Crohn's Chronicles: A blog about Crohn's Disease

I went to this panel/performance at Access Living  last Friday. It was on the intersections between disability, race and community. Very interesting. There was one thing that the moderator said, though, that really struck me. It's something I've read and taken note of before, but for some reason hearing it in this context really drove the point home. He made the point that disability and disease challenge the idea of "the individual." In American society, we're pretty much taught to take care of ourselves. Individualism is extremely important to the way we conceptualize our bodies and our minds. The "I" is at the center of the American dream. If I work hard and educate myself, I can rise through the ranks of society. So, what happens to this concept when a body must depend on others to perform certain tasks, or even to make it through the day? This is more of an issue for some types of disability than others. With Crohn's, for instance, as long a...

Possibly worse than feeling awful all the time is feeling great for a while and then flaring up. Okay, maybe not worse, but incredibly frustrating nonetheless. For the first time in years, I have felt like myself for more than a couple months. (Although, as I have come to realize, Crohn's is part of my "self.") I go places and my first thought is not whether there is a public bathroom close by. I wear heels without having to worry whether I will be able to walk the next morning. I treasure these things, which so often go overlooked, because they are not default for me, they are luxuries. For years I worried about these things almost constantly, and I had forgotten how freeing it is to be able to let those go, not entirely, but a little bit. But then some small thing happens. I am stressed about school, rehearsals, or issues in my personal life and Myrtle begins to reflect that stress. The weather changes and my joints freeze up. I get my period and the flare that ofte...