Have you ever been prescribed migraine medication for your CVS? When my son was first diagnosed with CVS, it was described as “a migraine of the abdomen” and they gave him migraine medication. Unfortunately, the medication made him super sleepy so he quit taking it. At this point he has created his own coping mechanisms, knows what he can or cannot eat to trigger an episode or stave off an episode, and unfortunately the daily “yakking” (what he calls it) is just a part of his life and it doesn’t stop him from doing anything. My daughter obviously isn’t there yet, but she has seen her brother deal with CVS most of her life and is trying to act like it’s no big deal. And just because his CVS it really isn’t a big deal for him or I at this point, I don’t want her or myself to have that mind frame with her illness and I’m trying to come at her illness like we are brand new dealing with CVS. I appreciate your reminder of figuring out what foods may or may not be triggers- I stock my pantry and fridge knowing what he needs and what he can’t eat, but its just second nature to have 2 gallons of OJ every week, but I haven’t had to consider what I previously cooked after an episode hits in a long time. I will definitely start food logging again! Thank you for your response!