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Dear Martha, Colistin is what almost EVERY patient gets. When in we always joke about how it screws up the memory and body and whatnot.

Dear Melissa, Yeah, I have been through a lot and am still fighting. I must admit that I have stopped fighting at times and nothing good has come of it. Yeah, I am always willing to share the information I have with others and I'm glad I found this site. My girlfriend actually came upon...

"The New Kid in Town Dear, all Hello, my name is Bryan and I am 19 years old. I was diagnosed with Cystic Fibrosis at approximately one month old, and that was due to my brother having it my parents recognized the symptoms and got me tested quickly. I am the younger of two children, my...

Dr. Stern is, in my opinion, amazing! I have gone to him for about 10 years or so maybe even more. The man is just amazing, what else needs be said. He is the only reason that my brother (21 y/o with CF) is alive. I'm glad to hear you liked the hospital, it is amazing also, but usually...

Coldplay - Don't Panic "If I looked all over the world And there's every type of girl But your empty eyes Seem to pass me by"

Dear all, I have not had a transplant, but I know approximately 4 people who have had them. I am also currently testing to see if I'm able to get a transplant. The testing probably depends on where you go, and I'm going to the Cleveland Clinic for testing. It is a long and drawn out process and...

Hey, I'm Bryan. I'm 19 and have CF. IM me or e-mail me and I'll be glad to talk to you.