Welcome to the Endometriosis Forum.
When I read your story it reminds me a lot of me. I was diagnosed with Endo at 27 but lived with it for 14 yrs undiagnosed and I had symptoms from the age of 13.
I was diagnosed with mild dysplasia around 4 yrs ago. I had 2 paps that show mild grade cells, doctor wasn't too worried about it but I was because all the health conditions I have had. Long story short I was diagnosed with high grade lesions which were removed and came back again. I was bleeding every time I had sex which can be caused by dysplasia, Endo, Adeno, cervical erosion, STD etc. Finally had a leep to remove it as it was persistent.
So that being said it is possible the bleeding is from the cervix or a variety of things. I read this over and over again to try to figure out what was causing it and for me it was the cervix http://womenshealth.about.com/cs/menstruation/a/bleedaftersex.htm
If it doesn't show the link I will message you it. :)
When you were on Yaz did it help? Sometimes being on a BCP masks the Endo symptoms.
When you orgasm does it hurt or you bleed when you orgasm?
Hey there-
Given your symptoms I would say that yes, these are concurrent with endometriosis symptoms. You need to see an endometriosis specialist. The only way to conclusively determine endo is through laproscopic surgery. It very rarely shows on any ultrasound, mri, ct, or xray and certainly not in blood or pap tests. I had HPV and cervical cancer when I was 19 which I had 3 surgeries for. 10 years later I was still having terrible symptoms (like you described to the power of ten) I completely lost my ability to function- could not work, or perform basic daily activities, sex was a no-go. I also have Crohn's disease so the docs passed it off as that until my scopes started coming back normal. I was finally referred to a pain specialist who listened to my symptoms and story and found it almost identical to that of his wife. He referred me to one of the best obgyn endometriosis surgeons in the country and she performed the surgery- confirming that I had stage 4 endo and it was absolutely everywhere- on my uterus, bladder, bowel, etc. I had two excision surgeries, the last in 2010 and was symptom free for 3.5 years. My symptoms returned 6 months ago and I am to have another surgery this summer after which I hope to conceive immediately.
Know that you are not alone and this is a disease that few docs understand, and can only be diagnosed through a lapreroscopy. You have to do a lot of research and find a good surgeon. Be a strong advocate for yourself (the squeaky wheel gets the oil) Seriously, this disease is insidious and took 7 years from me. The only way to relieve the symptoms is through excision- not laser surgery, not medication. So fight to get heard. You deserve it.
Keep posting- here for you...
Lu