My DS had a higher than normal nuchal fold measurement and combined with the other factors we had a 1 in 284 risk of downs. Our hospital considered anything less than 1 in 300 to be high risk, however we didn't. I refused to have an amnio and opted to see the genetic counsellor at our 18 week scan to determine if there were any other indicators.

Nothing was found at our 18 week scan, and we now have a beautiful healthy 10 week old.

Have you been given any other information?