Thank you for visiting our family walk page! We work hard to keep Andrew as healthy as possible. All of the resources we rely on are thanks to the Cystic Fibrosis Foundation. Without their dedication to stopping this disease, we would not be able to control the 5+ bacterial and fungal infections that Andrew constantly battles every single day. Some of these treatments may not be easy, (and certainly are not fun), but they are necessary. We are thankful for them.
The CFF receives no government funding. So folks, You're It!! You make the magic happen for Andrew and the others like him. You are the reason he has these not-fun but ever-so-appreciated medications and therapies. You are the reason we will cure CF!
I will let the CFF pre-written message do the rest (see below). We would love to have you join us...in person, in spirit, or both!
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.
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.