Thanks for the suggestion Ivy, I found someone who sounds similar to my symptoms. I'm going to check out the article she linked.
It's funny, because when I mentioned briefly on the phone to my (male) GI about how that area was hurting he didn't seem to think of any corrolation, then I see the woman GI and dont even think there's a connection 'cause of what my gyno told me the day before and the female GI was the one who said the crohns can affect that area. I mean, it makes sense to me, seeing as the areas are so close, and my crohns is the worst it has ever been and all of a sudden I seem to be getting new symptoms left and right that are unlike my usual out-of-remission symptoms. But who knows? I hate this. I hate not knowing.
25 year old female, diagnosed with Crohn's in 2002 after being misdiagnosed with Lyme Disease for a year. Have been on Prednisone, Asacol, Entocort, Remicade, random antibiotics (cipro, flagyl, avalox, etc), and Mercaptopurine, (even the lowest dosage was messing up my liver, argh) in the past.
Currently on Predisone and (finally!) just started Humira.