My MINI BFF is my own super hero. I am in awe everyday by Greyson and the whole Carter/Vache family. Please see Greyson's story below.
Greyson was born with Cystic Fibrosis and after the last 7 years, we are determined more than ever to raise more money to continue research to find a cure for CF! Greyson is turning 8 August 3rd and we are so thankful to family and friends who have helped us so far! Greyson loves his family, his baby sister, playing baseball, collecting Pokemon Cards, riding his bike and generally being active! He is so vibrant and has such a good attitude when dealing with his daily therapies and medications. He is able to be on CF Modulators because of the work that the CF Foundation fundraises for so tirelessly. Greyson is truly wise beyond his years when working on his treatments and taking care of himself.
We are walking in person this year for Great Strides again and we are so excited! Please join us on May 19th at 1PM for a walk around the Seattle Center!
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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.