Our sweet Henry was diagnosed with Cystic Fibrosis when he was 10 days old. At the time, it was devastating to our growing family, with my husband and I not knowing anything about CF and feeling overwhelmed and helpless at protecting our son.
But now, two and a half years later, we are filled with hope. Over the past decade advancements have been made that will be life saving for Henry. And those advancements were possible because of the people before us – the ones that fought to fund the science and the research.
This year will be our third walk, and definitely not our last. We will walk every year for Henry and for everyone living with CF. Until there’s a cure.
With love, Shane & Tiffany Recicar
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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.