I went for my anatomy scan at 18 weeks. Everything looked normal aside from the EIF (bright spot) they saw in my son’s heart. I went for a level II ultrasound today and was told my son has a small VSD. I was also told that both of these are soft markers for Down syndrome. I go for an echo in a month so they can get a closer look at how his heart is functioning. Has anyone gone through this with their child? I also haven’t done any genetic testing (I’m 27, no family history of anything, have one healthy child) but was asked today if I’d like to do NIPT or an amnio to see the odds for Down syndrome. I’m not sure what to do and was hoping I could get some advice or reassurance from anyone who has gone through anything similar. I’m a nervous wreck.