Rise against Cystic Fibrosis! Join CF Bane's Army and join the fight to Raise awareness and funds for a cure.
Running for Those Who Can't.
Imagine waking up with a cold, the kind that sits in your lungs and burns when you breathe. Now imagine you are told that while you have this cold you must pinch your nostrils shut and breathe through a straw. Lastly, imagine you have to go to work, run errands, and do everything else that occurs in most people’s daily life.
Every. Single. Day.
This is not a life one would choose and not one many people can imagine tolerating. However, this is the reality of children and adults affected, living, and thriving with Cystic Fibrosis. We have witnessed Cystic Fibrosis through the eyes of a dear friend affected with this genetic disease. We have witnessed her resiliency, strength and positive outlook on her life as well as the resiliency and strength of many others affected by CF.
I was inspired to "see what it felt like" to have Cystic Fibrosis. Through the unwavering support of the Lucosky Brookman Foundation, the idea for running with the mask was born. As I run, I sometimes struggle to breathe, to finish the race and take each step. My luxury is one that those with Cystic Fibrosis do not have; I can remove my mask at any time. My struggle is temporary.
CF Bane was born to illustrate to the world through wearing a memorable mask what it is like to live with CF. I try to provide a tiny glimpse into the struggles of a life with CF. Sometimes concepts and struggles are hard to imagine. The mask serves as a stark reminder to everyone that the struggle is real.
Everyone deserves to just breathe.
All proceeds are going to the Lucosky Brookman Foundation and donated to bona fide Cystic Fibrosis Charities.
Made with 100% Polyester Moisture Wicking Fabric
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I was so happy to get it so fast, in time for May CF Awareness Month. It fits great. I'm very pleased with it!!