Thanks JDX and Satya. The 'to do' list is great!! I'm a BIG list maker!! I think that's why I've been panicking so much. The CVS tests are chorionic villus sampling which are done like an amnio at 11 weeks. They have to anaylse the baby's genes to determine whether it has a full mutation of the condition I carry. For that reason I think DH and I don't really want to do anything too early to try not to become to attached to the idea of being parents (although that's easier said than done).We made a decision years ago when we knew about my situation that we wouldn't tell anyone until we knew that every thing was ok at 13 weeks.So it's really hard! And for that reason it feels like we're tempting fate to have doc appointments and scans/ hospital visits booked in until after then. Silly, but that's the way I am.
I guess I'm going to have to just get on with it but I'm pretty nervous.
Thanks for the advice. I'll be brave and see the doc next week.... I think!
Lol




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