Devastated to learn today that Nurse Malone has moved to Boston. She was the only provider who actually "got it" when it comes to this issue. Of course, the practice has recommended we see another one of their docs. Specifically, Rehtman. I've read bland reviews on her treatment of kiddos with this condition. We've been dealing with this issue for 1+ year and it has most recently returned with some frequency. Ugh. Would appreciate hearing recs for other pediatric GI doctors/nurses in the area with whom folks have had success (good bedside manner, understands what's going on, not just Miralax tmt). Our experience at CNMC was terrible so not intersted in returning there.
Thanks!