This afternoon we go to the poop doctor. (That’s a pediatric gastroenterologist for you adults reading.)
I get so nervous going to these "special" doctors. I want to get help for Spence so badly, but I don’t want them to have to do any tests on him or for him to have a bad experience. To calm my nerves, I wrote out everything about Spence’s diet and poop habits that I could think of. I tried to reconstruct the last 9 weeks(!) so I can accurately tell the doctor what’s changed or hasn’t changed in Spence’s diet since the problems started. At the very least, I’m prepared.
I’m also nervous for the nanny to bring Spencer into Manhattan. (They are meeting me at the doctor since I work nearby.) She’s never taken him on the subway before. But, she’s totally capable and I’m sure she’ll have no problem, so I should just chill now.
Update later today when we get back. To be continued…
Update:
So, after a very, very long hour+ in the waiting room, the diagnosis is severe constipation. We have a prescription to try since the food-based solutions haven’t worked. Dr. Poopy ruled out colitis and a milk allergy, but wants him to get tested for celiac disease. I was happy to leave with something new to try – I just hope it works and it’s not too harsh for my little guy. He told me that it’s not technically approved for infants, but they’ve been using it successfully for a number of years. If I weren’t at such a big hospital, I might have balked. But, I do feel like they probably have a pretty sound basis for their judgement because of the number of patients they see and have tried it with.