Hi, I am Leah! I was born with a genetic disease called Cystic Fibrosis.

RIGHT NOW, THERE IS NO CURE FOR CYSTIC FIBROSIS.
​But there is hope for a better future.  Much research and drug development are being done to increase the quality and length of life for someone with cystic fibrosis.

My team, Leah’s Front Line, helps promote awareness about cystic fibrosis and raise money to support the Cystic Fibrosis Foundation (CFF). 

​Every year, Leah’s Front Line walks in the GREAT STRIDES walk to help fund vital CF research.  Please consider partnering in our efforts by giving a donation and/or joining our team as a walker.  

Every day I work to add tomorrows. Would you help support me through fundraising research to find a cure. 

THANK YOU!