Everyone meet my beautiful daughter Drea. She is the absolute love and light of my life. Drea was diagnosed with cystic fibrosis at 2 weeks old. Luckily starting her treatments so young gives her such an advantage to live a long healthy life. With everything Drea deals with on a daily basis she continues to always have a smile on her face. She is by far the strongest little girl I know. The past couple years have been an emotional rollercoaster for me but with the help of my family, friends, all her doctors and the Cystic Fibrosis Foundation, CF is just my new normal and a part of my life. With your help and generous donations medical research can advance and new medicines can be produced.
There are still 30,000 Americans who suffer from this disease which is far too many! Please will you join us in raising funds and awareness for this disease, so one day Drea's disease has a cure! We would like to thank everyone for their generous donations and for joining Drea's Dream Team. By walking today, we are adding tomorrows for everyone living with Cystic Fibrosis. Thank you all for your support through this journey.
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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.