I read the earlier posts regarding genetic diseases potentially associated with being Askenazi Jewish but the threads were unclear about some things and are likely dead now. I am half Jewish (raised Jewish but genetically half) and this was not something they asked about or something I mentioned at my initial OB visit. I got screened as a carrier for CF (negative) but nothing else because again, I was unaware. My husband is not Jewish, he's Hispanic, and we are meeting with a genetic counselor on Tuesday (scheduled an appointment today after the midwife said I was really low risk but she likes the counselor and thought it wouldn't hurt). On the one hand, I can write it off and say even if we were both carriers it's a 25% chance of Tay Sachs, and the chances of us both being carriers are very low. On the other hand, after a miscarriage in February, it's easy to get worked up about every new level of thing that could possibly be wrong. Anyone have any experience with this? Any helpful words? I'm hoping the counselor just reassures us that no testing would be necessary because of how low the risk seems. And at 19 weeks pregnant, that's all the hope I have to hang on to. I feel like a failure for not doing this earlier.                
                TTC since 12/12 BFP#1 1.11.13 Natural MC 2.11.13
             
        
Re: Ashkenazi Jews
https://www.jewishvirtuallibrary.org/jsource/Health/genetics.html
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