J
julieta79
Guest
My newborn baby boy was screened and showed Del F508 and 5-T 12 TG, no other mutation is present. His initial sweat test is 20. Doctors can not tell me what happens next, as this combination could produce mild symptoms or none. Please share if you have a child or you are an adult with this. When were you diagnozed and what kind of symptoms did you have? Any info is GREATLY appreciated(VEST)