watchful eye on everything that’s going on. And unlike Kevin Costner, there’s not a whole lot I could do except be there. I can’t make the disease go away. I can pray, and I can be there whenever my wife needs me. When my wife was sick in the middle of the night, I was awake with her. When she was too weak to get out of bed on her own strength, I helped her up. When all she could or wanted to do was lay on the couch, that’s all I did, too. I instantly became a professional chauffeur, personal assistant, and expert dog taker-outer. If I wasn’t at home or at the hospital, I was at the pharmacy, standing off to the side while the staff gathered up the hundreds of dollars worth of home injections and pills that I didn’t have the capacity to afford. As a caregiver, you do whatever it takes.

In those times, I’d often think back to the day I married Stephanie. “For richer or poorer… In sickness and in health.”

So this is what that meant. This is what I meant.

Being a caregiver is not a glamorous gig. As a caregiver, you hold down the fort. Your partner is down, and it’s all on you now: the house, the kids (or, in our case, the dogs), the money, the bills, making sure your family is fed, that they have a roof over their heads, clothes on their backs… and the whole “giving care” part. That’s your job now. Your job is no longer just your job. You will lose sleep. You will not be able to do some of the things you used to enjoy. You will sacrifice your own health to ensure the health of your loved one. And you will need never-ending amounts of grace and forgiveness.

You will do all of this, and you will likely not be recognized for any of it. You will feel left out. You’re in the wings, remember? When things go bad, prayers and support are 99.9% directed at your loved one. When things go well, congratulations and well-wishes will also be 99.9% directed at your loved one.

You’re the unsung hero, the bodyguard. Stay out of the way and save the day.

Often times, my wife gets told that she is someone’s hero. Nearly every day, she hears that from someone. People lavish her with praise, saying she inspires them. They want to make sure that Stephanie knows how much she means to them.

For me, my wife is the one telling me that I’m her hero. When she is everyone else’s hero, I’m hers. She sees what I do, the sacrifices I’ve made to make her as comfortable as possible as she fights the hardest fight of her life. She appreciates me. That’s awesome. That being said, if you know someone who is a caregiver, tell them how you feel about them. Do you appreciate them? Tell them. It’s amazing what encouragement can do. For every person you know who is faced with cancer or some other life-altering affliction, there is also someone in their corner who, if you’re honest with yourself, you likely have never noticed.

No one is meant to fight alone.

Philippians 2:4 (ESV)

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

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Complicated Results and Abundant Faith

It’s that time of the year again. My three month follow up scan has arrived. If you follow me on Instagram, Facebook, or Twitter, you know that I laid on the hard, metal table one week ago. The results are in…

There’s a spot on my left adrenal gland.

Before you begin jumping to conclusions, let me explain. We aren’t positive that this lesion is even cancer. This is a spot that has lit up on the last few of my scans, and first made it’s appearance in October. Since then, I’ve had several rounds of chemotherapy. Throughout it all, this unknown mass has remained. It has grown slightly in size over the last seven months, but doesn’t seem to be affecting my body’s function.

When I was first told of the news, I didn’t even know what an adrenal gland was. One of our close friends is a doctor in this field and was able to explain to us in non-medical terms what we were dealing with. The adrenal gland is essentially a hat on top of the kidney. It’s purpose is to produce hormones such as stress and adrenaline. Each kidney gets it’s own adrenal gland, so, naturally we all have two. This lesion could potentially be one of three things.

  1. A benign non-functioning tumor. In which case, it’s a mass that serves no purpose and isn’t affecting my adrenal function.
  2. A benign functioning tumor. This is a tumor that is releasing it’s own hormones like stress and adrenaline.
  3. A malignant tumor. Also known as, cancer.

Of course, we won’t definitively know what this spot is until it is biopsied and sent to a pathologist. However, based on my history in Cancerland, we can conjure up an idea of what it may or may not be. Most likely we can rule out it being a benign functioning tumor. If this were the case, I would be experiencing symptoms like heart racing and bloodshot eyes, which I’m not. It would be obvious if this mass was functioning on it’s own, and from what we can see, it’s not doing much.

There is a chance that this could be another recurrence. However, taking my history of malignancies into account, although this lesion has grown, it has not increased as rapidly as my other recurrent tumors. If you recall, my first recurrence was a softball-sized tumor that developed within three months. That mass grew rapidly and aggressively and even began affecting my hormonal functions. In addition to the difference in growth, my body has proven to respond very well to chemotherapy. If this were a malignancy it would be quizzical to have had no response to treatment. For these reasons and more, we believe this is not a malignant tumor.

This leaves the possibility of it being a simple mass that serves no purpose other than to annoy us by showing up around my left kidney. A little pest that has chosen to, for whatever reason, hang out on my adrenal gland. Matt and I strongly believe that a non-functioning tumor is what’s lurking inside of me.

We have abundant faith that this is not cancer.

Arguments can be made for both sides — malignant and benign. Yes, based on these last two years, an unknown mass can lead many to immediately think cancer. However, just as likely, it could be something completely unrelated. Not everything inside of me has to be marked by this disease.

Regardless of what this lesion is, it will need to be removed. Cancer or not, I don’t need something harassing my adrenal gland. Therefore, I will have surgery at some point. Honestly, I am not fazed in the slightest. I’ve already been through three major surgeries in the last couple of years. I’m familiar with the process and recovery. I know all too well about the discomfort and pain. Surgery no longer scares me. I trust that God has my life in His hands; Just as He orchestrated what has been, He orchestrates what will be.

This morning I venture back into the hospital to lay on another hard table while a loud spinning machine takes several images of my insides. This scan will be a full body PET scan and will show all of my internal organs, including my brain. Compared to the CT scans that I receive every three months, a PET goes deeper in it’s imaging and is far more comprehensive. We may or may not learn more information from this scan. This step is necessary to make sure there are no other masses growing elsewhere in my body.

Next week a new doctor will be added to our team, and we will meet with him to discuss surgery. He will go over the hundreds of documents that have chronicled my medical journey and review each scan image that has been taken. He officially has a new patient that comes baring a lot of medical baggage, and it’ll be interesting to hear his opinion on my case.

For now, we hope and pray. As I mentioned, Matt and I are not fearful, but full of abundant faith. We aren’t anxious, nervous, or even the slightest bit afraid. Standing in faith, we believe this growing lesion is not cancer. We believe that I am still cancer free and will remain so for the rest of my life. We believe that the chapter of cancer has closed and we are entering in to the next season of our lives. We are not only believing, but declaring this. God is so mighty in His power, we are calling upon Him to perform a miracle. He beckons us to have faith, to knock so He can answer, and to trust in Him. Therefore, while believing and trusting in Him, we are asking that this mass that has shown itself on my scans for seven months, will not appear on my PET scan. We are praying that whatever this spot is, will vanish. I actually laugh as I pray, because I can picture my team of doctors jaw-dropped as they read the report and view the images, and see the once 2.6cm mass completely gone.

So, while I don’t have the best news to share, I don’t have the worst news either. The results from my CT scan are merely a speed bump on the journey. This is a moment that the enemy is attempting to lead us to question God. I know he is asking us, “Are you sure you’re healed?” He wants to lead us down the path of emotional and spiritual destruction, but we stand against it. We aren’t entertaining the thoughts and fears that try to creep in. We won’t open a door until God tells us to. For now, we are firm in our faith, and believe in healing. We ask that you would stand with us and believe for a cancer free report.

Luke 8:50 (ESV)

“But Jesus on hearing this answered him, ‘Do not fear; only believe, and she will be well.’”

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