Our daughter Sunny is a soon to be 14 year old who loves theater, songwriting, digital art, and hanging with her friends. When she was 9 days old we received a phone call that we will never forget: Sonya has Cystic Fibrosis. Completely shocked and devastated, we eventually picked up the pieces of our shattered hearts, learned all we could about the disease and made it our mission to help find a cure for CF within Sonya's lifetime. We will not stop fundraising until a cure is found. Please help us raise awareness and much-needed funds for the CF Foundation by joining our team and walking with us.
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.
Thank you for your support.
Achievements:
Jennifer Tower
Event: Easton
| Team: Sunny Days Ahead
Jennifer's Fundraising Goal: $1,000.00
| Amount Raised: $1,632.72
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.