Hello, my name is Kristen. This Hirschprung Disease blog all started because of a project for my Anatomy & Physiology class. We all picked a disease or illness that someone we knew had and then interviewed them. My brother had hirschprung's disease (HD) about 20 years ago. I've always known that he's had to suffer with this disease but I never could fully understand what he went through. I'm certainly not saying that I can now because I personally didn't have to go through with this disease. However, I feel that now I know more about him and the problems he's been through, and he sure is a trooper!
I wanted to make a blog for the people who've had to deal with HD or is dealing with it right now. This blog with be fairly informative and have to stoma bag suggestions (from my mom) and stores for those of you who are looking for some. I hope that questions and stories are shared for those of you who are interested.
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