Welcome to Brady John's Page
Brady John
I am honored to be nominated for the Cystic Fibrosis Foundation’s 30 Under 30 in Nashville. Being included in this group is incredibly meaningful to me, and I’m grateful for the chance to use this recognition to support a cause that matters so much. I do not take this nomination lightly, and I truly see it as both an honor and a responsibility. Through this campaign, I’m raising funds to help the Foundation continue its work toward curing cystic fibrosis and giving people living with CF the chance to live a long, healthy, and fulfilling life.
I would be truly grateful for your support in helping me reach my fundraising goal. Every donation, no matter the size, helps fund critical research, treatment advances, and care for those living with cystic fibrosis. Contributing to this effort is a meaningful way to stand with individuals and families affected by CF and to be part of the progress toward ending this disease. Please consider making a donation and joining me in supporting this important mission.
Nearly 40,000 people in the United States are living with cystic fibrosis, a progressive genetic disease that affects the lungs, pancreas, and other organs. Sixty years ago, most children with CF did not live long enough to attend elementary school. Today, thanks to Foundation-supported research and care, the median survival age for people with CF is now over 50. Working alongside the CF community, the Cystic Fibrosis Foundation has helped drive the development of more than a dozen treatments and add decades of life for many people living with this disease. Still, many individuals do not benefit from existing therapies. That is why the Foundation remains committed to its vision of a cure for every person with cystic fibrosis and a life free from the burden of this disease, leaving no one behind.
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. Thank you for supporting the mission of the CF Foundation!
Comments