-- Shares Facebook Twitter Reddit Email Rebecca Vincen-Brown was still in her first trimester of pregnancy, in the late fall of 2022, when things started to go wrong. She had blood drawn for a standard genetic test called noninvasive prenatal testing, or NIPT, which can detect increased risks for various chromosomal disorders. The results of the test took slightly longer than normal to come back, and when they did, Vincen-Brown received a troubling phone call: The test was “inconclusive” because not enough fetal DNA was detected in her blood.
NIPT cannot diagnose fetal disorders conclusively, but the possibilities were troubling: Her fetus might have triploidy, trisomy 13 or trisomy 18, rare and serious genetic conditions involving either an extra set of chromosomes or an extra copy of one chromosome. While the specifics vary, most infants born with these conditions will live only days or weeks, and almost none will survive to adulthood. When Vincen-Brown and her husband first learned she was pregnant with their second child a few weeks earlier, they were “over the moon,” she said.
They’d been trying to conceive for nearly a year. She went to the attic of their house in Kuna, Idaho, a small town south of Boise, and began digging out some of the favorite baby clothes that her older daughter, then two years old, had outgrown. She even started to get the nursery set up for their new arrival.
(Vincen-Brown has requested that Salon not identify her husband by name or occ.
