The 3 kids went to the Pulmonologist today. They all did well with the lungs and we are going to start adjusting some of Ashley's medicine. The babies will still be on the same steroids. They were concerned about CJ's weight because instead of gaining weight over the last month he actually lost weight. They gave us a new food action plan for him. They also want him to have the Cystic Fibrosis Sweat Test done again. This was a major concern for us while he was in the NICU and now it is a concern again. He will also be having some chest a x-ray done again. Savannah goes to the ENT on Thursday for a follow-up and to make sure the cyst in her throat didn't get any bigger. That's all for now.