Our son Dayne fights daily, the dreadful life-shortening genetic disease, cystic fibrosis (CF). When he was first diagnosed in 2007, it became a mission of mine to raise both awareness and funding to improve treatments (care and/or medications), and eventually, to find a control or cure.
Through my Breathe Easy Ride events, the motorcycle community rallied to learn about cystic fibrosis and importantly, we raised money to support lifesaving and non-government funded research. Since that time, there have been truly remarkable advancements in care and medications (Read about Vertex Pharmaceuticals breakthrough drug, Trikafta) thanks to the kind hearts and generosity of those who have financially supported this cause.
Sadly, there is still no cure for this devastating disease, and I humbly ask you to please consider making a 100% tax-deductible donation of any size (one that you are comfortable with, and nothing is too small to make a difference) to the Cystic Fibrosis Foundation through our Team DayneGerous .
With heartfelt gratitude,
The Glover Family and worldwide cystic fibrosis community
Connect With Us
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.