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Why I Relay

April 15
by
Chandler Johnson
in
Creative Outlets
with
.

“It’s the size of a grapefruit.”


I imagined the bitter, fleshy pink fruit. In my mind’s eye the fruit sat, covered in layer of white, granular sugar, untouched with a silver spoon gleaming beside it. My trance dissipated like a curling cloud of smoke as I listened to my mother’s voice through the phone.

“It doesn’t look good,” she murmured.

I knew it was too late. It was too big. It wasn’t caught soon enough. It was a tumor, and it was draining my last surviving grandparent of her life.

The air was hot and humid, with the smell of food simmering on the stove. It was the kind of air that makes you feel like just one breath could give you a mouthful of whatever was cooking. I walked further into my oma’s kitchen and peered into the bubbling pot on the stove. With her giant spin in her hand, she wagged it towards me as she asked, “Hungry?” with her mouth pulled back into a sly grin.

She already knew the answer; no one could resist her spaetzle dumplings, dripping with browned butter. I gave her a long hug, pressed against the cool silk of the draping mumu that provided her a sort of sanctuary in the hot kitchen. Then I took the heaping plate.

“Wait, so how far along is she? Like, how advanced is it,” I questioned, still in shock, still hoping.

“Honey, she’s very sick.”

“Should I come home? Is it bad?”

“If you can, I think you should come…” To say goodbye?

It wasn’t said, but then again it didn’t have to be. The short exchange, now seared into my memory, was enough to tell me everything I needed to know. Tears began to well in my eyes, salty and stinging as they ran down my face. The cold night air rested on my tear-stained cheeks like a cold kiss, the dark silhouettes of buildings forming a voyeuristic audience to my grief. Almost shocked by the sound of my sobs, I went back to my apartment and feel into my bed.

“Hoopah-radah-ridah-da-felda-in-da-craada. Oops, there goes the baby in-da-craada.”

Memories of lullabies from a foreign land, dripping with harsh German enunciations, dance through my mind as I look at photos of my grandmother, cradling me as a baby. She was there, gazing down at my thick, black hair, my closed eyes, my rosebud lips, cherishing the simplicity of my total innocence. But now I’m here, cradling this photo of her, observing her in her youth. I take notice of her dark hair that’s so much like my own, and her air of seriousness that seems to radiate from the glossy image.

I can’t help but to pause and think of the authority of time.

It never stops—an infallible machine that never needs greasing or turning, wrenching or polishing. Who takes care of time? It certainly doesn’t take care of us. I wondered how long it took for the cancer to metastasize to form the massive tumor, situated atop my oma’s liver. How many seconds, minutes, hours, weeks, it took for the malignant mass to form, and for the cancer to stake its claim.

It took three hours to drive back to Rome, straight to the hospital, when my last class ended on Friday. My mother came to the lobby, to bring me to the sterile hospital room, where my grandmother lay surrounded by family. My mother whispered in my ear, “She doesn’t have long. I didn’t realize she would go this quickly…”

I nodded, and then neared the hospital bed, the ambient lighting casting a glow on my oma’s pale skin. I reached out to touch her hand, still as lovely as it had always been. I heard my aunt murmur, “She’s always had beautiful skin, hasn’t she?” I gazed down at her fingers, interlaced with mine. Over fifty years my senior and little differed between ours, besides my slightly darker complexion.

I gripped her hand a little firmer, feeling the warmth it radiated, wondering if I could feel the blood pulsing through her veins if I was still enough.

Of course, she didn’t stir from her sedated state, propped on her side as to avoid pressing on the painful tumor. All I could do was stare at her, sleeping so peacefully, only the slightest signs of her regular breaths. Inhaling and exhaling, her chest mimicked the ocean tides, and I felt soothed for a little while.

The hardest part wasn’t the funeral. It wasn’t the process of cleaning out her home, full of memories from my youth. It wasn’t that seeing my oma’s twin sister when she came to town was like seeing a ghost. It was saying goodbye to her, in that dimly lit hospital room, knowing that it was the last time. It’s an eerie thing, saying your last goodbyes to someone who is still alive. So unnatural and shocking it seemed to me at the time that I couldn’t utter a simple goodbye out loud.

