There are approximately 30,000 Americans living with cystic fibrosis. My daughter Brooke is one one of them. She was diagnosed with Cystic Fibrosis when she was 3 weeks old. Needless to say, my husband and I were devastated.... Our precious little girl was given a disease that could cut her life short. So now, we fight. We do what needs to be done every day. This includes several breathing treatments per day, airway clearance 2x per day to break up the thick sticky mucus that builds up in her lungs, take her oral medication and exercise. This is when she is healthy. When she gets sick these treatments increase. The current average life expectancy is 48 years old. That is NOT acceptable to me. I walk for her and the other 30,000 people who suffer from this horrible disease. I 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.