Stephanie Liss is an adult living with CF with two nonsense mutations. "Because of my CF mutations, I am part of the group of people with CF who cannot benefit from current therapies. It is sometimes difficult to read success stories about how lives have been changed by these drugs because, despite being happy for those who have been helped, there are moments I wish I could be in their shoes."
Yet, Stephanie keeps a positive outlook and stays focused on her dream, knowing that CF will not hold her back.
The Foundation has led the way in the fight against cystic fibrosis, fueling extraordinary medical and scientific progress and enabling many individuals with CF the chance to chase their dreams. But we must fulfill our vision of a cure for every person with cystic fibrosis. We will not leave anyone behind.
Today, we challenge you to make a monthly gift that will drive our momentum forward by helping to fund research, creating meaningful new programs that enhance lives, and supporting all that we do each day for people with CF.
Join the 65 Roses Club today and help us make CF stand for Cure Found.