I turned to my family who watched me as I stood by the hospital bed, and sobbed, “I can’t do it. I can’t say goodbye…” But what I could do was hold her hand, and I did.

This is why I relay.

So that no one else has to feel the pain of saying goodbye, for the last time, to loved one dying of cancer. I relay because cancer has gone too far. It’s taken one too many wonderful beings from this world. For all those who are battling cancer, know someone who is battling cancer, or hope that they will never have either of these connections: I’m implore you to direct your passion to this cause. Whatever your motives are, everyone who relays has the same goal—to beat cancer.

We can.


 

The “C” Word

April 15
by
Courtney Grap
in
Health
with
.

She found the lump.


She was told it was breast cancer and that it needed to be removed. The lumpectomy did the job, and she was considered cancer free shortly thereafter.

At age forty-eight, it must be empowering to look cancer in the face and give it the finger. It must be harder when twelve years down the road, it comes knocking angrily at your door again. The breast cancer was more aggressive this time, and a lumpectomy simply was not sufficient. The cancer had spread and more extreme measures needed to be taken.

She would need to undergo a mastectomy, a surgery that would take away part of what we consider our womanhood. But if we’re being honest, she handled it like a champ, and she was once again considered cancer free.

They say the third time is the charm.

The cancer was back and pretty pissed off that she had beaten it not once, but twice.

It had spread to her other breast and she knew this meant a double mastectomy. We had never seen her so frail and fragile, but never once did her will power and audacity cease.

Doctors say my Nana is a very rare case. Being diagnosed with breast cancer three times over the course of fifteen years, and beating it every time, is unheard of. She once told me, “It’s not the obstacles you face, but how you overcome them.”

Persevering through the loss of both of her breasts, rounds of radiation, chemotherapy, and the loss of her hair, she not only inspired me to get involved with organizations that support finding a cure, but also to live by that quote each and every day.

Breast cancer awareness is obviously something that is near and dear to my heart. It is astounding that about one in eight women in the United States will develop invasive breast cancer over the course of her lifetime.

Courageous, spirited, independent, and strong are just a few words I would use to describe my Nana. But these words describe all cancer survivors. It’s our job to support them and raise awareness and funds so that we can eliminate the “C” word forever.


 

Fighting Back Against Cancer

April 15
by
Sarah Morgan
in
Health
with
.

The summer before my sophomore year of college, I took my dad to his annual colonoscopy.


As he was waking up from under his anesthesia, the nurses called me back to see him, where he was in a room with other patients waking up from their procedures. My mom had warned me that morning that his Parkinson’s disease would make him take longer to wake up.

I was joking with him about how groggy he was when the doctor came in. The doctor sat me down and said, “It doesn’t look good. It’s probably cancer. Once your dad is more awake, I want to meet with both of you in my office,” but all I heard was “CANCER.”

Cancer had already had a huge impact on my life.

I watched as it took three of my friends’ parents, one of my high school classmates, and other cousins and aunts. I was numb. That day we scheduled scans for the next week and more doctor appointments.

The doctor said he wanted to go ahead and do everything they could as soon as possible, so we did. Dad had scans done that confirmed he did indeed have colon cancer, and it had already spread to his liver. Doctors removed the cancerous part of his colon. Then he went through countless rounds of chemo to decrease the size of the cancerous spots on his liver so the cancerous part of his liver could be removed with more surgery.

That summer, my family became much closer. I had always been a daddy’s girl, but while I was in high school, we argued a lot. After his cancer diagnosis, we definitely grew closer again. I enjoyed being a part of my dad’s recovery: spending the nights with him at the hospital and going to his chemo appointments.

My dad completed more chemotherapy treatments, just in time so that he could be finished for our trip to Daytona Beach. But as soon as we returned home, the doctor told us that Dad’s cancer wasn’t gone. There were still some spots on his liver, so he went through more rounds of chemo and some radiation.

The cancerous spots decreased in size but haven’t completely gone away yet. He just finished his third round of treatments three years after his cancer diagnosis. After watching him endure so many rounds of chemo and radiation, eventually I started to feel a little frustrated.

I kept thinking why does it have to be my dad?

Why couldn’t I have been one of those people whose family was totally unaffected by cancer?

This fall, my grandfather was also diagnosed with colon cancer. He took chemo pills and went through radiation.

