So my 11 week ultrasound flagged some major concerns. My son has fluid edema around his head. OB was concerned about Downs, heart failure or anemia. My genetic testing all came back low risk, which was encouraging. But at my 13 week follow, tbe fluid is still there and is pretty substantial at 1cm. I am being referred to MFM. But beyond genetic/chromosomal defects like trisomies, my OB has speculated omphalacele or gastroschisis. This would mean having to travel to a city 1.5 hours away for a csection and immediate surgery for the baby, long with weeks in NICU away from home and my toddler. Outcomes are generally good for baby. But nothing is know definitively right now. The weeks of uncertainty have been unbearable. This is all also following a miscarriage earlier this year. Any advice or anyone with experience who wants to comment is appreciated. My husband and i are at a loss and beyond stressed and worried.
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