Hi All,
Thanks for visiting our page. As you know our son Dominic was diagnosed with Cystic Fibrosis at 5 days old. We were terrified in the beginning about what this would mean for our little super hero. He has had a pretty healthy journey and we are super grateful! There is still a lot research to be done to find a cure!
The constant research that is happening arround the world right now has come so far in just the last 10 years and it wouldn't be possible without the donations made to the Cystic Fibrosis Foundation. Please know that none of the money raised will go to our family, but to the foundation to help find a cure, so that one day Dominic and his CF friends may breathe a little easier and grow with greater ease.
There are approximately 30,000 Americans living with cystic fibrosis. They are moms, dads, sisters, brothers, daughters, sons, friends and co-workers who struggle every day just to breathe. I walk for them and hope you will support me in my efforts.
Real progress has been made in the search for a cure, but the lives of people with CF are still cut far too short. There still is no cure for this devastating disease. By walking today, I am helping add tomorrows to the lives of people living with cystic fibrosis. Will you join me? Support me by making a donation to my Great Strides fundraising campaign today!
Great Strides is a fun, family-friendly event that raises awareness and support for people with CF and their families.
Please support me!
Help me reach my fundraising goal by donating to my Great Strides fundraising campaign. Your gift will help add tomorrows to the lives of people with cystic fibrosis by supporting life-saving research and medical progress. 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.