My family thought that since we had already gone through so much chemo and radiation with my dad, we would know what to expect with my grandfather’s treatments. However, instead of really helping, his chemo and radiation treatments just seemed to hurt him more.

After numerous hospitalizations and a COPD diagnosis, Hospice moved my grandfather into my parents’ home. Over spring break, I got to come home and spend lots of time with him. During that week, he really perked up and stood up for the first time in almost two months.

My parents started to talk about the possibility of taking him out of Hospice because it really looked like he was going to get better. I left home the last Sunday of spring break and kissed my grandfather goodbye and he told me to “look out for the car behind the car in front of you” like he always did.

I was planning on coming back home just two weeks later to celebrate Easter with my family, so I didn’t think much of our goodbye that day. Just three days later, my grandfather passed away.

My sophomore year, I joined UGA Relay For Life soon after my dad’s first cancer diagnosis. Relay gave me a way to help in his fight against cancer. As an executive board member of Relay this year, I have become friends with so many others whose lives have been affected by this terrible disease. Many have lost family members to cancer and yet continue to fight for a future without cancer.

For a long time, I felt helpless against cancer. I can’t help but think that if my grandfather had just lived two weeks longer, I could have said a real goodbye to him. I Relay for that two weeks.


I Relay so that one day some girl can have two more weeks with her grandfather because I know how much that time would mean to me.

 

Finding Hope Two Hemoglobin Levels Away From Death

April 14
by
Gabbi Benton
in
Health
with
.

Cancer… That disgusting, evil, dreadful, horrifying, life-changing disease that affects each and every one of us in some way or another.


Why does it exist? I am not really sure. But I do know for sure that we must stand up and battle it until the day that it no longer exists. My very close friend of two years has been battling Stage 4 Liver Cancer for about five years now.

First meeting her, I would have never known she was fighting such a horrible disease because of the smile that she never lets slip away from her face. That smile makes coming back to college after every break only that much harder.

Back in early October, life seemed to be going pretty smooth for her.

She was living the life of a normal nineteen year old. She attended all of her brother’s high school football games and all of the big events in town. She was not letting her cancer affect her in any way.

Then one morning, I got the call that she was being rushed to a hospital an hour from home due to some major complications. I will never forget answering that call in class and completely losing it. I debated on walking out of class to make the five hour drive home to be with her, but I did not know if I was strong enough to get behind the wheel of the car. Until… I got a phone call from her begging me to leave class to come be by her side.

Without hesitation, I took off.

The drive to the hospital was probably the longest drive of my life. There were a million thoughts running through my head, thoughts of overcoming and thoughts of pure sadness. I was not sure if I would make it in time to give my friend that one last hug. I was not sure if I would make it in time to let her know how much I love her.

Thankfully, I arrived at the hospital with a red face and swollen eyes and sprinted to her room. Only to find my friend with that same smile on her face that makes it hard to go back to college after every break. That smile that brings so much joy to my heart. I wondered how she was able to carry this smile while being literally two hemoglobin levels away from death.

I was a bit frustrated with myself because I knew that my sadness and fear was radiating, yet all she wanted was happiness. After arriving at the hospital Tuesday, I did not leave her side until we walked out together with discharge papers in hand and a smile on her face.

Needless to say, her battle with cancer is not over yet. But the moral of this story is to never let your smile slip away from your face. My friend is battling some of the nastiest stuff on this planet, yet she still finds a way to let that smile shine. She can be in the most pain and be filled with so much fear, but she lets that smile shine.

Look into every situation for the positive. For when you can take that view on life, your smile will radiate. It is not just a smile that people see. It is a smile that affects people. It changes people to realize all that they have and to find greatness in the most troubling situations. Be the light of the world by smiling a contagious smile today.


Who knows, that one small smile could change the life of someone who really needs it.


 

Cancer and the Creek, An Epiphany

April 13
by
Brittany Lewis
in
Health
with
.

It’s the fall of my sophomore year. I’m settled, feeling confident, and more ready than ever to start pumping up my resume with extracurricular activities.


I’m interested in health science, so when presented with the idea of joining Relay for Life at the University of Georgia, an organization that raises money to support the American Cancer Society, I said “sure, why not?” I knew it would look great to future employers and my great grandmother had cancer so it meant a lot to me to fight back against a terrible disease. So, I joined a committee.

