My Great Strides Story
Ever since my daughter Pia was diagnosed with Cystic Fibrosis at just 9 days old, our journey has been one of unwavering determination and profound purpose. From that moment, we embarked on a mission to illuminate the path towards greater awareness and understanding of this condition, with a singular goal in mind: to pave the way for advancements in medication and treatment. Through our tireless efforts and boundless hope, we have forged a beacon of light amidst the darkness, inspiring others to join us in our quest for a brighter, healthier future for all those affected by Cystic Fibrosis.
Cystic fibrosis affects the lungs, pancreas, and other organs. The symptoms can vary from person to person, and as people with CF live longer than ever before, their disease can become more complicated, leading to serious health issues.
The Cystic Fibrosis Foundation has made extraordinary progress — including fostering the development of more than a dozen CF treatments — but these treatments are not a cure and not everyone can benefit from them. We must keep going.
Your support makes a difference.
By donating to my fundraising goal, you will help advance our mission for a cure for all. Please consider joining us and helping 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.