I decided to start this blog for a couple of reasons…First, to shed some light on what some people would refer to a an invisible illness (i.e. an illness or disease people can’t see visibly). Second, to bring as much of the knowledge/experience I have collected over the years through enduring a lot of hard times to anyone dealing with health issues, or having some kind of life-long struggle. Finally, to reach out and share my story, somewhat for personal reasons, but also if I can help/connect with one person who feels like they’re out in the world alone, scared and uninformed then I will have accomplished what I set out to do.
Published by cysticfibrosislifeblog
I am a 29 year old CF patient...I've been through really fun times, and really shitty times...in recent years it has been the latter. I am creating this in hopes of reaching just one person who feels alone, scared, tired of being sick and tired, etc. Having CF is a really tough situation because it is what is considered an invisible disease, so unless youre hooked up to a oxygen tank most seem fine at first glance... and people tend to overlook the obvious illness right in front of them, also one of the things about having CF is you don't want to only talk/think about CF ....I could go on and on complaining but we'll leave that for another post. View all posts by cysticfibrosislifeblog