Another angel on my list...and questions.
I have to do a D&C this time - never had it for my last four mc because my body did it all on it's own. I know this has been posted numerous times...but can someone give me an idea what to expect for the D&C?
I guess the only 'good' thing I can see in this right now - and it's no guarantee - is that there's a university here that has a huge genetics program, and they've advised that if the dr can do the D&C w/o totally destroying everything, they can try to do genetics testing - even on a 6w size embryo - to see if it's a genetic cause or not. Not that that can answer for the other four - but at least if I know this one was genetic or just my ****** up body (sorry...I'm a little frustrated and bitter right this minute) it gives me some place to start looking.
I was drugged up to the gills on this one - progesterone 3x a day, lovenox 1x a day, 2 baby aspirin a day, folic acid coming out my ears...and still the same results. Of the 5 mc now...three have been within 1-2 days of exactly 6 weeks. One was 7.5 weeks, one was about 8 weeks...but the last two, even though there was a hb at 7.5 and 8 weeks, were small for their 'age,' lagging several days behind where they should have been.
I talked to the dr whom I saw two years ago - after mc #2 - at Oregon Health Science University. Before I even mentioned the D&C, he told me to get one done and have them do genetics testing and to call him back with the results of that. He said that if it shows a genetic problem, they will assume that's the cause of this miscarriage...but if there's nothing in the genetics, there are not a lot of tests left that they can try...that it would just be a matter of finding the right 'treatment' for me. I've no idea what 'treatment' is left if they can't even confirm the reason...but don't have a lot of choice on 'waiting and seeing' what the results of the testing are - if they're able to do it - then see what the OHSU dr says about alternative treatments.
I asked the dr I was seeing here for this pregnancy re IVF and doing the genetic testing (which is also available here for reasonable prices) and she said that w/five mc now...she does not think that it's genetic...that she thinks it's something to do with my blood clotting mutations. She said I could do the IVF...but that it's just a 'business' to the IVF drs...and that there are still no guarantees. I'm looking at it more that if I did the IVF w/the genetic testing...at least I'd know if I mc'd again that it was not a genetic thing and that it was definitely my body causing the problems. It's also a matter of convincing DH - who waffles back and forth re IVF - to do the IVF and give that a try.
Holly
January 2008,
July 2008
December 2008
July 2009
September 2010
July 2011
Mom to Khaled
Holly
January 2008,
July 2008
December 2008
July 2009
September 2010
July 2011
Mom to Khaled
Thanks Jenn. You hit the nail on the head...the emotional part is the part I'm dreading most. I don't know whether to hope the testing comes up with something genetic or not. If it's not...then what are the alternative treatments...and if so...then will I be able to convince DH to do the IVF. Right now - because we're both an emotional mess - he's telling me 'whatever you want,' but will he stick to that? We'll see...I've got time to worry about it.
Holly
January 2008,
July 2008
December 2008
July 2009
September 2010
July 2011
Mom to Khaled