Life is hard for everyone! Some people have issues that go a bit above and beyond, i’ve always wanted to be able to reach out to those people to tell them they aren’t alone. So, this is a site/blog specific to people with Cystic Fibrosis or other terminal illnesses, their family member’s, their friend’s, or anyone who wants to understand a bit better what life is like with a degenerative disease that will only get worse until the end. Especially since most of these fall somewhat into the category of (invisible illness)… It will also be a guide on how to do everything from daily activities to coping with the stressors of being sick continuously.  “Will’s CF Life” is going to be a place where people can get a bit of useful information, rare insight, or just a story about a day in the life of a CFer.

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