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I Hate Evan's Guts

Organized by Evan Mundine
Front large extended
I Hate Evan's Guts Fundraiser - unisex shirt design - front
I Hate Evan's Guts Fundraiser - unisex shirt design - back
I Hate Evan's Guts shirt design - zoomed
Gildan Ultra Cotton T-shirt

I may have Crohn's Disease but it will never have me! Help me support the fight for a cure.

Custom Ink
All funds raised will go to Evan Mundine, the organizer for CCFA Take Steps team - I Hate Evan's Guts.
$330 raised
24 items sold of
100 goal
Thanks to our supporters!
$20
Gildan Ultra Cotton T-shirt, Unisex - White
Gildan Ultra Cotton T-shirt
Unisex - White
Organized by Evan Mundine

About this campaign

My name is Evan, I was a soccer player, and in 2011 I was diagnosed with non-responsive Crohn's Disease. I never knew what inflammatory bowel disease was or how life changing it could be. My goal is to raise awareness, help fight for a cure and to live a life that makes a difference.

I'm a sophomore in high school and I was a soccer player who dreamed of going pro. Just about my whole life I've had stomach pains, nausea, and random fevers. Looking back, I didn't know how much all of that impacted my life. I avoided eating anywhere except at my home, because I was never sure when I might get sick, and if I were to get sick, I preferred that it be in my own home. There were times when I'd be playing with other kids at the park when all of a sudden my stomach would start hurting and I'd have to go home to lie down. As I got older I realized that I had to use the restroom more than everyone else. My parents took me to the doctor several times over the years, but after all the check-ups and the tests I was diagnosed repeatedly with anxiety. Even though I never thought that I felt anxious, it was almost easier to accept that diagnosis because my doctor and my family kept telling me that’s why my stomach hurt. It really started affecting my life once I was in elementary school. Kids notice things like another kid who never eats at school parties or at birthday parties. Actually parents notice that too and sometimes it makes adults uncomfortable to have a kid at a party who won’t even eat cake. I guess I was around 7 or 8 when I stopped being invited to friend’s birthday parties. How do you explain that your stomach just doesn’t ever really stop hurting and that food seems to make it worse? As far as my family and I go, none of us knew about Crohn's disease so of course none of us recognized what it really was that I was going through. Crohn’s disease isn’t just an upset stomach that medicine clears up. It can be a very bad life altering and a lifelong battle. And it can steal your dreams. It took soccer from me but I’m hoping to help other kids hold on to their dreams by gaining support in the fight for a cure.

Someone once asked me when I became interested in soccer. I remember stopping to really think about it and I realized my earliest memories were all soccer related. I don't recall a time when it wasn't part of my day to day life. I joined my first team shortly after my 3rd birthday. Within a few years my goal was about learning as much as I could from older experienced players from my club, and of course pro players ,so that I could become the strongest player possible. While my friends would be out skating or biking, I would be working on free kicks or juggling in my backyard. After my 8th birthday I started dealing with regular daily stomach pains. The truth is the only time I could really block the pain was while I was training, playing or watching soccer. Soccer was the only time I felt fully like every other kid. With a ball at my feet I was free from the deep burn in my stomach. At least until I got to be 13. Then it started getting to where I needed to ask to be subbed. Something I didn’t realize then was that running makes your digestive tract move faster. Maybe I would start the game with a slight cramp in my intestines but as I played the cramp would grow in strength. I remember having to stop and hold my stomach because it was just hurting so bad. I wasn’t able to compete at the level I needed to as a select player and I started to feel my dream slipping away.

My dream is for my generation to be the last one to know IBD as having no cure. For me it’s about all the little kids who deserve to have a true childhood. I’ll never know that feeling but if I can help change that for others then that’s good enough for me. I tell people I do the Take Steps walks for now but I fully expect them to become the “We Took Steps” celebrations one day. I believe that day can and will be reached. The day that we will finally be able to say we found the cure for IBD. Please help me in the fight for a cure. Thank you!










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Supporters

Anonymous 5 items
A friend who believes in you! 3 items
Cynthia Cardenas 1 item

Evan's story really tugged at my heartstrings. You can tell his a strong person and one that cares deeply about others. I cannot even imagine what he goes through everyday but it's amazing that he chooses to inspire others with his story. Keep it up!

@Folg 1 item

One of the most positive people I've ever met.

Anonymous 1 item + $10

You arr an inspiration Evan...God Bless!xo

Micheal azira 2 items

Evan is inspiring to me, he has not let this disease define him, instead he is living life and always encouraging other people to live their dreams.

Kandi B. 1 item

I've been following Evan for some time and I want to support him! I'm praying for you, Evan, and I'm praying for a cure!

Anonymous 1 item
Derek Johnson 1 item
M5 1 item

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