As the parent of a very complex CDH kiddo (16+ yrs old, who lost a large portion of intestine both small and large as an infant due to NEC) we were told that he is not allowed to have any live vaccines. I asked at his most recent appt and that is still the case, per his surgeon. When Sean was a baby he also suggested it would be prudent to consider doing just one vaccine at a time rather than doing them as typical babies, several per visit, even if that meant delaying some of the vaccines a little bit. What are your thoughts on this?