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Teema

Updated 1y ago

Newly Diagnosed with UC: So Many Questions, No Answers

I’m newly diagnosed (or almost diagnosed) with UC. Flare up started in the beginning of October and while I’m feeling a lot better now it just feels like there’s a million questions I can’t get answers to. I don’t even officially have a doctor assigned to me yet! I had a quick visit to get established with the practice, a colonoscopy, a calprotectin test, I’ve been prescribed a medication that I haven’t started yet. It just feels like I haven’t really been able to talk to anyone.

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SlipSlide

1y

So glad you reached out! I can’t imagine how you must be feeling right now; I’m sure your mind must be swimming at times as you adapt to this new diagnosis and try to figure out what life is going to look like now. I’ve had ulcerative colitis for about 24 years at this point, and it’s definitely a journey. Two sources that are very helpful are the Crohn’s and Colitis Foundation’s website, and the new Crohn’s and Colitis for Dummies book (not that you’re a dummy; just the name of the series of books 😊). These can help answer a lot of questions you have with your new diagnosis, and can also help connect you with support groups. We’re here for you as well!
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Teema

1y

oh my gosh I love the For Dummies series haha I never knew they covered something like this! I’ve been looking into local support groups too, it just has felt like I have a new question every day.

The content in this post is not intended to be a 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.

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