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My CF Cycle for Life Story

Nearly 40,000 people in the United States have cystic fibrosis: a progressive, genetic disease that affects the lungs, pancreas, and other organs. They are moms, dads, sisters, brothers, daughters, sons, and friends who face the sobering prospect of a shortened lifespan. 

My son Aiden had Cystic Fibrosis. He loved every moment to the fullest. Even though he had to do hours of treatments every day, he always found time to enjoy spending time with family, eating, drinking coffee and playing video games with his cousins, brother and friends. Unfortunately his life was cut short due to his illness and the lack of treatments for his specific CF mutation. That’s why is so important to me to help this cause. 

Working alongside the CF community, the CF Foundation has fostered the development of more than a dozen CF treatments and helped add decades of life for people with CF. Yet, many people with CF do not benefit from existing therapies. Our vision is a cure for every person with cystic fibrosis – a life free from the burden of this disease – and we will not leave anyone behind.

You can support me!

By supporting my fundraising goal, you have an opportunity in your lifetime to be part of ending this disease. Please consider joining us and help make medical history.