Please watch the video below to learn more about Cystic Fibrosis, our family's journey navigating this disease and the recent Foundation driven advancements in its pursuit of a cure.
My 18-month-old son, Wyatt, is living with Cystic Fibrosis, and I am advocating for him and all of those affected by CF by participating in a fundraising competition culminating in a special event later this year.
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. 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.
Please join Wyatt’s team by donating today, because investing in research requires significant funding. We are stronger together. Even the smallest donations can have a huge impact. 100% of your donations goes to the Cystic Fibrosis Foundation where their experts will help make CF stand for Cure Found.
To learn more about CF and the CF Foundation, visit cff.org. Thank you for supporting the mission of the CF Foundation!