I just wanted to reintroduce myself!
I posted here a loong time ago, right after we got the results from my DH's SA, but I have been MIA because we took a break for a while.
Dh has had 2 SA's, both of which were pretty much the same. His count was 1 million, he has a liquefaction defect, and some morphology issues.
We just got some bloodwork results back. They tested for Y Chromosome Microdeletion and Cystic Fibrosis, both of which were negative. Which is good, but it just means we still don't know why his count is so low. We are supposed to make an appointment with the RE in the next couple of weeks, and then I guess we will see what they say. What they had said before is that if all the tests were normal, we would need to go right to IVF with ICSI, so I expect them to say the same. I really don't know what we will do for sure, because I know that is going to be reeeeaaally expensive.
Anyway, thanks for reading!
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"Let us not become weary in doing good, for at the proper time we will reap a harvest if we do not give up." - Galatians 6:9

TTC on our own for over 2 years
Dx with Severe MFI- Blood work shows no Microdeletion and no CF mutations
Ultrasound scheduled 3/22- DONE! Everything looks normal, other than some cysts on my right ovary.
HSG scheduled 4/14- DONE! Tubes are clear!!

On BCP until our IVF w/ICSI scheduled for August!!!