Has anyone skipped straight to a CVS (by-passing NIPT type testing) in pregnancy for definitive answers early on? I had a follow up appointment with MFM doctor last week and one of the things he mentioned for a possible future pregnancy is skipping straight to a CVS as 10 weeks to get definitive answers on chromosomal issues early on. Basically, he suggested this because we found out about our poor fetal diagnosis so late in pregnancy last time.

If you did the CVS early, how did it go? What were your reasons for pursuing it rather than the NIPT screening test first?