SND - that sounds like good development to me, concerning your follies ... and I am pretty sure that number will increase a bit by the time of your ER. Shooting pains I haven't had near my belly button for any of the tries, but like Getting says, everyone's different.
Heidi - that would be fine for me too - being able to see the first page and then continue the conversations, I guess it doesn't really matter where we do that... Wow - we really must have broken some record
So the doctor really took his time with us yesterday. In his opinion, this really just is a case of embryos that are chromosomally abnormal and that they for this reason just don't carry on developing / it doesn't lead to a viable pregnancy. He says it is impossible to know whether this is due to the really poor quality of sperm - or if perhaps my eggs contribute to it.
Both of us are chromosomally normal - however that doesn't mean that our "produce" has to be. It is a question of chance really and we have so far just been unbelievably unlucky. He does believe it will work, that we are on a good track, since for our last two tries, our embryo development has been so much better than for all the other 6, so we are doing something right.
He showed us a study of a lady, quite a bit younger than me, who had had 2 miscarriages, followed by a baby, followed by 4 miscarriages. She was tested to see how her chromosomes are and it turned out that two (#4 and #14) were abnormal. For her, that made no difference, but it clearly seemed to have an effect when she wanted to have children. So they stimmed her, managed to get 5 blastocysts, which they then did PID on. Turned out, that for four of the embryos, there were some chromosomal abnormalities (one had chromosome #9, another had #2, #4, #14, a third had all sorts, only including #14 and a fourth was all over the place) - the 5th was healthy and that turned into her baby - it worked. But the analysis of their "produce" showed, that there wasn't a link between her abnormal chromosomes, since the result of their chromosomes was totally different.
Now we had already considered doing PID for us - however a) they can only be done on blastocysts and our history of blastocysts hasn't been that great and b) our clinic can't get the genetic analysis done in 24 hours which means that it can't be a fresh transfer ... and based on all our tries, it is very clear that our frozen embryo development has been significantly worse than fresh development - and we want to avoid freezing and thawing if we can. Our doctor also said that PID is horrendously expensive, so at this point he wouldn't recommend it. Especially, if he looks that the first few tries that we had, what was transferred really didn't have that good a chance and it is only our last couple of tries that we should "count" - which would mean, that I am still well within the statistics of how many blastocysts and average woman my age needs to get pregnant.
Finally, he recommended that DH go see a different urologist to see whether he recommends doing a PESE / mTESE - just in case the developmental issues are linked to how poor the sperm is. DH just rang that he has an appointment at this other urologist next week Friday.
So I have the prescriptions for the meds ... after AF comes, I will start stimming again on day three (seeing that I ovulated day before yesterday, I guess that is in roughly two weeks, give or take a day or two).