EDIT: I will one day revisit this topic...in a more eloquent manner.
Oh hey, I have Crohn's disease (warning: there are some pictures, a few of which are not for the squeamish). That might sound casual but that's kind of how I live with it. Every eight weeks or so my symptoms flare and I think "oh yeah..." This isn't to say Crohn's isn't a big deal, I mean look at those pictures...it can be a huge deal (e.g. stomach/colon/intestine removal, extreme diet change, bag for a stomach, etc). But I've been lucky, what can I say. I had great doctors that found it, found what drugs worked for me, health insurance to cover it, and I've been good for 4 and 1/2 years, ish.
I used to get infusions of Remicade (my personal miracle drug) every 12 weeks and the last month before my treatment I would start feeling terrible. When I couldn't stay awake during class, or even get to my morning classes on time, or would be late for work, (fatigue from Crohn's is a big kick in the teeth for me), or would regret eating because I knew eventually I'd have to go to the bathroom, I'd get frustrated that I'd acted so nonchalant the eight weeks prior. Then I realized the disease was nonchalant for the eight weeks prior, there wasn't really anything I could do about it. I wasn't about to wish for a more extreme case of Crohn's (I'm not that masochistic) so there was maybe the most troubling part of my illness: that I couldn't claim it all the time, because most of the time, there was nothing to claim.
But then, I actually got to talk to a doctor who made my treatments more frequent and now my bleed-through might be a few days, (which still suck, but it's better than a month) but nothing too extreme. Today I got my infusion at a new place, and it was good. The nurse was really nice, I was in a room by myself, the IV didn't start itching or hurting, and I just studied French for 2 hours.
So now you're saying "Laurie, get to the point." I guess I can't stop thinking about how lucky I am. Sometimes I almost feel guilty, people hear I have Crohn's and start gushing about my life, trying to alter potlucks around my "eating habits", and I have to clear my throat and say "actually, aside from the ridiculous financial aspect of this garbage, I'm 98% fine. Sometimes if I eat too much candy/ice cream/soda, it bothers my stomach, whereas before it didn't. ...Sorry." (seriously, I never got sick from excessive junk food before Crohn's...it was a mind blowing gift). I'm sure there will be complications later in my life (there just has to be...I'm just going to bank on it) and I should count all financial garbage (I keep saying garbage so I don't swear about it...garbage) as sickness enough.
But when I Google Crohn's out of morbid curiosity, and I see people with massive scars and attached to bags and listing their restricted diets, I just close my internet browser and sit outside for awhile.
2 comments:
So not stupid! I demand that you remove that edit! I will not have people saying things like that about people that I love. <3 :)
Done and done :)
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