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Death and CF
I’ve known for over half of my life that CF was a terminal disease that shortened our life. It’s a harsh reality that all adults with CF had to discover at some point, and while it’s heavy, it’s an important element of our life that we have to acknowledge.
- How old were you and how did you find out about people with CF having a shorter life expectancy?
- How do you approach this as an adult? Do you approach it by being open? Or other ways?
- What do you wish other people understood about the way CF forces us to have this burden?
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