The year marched on and I lost touch.

Not really invested in anything the organization put on, but rather just going through the motions and showing up to meetings when it was convenient. I wasn’t proud of this, but at the same time I was a busy college student, so that’s a great excuse, right?

Second semester arrived and I had this unexplainable gut feeling that I needed to step my game up. I needed to get involved, get motivated, and do whatever I could to help this organization because its passion and heart was worth investing effort into. I kicked it into high gear and started fundraising, being involved with fellow committee members, and getting to know the girl that oversaw our committee.

%tags Health

Fast forward to the week before the big event. It was a normal Friday morning, except I was planning to travel home for Easter weekend. My dad called me and said with a serious tone “call me when you get home, we need to talk.” Those words are never good.

Of course the whole way home all the possibilities of news I could receive raced through my head, but didn’t prepare me for what was to come. I finally arrived, and anxiously called my dad as he requested. He said, “Brittany, Granddaddy has cancer and it does not look good.”

Shattered. My heart. My world. Turned upside down and back again.

I didn’t know what to say or do, so I just hung up and took off running down the road. I ran until I was out of tears, and sat down in my favorite spot by the neighborhood creek. I sat there watching the water pass just as fast as the emotions ran through my heart. I kept thinking of anything, anything I could physically do to stop this or make it go away.

And then it hit me.

There was nothing I could do to fix the cancer in Granddaddy’s body, but there was an opportunity to stop this disease from shattering other lives in the future. Relay for Life was that channel of energy and emotions I could utilize for grief, coping, but most importantly, a beacon of hope.

Fundraising, planning the night-of, and my commitment to this organization is my way of standing up to cancer, honoring those lives lost, and celebrating the ones spared. I believe God uses us as the hands and feet of His mighty power to carry out His will for the world, and I believe we are His vessel for making a difference in a world full of cancer.

I continue to serve this organization now as the Logistics Chair, and wouldn’t trade my time here for anything.


To me, Relay is more than just another detail of my resume; it is my Hope and heart to say that one day in my lifetime, I believe this world will finally be cancer free.


 

Life With My Step Brother Works Out

April 13
by
Sam Straker
in
Overcoming Challenges
with
.

I was nine years old. I had a seven-year-old younger sister Kate. My mom had just passed away from breast cancer, and my dad felt hopeless.


Things didn’t seem like they could get any worse. The next year or so is a complete blur in my life; I think I have subconsciously blocked out that time because it was so difficult for my family and me. My dad about a year later began to date who would become my step-mom, Debbie.

My family had known Debbie and her family for years before, and her son Mark was my best friend growing up. His parents got divorced right around the time of my mother’s passing, and the timing just seemed to work out perfectly for my dad and Debbie.

This time seemed to absolutely fly by, and before I knew it my family was moving into a brand new house with Debbie, Mark, and her daughter Jackie. There were six of us now in a house. Things had moved so quickly I don’t think any of the kids were ready for such a big change.

There was so much resentment between the opposing families. Kate and I had loads of tension with Debbie, while Mark and Jackie couldn’t stand my dad. They were disgusted with the new situation because they obviously wanted their real dad instead of mine.

Understandable, but not pretty.

Mark and I, best friends growing up, couldn’t stand each other more. We never spoke, never hung out, and talked bad about each other behind each other’s backs. I hated that he disliked my dad, and he probably hated me for disliking his mom.

All I wanted was to move back to my old house with Kate and my dad. We were finally starting to get stronger after my mom’s passing, and now we had to deal with this? It seemed totally unfair.

Those next three years were really rough, and it was probably a stereotypical step family situation. Lots of resentment and tension, but our parents were happy together. Finally, however, there was a defining moment that brought Mark and me back together.

My best friend from high school, Graham, was a big basketball player like Mark. We always hung out, and he couldn’t stand Mark either because of everything I would tell him. However, during the summer going into junior year, Mark and Graham worked at the same basketball camp. They spent 8 hours together for two weeks and grew pretty close.

One Friday night, Graham invited me to come over and hang out for the night and when I got there, Mark was there too. At first I was pissed and thought about just going home.

But I decided to stay, and I couldn’t be more grateful that I did.

