Our Story
Hello.
Hope you are well...Hugh has gone through a lot these past 6 months. We are reaching the point where we really need to find more medicines that will help him fight off the seemingly endless bacteria that keep finding their way into Hugh's lungs. Better yet...we need to FIND A CURE. and we need your help! Melanie and I hope you will join us Saturday May 17 at 9:30 am on the Georgia Tech campus as we walk for our 6th year in the Great strides walk to raise money to find a cure for Cystic Fibrosis. If you are unable to walk...your donations of any size are greatly appreciated.
More information follows about CF and the Walk...hope to see you there.
Cheers!
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. We walk for them and hope you will support us in our 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, we are helping add tomorrows to the lives of people living with cystic fibrosis. Will you join us? Support Hugh by making a donation to our 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 TEAM GREENE!
Help us reach our fundraising goal by donating to our 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.
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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.