At my 12 week scan I was told I had an increased NT of 4.6mm and my pregnancy is ‘high risk’, my NIPT test came back as low risk for the T13, T18 and T21. Currently awaiting my 16w scan and amnio
looking for cases where baby has been born with no abnormality / chromosomal disorder? I fear metal medicine miss something and baby is unwell, I currently have 1 child under 2 and am a single parent so I fear how could I split myself in 2 for hospital appointments. Endless worrying