Lauren Gray's Fundraiser for the Cystic Fibrosis Foundation

Cystic Fibrosis is a genetic disease that predominately effects the lungs and pancreas, that occurs in 1 in every 25,000 Americans. With a cure for the most common mutation awaiting FDA approval, please help us in funding further research and development. The Cystic Fibrosis Foundation (www.cff.org) has made great strides for the betterment of CF patients like myself, Lauren Gray. I have been very fortunate with my disease in the past, but now it's starting to catch up to me, which is why I am fighting even harder than ever, and decided to become more active in my community. Although, many others cannot say the same. The Cystic Fibrosis Foundation, or CFF has, for example of the great work they've done, risen an average CF patient's life expectancy from 4 years old in the 1950's, to over 40 years of age today. In just the 14 years that I have been alive, a CF patient's life expectancy has risen from 18 to 40. 35 to 40 in just the past few years. That's a significant leap. Please help me and others like me become Cystic Fibrosis survivors, and help CFF "add tomorrows." Thank you.