We have a sense of purpose that compels us to do all that we can to make a difference in the lives of others. Therefore, we are committed to focus our efforts to find a cure for Cystic Fibrosis. We have supported The Cystic Fibrosis Foundation since 2011 and have donated more than $1,200,000 and counting with the help of our partners.
The Cystic Fibrosis Foundation, a non-profit organization, is impacting the lives of 70,000 individuals around the world diagnosed with this genetic disease through funding research and providing support programs for patients and their families.
Each year, there are more than 1,000 cases of Cystic Fibrosis diagnosed in the United States. More than 70% of those are children.
Diagnosed when she was three months old, Emily is now a teenager living with Cystic Fibrosis. Here, she explains her life with CF. She explains what Cystic Fibrosis is, how it impacts her life, and how the Cystic Fibrosis Foundations’ Great Strides walk has made a difference in her life.
The Cystic Fibrosis Foundation is the world’s leader in the search for a cure for cystic fibrosis. The Foundation funds more CF research than any other organization, and nearly every CF drug available today was made possible because of Foundation support.
Through our work together with our partners for the cure, we have been able to make an impact. This year, we hope to raise $350,000 and continue our efforts in finding this cure!