Humidifier or Vaporizer
I'm new on this board. My 3 year old daughter was diagnosed 5 months ago. It has been really hard to learn she has CF after 2 years of not knowing what was wrong. It has been an emotional r coaster. Since she was a yeard old she was having 7 or more bowel movements a day and eating constantly but her pediatrician would say she was fine and she was just a "hungry baby" . Finally I changed pediatrician and she sent me to a GI. The same week she was diagnosed. Now she is taking enzymes and she is not eating as much as she used to. We are doing ACT. She is very allergic to pollen and her nose is constantly stoped up. There are 5 pulmonologists at her CF Center. They said different things about using humidifier or vaporizer. Do you recommend using them?
Thanks so much and I appologize for my silly grammar.