The three of us played basketball, ping-pong, video games, built a bonfire, and watched a movie. We all had a blast, and it was at that exact moment that Mark and I became friends again. This transformation in our relationship not only helped us grow closer, but it helped our family as a whole bond.

Mark and I’s struggling relationship was a prime reason why our family had so much tension, and fixing that friendship was a turning point for our family. Since then, our family has only been growing stronger. Mark and I went off to UGA last year, and we even roomed together.

Four years ago if somebody told me that Mark would be my roommate in college, I would have laughed in their face because I couldn’t think of anything worse. But we did, and it was an unbelievable year. All of the kids are in college now, but when we go back home for holidays and breaks, we always pick it up right where we left off.

I couldn’t be happier with how my life is now; I can truly say that life will always go on and everything happens for a reason.


 

Countering The Reality Of Cancer With Relay For Life

April 6
by
Morgan Carson
in
Health
with
.

We live in a day and age where it’s difficult to find someone who’s life hasn’t been affected by cancer in some way. Unfortunately, like many others, I can’t remember the point in my life where cancer wasn’t in my vocabulary.


From a young age I have been exposed this disease that has robbed me and my family of so many memories with the ones we love. It became all too real in high school, when my best friend was sleeping over on school nights while her parents were away in Mexico on experimental chemotherapy trips to attack her father’s colon cancer.

It became all too real when my aunt was asking us to come visit to explain her terminal diagnosis in person, rather than over the phone. It became all too real when my cousin, and built in field trip chaperone, was told that only 3 hospitals on the east coast would even look at his case because it was so rare and unexplored.

It became too real when the man who knew how to light up a room with his belly laugh was told he had throat cancer that barely allowed him to speak at most points during his treatment. It all became too real, and too unbearable at a speed that took my anxiety to a whole new level.

Every time the phone rang, my heart sank into my stomach wondering if it would be an update that would change everything. I lived my life in fear of what cancer was taking from my loved ones.

Day in and day out, I couldn’t find solace that I was away at college and unable to help, even though all I could do was miniscule in compared to their daily fights against this horrible disease.

And then I found Relay For Life at Virginia Tech.

As a confused little freshman, I joined a random person’s team (shoutout to my now BFF), and arrived at the rainy and chilly event, unsure of what to expect of the night. I knew there was music, food, and community, but I didn’t expect to find the comfort my soul so desperately needed.

As I heard others speak about their battles with cancer, the loss of their loved ones, their continuing bouts, my eyes were gently opened to all that I could do to help. Even from hundreds of miles away, I could do something that would help change someone’s life.

Here I am, 3 Relays later, 2 committee families created, and one final Relay For Life at Virginia Tech approaching, and I am at a loss for words to express how much this organization has given to me. Opportunities to stray far outside my comfort zone, to not settle for mediocrity, and to express all the love I feel inside of me for the wonderful members of the executive team and committee of Relay For Life at Virginia Tech.

A Relay friendship is unlike any other. It is created on the basis that we’ve all been hurt by the whirlwind of cancer in our lifetimes, and while that hurt is immense, we can counter it with hard work and determination to make our event successful and spread the mission of the American Cancer Society.

In every event we put on or Cookout milkshake we eat, we bond a little more, learn a little more about each other, and eventually fill some of the hurting void that cancer left with a friendship that will last a lifetime. I find myself at a loss for words to explain what these friendships mean to me and I’m continually thankful for all the twisted paths that brought us all together.


I am thankful to Relay this year in memory of my Aunt Marilyn and Rich Conklin, in honor of my cousin Terry Carson, and in celebration of Jere O’Brien kicking cancer’s ass this year.


 

Juju

April 1
by
Rachel Helling
in
Faith
with
.

Her name was JuJu. A nickname from childhood that her dad had called her before he passed away. Juju was one of my campers in the Yellow unit of nine to eleven year olds and was a natural born leader.


She was only in elementary school, but carried herself as an outgoing young adult with a passion to create a brighter world through creativity and joy. I met Juju at Camp Kesem last summer. Camp Kesem is a place where kids can find solace, support, and love from others who truly understand losing a parent from cancer.

Losing a parent is difficult, and it is unimaginable to me to lose one when you are nine years old.

