Hello and Welcome!
I am so honored to be nominated by the Cystic Fibrosis Foundation at a special event recognizing outstanding young professionals in Nashville. In accepting this distinction, I have committed to raise money to help the Foundation realize its mission of controlling and curing cystic fibrosis (CF)!
The mission of the Cystic Fibrosis Foundation is to cure cystic fibrosis and to provide all people with the disease the opportunity to lead full, productive lives by funding research and drug development, promoting individualized treatment, and ensuring access to high-quality, specialized care. In this 16 week course, I will get exposure to other Tennesseans who live with this disease and learn just how it impacts day to day life. After hearing from local families who battle everyday with CF, I am beyond humbled to help make a difference in a cause that will truly benefit from every dollar raised.
Making a donation is easy and secure! Just click the Donate button (or buy a ticket to our gala!) on this page to make a donation that will be credited to my fundraising efforts. Any amount you can donate will be greatly appreciated!
Cystic fibrosis is a devastating genetic disease that affects the lungs and digestive system. More than ten million Americans are symptomless carriers of the defective CF gene. Advances continue to be made in finding a cure, but your help is needed now -- more than ever -- to help keep up the momentum of this life-saving research. Sixty years ago, children with CF usually did not live long enough to attend elementary school. Today, because of Foundation-supported research and care, the median survival age of people with CF is about 40. This is remarkable progress, but not good enough. We continue to lose precious lives to CF every day. To learn more about CF and the CF Foundation, visit www.cff.org. Together, we can make a difference in the lives of those with cystic fibrosis.
I am ecstatic to write this message with the intent and hope that you and I will be making a difference in the lives of people who are diagnosed with Cystic Fibrosis.
If you have any questions please feel free to reach out to me directly!!!!
Thank you for supporting the mission of the CF Foundation!
LET’S GOOOOOOOOOO,Braden Eutsler