Accidents with IBD
However, living with a chronic illness like ulcerative colitis has made me have to talk about crapping and other bowel habits. I only really talk about it to close family and doctors but still... it has made me have to be very knowledgeable about something I never ever wanted to even think about.
Accidents and urgency with Crohn's or UC
I wanted to write an article about having accidents because of IBD since a few people mentioned it in the comments section on our Facebook page. Whenever things are brought up, I like to bring them to the surface so even those few people know they are not alone.
Given Crohn’s disease and ulcerative colitis come with intestinal inflammation, sores, fistulas, among other things, it is not surprising that one of the symptoms of this disease is urgent, frequent diarrhea.
When I use the word “urgent,” I mean that sometimes a person with IBD has about 20 seconds to get to a bathroom. And given that isn’t always possible in the least bit, accidents unfortunately occur.
Accidents because of UC are embarrassing & mortifying
The possibility of them can make a person afraid to stay anyplace overnight other than home. This hinders a person’s social life.
While inflammatory bowel disease (IBD) is hardly just a bathroom disease, it can affect a person’s bowel habits a great deal. It does become very scary and anxiety-provoking.
Plus, accidents are supposed to happen when we are potty training, not NOW! This can really screw with the mind, in my opinion.
The mental impact of symptoms like urgency and accidents
I am not someone who is ever going to tell you to just “go out and live and if you happen to crap your pants, just move on!” because I personally would never want to hear that from anyone. It shows such a lack of understanding and empathy. I also am someone who doesn’t respond to tough love since I am tough enough on myself already.
So I am not going to give anyone reading this a tough love spiel. While I don’t have any amazing words of wisdom other than “you will get through it” - that doesn’t negate the physical and emotional turmoil that often comes with Crohn’s disease or ulcerative colitis.
This also brings up an entirely different subject about eating and diet. I highly encourage you to read some of those on our website if you are feeling kind of alone right now or if you just want to have a better understanding of how IBD impacts so many aspects of a person’s life.
Has this part of life with Crohn’s disease or ulcerative colitis impacted you a great deal? Can you relate at all? Have you been able to manage your disease better? If so, did it take a while to gain back some confidence? Or, do you still struggle with that part of things? Share your thoughts with us!
What is your comfort level disclosing your IBD to your employer?