This is a sample guest message. Register a free account today to become a member! Once signed in, you'll be able to participate on this site by adding your own topics and posts, as well as connect with other members through your own private inbox!
I am so so sorry. My son is 14 and I cannot imagine loosing him. He and I have been to counseling together as I too am the rock. I'm learning to be sad when Taylor's sad and allow him to express his feelings more openly to me. I don't know why I felt like I was going to cry and never be able...
Just wondering how others with this mutation are doing. My 14 year old son has this CF mutation and struggles with psudemonas. Seems like we can never get rid of it. He's a great athlete so exercise helps with airway clearance. Eating is a battle.
This site uses cookies to help personalise content, tailor your experience and to keep you logged in if you register.
By continuing to use this site, you are consenting to our use of cookies.