o.k. i need to have some opinions from cysters that have or had endo...or thought that they did...
way tmi...but during sex...W/O a condom sex hurts afterwards...but with a condom everything is fine...could be the lubrication thing...which I can agree with....but my sides hurts...it is kind of the mid. of my stomoche on the sides...my pcp thought it could be endo back in July and to talk to gyno about it....but once I quit my job the pain went away....gyno and I both agreed that the pain was probably caused from the stress of my job...now when I am stressed the pain crops back up...
The ? is next week I have a appt. with gyno to talk to him about endo...does anyone think that with the symptoms that I have that it could be endo?
Please any advice/opinions would be greatly appreciated! Thank you so very much!
I would think it'd be painful w/ or w/out a condom if it was endo. The only way they found out I had endo was from severe period cramps and heavy periods. They did a laporoscopy and removed some. Unfortunately it comes back. It's worth checking w/ the doc though. I also know that when the endo was sticking everything together internally, I was having bad colon/stomach pains and that would make other events not so fun. So if you had endo that could be what's going on too. Good luck and let's hope it's not endo and that it was just stress!
This might be something so simple it hasn't been thought of. Could you have a bacterial infection? Or even a minor yeast infection? I've had the same problem (pain only when he ejaculates inside me, but not otherwise), and that's what it was.
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first of all you shouldnt be afraid to talk to your doc about anything its always best to have an open relationship with your doc they hold your life in their hands you know.second of all like everyone said it could be just stress or something simple like an infection but if i were you id still ask the doc.i have endo and its the total opposite with me during intimacy i cant feel anything so ask your doc everyones different. Kat
Calches - The only true way to EVER know if you have endo or not is via a surgery (laparoscopy). Its frustrating... but true. The tissue does not show up on any tests/bloodwork/ultrasounds/etc... Now, Doctors are siding toward Lupron shots over the idea of surgery. Both are scary to me. I have endo and had a Laporoscopy over a year ago to remove it from my ovaries (like they weren't under enough stress with PCOS!). Rather than going back for another surgery... my doc wants to try the shots. I'm going to go have a second opinion after my PCOS symptoms calm down. I know what you mean about the sex. With a condom was not nearly as painful than without. Later I learned that I'm alergic to my husband's sperm! How crazy is that! Endo does bind everything up though... but it all depends on how serious your case may be. I have it between my bladder, uterus, and colon. A more invasive laporoscopy to remove that tissue would be to invasive. I guess I just want you to understand how different everyone's case is and let you know that we are here to support you. Any questions you my come up with about Endo... feel free to ask. We can share our stories, but just know in your heart that yours is unique and not let anyone else's scare you. Best of luck.
scared to talk to dr. about endo.... 
