Lab results started to come back today from Friday's draw, and we have decided to schedule a Rtx infusion for our daughter. This time last year she had just been released from the hospital after a flare almost took her kidneys. Treatment of pediatric WG is different in some ways, and one is the consideration of over-use; what if Rtx loses its efficacy, or what if unknown (or known) side effects wreck a person after 50 years of infusions? But PR3 is ticking upwards over the last couple months, and we want to forestall another actual flare. We are all comfortable with the decision to do the infusion (in fact she herself is relieved to have it, since pain and fatigue has been increasing), but as parents we're sad she has to face this. Mixed feelings, I guess.