
Hello to our dear friends and family. We are fundraising online for a cure for Ginger and Piper. Ginger is 14 years old now and Piper is 10. They have an incredible bond. They support one another through their treatments, doctors appointments, procedures and tests. Ginger has taken on the role of the brave leader. She goes first and talks Piper through everything. They wipe each others tears and celebrate their feats together. We will never give up on the dream of a cure for them. We will never give up the hope of a carefree childhood. We will never give up, period. Please continue to support us. We have so much love and gratitude in our hearts for you.
There are approximately 30,000 Americans living with cystic fibrosis. My 2 babies are two of them. There are moms, dads, sisters, brothers, daughters, sons, friends and co-workers who struggle every day just to breathe. I walk for them all 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.
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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.