As most of you know my sweet Kaisley Hope was born with Cystic Fibrosis. I walk for my sweet miracle baby and for all the other's who are living with Cystic Fibrosis. My wish is for my baby to live as normal and healthy life as possible, to grow old, to get married, have children and live her dreams without her disease slowing her down. Our hopes and dreams for our child's future is that this disease will not diminish her quality of life or cause her to miss anything that her life has to offer. We hope she has the same opportunities and experiences that any other child may have and that this disease does not control her life or inhibit her own hopes and dreams! So every penny donated matters!!!
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 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.