For the past 26 years, our family has supported the Cystic Fibrosis Foundation - and we haven't done it alone! So many of you have been on this journey with us, and we are so thankful for your support!
Decades ago, the CF Foundation was founded by families whose children were not living past elementary school. It is because of their grassroot advocacy and fundraising efforts that today, children with CF are living into adulthood, and why families like ours continue to fight for the cure.
When Andrew was born, we only dreamt of the medical advancements that have improved outcomes for people with CF. The CFF has proven itself time and time again to be an organization that uses their resources efficiently; funding science that delivers! Because of their research, we know our dream of a one-time cure for this disease will become a reality. And because of your continued support, we know this reality will happen for Andrew and the many others born with CF.
We thank you for sharing in our fight to end this disease.
Tom, Tonya, Andrew, Becca, and Sparty
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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 us!
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.
Love,
Tom, Tonya, Andrew, and Becca
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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.