I know a lot of the women on here have battled endo for a long time. I was diagnosed with Stage 3 fairly recently and I would like some opinions from the veterans.
DH and I have been trying to conceive since March of 05. In July of 06, my RE was suggesting that I have surgery for an ovarian cyst that wouldn't go away and mentioned in passing that while she was in there, she would check for fibroids, endo and any other possible problems. I had never had the heavy bleeding that most people associate with endo, but when I did some research on it, I realized that I did have several of the other symptoms.
The day that I went in to sign the consent for the surgery, she did a quick ultrasound to check on the cyst, but couldn't find it. She told me that she thought that the surgery would still yield valuable information, if I still wanted to go through with it. My gut told me that I should.
So she did the surgery and wasn't expecting what she found. First of all, the cyst was still there - the manner in which it was attached to my ovary made visualizing it on ultrasound difficult, unless you had exactly the right angle. Secondly, she saw that I had endo on my bowel, both ovaries and fallopian tubes, on my uterus, behind my uterus, and on my bladder.
I also had two large adhesions - one on my uteruas, and one on my bowel. The one on my bowel had caused my bowel to be moved up a lot higher in my abdomen than it should have been. (I realized afterward that was probably why my PCP couldn't complete a colonoscopy on me - he said that whenever he tried to get the scope past the first bend, I would start screaming. Thank god for Versed - I don't remember a thing!)
The other RE that was assisting with my surgery said that with the severity of the endo, she would have thought that I would have been missing work from the pain every month. Truth is, until after the surgery, I had no idea what "normal" felt like. I thought that my cramps *were* normal.
In retrospect, I've probably had endo since sometime in my teens - I remember that I'd miss school sometimes because of the pain. I was on birth control pills from the time I turned 18 until March of 05 when DH and I started TTC. I realize now that my symptoms improved while I was on the pill, because the pain got progressively worse after I stopped.
Here's my dilemma: I can't afford further fertility treatments at this point in my life. My RE agreed to let me try on my own for 3 cycles, but then she wants me on continous bcps to help prevent the endo from recurring. This means that unless I'm doing a fertility treatment, I have pretty much zero chance of getting pregnant.
I've gone through 2 of the 3 cycles on my own so far with no luck - didn't even ovulate. I'm about to start my 3rd and final cycle - basically, my last chance to have a baby anytime soon.
I don't ovulate very often, so I can go months without a period. I'm really tempted to not go on the pills and to just let my body do what it wants. I'm tired of all the treatments and medication to try to force it to act normally...*sigh*
Deep down I think I know that going back on the pill is the best thing for me right now. I just don't want to admit it. Even though I was lucky and the endo didn't do any bad damage, I may not be so lucky when it comes back... and I'm sure it will.
I guess I'm just looking for words of wisdom, encouragement, or whatever from those who have been there.
Thanks in advance,
Hollie