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Cystic Fibrosis and Sleeping Patterns
To be honest it is my friend that has this problem and I'm asking because he is far too stubborn to look admit this kind of thing and I'm worried about him, so here it goes..

He isn't attending school right now because of medicine he is taking at the moment and isn't committed to anything in the mornings so he has  messed up sleeping times. He will stay up until 3-5 in the morning and sleep until 2-3 the next afternoon. He says he feels a lot worse at night, and anytime he has had a certain problem with CF it has always happened at night.
Can how you sleep (amount of sleep, sleeping patterns) affect an illness like CF? Can it become more aggressive?

As I said, I'm just concerned and would appreciate any help.
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