I have an appointment with my OB-GYN tomorrow & it’s the 1st time I’ve seen him since I had our son (1 yr old SWCAH) -I saw his NP for follow-ups as my OB was too busy.  I want to discuss my pregnancy & delivery w/my son as nothing went smoothly & instead of boring you with all the details...I was just wondering if anyone ever had something called Polyhydramnios when carrying a CAH baby?  Basically it was too much amniotic fluid which put me on bed rest -and though my OB said the majority of the cases have no "cause" at one point he did mention concern over the baby having a metabolic disorder -but he was thinking more of a problem with digestion or something in the throat not being properly formed. So much went "wrong" during the pregnancy & delivery, -our son ended up in NICU for 3 days (this was a week before the CAH diagnosis) as he was in the birth canal too long & developed pneumonia...I have many concerns with another pregnancy & my choice of doctors & I’m sorry this got to be such a long post -I really just want to know if anyone else had too much amniotic fluid/bed rest issues when carrying a CAH child (nothing w/re:to using Dex). Thanks in advance for any info!!