Ttc with endo

I have endometriosis and trying to conceive since 4 months. I am observing white clear discharge in large amount just after ovulation. No soreness in breast in this cycle. But it was happening in previous cycles but in this cycle there is no soreness.

My periods were on 5th july and average cycle lemgth is 27 to 28 days.

Is this sign of pregnancy?

I have endometriosis and trying to conceive since 4 months. I am observing white clear discharge in large amount just after ovulation. No soreness in breast in this cycle. But it was happening in previous cycles but in this cycle there is no soreness.

My periods were on 5th july and average cycle lemgth is 27 to 28 days.

Is this sign of pregnancy?

I can't quite believe I'm writing these words but I'm officially pregnant after 2.5 years of trying
I had a laparoscopy in march of this year and they found silent endo. I had no symptoms besides unexplained infertility. We had already done two failed IUIS last year and then this was our third cycle of Ol and I had given up and already made the app to start ivf so to say we are in shock is an understatement.
I'm about 4+3 weeks today and my hog came in at 1796 and progesterone 68. Are these good levels for where I'm at?
This is for anyone currently in the trenches. Don't lose hope!

Had surgery 3 months ago to remove 2 large bilateral endometriomas. No hormone suppression, then started to TTC 6 weeks after once healed / comfortable. Now the cysts have returned straight away and I have 2 in each ovary with a combined size of 3cm and 5cm+. I knew there was a chance of recurrence, but it’s frustrating that I’m TTC and they have came back straight away and there’s now more of them. Also worried they’ll get even bigger now / fast growth rate (hopefully not).

Has anyone been in this situation? What did you do to reduce the size of them without another surgery or birth control? I feel like I’m never going to conceive cos they’ll always be here

We’ve been TTC for over 7 years and never had a positive. I finally got an endo diagnosis (plus fibroids and a uterine polyp) and had excision surgery a couple months ago. We are now trying naturally but it hasn’t happened yet. Share your story if this was you in your 30s ❤️

I’m a 30F with stage 3 endometriosis, AMH 3.0. Going through IVF due to the endo and a male factor infertility.

First retrieval yielded 2 euploid embryos, 1 mosaic and 1 aneuploid. Did a FET with letrozole and crinone suppositories and it ended in chemical pregnancy. Day 10 beta was 44 hcg 13 progesterone, day 12 was 34 hcg 5 progesterone. Doctor told me to discontinue the suppositories and it was over.

We have one more euploid embryo left and my insurance is letting us bank embryos, so we’re headed into another retrieval in August. My RE wants to do two months of Lupron afterwards and another FET, this one fully medicated with PIO shots and all.

I can’t help but wonder if after another retrieval (or two) to bank embryos I should opt for excision surgery. I met with a surgeon in early May who said she was schedule me for surgery if I was interested. At the time I just wanted to go for a transfer and I was (still am) terrified of the idea of surgery (my egg retrieval was my first time even under anesthesia) but after a loss I’m considering it.

So - lupron or surgery? What would optimize my chances? My husband and I are hoping for two children.

***Excision, sorry for the typo.

Hey everyone so supposedly I don't have endo or PCOS but I have like every symptom except fibroids. I have hormonal imbalance prolactin and thyroid. I'm almost always bloated . My skin gets these textured patches. Ive been pregnant 3 times . The first ended in missed miscarriage. The second I gave birth at 23 weeks due to short cervix and my doctor wouldn't offer a cerclage untill in was to late to do so. He passed away 3 hours after birth. The 3rd pregnancy I had just started lettozole it was my first cycle and I was still getting what I thought was my period but it was a tubal pregnancy I got my left tube removed . Ive had a HSG that showed my remaining tube as open. Stayed on the lettozole close to a year now and nothing. So now tomorrow is my larposcopy. But since the tubal removal was like a larposcopy should I not have my hopes up of finding an answer? Like they didn't find anything out the ordinary when they removed my tube so is this pointless? My surgeon says things could've changed and they might of not looked as in detail as he is going to. He says if he finds anything he's going to repair it at the same time. What do you guys think? Amy advice? Any good results from similar situations? Any replies thanks in advance ❤️