Join our team and help add tomorrows!
Our son Nate was born with Cystic Fibrosis (CF), a genetic disease that causes damage to his lungs and digestive system. He needs medications and breathing treatments multiple times a day to help prevent damage to his body and to stay healthy! Nate manages all of this, plus extra doctor appointments, with a smile and a great attitude. We are so proud of him!
The Cystic Fibrosis Foundation has launched a Path to a Cure - devoting $500 million dollars through 2025 into a finding a treatment for every person living with CF and finding a cure. Nate has benefited a lot from the CF Foundation already, with the research and quick FDA approval of a groundbreaking medication called Kalydeco. We feel so lucky, but sadly it is not a cure, and we still desperately need one!
To learn more about Cystic Fibrosis and the imapct the Cystic Fibrosis Foundation has on the lives of those living with CF, please go to CFF.org .
To become a member of our team, just click on the "Join our Team" button. From there you can join, make a donation and start your fundraising.
*** This is our first time walking in person since the Covid-19 pandemic began. As the CF Foundation requested to protect the vulnerable population attending, we are expecting all eligible in-person teammates to be fully vaccinated against Covid-19 ***
By becoming a member and making a donation, you are joining a growing group of people committed to finding a cure for cystic fibrosis.
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IMPORTANT NOTE ON ATTENDANCE AT FOUNDATION EVENTS:
Updated June 15, 2022. To reduce the risk of COVID-19 the Foundation is taking steps to host safe events for our community. Please be advised that events may be subject to change at any time based on guidance from the Centers for Disease Control and Prevention and local health officials.
To minimize the risk of COVID-19 infection, we ask that attendees at CF Foundation events follow these steps:
FOR YOUR SAFETY AND THE SAFETY OF OTHERS: