Hello all! I just wanted to quickly invite you all to check out my new guest post, Figuring Out the Body-Mind Connection, over on Every Person Is A Philosopher, the Neighborhood Writing Alliance's blog. They are a truly wonderful org that I have the pleasure of volunteering with every once in a while. Anyway, please head on over there, read the post, and leave some lovely comments if you feel so moved!
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.
I was diagnoed with chrohns at age 33, other than a few hospital stays a year I have been able to manage it with ibuprofin. I had surgery on my shoulder and was on pain meds for a few months. Now that I have been off meds I cant eat without hurting really bad in my stomach and having diareah within minutes after eating. I feel feverish and weak. I cant take asacol and have heard the remicaid infusion can cause heart attacks. This is interfering with my life. Are there any new uninvasive treatments?
ReplyDeleteYou've been nominated for a Liebster Award :)
ReplyDeleteFor more details check it out here: http://fibrovslife.blogspot.com/2013/07/the-liebster-award.html