Life in a matters of seconds
I was diagnosed with Cystic Fibrosis when I was months old, I am now 19 years old.
This disease causes my body to generate excessive mucus, causing problems in my lungs, pancreas and other organs. There is no cure, but there is a treatment. There is also the possibility of a lung transplant, I have been on the waiting list for years, although if you ask me my hopes of having new lungs have gone down a cliff. I don't care anymore, I guess I have entered the acceptance phase, where if they talk to me about my life expectancy and confess that I only have a few months left I might sigh with relief, a break from all this what you call "life" wouldn't hurt.
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