How do we begin to explain the importance of funding the Cystic Fibrosis Foundation?
Leanna and Bou's son was diagnosed with CF at 2 weeks old. He is now 6 years old and healthy! However, his health would not be possible without the advocacy and advancement of treatments by the Cystic Fibrosis Foundation. The medicine he takes, the treatments he undergoes on a daily basis, and the outstanding care of his CF team are all available to him because of the Cystic Fibrosis Foundation’s determination to make each CFer’s quality of life better.
Riley's fight with this disease is not over. He will face challenges as he gets older, and thankfully, there is an organization that will not stop until a CURE is found! ***Just in the past month, the CFF has successfully put another drug therapy before the FDA. It was approved! This drug therapy has shown such promising data for those with CF.
This is why we support the Cystic Fibrosis Foundation and why we are attempting to continue funding the organization that will allow Riley to grow and prosper.
We invite you to join us at the Great Strides walk in May. And, please, consider making a donation to this life changing organization. Every dollar matters.