Living with UC? Tell us about your experience. Take our survey here.

Every day is a different day

Diagnosis came March 1999. Over the years, it has definitely been a challenge. People say "I can only imagine". Well, I'll have to disagree with that statement. No one has any idea what this is like. I've been through too many colonoscopies, plus trying so many biologics to count and trying a new one now. Without prayers from my Father and Mother-in-law, and my husband's always there for me, what can I say. Stomach pain is the worst pain. I think with this stuff, it's the worst. It effects so many things, your eyes, joints, Nausea, cramping. etc. The lists goes on. I just hate that little children have to deal with this. We will overcome, with God's help nothing is impossible.

By providing your email address, you are agreeing to our privacy policy.

This article represents the opinions, thoughts, and experiences of the author; none of this content has been paid for by any advertiser. The InflammatoryBowelDisease.net team does not recommend or endorse any products or treatments discussed herein. Learn more about how we maintain editorial integrity here.

Join the conversation

Please read our rules before commenting.

Community Poll

How open are you about being diagnosed with IBD?