[cpfohl]

Yeah, my son's issue was rare and congenital. I wish I still had the conversation, but I can't remember which LLM it was and it's not in either my Claude or GPT history. It got it in two shots.

1. I described the symptoms the same way we described it to the ER the first time we brought it in. It suggested all the same things that the ER tested for. 2. I gave it the lab results for each of the suggestions it made (since the ER had in fact done all the tests they suggested).

After that back and forth it gave back a list of 3-4 more possibilities and the 2nd item was the exact issue that was revealed by radiology (and corrected with surgery).