Hi ladies, I’d be really grateful for anyone’s thoughts. We’ve just had multiple FET failures with top quality blastocysts. Over the past few years I’ve had 4 chemicals (always before 5 weeks), maybe 6 (single faint positive with the additional 2).
I want to look in to embryo testing and immune testing, but not sure I can afford both.
Does this sound like more of an embryo problem, or a maternal/womb issue?
As my chemicals always follow a similar pattern, I’ve had no MMCs before, deep down it doesn’t feel like a chromosome thing, surely this would mean you’d have MCs at varying stages?
I read a quote from a well known consultant that said “the most common reason for a miscarriage is chromosome anomalies, but it is not the most common reason for recurrent miscarriage”.
Does this sound like an embryo or womb issue to you?
The only other things we haven’t tested are sperm DNA fragmentation and karotyping.
Thank you xx