I had a somewhat similar worry not long ago when my brother’s wife was pregnant. I asked them if they were going to request screening, and they said that the doctors said CAH was too rare to worry about. After Brandon was born, premature, I again asked if they were going to test for CAH, and they said the same. Brandon died not long after that with no CAH testing ever being done.

It’s like people think that if they pretend they aren’t at a greater risk, then they won’t be.