Hi everyone. I'm a mother of 9 month old twin boys both diagnosed at birth with cystic fibrosis (delta f508 mutation). I just had a question for other parents here who are dealing with cf on a daily basis. How did you cope when you had to go back to work full-time. How did you trust someone else to take care of your child and to be diligent with the medications/physical therapy? & for older aged children, how does it get dealt with in the schools? I have fears about how things will change when the twins go to school, if they will be made fun of for being different, if the teachers will be diligent and help them take their medications, etc. I have so many worries and it all weighs so heavy, just looking for some sound advice from someone who has already "been there and done that" : ) thankyou to anyone who responds.