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.
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?
- 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 🙂