Our Great Strides Story
Almost 5 years into our CF journey, and Hazel truly is a super hero! She does her treatments every day (mostly) without complaint. She is brave and strong through clinic visits, blood work, chest x-rays and daily medications.
She asks more questions than anyone we've ever met. She runs like an Olympian. She eats so much bacon. She sings and dances with reckless abandon.
We're thankful every day for Hazel's good health and credit a great deal of that to the treatments made available by the research done by the CF Foundation.
It's our joy to walk alongside other CF fighters and families to support them.
God bless you. -Megan, Alex, Hazel, and Finley Nelson
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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.