Thank you everyone for sharing your experience with the IV antibiotics infusions. It has really been helpful and calmed my nervousness down about starting them. I’m curious as to how you know if they are working. Do you feel better, less flare ups, less coughing up mucus, etc,? I have M Abcesses and had a really bad flare up with bronchitis and pneumonia so my Stanford pul wants to start me. I don’t know what drugs they will be. Also he told me the goal is on the IV for a year but do it just as long as I can. Thank you all again for sharing as I don’t know what I would do without this site to talk about BE and all that comes with it.