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. One of those is Livi, my baby girl (who is not such a baby anymore). This year we celebrated her 15th birthday. 15 years with the toughest chick I know. Livi is shy yet loud, she is reserverd yet crazy, she is serious yet a jokster. Only those who really know her,know what a colorful and determinded person she really is.
Livi lives her best life everyday. Her health is directly related to the fundraising done through the amazing foundation. You see, she is now taking a medicine that has changed her quality of life. She is not the tiny fragile little girl she once was. She is strong! Her body is heathy and her lungs are clear. This is because the fundraising directly supports the research which directly helps those with CF!
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 and our fight against CF!
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.
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.