Friday I went to the doctor, and he told me I was eliagible for the phase 3 study of ataluren, the drug that fixes the "nonsense" CF mutation. My mutation is R553X/F508del, meaning that the CFTR gene is there, its just cut short, so it doesnt work. Ataluren finishes this protein, basically fixing the underlying cause of CF. Ive done a ton of research on it, and I feel like theres no downside, theyre going to pay me to get better?! I am a bit freaked though (since they dont yet know the long term side effects), and I have to drive down to Chicago once a month (I live in Milwaukee). Im wondering if anyone else is taking part of this study, or took part in the first two? Or if youve heard how it worked in other CFers...? Im kinda going in blind here and I was just hoping someone else had experience, or if ANYONE had advice? Im just looking for support, i guess.