Could UCers and Crohnies develop BOOP?
I'm unsure if this is a real problem for IBDers. Here's a possibly more legitimate link for Wiki-waries.
I first got pneumonia the winter after my diagnosis. Nothing like BOOP, it began as a cold and then developed into what felt like an iron patch in my chest, pressing me into a doubled-over position when I tried to climb the five flights of stairs to the apartment. I must've looked like such a smoker! But the whole time, I thought, hey, I should go to the doctor again because the first Cobra-covered CT scan had found nothing. They would believe me now, I could barely walk up the stairs. I could barely ... damn it.
They found an eeny spot on the left lung. They gave me a shot. No BOOP, no COP, no Popcorn Workers Lung (though not for lack of trying, mmm...), just a baby pneumonia with no exit strategy.
Still, the idea of BOOP interests me, and not just because it's fun to say. Boopboopboop. But "Bronchiolitis Obliterans Organising Pneumonia" seems to be a related disease, rather than a result of ulcerative colitis or other inflammatory autoimmune disease (as Wikipedia says). I suppose I shall have to ask a damn doctor.
With the pneumonia scare, I met the first general practitioner I've ever liked. He had one ear. Ours was a short, sweet yet blood-curdlingly tragic tale.
I have a history of bronchitis. Also, I used to eat Microwave popcorn, which is apparently almost as bad as smoking for your lungs.
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ReplyDeleteI was diagnosed with UC in April of 2007. In the summer of 2007 I began having a bad, persistent cough. After seeing a variety of doctors, x-rays, a CT scan, and a bronchoscopy, I was diagnosed with BOOP.
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