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The Sick Adventures of a Semicolon Girl

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About Me

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Hi, I’m Julie and I’ve had Crohn’s Disease for almost 20 years. I’ve been in and out of the hospital, multiple surgeries, nearly lost my life, and currently, have an ileostomy (after having two colostomies). I am more than my disease, follow me along as I discuss the ups and downs of life with a chronic illness.

Why Semicolon Girl? Well, after having multiple surgeries I’ve had portions of my colon removed, leaving me with a “semicolon”. Get it? I crack myself up sometimes. I even have a semicolon tattoo. I own it. *Update* I no longer have a colon, but No Colon Girl just doesn’t have the same ring to it.

This blog serves many purposes for me, first, it’s an outlet, second, I want to share my stories with others that might feel alone and isolated and last, I want to try and normalize the conversation when it comes to IBD. Talking about bowels and being sick has always been taboo in the past, but if we don’t talk about it how can we get through it?

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Follow me on Twitter , Facebook, and Instagram for more fun stuff.

Thank you for taking the time to read my blog.

Medical Disclaimer: This content is not intended to substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this site.

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Medical Disclaimer

This content is not intended to substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this site.

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