My name is Hannah, and I’m a twenty-year-old college student
that just so happens to have Ulcerative Colitis.
And just what is Ulcerative Colitis?
I describe it to most
people as an autoimmune disease that causes ulceration and inflammation in the large
intestine; a type of Inflammatory Bowel Disease (IBD) similar to Crohn’s Disease but
localized in the colon. While this is an accurate description, the disease—and what
those of us with IBD go through—is not so simple.
With Ulcerative Colitis, going to class, going out, meeting
up with friends, eating food, and even just getting out of the house suddenly becomes
complicated. It’s not just the disease that we “UC-ers” have to deal with, but also
side effects from medications and being more vulnerable to certain infections. Not
to mention the sheer amount of pain that
the UC can cause when it’s active. Because an exact cause has not been
determined and the only “cure” as of now is to surgically remove the colon, we
are forced to deal with a lot of unpleasant things that can make a person’s
life quite a bit more complicated.
I find that most people I talk to, if they have heard of Ulcerative
Colitis at all, usually have only a vague understanding of Irritable Bowel Disease,
and more often show greater recognition of the label of Crohn’s Disease. While
it is easy to define Ulcerative Colitis, it remains a challenge to truly convey
the magnitude of the disease; especially when your outward appearance may not
reflect the chaos transpiring in your colon.
Thus, I’ve decided to begin this
blog to share my experiences with other people who have UC, as well as provide
a more personal insight to people without the disease that might be curious to
learn more about it. I hope to help raise awareness about IBD and, with any
luck, this blog may serve as helpful to others that also suffer from this
disease!
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