Miles for Millie returning for our third year. Amelia has continued to be a rockstar. She continues to take her medicines and do her therapy. She does like to challenge her therapy some days, but she still gets it done. (I am proud of you girlfriend, if you ever read this!) She is a tough little girl, with some sweetness and sass. This year some of her favorites were Halloween, art, chicken nuggets, and Target. She has also mastered to take her creon whole by mouth with some water. She loves to snack and go after our dog or her big brother, Liam. Turning three definitely brought the personality for her!
We are looking forward to great strides 2024. We hope you will join us in walking, donating, or even just simply sharing our story.
We can’t wait to see everyone!
Join our team and help us get one step closer to a cure for cystic fibrosis – a rare, genetic, life-shortening disease that makes it difficult to breathe.
With supporters like you by our side, the Cystic Fibrosis Foundation continues to lead the way in the fight against CF, fueling extraordinary medical and scientific progress. The life expectancy of someone born with CF has doubled in the last 30 years. Despite this progress, many people with CF do not benefit from existing therapies either because their disease is too advanced or because their specific genetic mutations will not respond. They are moms, dads, sisters, brothers, daughters, sons, friends, and co-workers who struggle every day in the face of this devasting disease.
We walk in Great Strides for them.
Will you join us?
Great Strides is a fun event that provides a fantastic opportunity for family, friends, students, and colleagues to come together to make a difference in the lives of people with CF.
To participate, just click on the "Join our Team" button. From there, you can make a donation and start fundraising.
By joining our Great Strides team and making a donation, you will be part of a tenacious and passionate group of people committed to ending this disease. Together, let’s make CF stand for Cure Found!
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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.