I was wondering if others also suffer from severe diarrhea despite not having the endo in the rectum.
I have been diagnosed with Endometriosis in the Pelvic Peritoneum and Endometriosis uteri.
My doctor said that the diarreah shouldn't be related to my endometriosis.
But it always comes before my period and after my lypo last year it went away for some time. After half a year it came back though as my other symptoms have. (Trying a different contraception pill now to get it in control)
So I am sure the diarrhea (coming with cramps & leg pain) is related to the endo. Does anyone else with Endometriosis in the Pelvic Peritoneum have these symptoms?
And if so, have you found any diet change to help?
I can deal with my other symptoms, the constant pain in the lower stomach and in the lower back, or just the general feeling of being tired and weak.
But sometimes it hits me out of the blue, when I'm at work or out. It hurts so much that I need to stop what ever I'm doing and (if I could) just lay down till it is over. But if I am in meetings that's obviously not possible. I don't want anyone to know what's going on in those situations but it is hard to deal with especially since I know I will need to find a toilette within the next 10 minutes. I tend to just press on my stomach to suppress the pain somehow. But then I will not be able to concentrate on the situation around me (like the meeting).
I really just want to find out if there are girls out there who deal with the same problem and if so, if they have tips of how to do it better.
I appreciate your comments.