Cameron has been on this journey for 4 years now. We have watched him grow into a a happy and strong little boy who just happens to have cystic fibrosis. Thanks to the backing of The Cystic Fibrosis Foundation, we have seen Cameron benefit from major medical advances.
As grateful as we are for these advances, there is still much work to be done. When healthy, Cameron takes about 8 different medications per day, two nebulizer medications per day, plus 30 minutes of chest therapy two times a day. When he is sick, medications and time doing chest therapy increase. We need research into new medications, new therapies, and a cure. The Cystic Fibrosis Foundation uses your donations to back this research. We simply can not do this alone.
Cameron, our family, and the entire CF community thank you for joining our fight to find a cure.
Until It's Done!
Darlene Cave
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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.