My son was first misdiagnosed with a milk protein allergy and reflux at around 2wks old then two weeks later he was finally diagnosed with pyloric stenosis after constantly bugging drs.

It’s been one month since my sons pyloromyotmy and now he’s having the same symptoms that he had before his surgery. I’ve called the pediatrician MULTIPLE times and explained to her that I’m seeing the same things I saw when he had HPS (before surgery).

Children’s hospital New Orleans is trash and thinks I’m just some overreactive first time mom but my intuition is telling me something is wrong and this isn’t just reflux. The amount of spit up is just way too much.

If anyone has had a child with HPS please tell me your experience before and after surgery!!