She's been complaining about
belly aches for years, and we've been dealing with it only as far as it intrudes on her daily life, like preventing her from going to soccer or school. She's almost 11 and I wanted to delay as long as possible so she wouldn't have to go through the incredibly invasive diagnostics we're all too familiar with.
Her issues were pretty well controlled with a PPI and avoiding lactose. But last weekend she had two bloody stools (not too much, but enough to notice) and started feeling pretty awful. This week she's only managed to be at school for 2 days and hasn't eaten much or taken significant fluids. We brought her to her ped on Monday for the needed referral to the local GI clinic. But on Thursday, having heard nothing from either office about our referral, and seeing her pale face refusing to go to school, I took her to the ER. sigh. They were of no help (except getting us a prescription for zofran) - I was hoping to force the system and get her a GI consult that way, but no luck.
Then I spent the afternoon on the phone and finally got an appointment for Monday. whew.
Meanwhile she still feels miserable. She's taking prilosec, and took her 2nd dose of zofran this morning. After my 10 years of Crohn's and 11 years of parenting I still feel clueless on how to get her to eat or drink. She isn't vomiting and she doesn't have diarrhea - just malaise and misery. I suppose I can offer her jello; she's refused chicken broth, yogurt, water....ugh.
I'd love to hear about what diagnostic practice is for children - if she has to get scoped next week, do they do the prep as an inpatient, or are we going to be sitting up with her all night trying to get her to drink the nasty stuff and pound water?