I'm after a little advice/ stories from people who have experienced.
I found out yesterday I'm expecting twins 🤯.
I spoke to one of the screening doctors after my scan about screening and what it means with twins. They say I have MCDA twins but I wasn't quite As ahead as originally thought so can't 100% confirm, so I am back next week for another scan. They have told me that I don't have to have it and they can just see what the scan comes up with (with regards to fluid on neck etc) and if it's increased they may suggest screening but that if they are identical it's likely to give a more accurate result as if one twin has high risk of downs then so will the other but if they are non identical if one is showing increased fluid then to have the screening might not actually give an accurate risk number because one the blood test might be scewed by one twin giving more of an influence if that make sense!
Who here with twice (either sort) had the screening and did you find it helpful/worth it? Or did you have it and it make you feel more confused?