I'm looking for a bit more info on endo & fertility -- beyond the idea that it is bad!!
I have stage II/III endo w/adhesions & cysts + adenomyosis & adenomyomas + fibroids, but my tubes are good, my general uterine & ovarian appearance & function seems fine (none of the growths are blocking anything, the shape is good, etc). I don't seem to have a lot of bowel or other endo involvement. My main symptoms are terrible periods, pain in my left side with ovulation & bleeding of any kind. I had a LAP in October 2009, & I already have quite a build-up of stuff, & my left ovary is again pasted to the wall (but still works fine). I am EXTREMELY lucky to have only started having symptoms a few years ago, & I do not have such terible ones at that, so I am not complaining.
We are constrained to IVF with ICSI due to severe male factor. My eggs SEEM perfect, but we have never done genetic testing of embryos. We've done 2 fresh & 2 frozen transfers, & it hasn't taken so far (either 3-4 total failures or 1-3 chemicals, not sure as I was doing hCG injections afterwards so positive betas were unable to be believed). I am also 41, so even if things look good & AMH is fine, we know that there is less chance of OK eggs.
Before this last FET, I was put on continuous birth control for 3 months to "control the endo-induced inflammation." The drugs were not strong enough & I bled for 40 days before the doc finally doubled the dose. (Don't have a lot of choice of BCPs as I have some allergies to excipients.) This at least stopped bleeding, but I hated the side effects, & not sure if it worked to calm the endo, but whatever. I know that the more accepted treatment for endo is to do agonist injections for 3 months, but due to my age my doc didn't want to do it.
My lining is very slow-growing for a FET, altho it ends up fine. I also don't seem to metabolize hormonal supplements well -- we always have to up the doses of oral estrogen & change to mostly suppositories before my lining grows.
In preparation for my 4th WTF appt on 4th February, I am trying to get my head around what we may be doing wrong & right, what our chances are (we've NEVER been quoted chances, except that we've been told it is impossible to get pregnant without ICSI due to the MF), if my endometrium is just no good do we have to forget even about donor options, etc. etc.
Are there any recommendations for testing to be done? Treatments that are supposed to help? Chances of getting pregnant if you have endo? Things to avoid? How do you know when a failure might be due to endo? Is there a way of measuring the inflammation or other endo effects?
Any ideas would be fantastic...
I have stage II/III endo w/adhesions & cysts + adenomyosis & adenomyomas + fibroids, but my tubes are good, my general uterine & ovarian appearance & function seems fine (none of the growths are blocking anything, the shape is good, etc). I don't seem to have a lot of bowel or other endo involvement. My main symptoms are terrible periods, pain in my left side with ovulation & bleeding of any kind. I had a LAP in October 2009, & I already have quite a build-up of stuff, & my left ovary is again pasted to the wall (but still works fine). I am EXTREMELY lucky to have only started having symptoms a few years ago, & I do not have such terible ones at that, so I am not complaining.
We are constrained to IVF with ICSI due to severe male factor. My eggs SEEM perfect, but we have never done genetic testing of embryos. We've done 2 fresh & 2 frozen transfers, & it hasn't taken so far (either 3-4 total failures or 1-3 chemicals, not sure as I was doing hCG injections afterwards so positive betas were unable to be believed). I am also 41, so even if things look good & AMH is fine, we know that there is less chance of OK eggs.
Before this last FET, I was put on continuous birth control for 3 months to "control the endo-induced inflammation." The drugs were not strong enough & I bled for 40 days before the doc finally doubled the dose. (Don't have a lot of choice of BCPs as I have some allergies to excipients.) This at least stopped bleeding, but I hated the side effects, & not sure if it worked to calm the endo, but whatever. I know that the more accepted treatment for endo is to do agonist injections for 3 months, but due to my age my doc didn't want to do it.
My lining is very slow-growing for a FET, altho it ends up fine. I also don't seem to metabolize hormonal supplements well -- we always have to up the doses of oral estrogen & change to mostly suppositories before my lining grows.
In preparation for my 4th WTF appt on 4th February, I am trying to get my head around what we may be doing wrong & right, what our chances are (we've NEVER been quoted chances, except that we've been told it is impossible to get pregnant without ICSI due to the MF), if my endometrium is just no good do we have to forget even about donor options, etc. etc.
Are there any recommendations for testing to be done? Treatments that are supposed to help? Chances of getting pregnant if you have endo? Things to avoid? How do you know when a failure might be due to endo? Is there a way of measuring the inflammation or other endo effects?
Any ideas would be fantastic...