But Camp is about finding light in dark situations and creating incredible friendships. At Camp when the sun goes down and the campers are all in their pajamas, we have Cabin Chat. This is a time when counselors lead a discussion with a series of questions. The first couple questions are lighthearted, but eventually they become more serious throughout the week.

On one of the first days, we asked the girls in our cabin “What is the most beautiful thing you’ve ever seen?” I was expecting the girls to say something like “a rainbow!” or “my dog is beautiful,” but instead I was floored from the answers they provided. Juju’s answer is the most vivid in my memory.

Calmly she asked, “Does it have to be something I actually saw or can it be something I know?”

The other counselors and I were curious. We let her continue, “The most beautiful thing I’ve ever seen was when my dad passed away and he wasn’t hurting anymore. He was finally peaceful…I know he’s up in heaven now playing golf with my grandpa and catching up.” We were all speechless. What nine year old should be able to say that? I started thinking about how young she was and how mature I could never be at that age.

I mean nine years old and accepting that your life will go on knowing this? Feeling at peace that you know he’s safe and one with God? When I was nine, I was playing with Barbies and cried when butterflies accidentally hit our moving car. But here she was, this little girl with the biggest heart and a calm voice. I however, was not calm. Internally I was wrecked, bawling like a typical elementary schooler.

I teared up and looked around to the other counselors, only to see similar teary eyes looking back at me. As we nodded heads towards each other, it was like a wordless agreement between the counselors that we would not let our emotions interrupt this beautiful time and that our lives were forever changed. Juju was only one of the campers who became one of my role models and inspired me to become a bigger, better person.

It is incredible to be part of an organization that brings children and teens together to share this experience with and make each summer unforgettable. This summer, Camp Kesem is providing two weeks of camp so even more kids struggling with a parent’s cancer can finally be a kid again and college kids can find inspiration from 3rd graders. I joined Camp to change lives, but this summer, I can’t wait to see who will change mine.


 

C-A-N-C-E-R

March 28
by
Andrea Everett
in
Health
with
.

The first time I heard the word ‘cancer’ was in the third grade when it was on one of my Words of the Week sheets.


The class received the sheet on Monday and by Friday we all had to know how to spell and the definition of the word. For me, the word itself was easy to spell but rather difficult to understand. C-A-N-C-E-R.

C. I looked up the word and the definition was along the lines of “an invasive and destructive tumor.”

So then, my third grader self had to also look up the word ‘tumor’ and after discovering what it was and putting it together, I realized that this was not a good thing.

I asked my teacher what this word really meant and all she told me that it was some terrible condition that makes a family come together. At that moment in time, I thought this woman was crazy; that’s not what the dictionary says. But as an awkward eight year old I just confusingly giggled and thanked my teacher for her time.

A. My second memory was when a girl I played basketball with lost her mother to breast cancer.

It affected the entire community. I wasn’t even good friends with the girl but I remember wanting to be there for her in any way possible.

%tags Health Overcoming Challenges

I could not imagine losing my motivation, my biggest supporter, my best friend- life without my mom is one I cannot mentally picture. This is when I began to try to understand the definition my grade school teacher gave me.

N. Memory number three came into my life when my mom’s best friend was diagnosed with breast cancer.

This is when my hatred for cancer really started to arise. My mom’s best friend, Donna, is one of the most amazing women on this earth. She is unbelievably intelligent, beautiful, and inspirational. So my main question: how did such an incredible, uplifting woman have such a malicious mass in her body? I understand that life isn’t fair but this was too much. Now I began to actually see what my teacher meant.

C. Relay for Life 2015 became a part of my life because of one of my good friends who made a team and wanted me to join it.

At first I signed up because I wanted to be apart of something here at Virginia Tech (and to make her stop bugging me about it) but after hearing her story, my entire perspective changed. Seeing something truly affect one of my best friends made me want to do something. She is one of the strongest young women I know yet when the word ‘cancer’ is said in conversation, I know it hits her hard. I never fully realized that cancer is so “well known” in almost every household. It made me think about how fortunate I was that I didn’t have a direct hit to the heart.

E. “I didn’t want you to worry.”

Of course when those words came out of my father’s mouth, I knew something was wrong. The summer before my second year of college, my dad said that statement to me. Little did I know that this sentence followed one along the lines of ‘I have cancer in my colon.’

