We are so excited to once again form a human (that's not virtual..) team to participate in the annual Cystic Fibrosis Great Strides Walk in Columbus, Ohio !!!
Our first Team Parker was formed in 2013 the year Park was born and diagnosed with CF. We have been so blessed to have so many family members and awesome friends join us in previous years not only to walk but to raise life changing funds for CF research.
Parker is positive proof that donations to CF research REALLY DO WORK ! He has been taking the life changing Trikafta medication for quite awhile now. He no longer has to wear the "vest" twice a day nor do daily breathing treatments. His lung function is FANTASTIC. He is an absolutely healthy active growing boy and we could not be happier, but .. he still has Cystic Fibrosis as do many others.
Trikafta, a miracle medication is still in its early stages and it does not help everyone with CF. It will always be a priority with our family to support the Cystic Fibrosis Foundation until and after a cure for all is found.
It's because of you, the generous people who continously donate hundreds of thousands of dollars each year that CF makes GREAT STRIDES towards improving the life of those who battle CF daily. Your commitment to CF and specifically Parker has been overwhelming and much appreciated. Please consider once again to donate to Cystic Fibrosis through Team Parker. We are and always will be humbled by your constant care and concern.
It's not all about donating though. You have no idea what it means to Parker (and his family) to have our people join us to walk each year. Please consider doing us this year to make it the largest Team Parker participation... EVER!!!
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.