There are approximately 30,000 Americans living with Cystic Fibrosis (CF). One of them is my son, Will. He was born with this disease but wasn’t diagnosed until 2015 on when he was 9 1/2 years old. That first year was tough as he spent over 40 days in the hospital but with continued research & advanced medications he’s doing so much better!!
Cystic Fibrosis is a life shortening disease that causes the body to produce a thick sticky mucus in the lungs. We all breathe in the same air but for those with CF the mucus creates a breeding ground for bacteria resulting in dangerous infections and chonic lung damage. It also affects the digestive system and other areas in the body causing multiple complications to the victims health and quality of life.
Fortunately through fundraisers like this they are developing new treatments & drugs to help extend the life of those fighting this disease. Will you join our Will's Warriors team? All you need to do to become a member of our team is click on the "Join our Team" button.
We appreciate your support & donation. You can also follow Will's fundraisers and health updates at https://www.facebook.com/Wills-Warriors-1709266412618751/
Your gift is 100-percent tax deductible.
Connect With Us
IMPORTANT NOTE ON ATTENDANCE AT FOUNDATION EVENTS:
Updated July 5th, 2023
The CF Foundation is committed to ensuring the health and wellbeing of individuals attending Foundation events. Individuals attending CF Foundation events must abide by the Foundation's Event Attendance Policy www.cff.org/attendancepolicy, which includes guidance for event attendees living with cystic fibrosis.