Amniocentesis Or Not – Part 2

Amniocentesis Or Not – Part 2

Amniocentesis Or Not – Part 2


Here is PART 1 of this Article.


I went home and cried while staring at our baby’s ultrasound pictures for hours, trying to figure out what to do. Should I get an amniocentesis or not? Could I wait it out and hope for the best? Could I live with the consequences of not knowing and having a baby with a potential genetic abnormality? Would we continue with the pregnancy if we knew the baby did have a genetic abnormality? How would this affect our then one-year-old son, Dylan?


I was terrified of the idea—the thought of a long needle invading my baby’s amniotic sac, the risk of infection, poking the baby, and, worst of all, the 1/1000 risk of miscarriage. For me, I didn’t want to live the rest of the pregnancy being fearful, worrying about the worst-case scenario. If our child did have a genetic abnormality, would he be well or unwell at birth? Was there another genetic abnormality that was masquerading as a positive Down’s screen that could be deadly? I needed to mentally prepare myself for all the possibilities.


Read the FULL CONCLUSION on Amniocentesis Here.

Dina M. Kulik, MD, FRCPC, PEM

About Dina M. Kulik, MD, FRCPC, PEM

Dina is a wife, mother of 4, and adrenaline junky. She loves to share children’s health information from her professional and personal experience. More About Dr Dina.

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