Hello ladies,

missbec recently mentioned a list of miscarriage exams in one of her posts, I did most of these and they were all fine, except MTHFR. It came back as indicating a genetical mutation ("compound heterozygotous MTHFR mutation"). Apparently this means that I have inherited this condition from one of my parents. It wouldn't be a problem per se if it was only one mutation, but there are 2 of them ("compound") which makes it a risk. I am taking 4mg of folic acid daily (ten times the normal dosis) and will be on heparin once I'm pregnant again. Does anybody have a similar condition and experience to share?



thank you!