HAWMC Day 26: Crohn's Chronicles Timeline

A tagline, huh?

Well, I really enjoy the one I have up now: Because Sh*! Happens.

It might be overused, but I like it. I think it sets pretty much the exact mood I look for in my blog. It's just a little profane. It's honest. It's funny.

I was going to try and come up with another one, but I'm deciding as I'm writing this that I'm sticking with it. So there.

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Overwhelming Nuance - Dancing Crohn's Disease

Below is small segment of my Dance Studies Research Project, "Cripping Dance: Radical Representations of the Disabled Dancing Body." It's the bit I wrote about my own work, Overwhelming Nuance (excerpted below), which, as you will see, was inspired by the feelings of denial that so often accompany disease. Nearly four years after I was diagnosed with Crohn's, it flared massively. Lost in the idea that "my disease will not define my life", I ignored for months the signs of the looming crash. This breakdown forced me to come to terms with the reality of my disease. I suddenly understood that the idea that the mind might overcome the body just supported the willful denial of my disease. After this experience, determined to force an openness about disease in my own life, I claimed disability as part of my identity and choreographed my own "crip" coming out.

Chronic Overshare

Every two weeks I take my Humira shot. No big deal. But, a couple days afterward the most wonderful thing happens. I poo. I mean, I take a dump . It's awesome. The thing is, I crap constantly. All the freaking time. Just not like this. This is one of those rare, deeply satisfying, glorious dumps. And I get to look forward to it every two weeks. It's a major source of joy in my life. And what's my immediate reaction every two weeks? What is the first thing I want to do as I saunter triumphantly from the bathroom? I want to tell people. I actively seek out someone to inform of the magnificent crap I just took. I'm genuinely disappointed if no one's around. My poor roommates.

The Trouble with Pep Talks

The scene: You're sitting on a comfy couch having a conversation with a good friend or a family member. Someone you're very close to. Maybe you're having a cup of coffee/tea or a glass of wine. It's been a good night of sharing with someone you trust. The issue you're talking about doesn't necessarily have to be Crohn's, but let's say it is. You're feeling comfortable, so you are very honest about your experience. You decide it's okay, just for a moment, to let go of that tone of optimism you normally adopt when speaking about your disease. It's not that you've actually given up hope, you're just tired. After you finish your tale, your friend/family member looks at you lovingly and says something like, "you're the strongest person I know" or, my personal favorite, "it'll just make you stronger in the end." I've been trying to write this post for a while now, and I've been having a lot of troub

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

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