Fund More Breaths

In 2015 I was diagnosed with Cystic Fibrosis and joined the roughly 70,000 people around the world who fight this genetic disease every day. Despite having spent my entire childhood with lung issues and stomach issues, I finally had a name for what I lived with and a wonderful medical team that now supports me in living a healthier, happier, and longer life.
Since my diagnosis my family and I have learned much more about Cystic Fibrosis. We have also learned a lot about the great progress research has made over the last few decades in offering treatments that extended life expectancy from less than 5 to 40 years old. Further research has the great potential to offer even longer lives to those with CF and hopefully some day a cure. We hope during the month of May you will join us in sharing information about CF to increase awareness and in raising money to support this important research. Thank you!