Crohn’s and the Endurance Athlete

Hi everyone! I hope you all had a good weekend. Today I have a little something different for you… and I hope you can learn a little something from it!

Last week was Crohn’s and Colitis Awareness Week (sorry a little late…oops). Someone very close to me has been affected by Crohn’s disease. They also just so happen to be the very same person who introduced me to the world of running, cycling, and duathlons. Crohn’s disease is a chronic inflammatory condition of the gastrointestinal tract. Crohn’s most commonly affects the end of the small bowel (the ileum) and the beginning of the colon, but it may affect any part of the GI tract.

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This would be my boyfriend, Drew who has been living with the disease for the past 5 years. He was kind enough to let me interview him and share his experience through diagnosis and living with the disease currently for this post. Drew started getting into cycling and duathlons a few years ago, and has been able to keep training and competing despite this annoying disease. Our hope in this little interview is to maybe enlighten others on the fact that you can certainly tackle the endurance world if you have Crohn’s.

When were you diagnosed with Crohn’s?

I was officially diagnosed with Crohn’s in August of 2007, which was my freshman year of college. I had been dealing with extreme fatigue symptoms and bowel issues for a few months before blood work finally showed that I was extremely anemic for a guy my age even lower than a girl. After that they ordered a colonoscopy and once they put both of those together they realized I had Crohn’s. Mine happens to mostly effect my lower GI tract.

Did  these symptoms occur out of no where or had you always had stomach issues?

I feel like they really came out of nowhere. I never had stomach issues growing up and they hit me all of a sudden.

How was the first year of dealing with Crohn’s?

Actually after the diagnosis, my whole freshman year the symptoms were under control. I was on a type of anti inflammatory. However, for whatever reason, right as the summer began I ended up with my worst flare up. I landed in the hospital for 6 days, no solid food had a colonoscopy and upper GI. Sometimes I go for a long time with no issues and then sometimes I feel like it wont stop. A couple months ago, I needed to go to the ER because the pain, cramping, and nausea in my stomach was unbearable. Once you start having a flare up and your stomach starts cramping you hope that its just something small and will go away. When they start getting extremely intense and you start vomiting and you can’t control it, you know you’re in trouble.

So, basically Crohn’s is very unpredictable. How does this affect your daily life?

It is very unpredictable. I know the foods that set me off but there are times where you could go from feeling great to absolute crap in about 30 seconds. It affects my daily life being constantly worried on how your going to feel especially with important days and work. It sucks to always be tired and not know how your going to feel. Also, with the bowl problems that are associated with it…They can be unpredictable and embarrassing at times. When your in the bathroom for 15 minutes everyone knows what your doing… not fun.
Being that you are an endurance athlete, how does Crohn’s affect you during your training or race performance?
Well obviously low iron (anemia) means less oxygen to muscles which is counter productive to anything endurance related. Days when your just so tired makes training extremely difficult or impossible. Also, crohns is trigered by stress so when race day comes around your nervous that stress might set off a reaction or symptoms which is the last thing any one wants.  Long training rides where you go for 3 hours can be really tough because you hope you don’t have to go to the bathroom and your out in the middle of no where. Really just trying to keep up with people who are equally trained and in equal shape makes it difficult when your anemic and tired your just at a disadvantage at any endurance sport when you have low iron. I take iron supplements but they are very rough on the stomach and really don’t seem to make a dramatic difference so it gets frustrating.

Well, that doesn’t sound fun… What is it that gets your through the tough training and what keeps you doing it?
I like to do it. I enjoy riding bikes. I’m part of a group in PA and I’ve met so many great people who share the same interest. Riding a bike is a great stress relief and gives you a different perspective of things around you that you dont get while in a car. It something i can do with my father and we both love spending time together.
DrewDuBike
So basically you giving a big screw you to Crohn’s and doing what you like right?
Exactly! You can’t live everyday afraid to get out of bed becasue your scared about how your going to feel. If you let it control you your just going to go insane.The first time I was in the hospital my parents and friends where very scared and nervous for me. But my rationale is that it could always be worse and i could have some worse disease or illness. Thats what i say to myself every time (or almost every time. Sometimes you cant but help feel a little sorry for yourself) it could always be worse. Im lucky i have parents that help me and have taken me to doctor appointments, found me doctors, driven me to the ER at 3:30 in the morning and ruined a camping trip. Oh, and an amazing girlfriend who helps me and understands that I just have bad days. (I didn’t pay him to say that- I swear 😉 )
Any tips for people with Crohn’s or GI issues who want to try endurance sports?
You can’t let it control you. Your going to have bad days and those are the days where the bike stays leaning against the wall and the running shoes stay in the closet. And you just have to say to yourself that tomorrow will be better and I’ll go after it tomorrow. Im not a sponsored athlete and no one is paying me to do this. I do it because  I enjoy it and you can’t let Crohn’s ruin it for you! You just have to listen to your body. If your feeling good, go for it. If your feeling crappy (haha- sorry), cut it back.
DrewDuRun
  • Any questions? I hope you all learned something and for anyone dealing with the disease know that you can also do endurance sports. Drew has gladly agreed to answer any questions you might have 🙂
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13 thoughts on “Crohn’s and the Endurance Athlete

  1. Really interesting post! And great attitude to it all! It woukd definitely make everything tough sometimes, let alone endurance comp! But you’re right do what you love and be grateful for what you do have!

  2. whoa I had no idea he had Crohns. Just last year my close friend was diagnosed and after spending nearly 3 months in the hospital and having to drop out of school he is finally able to get his life back together. it was scary to see how bad it could be but now he is learning how to live with it and best of all be that kick ass swimmer he was before it. Congrats to Drew for seriously pushing past a lot of the limitations it has

  3. This was so informative and so interesting to hear how it affects him…i can’t imagine having to deal with that on top of the normal adjustments of being a college freshman! thanks for sharing, Drew 🙂 … I act like he knows who I am… whatever.

  4. I have Cohn’s too and I actually had my large intestine taken out because of it (it twisted into a knot)… Sadly, taking my large intestine really only made things worse, but luckily my positive mind set about everything really helps me get through the pain, gas, bloating, etc… And I honestly just make fun of myself when I have flair ups (pain makes me even more of a comedian than I alreayd am for some reason lol)

    • Wow, thats one of my biggest fears with crohns, that it will progress to the point of surgery and partial or whole intestine removal. All you really can do is keep a positive mind. Stressing and worrying about it only makes things worse.

  5. This was such an informative post and your man has a good attitude about his disease! He’s right, it could always be worse. No one likes to think about the people in the world suffering worse than you but sometimes that’s all that makes me feel better. I was SO down on myself when I had a month of GI issues this past fall but now they are gone, and I think back to how down I was and wonder how I could’ve been when people like your bf live with this all the time! This post is a great way to raise awareness.

  6. What an amazing, inspiring, motivating & informative post. It was so great to read what Drew had to say in regards to Crohns. I give him the utmost credit for always remaining positive in regards to his situation!

  7. DUde I had no idea Drew had Crohns! He’s so badass! And now he is officially even more badass. You may tell him I said that lol. This is really great info, too – one of my best friends just got diagnosed with Crohns – she’s a runner too and she’s been devastated over it. I should have her read this, I think she’ll be relieved and motivated 🙂

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