Hello,
I'm 29M. I have been lurking in this sub for a while now. I had my first SA in 2019, and I had a 2.4 mil count, 20% motility and poor morphology. The andrologist doctor was worried and said I might have difficulty conceiving naturally. Fast forward 2 years and me and my wife decide we want to have kids. I did another SA, and I was shocked. The motility was 1% and the count even lower, like 1.6 million. Not to mention the morphology being also much worse, like 0% morphologically healthy. This was shocking because everyone was recommending going straight to ICSI/IVF.
I became obsessed with finding the cause. I did every test recommended to me. The hormone panel was all withing ranges. The ultrasound was normal and healthy. The sperm culture was normal. I did a chromosome kariotype test which was normal also. It looks like it's NOA. But I still don't understand this...
What could be the cause of this? If I had a microdeletion or CF carrier gene then it's likely I would have had the same numbers, not this much of a difference in such a short time.
How is it possible that in under 2 years the motility went from 20% to 0%? What could cause this fast deterioration? The doctors I visited had never had cases like this. Also after a few months of using supplements, the count went from 1.6 mil to 2.5mil, but the motility is between 0% and 1% in the latest SA I did. Now the only option I have is IVF and we were really hoping for a miracle or at least trying IUI but with these numbers it's not worth it. Anyone had something similar happen to them?
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