You never think it will happen to you and even when it does, you still don’t believe that it did. It hit me like a cannonball in the gut. I felt like air couldn’t get to my lungs- I could barely speak two words. He ‘didn’t want me to worry’ because I’m a busy person here at college. Yes, I’m a double major.

And yes, I’m in a sorority. And yes, I’m already stressed about being five and a half hours away from home. But NO, these things do not come before my own father. After trying to explain this to my dad he still didn’t agree. And that’s the thing about cancer: it makes everyone who is dealing with it so much more selfless. You don’t want to force it upon other people but you can’t deal with it by yourself.

R. Relay for Life 2016 is where I stand today. After all of my encounters with cancer, I took it upon myself to make sure I made a difference.

Fortunately, I was chosen to be a part of the Relay for Life Fundraising Committee (aka the best one). My relay family is one of the greatest ones I’ve been a part of at Virginia Tech. Each and every one of them has dealt with cancer in some way and they are the most supportive and loving people on this planet. They are here for me through every struggle I have and I am beyond blessed to be apart of such an amazing group of people.

In case you were wondering, I got a perfect score on my Words of the Week test that week, which was expected because I was an overachiever in elementary school. However, I would’ve never guessed that this one word I was forced to learn in the third grade would affect my everyday life and shape me into the individual that I am today.


I can honestly say that cancer is one of the worst things to ever cross someone’s life, but, with support, dedication, and love, anyone can overcome the battle.

Finish The Fight- Relay For Life

January 12
by
Juliana Leczas
in
Inspirational People
with
.

(Written by Juliana Leckszas)


I have been given the amazing opportunity to be on the executive board for the 2015- 2016 Relay For Life at Virginia Tech. I was not given just a board of fellow peers and students to work with to plan the event this year…I was given a family.


Throughout the fall semester we grew from just a group of single individuals meeting each other for the first time into something so cohesive and wonderful. We all complement each other and help each other grow and flourish so that we can put on the best Relay For Life event that we can.

When you are apart of such a big event like Relay For Life especially at Virginia Tech where we are the largest collegiate Relay For Life in the world you always get the question so why are you involved in an event like this. Whenever I am asked this question I could talk your ear off for hours about the many different reasons as to why I want and love to be apart of Relay For Life.

However, the beauty of Relay For Life is that you don’t have to be personally affected by cancer to be apart of the event.

Yes, the majority of people that participate have been affected somehow by cancer in their life whether it be the grandmother had cancer, their dad had cancer, their neighbor had cancer, etc., but you also see the people that come out and participate just because they want to support the cause and that is one of my favorite parts about Relay For Life.

%tags Inspirational People

Relay For Life is about everyone coming together to support one cause and that is the fight against cancer.

One of the main reasons why I relay takes me back to when I was 10 years old. My parents sat me and my older brother down and told us that Grampy had lung cancer. Now, as a 10 year old I had a hard time wrapping my brain around what exactly cancer was and how it was going to affect my Grampy. My parents did their best to explain what was going on to a 10 and 13 year old, but they could only tell us so much.

Finally, the question surfaced, “is Grampy going to die?”

Those words coming out of a little child’s mouth should never have to be said, but my parents knew they had to answer.

My mom was gone a lot the next couple of months traveling to and from home to be with Grampy. We would visit him a few times a month, but each time we went we could see the progression of him getting worse and worse and the visits would get harder.

One day, my brother and me came home from school and our stepfather picked us up from the bus stop. He brought us inside and sat us on the couch and gave us the news that Grampy had passed peacefully in his sleep. The cancer had become too much for his body and he couldn’t hold on any longer.

Tears immediately burst from both of our eyes as we realized that we were never going to see Grampy again. That night we drove to Maryland to be with our mom and the rest of the family to get ready for the funeral.

I will never forget the last moments I had with my Grampy and all of wonderful memories before he was sick.

I relay so that no one has to say good-bye to a loved one because of cancer. I relay because no one should have to grow up without a mom or a dad or a sibling because of cancer. I relay because cancer has taken too many lives.


Virginia Tech Relay For Life has given me an amazing opportunity to make a difference in so many lives. I am proud of what we have accomplished so far this year and I look forward to what the spring semester has in store. We won’t stop fighting until cancer is no more. For more infromation visit vtrelay.org.

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